General Information of This Payload
Payload ID
PAY0KPOZO
Name
Genistein
Synonyms
Genistein; 446-72-0; Prunetol; 4',5,7-Trihydroxyisoflavone; Genisterin; Genisteol; Sophoricol; 5,7-dihydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one; 5,7,4'-Trihydroxyisoflavone; Bonistein; Genestein; Differenol A; NPI 031L; 5,7-dihydroxy-3-(4-hydroxyphenyl)chromen-4-one; 5,7-Dihydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one; 4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(4-hydroxyphenyl)-; C.I. 75610; SIPI 807-1; MFCD00016952; NSC 36586; CCRIS 7675; 4',5, 7-Trihydroxyisoflavone; 5,7-Dihydroxy-3-(4-hydroxyphenyl)-4-benzopyrone; NSC36586; EINECS 207-174-9; UNII-DH2M523P0H; NSC-36586; Genistein [USAN]; Lactoferrin-genistein; BRN 0263823; DH2M523P0H; NPI-031L; DTXSID5022308; ISOFLAVONE, 4',5,7-TRIHYDROXY-; CHEBI:28088; HSDB 7475; BIO-300; SIPI-807-1; CHEMBL44; FW-635I-2; Bio 300; PTI G4660 (Genistein); MLS000738127; DTXCID002308; STO514; PTI G4660; PTI-G4660; SIPI-9764-I; PTI-G 4660; 5-18-04-00594 (Beilstein Handbook Reference); TNP00151; Genistein (USAN); GENISTEIN (ENDOCRINE DISRUPTER); GEN; NCGC00015479-09; GENISTEIN (MART.); GENISTEIN [MART.]; G 6649; GENISTEIN (USP-RS); GENISTEIN [USP-RS]; 5,7-dihydroxy-3-(4-hydroxyphenyl)-chromen-4-one; ENDOCRINE DISRUPTOR (GENISTEIN) (SEE ALSO GENISTEIN (446-72-0)); 690224-00-1; CAS-446-72-0; 4,5,7-Trihydroxyiso-flavone; SR-01000075498; 3kgt; 3kgu; 4′ Genistein, 8; Genistein,(S); Genistein (GEN); IN1327; Genistein (flavonoid); Spectrum_000320; Tocris-1110; 1x7r; 2qa8; Genistein 85% HPLC; GENISTEIN [INN]; SpecPlus_000305; GENISTEIN [MI]; GENISTEIN [HSDB]; GENISTEIN [INCI]; Spectrum2_000638; Spectrum3_000678; Spectrum4_001543; Spectrum5_000106; Lopac-G-6649; ,5,7-Trihydroxyisoflavone; 4',7-Trihydroxyisoflavone; D0L4FS; MolMap_000022; UPCMLD-DP096; G10000; GENISTEIN [WHO-DD]; 4,5,7-Trihydroxyisoflavone; Isoflavone,5,7-trihydroxy-; Lopac0_000520; Oprea1_224620; Oprea1_437815; SCHEMBL19166; BSPBio_002375; KBioGR_002006; KBioGR_002564; KBioSS_000800; KBioSS_002573; NPI031L; SPECTRUM210296; BIDD:ER0113; DivK1c_006401; Genistein, analytical standard; SPBio_000636; 4',5,7-Trihydroxy isoflavone; 4',5,7-trihydroxy-Isoflavone; GTPL2826; MEGxp0_000568; 4,5,7-Trihydroxy Iso-Flavone; UPCMLD-DP096:001; ACon1_001065; BDBM19459; C.I. 75610(ChemID); cid_5280961; KBio1_001345; KBio2_000800; KBio2_002564; KBio2_003368; KBio2_005132; KBio2_005936; KBio2_007700; KBio3_001595; KBio3_003042; CHEBI: 28088; cMAP_000086; Bio1_000445; Bio1_000934; Bio1_001423; HMS2271K09; HMS3261H21; HMS3267K14; HMS3412I13; HMS3428M01; HMS3649B22; HMS3654D17; HMS3676I13; HMS3742I07; AMY25676; BCP07581; Tox21_110161; Tox21_201428; Tox21_300585; Tox21_500520; AC-472; BBL010484; CCG-38551; HB2775; LMPK12050218; s1342; STK801619; WHO 11073; AKOS001590147; Tox21_110161_1; CS-1534; CS-O-01020; DB01645; KS-5128; LP00520; LS-1266; SB17235; SDCCGSBI-0050503.P003; SMP1_000133; Genistein; 4',5,7-Trihydroxyisoflavone; NCGC00015479-01; NCGC00015479-02; NCGC00015479-04; NCGC00015479-05; NCGC00015479-06; NCGC00015479-07; NCGC00015479-08; NCGC00015479-10; NCGC00015479-11; NCGC00015479-12; NCGC00015479-13; NCGC00015479-14; NCGC00015479-15; NCGC00015479-16; NCGC00015479-17; NCGC00015479-18; NCGC00015479-19; NCGC00015479-20; NCGC00015479-38; NCGC00025005-01; NCGC00025005-02; NCGC00025005-03; NCGC00025005-04; NCGC00025005-05; NCGC00025005-06; NCGC00025005-07; NCGC00169711-01; NCGC00169711-02; NCGC00254275-01; NCGC00258979-01; NCGC00261205-01; HY-14596; NCI60_003369; SMR000112580; SY050124; EU-0100520; FT-0603395; FT-0668961; FT-0668962; G0272; GENISTEIN (CONSTITUENT OF RED CLOVER); SW203763-2; C06563; D11680; EN300-210743; G-2535; Genistein, synthetic, >=98% (HPLC), powder; K00046; US8552057, 2; AB00052696_09; AB00052696_12; A826657; GENISTEIN (CONSTITUENT OF SOY ISOFLAVONES); Q415957; GENISTEIN (CONSTITUENT OF RED CLOVER) [DSC]; Genistein, primary pharmaceutical reference standard; Q-100484; SR-01000075498-1; SR-01000075498-3; SR-01000075498-6; 3-(4-hydroxyphenyl)-5,7-bis(oxidanyl)chromen-4-one; 4 inverted exclamation marka,5,7-Trihydroxyisoflavone; BRD-K43797669-001-02-3; BRD-K43797669-001-03-1; BRD-K43797669-001-10-6; Genistein, from Glycine max (soybean), ~98% (HPLC); SR-01000075498-10; 5,7-dihydroxy-3-(4-hydroxyphenyl)-1-benzopyran-4-one; F0001-2388; GENISTEIN (CONSTITUENT OF SOY ISOFLAVONES) [DSC]; 4H-1-Benzopyran-4-one,7-dihydroxy-3-(4-hydroxyphenyl)-; 4h-1-benzopiran-4-ona, 5,7-dihidroxi-3-(4-hidroxifenil)-; 5,7-Dihydroxy-3-(4-hydroxyphenyl)-4 H-1-benzopyran-4-one; Genistein, United States Pharmacopeia (USP) Reference Standard; 4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(4-hydroxyphenyl)-(ChemID); Genistein, Pharmaceutical Secondary Standard; Certified Reference Material
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Target(s) Pro-epidermal growth factor (EGF)
Structure
Formula
C15H10O5
Isosmiles
C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O
PubChem CID
5280961
InChI
InChI=1S/C15H10O5/c16-9-3-1-8(2-4-9)11-7-20-13-6-10(17)5-12(18)14(13)15(11)19/h1-7,16-18H
InChIKey
TZBJGXHYKVUXJN-UHFFFAOYSA-N
IUPAC Name
5,7-dihydroxy-3-(4-hydroxyphenyl)chromen-4-one
Pharmaceutical Properties
Molecule Weight
270.24
Polar area
87
Complexity
411
xlogp Value
2.7
Heavy Count
20
Rot Bonds
1
Hbond acc
5
Hbond Donor
3
The activity data of This Payload
Standard Type Value Units Cell line Disease Model Cell line ID Reference
Half Maximal Inhibitory Concentration (IC50) 0.1 ug/mL
A-431 cells
Skin squamous cell carcinoma
CVCL_0037 
[1]
Half Maximal Inhibitory Concentration (IC50) 0.54 ug/mL
Neutrophil cells
Normal
Undisclosed [2]
Half Maximal Inhibitory Concentration (IC50) 0.7 ug/mL
A-431 cells
Skin squamous cell carcinoma
CVCL_0037 
[1]
Half Maximal Effective Concentration (EC50) 13.9 ug/mL
C8166 cells
Leukemia
CVCL_1099 
[3]
Half Maximal Inhibitory Concentration (IC50) 4.18 ug/mL
B16-BL6 cells
Melanoma
CVCL_0157 
[4]
Half Maximal Inhibitory Concentration (IC50) 6.99 ug/mL
Neutrophil cells
Normal
Undisclosed [2]
Half Maximal Inhibitory Concentration (IC50) 1.3 nM
HEK-293T cells
Normal
CVCL_0063 
[5]
Half Maximal Effective Concentration (EC50) 1.7 nM
SH-SY5Y cells
Bone marrow neuroblastoma
CVCL_0019 
[6]
Half Maximal Inhibitory Concentration (IC50) 1000 nM
MCF7-F (fulvestrant resistant) cells
Invasive breast carcinoma
CVCL_0031 
[7]
Half Maximal Inhibitory Concentration (IC50) >1000 nM
RAW264.7 cells
Monocytic-macrophage leukemia
CVCL_0493 
[8]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 10000 nM
CCRF-CEM cells
T acute lymphoblastic leukemia
CVCL_0207 
[9]
Half Maximal Inhibitory Concentration (IC50) 10000 nM
LNCaP cells
Prostate carcinoma
CVCL_0395 
[10]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 10000 nM
MCF7-F (fulvestrant resistant) cells
Invasive breast carcinoma
CVCL_0031 
[11]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
PC-3 cells
Prostate carcinoma
CVCL_0035 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
K-562 cells
Chronic myelogenous leukemia
CVCL_0004 
[9]
Half Maximal Inhibitory Concentration (IC50) >100000 nM
U-937 cells
Adult acute monocytic leukemia
CVCL_0007 
[12]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
U-251MG cells
Astrocytoma
CVCL_0021 
[9]
Half Maximal Inhibitory Concentration (IC50) >100000 nM
Caco-2 cells
Colon adenocarcinoma
CVCL_0025 
[13]
Half Maximal Inhibitory Concentration (IC50) >100000 nM
Hep-G2 cells
Hepatoblastoma
CVCL_0027 
[14]
Half Maximal Inhibitory Concentration (IC50) >100000 nM
DU145 cells
Prostate carcinoma
CVCL_0105 
[15]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
COLO 205 cells
Colon adenocarcinoma
CVCL_0218 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
HT-29 cells
Colon adenocarcinoma
CVCL_0320 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
MDA-MB-435 cells
Amelanotic melanoma
CVCL_0417 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
SK-MEL-28 cells (BRAF inhibitor resistant)
Cutaneous melanoma
CVCL_0526 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
SK-MEL-5 cells
Cutaneous melanoma
CVCL_0527 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
T-47D cells
Invasive breast carcinoma
CVCL_0553 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
NCI-ADR-RES cells
High grade ovarian serous adenocarcinoma
CVCL_1452 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
NCI-H23 cells
Lung adenocarcinoma
CVCL_1547 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
OVCAR-5 cells
Ovarian serous adenocarcinoma
CVCL_1628 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
OVCAR-8 cells
High grade ovarian serous adenocarcinoma
CVCL_1629 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
SF539 cells
Gliosarcoma
CVCL_1691 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
SF268 cells
Astrocytoma
CVCL_1689 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
MCF7-F (fulvestrant resistant) cells
Invasive breast carcinoma
CVCL_0031 
[9]
Half Maximal Inhibitory Concentration (IC50) >100000 nM
HEK293 cells
Normal
CVCL_0045 
[16]
Half Maximal Inhibitory Concentration (IC50) >100000 nM
Sf9 cells
Normal
CVCL_0549 
[17]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
HCC 2998 cells
Colon adenocarcinoma
CVCL_1266 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
HOP-92 cells
Non-small cell lung carcinoma
CVCL_1286 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
KM12 cells
Colon adenocarcinoma
CVCL_1331 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
M14 cells
Melanoma
CVCL_1395 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
Malme-3M cells
Melanoma
CVCL_1438 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
OVCAR-4 cells
Ovarian adenocarcinoma
CVCL_1627 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
TK-10 cells
Renal carcinoma
CVCL_1773 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
UACC-62 cells
Melanoma
CVCL_1780 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 100000 nM
MDA-N cells
Breast carcinoma
CVCL_1910 
[9]
Half Maximal Inhibitory Concentration (IC50) >100000 nM
L02 cells
Cervical carcinoma
CVCL_6926 
[14]
Half Maximal Inhibitory Concentration (IC50) 10469 nM
Farage cells
Normal
CVCL_0214 
[18]
Half Maximal Effective Concentration (EC50) 108000 nM
A-431 cells
Skin squamous cell carcinoma
CVCL_0037 
[19]
Half Maximal Inhibitory Concentration (IC50) 10924 nM
U-937 cells
Adult acute monocytic leukemia
CVCL_0007 
[18]
Half Maximal Inhibitory Concentration (IC50) 11000 nM
MCF7-F (fulvestrant resistant) cells
Invasive breast carcinoma
CVCL_0031 
[20]
Half Maximal Inhibitory Concentration (IC50) 11000 nM
Ventricular myocyte cells
Normal
Undisclosed [21]
Half Maximal Inhibitory Concentration (IC50) 11000 nM
Ventricular myocyte cells
Normal
Undisclosed [22]
Half Maximal Inhibitory Concentration (IC50) 11013 nM
Platelet cells
Normal
Undisclosed [18]
Half Maximal Inhibitory Concentration (IC50) 1110 nM
Neutrophil cells
Normal
Undisclosed [23]
Half Maximal Inhibitory Concentration (IC50) 11400 nM
RAW264.7 cells
Monocytic-macrophage leukemia
CVCL_0493 
[24]
Half Maximal Inhibitory Concentration (IC50) 1300000 nM
MDA-kb2 cells
Breast adenocarcinoma
CVCL_6421 
[25]
Half Maximal Inhibitory Concentration (IC50) 135 nM
Sf9 cells
Normal
CVCL_0549 
[18]
Half Maximal Effective Concentration (EC50) 14200 nM
FRT cells
Normal
CVCL_A6IE 
[26]
Half Maximal Effective Concentration (EC50) 14400 nM
Huh-7 cells
Adult hepatocellular carcinoma
CVCL_0336 
[27]
Half Maximal Inhibitory Concentration (IC50) 14910 nM
Farage cells
Normal
CVCL_0214 
[18]
Half Maximal Inhibitory Concentration (IC50) 15100 nM
MCF7-F (fulvestrant resistant) cells
Invasive breast carcinoma
CVCL_0031 
[28]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 15848.93 nM
SNB-75 cells
Glioblastoma
CVCL_1706 
[29]
Half Maximal Inhibitory Concentration (IC50) 16500 nM
HEK293 cells
Normal
CVCL_0045 
[30]
Half Maximal Inhibitory Concentration (IC50) 16918 nM
Farage cells
Normal
CVCL_0214 
[18]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 16982.44 nM
NCI-ADR-RES cells
High grade ovarian serous adenocarcinoma
CVCL_1452 
[31]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 17000 nM
MDA-MB-436 cells
Metastasis of ductal carcinoma
CVCL_0623 
[11]
Half Maximal Inhibitory Concentration (IC50) 17442 nM
HEK293 cells
Normal
CVCL_0045 
[18]
Half Maximal Inhibitory Concentration (IC50) 17560 nM
K-562 cells
Chronic myelogenous leukemia
CVCL_0004 
[32]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 17782.79 nM
NCI-H522 cells
Non-small cell lung carcinoma
CVCL_1567 
[29]
Half Maximal Inhibitory Concentration (IC50) 18100 nM
RAW cells
Monocytic-macrophage leukemia
Undisclosed [33]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 18197.01 nM
LOX IMVI cells
Melanoma
CVCL_1381 
[29]
Half Maximal Inhibitory Concentration (IC50) 183900 nM
BALB/3T3 cells
Normal
CVCL_0184 
[34]
Half Maximal Effective Concentration (EC50) 19.95 nM
HEK293 cells
Normal
CVCL_0045 
[35]
Half Maximal Inhibitory Concentration (IC50) 19100 nM
RAW264.7 cells
Monocytic-macrophage leukemia
CVCL_0493 
[36]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 19498.45 nM
ACHN cells
Renal adenocarcinoma
CVCL_1067 
[29]
Half Maximal Inhibitory Concentration (IC50) 19904 nM
CHO cells
Normal
CVCL_0213 
[18]
Half Maximal Inhibitory Concentration (IC50) >19952.62 nM
Vero C1008 cells
Normal
CVCL_0574 
[37]
Half Maximal Inhibitory Concentration (IC50) 2.88 nM
Sf9 cells
Normal
CVCL_0549 
[18]
Half Maximal Inhibitory Concentration (IC50) 20000 nM
Huh-7 cells
Adult hepatocellular carcinoma
CVCL_0336 
[38]
Half Maximal Inhibitory Concentration (IC50) 20000 nM
Ventricular myocyte cells
Normal
Undisclosed [21]
Half Maximal Inhibitory Concentration (IC50) >20000 nM
Vero C1008 cells
Normal
CVCL_0574 
[37]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 21877.62 nM
DMS-273 cells
Small cell lung carcinoma
CVCL_1176 
[29]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 21877.62 nM
MCF-12A cells
Normal
CVCL_3744 
[31]
Half Maximal Inhibitory Concentration (IC50) 22000 nM
HEK293 cells
Normal
CVCL_0045 
[39]
Half Maximal Inhibitory Concentration (IC50) 2210 nM
HEK293 cells
Normal
CVCL_0045 
[30]
Half Maximal Effective Concentration (EC50) 240 nM
Ishikawa cells
Endometrial adenocarcinoma
CVCL_2529 
[40]
Half Maximal Inhibitory Concentration (IC50) 24000 nM
LNCaP cells
Prostate carcinoma
CVCL_0395 
[10]
Half Maximal Inhibitory Concentration (IC50) 24000 nM
NIH3T3 cells
Normal
CVCL_0594 
[28]
Half Maximal Inhibitory Concentration (IC50) 24800 nM
Hep-G2 cells
Hepatoblastoma
CVCL_0027 
[41]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 24945.95 nM
UO-31 cells
Renal carcinoma
CVCL_1911 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 25118.86 nM
HCT 116 cells
Colon carcinoma
CVCL_0291 
[29]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 25118.86 nM
MKN-1 cells
Gastric carcinoma
CVCL_1415 
[29]
Half Maximal Inhibitory Concentration (IC50) 25120 nM
HEK293 cells
Normal
CVCL_0045 
[16]
Half Maximal Inhibitory Concentration (IC50) 2520 nM
BTI-TN-5B1-4 cells
Normal
CVCL_C190 
[18]
Half Maximal Inhibitory Concentration (IC50) 26000 nM
MCF7-F (fulvestrant resistant) cells
Invasive breast carcinoma
CVCL_0031 
[42]
Half Maximal Inhibitory Concentration (IC50) 26000 nM
RAW264.7 cells
Monocytic-macrophage leukemia
CVCL_0493 
[43]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 26302.68 nM
A-549 cells
Lung adenocarcinoma
CVCL_0023 
[29]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 26302.68 nM
NCI-H460 cells
Lung large cell carcinoma
CVCL_0459 
[29]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 26302.68 nM
SF539 cells
Gliosarcoma
CVCL_1691 
[29]
Half Maximal Inhibitory Concentration (IC50) 26500 nM
RAW264.7 cells
Monocytic-macrophage leukemia
CVCL_0493 
[44]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 26915.35 nM
NCI-ADR-RES cells
High grade ovarian serous adenocarcinoma
CVCL_1452 
[31]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 26915.35 nM
HBC-5 cells
Breast carcinoma
CVCL_B497 
[29]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 27542.29 nM
NCI-H226 cells
Pleural epithelioid mesothelioma
CVCL_1544 
[29]
Half Maximal Inhibitory Concentration (IC50) 27700 nM
WiDr cells
Colon adenocarcinoma
CVCL_2760 
[28]
Half Maximal Effective Concentration (EC50) 278000 nM
A-431 cells
Skin squamous cell carcinoma
CVCL_0037 
[19]
Half Maximal Inhibitory Concentration (IC50) 28400 nM
BV-2 cells
Normal
CVCL_0182 
[45]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 28840.32 nM
SF-295 cells
Glioblastoma
CVCL_1690 
[29]
Half Maximal Inhibitory Concentration (IC50) 29.4 nM
HEK-293T cells
Normal
CVCL_0063 
[5]
Half Maximal Inhibitory Concentration (IC50) 29200 nM
NHEM693 cells
Normal
CVCL_B448 
[46]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 29716.66 nM
ACHN cells
Renal adenocarcinoma
CVCL_1067 
[9]
Half Maximal Inhibitory Concentration (IC50) 30000 nM
BxPC-3 CDX model cells
Pancreatic ductal adenocarcinoma
CVCL_0186 
[47]
Half Maximal Inhibitory Concentration (IC50) >30000 nM
MCF7-F (fulvestrant resistant) cells
Invasive breast carcinoma
CVCL_0031 
[42]
Half Maximal Inhibitory Concentration (IC50) 30000 nM
Sf9 cells
Normal
CVCL_0549 
[17]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 30199.52 nM
HCT 15 cells
Colon adenocarcinoma
CVCL_0292 
[29]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 30199.52 nM
MKN7 cells
Gastric tubular adenocarcinoma
CVCL_1417 
[29]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 30199.52 nM
SF268 cells
Astrocytoma
CVCL_1689 
[29]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 30199.52 nM
MCF-12A cells
Normal
CVCL_3744 
[31]
Half Maximal Inhibitory Concentration (IC50) 30650 nM
LNCaP cells
Prostate carcinoma
CVCL_0395 
[13]
Half Maximal Inhibitory Concentration (IC50) 31000 nM
HEK293 cells
Normal
CVCL_0045 
[39]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 31622.78 nM
OVCAR-3 cells (FZD7 overexpression)
Ovarian serous adenocarcinoma
CVCL_0465 
[29]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 32359.37 nM
MKN45 cells
Gastric adenocarcinoma
CVCL_0434 
[29]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 32359.37 nM
NCI-ADR-RES cells
High grade ovarian serous adenocarcinoma
CVCL_1452 
[31]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 32359.37 nM
MCF-12A cells
Normal
CVCL_3744 
[31]
Half Maximal Inhibitory Concentration (IC50) 32900 nM
Vero cells
Normal
CVCL_0059 
[48]
Half Maximal Inhibitory Concentration (IC50) 34900 nM
HCT 116 cells
Colon carcinoma
CVCL_0291 
[13]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 35481.34 nM
OVCAR-8 cells
High grade ovarian serous adenocarcinoma
CVCL_1629 
[29]
Half Maximal Effective Concentration (EC50) 35695.8 nM
UoC-B1 cells
B acute lymphoblastic leukemia
CVCL_A296 
[49]
Half Maximal Inhibitory Concentration (IC50) 36000 nM
SK-MEL-2 cells (MEK inhibitor-resistant)
Melanoma
CVCL_0069 
[50]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 36307.81 nM
NCI-H23 cells
Lung adenocarcinoma
CVCL_1547 
[29]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 36307.81 nM
MKN-74 cells
Stomach adenocarcinoma
CVCL_2791 
[29]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 36391.5 nM
NCI-H522 cells
Non-small cell lung carcinoma
CVCL_1567 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 37153.52 nM
MDA-MB-231 cells (5T4 overexpression)
Breast adenocarcinoma
CVCL_0062 
[29]
Half Maximal Inhibitory Concentration (IC50) 37400 nM
LNCaP cells
Prostate carcinoma
CVCL_0395 
[15]
Half Maximal Inhibitory Concentration (IC50) 3890.45 nM
CHO cells
Normal
CVCL_0213 
[51]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 38904.51 nM
LNCaP cells
Prostate carcinoma
CVCL_0395 
[31]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 38904.51 nM
SNB-78 cells
Glioblastoma
CVCL_B321 
[29]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 39810.72 nM
MKN-28 cells
Gastric epithelial carcinoma
CVCL_1416 
[29]
Half Maximal Effective Concentration (EC50) 4.1 nM
HeLa cells
Endocervical adenocarcinoma
CVCL_0030 
[6]
Half Maximal Effective Concentration (EC50) 403000 nM
SK-BR-3 cells
Breast adenocarcinoma
CVCL_0033 
[19]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 40364.54 nM
MOLT-4 cells
Adult T acute lymphoblastic leukemia
CVCL_0013 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 40738.03 nM
RXF 631 cells
Renal carcinoma
CVCL_A780 
[29]
Half Maximal Inhibitory Concentration (IC50) 41670 nM
AGS cells
Gastric adenocarcinoma
CVCL_0139 
[13]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 41975.9 nM
NCI-H460 cells
Lung large cell carcinoma
CVCL_0459 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 42657.95 nM
PC-3 cells
Prostate carcinoma
CVCL_0035 
[31]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 42657.95 nM
U-251MG cells
Astrocytoma
CVCL_0021 
[29]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 42657.95 nM
MCF7-F (fulvestrant resistant) cells
Invasive breast carcinoma
CVCL_0031 
[29]
Half Maximal Inhibitory Concentration (IC50) 43000 nM
MDA-MB-231 cells (5T4 overexpression)
Breast adenocarcinoma
CVCL_0062 
[50]
Half Maximal Inhibitory Concentration (IC50) 43090 nM
A-549 cells
Lung adenocarcinoma
CVCL_0023 
[13]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 43151.91 nM
786-O cells
Renal cell carcinoma
CVCL_1051 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 43651.58 nM
OVCAR-4 cells
Ovarian adenocarcinoma
CVCL_1627 
[29]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 43651.58 nM
BSY-1 cells
Breast carcinoma
CVCL_B499 
[29]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 43651.58 nM
HBC-4 cells
Breast carcinoma
CVCL_B496 
[29]
Half Maximal Effective Concentration (EC50) 4400 nM
NIH3T3 cells
Normal
CVCL_0594 
[52]
Half Maximal Inhibitory Concentration (IC50) 44000 nM
LN-229 cells
Glioblastoma
CVCL_0393 
[50]
Half Maximal Inhibitory Concentration (IC50) 45200 nM
Hepa-1c1c7 cells
Hepatocellular carcinoma of the mouse
CVCL_0328 
[53]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 45708.82 nM
MCF7-F (fulvestrant resistant) cells
Invasive breast carcinoma
CVCL_0031 
[31]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 45708.82 nM
HCC 2998 cells
Colon adenocarcinoma
CVCL_1266 
[29]
Half Maximal Inhibitory Concentration (IC50) 46000 nM
BT-20 cells
Invasive breast carcinoma of no special type
CVCL_0178 
[47]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 46773.51 nM
St-4 cells
Stomach carcinoma
CVCL_H265 
[29]
Half Maximal Inhibitory Concentration (IC50) 47000 nM
NCI-H460 cells
Lung large cell carcinoma
CVCL_0459 
[50]
Half Maximal Inhibitory Concentration (IC50) 47290 nM
DU145 cells
Prostate carcinoma
CVCL_0105 
[13]
Half Maximal Effective Concentration (EC50) 48 nM
HeLa cells
Endocervical adenocarcinoma
CVCL_0030 
[6]
Half Maximal Inhibitory Concentration (IC50) 48000 nM
U-937 cells
Adult acute monocytic leukemia
CVCL_0007 
[12]
Half Maximal Inhibitory Concentration (IC50) 48000 nM
T-47D cells
Invasive breast carcinoma
CVCL_0553 
[50]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 48977.88 nM
DMS 114 cells
Lung small cell carcinoma
CVCL_1174 
[29]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 49203.95 nM
SW620 cells
Colon adenocarcinoma
CVCL_0547 
[9]
Half Maximal Inhibitory Concentration (IC50) 50000 nM
PC-3 cells
Prostate carcinoma
CVCL_0035 
[47]
Half Maximal Inhibitory Concentration (IC50) 50000 nM
HT-29 cells
Colon adenocarcinoma
CVCL_0320 
[50]
Half Maximal Inhibitory Concentration (IC50) 50000 nM
COLO357 cells
Pancreatic carcinoma
CVCL_0221 
[47]
Half Maximal Inhibitory Concentration (IC50) >50000 nM
RAW264.7 cells
Monocytic-macrophage leukemia
CVCL_0493 
[54]
Half Maximal Inhibitory Concentration (IC50) >500000 nM
Melan-a cells
Normal
CVCL_4624 
[55]
Half Maximal Effective Concentration (EC50) 501.19 nM
HEK293 cells
Normal
CVCL_0045 
[35]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 50118.72 nM
DU145 cells
Prostate carcinoma
CVCL_0105 
[31]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 50118.72 nM
OVCAR-5 cells
Ovarian serous adenocarcinoma
CVCL_1628 
[29]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 50118.72 nM
KM12 cells
Colon adenocarcinoma
CVCL_1331 
[29]
Half Maximal Inhibitory Concentration (IC50) 510 nM
Ishikawa cells
Endometrial adenocarcinoma
CVCL_2529 
[56]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 52480.75 nM
SN12C cells
Renal cell carcinoma
CVCL_1705 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 52480.75 nM
MCF7-F (fulvestrant resistant) cells
Invasive breast carcinoma
CVCL_0031 
[31]
Half Maximal Inhibitory Concentration (IC50) 52780 nM
HT-29 cells
Colon adenocarcinoma
CVCL_0320 
[13]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 53703.18 nM
HT-29 cells
Colon adenocarcinoma
CVCL_0320 
[29]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 54954.09 nM
SF-295 cells
Glioblastoma
CVCL_1690 
[9]
Half Maximal Inhibitory Concentration (IC50) 55000 nM
U-87MG ATCC cells
Glioblastoma
CVCL_0022 
[50]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 56754.46 nM
SR cells
Leukemia
CVCL_1711 
[9]
Half Maximal Inhibitory Concentration (IC50) 57500 nM
Cardiac Muscle cells
Normal
Undisclosed [22]
Half Maximal Inhibitory Concentration (IC50) 57830 nM
Melan-a cells
Normal
CVCL_4624 
[55]
Half Maximal Inhibitory Concentration (IC50) 58180 nM
HEK293 cells
Normal
CVCL_0045 
[16]
Half Maximal Effective Concentration (EC50) 59338 nM
SEM cells
Leukemia
CVCL_0095 
[49]
Half Maximal Inhibitory Concentration (IC50) 61.33 nM
SF-126 cells
Glioblastoma
CVCL_1688 
Half Maximal Cell Growth Inhibitory Concentration (GI50) 61659.5 nM
MCF7-F (fulvestrant resistant) cells
Invasive breast carcinoma
CVCL_0031 
[31]
Half Maximal Effective Concentration (EC50) 6170 nM
FRT cells
Normal
CVCL_A6IE 
[26]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 62373.48 nM
A-549 cells
Lung adenocarcinoma
CVCL_0023 
[9]
Half Maximal Inhibitory Concentration (IC50) 62710 nM
MCF7-F (fulvestrant resistant) cells
Invasive breast carcinoma
CVCL_0031 
[13]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 63095.73 nM
EKVX cells
Non-small cell lung carcinoma
CVCL_1195 
[9]
Half Maximal Inhibitory Concentration (IC50) 64000 nM
A-549 cells
Lung adenocarcinoma
CVCL_0023 
[50]
Half Maximal Inhibitory Concentration (IC50) 65000 nM
LNCaP cells
Prostate carcinoma
CVCL_0395 
[57]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 65162.84 nM
Hs 578T cells
Invasive breast carcinoma
CVCL_0332 
[9]
Half Maximal Inhibitory Concentration (IC50) 65170 nM
PC-3 cells
Prostate carcinoma
CVCL_0035 
[13]
Half Maximal Inhibitory Concentration (IC50) 6720 nM
Neutrophil cells
Normal
Undisclosed [58]
Half Maximal Effective Concentration (EC50) 67694.5 nM
Hep-G2 cells
Hepatoblastoma
CVCL_0027 
[49]
Half Maximal Inhibitory Concentration (IC50) 67990 nM
HEK293 cells
Normal
CVCL_0045 
[16]
Half Maximal Inhibitory Concentration (IC50) 68600 nM
PC-3 cells
Prostate carcinoma
CVCL_0035 
[15]
Half Maximal Inhibitory Concentration (IC50) 690 nM
Neutrophil cells
Normal
Undisclosed [58]
Half Maximal Inhibitory Concentration (IC50) 6900 nM
MDCK cells
Normal
CVCL_0422 
[59]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 69823.24 nM
HL-60 cells
Adult acute myeloid leukemia
CVCL_0002 
[9]
Half Maximal Effective Concentration (EC50) 7000 nM
FRT cells
Normal
CVCL_A6IE 
[60]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 71614.34 nM
IGROV-1 cells
Ovarian endometrioid adenocarcinoma
CVCL_1304 
[9]
Half Maximal Inhibitory Concentration (IC50) 72000 nM
U-937 cells
Adult acute monocytic leukemia
CVCL_0007 
[12]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 72945.75 nM
HCT 15 cells
Colon adenocarcinoma
CVCL_0292 
[9]
Half Maximal Effective Concentration (EC50) 73 nM
HeLa cells
Endocervical adenocarcinoma
CVCL_0030 
[61]
Half Maximal Inhibitory Concentration (IC50) 73000 nM
COLO 201 cells
Colon adenocarcinoma
CVCL_1987 
[50]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 74131.02 nM
NCI-H226 cells
Pleural epithelioid mesothelioma
CVCL_1544 
[9]
Half Maximal Inhibitory Concentration (IC50) 77000 nM
MCF7-F (fulvestrant resistant) cells
Invasive breast carcinoma
CVCL_0031 
[20]
Half Maximal Inhibitory Concentration (IC50) 7720 nM
Platelet cells
Normal
Undisclosed [18]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 77803.66 nM
RPMI-8226 cells
Plasma cell myeloma
CVCL_0014 
[9]
Half Maximal Inhibitory Concentration (IC50) 79000 nM
BxPC-3 CDX model cells
Pancreatic ductal adenocarcinoma
CVCL_0186 
[50]
Half Maximal Inhibitory Concentration (IC50) 79210 nM
B16-F10 cells
Mouse melanoma
CVCL_0159 
[4]
Half Maximal Inhibitory Concentration (IC50) 8000 nM
ANN-1 cells
Normal
CVCL_9242 
[28]
Half Maximal Effective Concentration (EC50) 8200 nM
CHO cells
Normal
CVCL_0213 
[26]
Half Maximal Effective Concentration (EC50) 8480 nM
CHO cells
Normal
CVCL_0213 
[26]
Half Maximal Effective Concentration (EC50) >86206.9 nM
SUP-B15 cells
B-lymphoblastic leukemia
CVCL_0103 
[49]
Half Maximal Effective Concentration (EC50) >86206.9 nM
KOPN-8 cells
Leukemia
CVCL_1866 
[49]
Half Maximal Effective Concentration (EC50) >86206.9 nM
BJ cells
Normal
CVCL_3653 
[49]
Half Maximal Inhibitory Concentration (IC50) 87000 nM
PANC-1 cells
Pancreatic ductal adenocarcinoma
CVCL_0480 
[50]
Half Maximal Inhibitory Concentration (IC50) 8800 nM
MCF7-F (fulvestrant resistant) cells
Invasive breast carcinoma
CVCL_0031 
[59]
Half Maximal Inhibitory Concentration (IC50) 88000 nM
Human umbilical vein endothelial cells(HUVEC)
Normal
Undisclosed [62]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 88307.99 nM
BT-549 cells
Breast ductal carcinoma
CVCL_1092 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 89125.09 nM
SK-OV-3 cells (FZD7 overexpression)
Ovarian serous cystadenocarcinoma
CVCL_0532 
[29]
Half Maximal Inhibitory Concentration (IC50) 89410 nM
T98G cells
Glioblastoma
CVCL_0556 
[13]
Half Maximal Inhibitory Concentration (IC50) 9100 nM
Balb/MK cells
Normal
CVCL_1B29 
[63]
Half Maximal Inhibitory Concentration (IC50) 9120.11 nM
CHO cells
Normal
CVCL_0213 
[51]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 92044.96 nM
SNB-19 cells
Astrocytoma
CVCL_0535 
[9]
Half Maximal Cell Growth Inhibitory Concentration (GI50) 92469.82 nM
DU145 cells
Prostate carcinoma
CVCL_0105 
[9]
Half Maximal Effective Concentration (EC50) 956 nM
HeLa cells
Endocervical adenocarcinoma
CVCL_0030 
[61]
Half Maximal Inhibitory Concentration (IC50) 96700 nM
SK-BR-3 cells
Breast adenocarcinoma
CVCL_0033 
[13]
Half Maximal Effective Concentration (EC50) 97000 nM
SK-BR-3 cells
Breast adenocarcinoma
CVCL_0033 
[19]
Each Antibody-drug Conjugate Related to This Payload
References
Ref 1 Protein-tyrosine kinase inhibition: mechanism-based discovery of antitumor agents. J Nat Prod. 1992 Nov;55(11):1529-60. doi: 10.1021/np50089a001.
Ref 2 A novel alkaloid, aristopyridinone A and anti-inflammatory phenanthrenes isolated from Aristolochia manshuriensis. Bioorg Med Chem Lett. 2011 Mar 15;21(6):1792-4. doi: 10.1016/j.bmcl.2011.01.067. Epub 2011 Jan 22.
Ref 3 Design and discovery of flavonoid-based HIV-1 integrase inhibitors targeting both the active site and the interaction with LEDGF/p75. Bioorg Med Chem. 2014 Jun 15;22(12):3146-58. doi: 10.1016/j.bmc.2014.04.016. Epub 2014 Apr 19.
Ref 4 Insights into tyrosinase inhibition by compounds isolated from Greyia radlkoferi Szyszyl using biological activity, molecular docking and gene expression analysis. Bioorg Med Chem. 2016 Nov 15;24(22):5953-5959. doi: 10.1016/j.bmc.2016.09.054. Epub 2016 Sep 22.
Ref 5 Estrogen receptor beta selective ligands: discovery and SAR of novel heterocyclic ligands. Bioorg Med Chem Lett. 2005 Dec 15;15(24):5562-6. doi: 10.1016/j.bmcl.2005.08.010. Epub 2005 Oct 10.
Ref 6 Toward selective ERbeta agonists for central nervous system disorders: synthesis and characterization of aryl benzthiophenes. J Med Chem. 2002 Mar 28;45(7):1399-401. doi: 10.1021/jm015577l.
Ref 7 Dihydro-resveratrol--a potent dietary polyphenol. Bioorg Med Chem Lett. 2010 Oct 15;20(20):6149-51. doi: 10.1016/j.bmcl.2010.08.002. Epub 2010 Aug 5.
Ref 8 Chemical Constituents of Apios americana Tubers and Their Inhibitory Activities on Nitric Oxide Production in Lipopolysaccharide-Stimulated RAW 264.7 Macrophages. J Nat Prod. 2018 Jul 27;81(7):1598-1603. doi: 10.1021/acs.jnatprod.8b00182. Epub 2018 Jun 22.
Ref 9 PubChem BioAssay data set.
Ref 10 Design, synthesis, and evaluation of the antiproliferative activity of hydantoin-derived antiandrogen-genistein conjugates. Bioorg Med Chem. 2018 May 1;26(8):1481-1487. doi: 10.1016/j.bmc.2018.01.009. Epub 2018 Feb 16.
Ref 11 Isoflavones with unusually modified B-rings and their evaluation as antiproliferative agents. Bioorg Med Chem Lett. 2009 Nov 15;19(22):6473-6. doi: 10.1016/j.bmcl.2009.08.084. Epub 2009 Aug 28.
Ref 12 Rotenoids and flavonoids with anti-invasion of HT1080, anti-proliferation of U937, and differentiation-inducing activity in HL-60 from Erycibe expansa. Bioorg Med Chem. 2007 Feb 1;15(3):1539-46. doi: 10.1016/j.bmc.2006.09.024. Epub 2006 Dec 8.
Ref 13 Synthetic conjugates of genistein affecting proliferation and mitosis of cancer cells. Bioorg Med Chem. 2011 Jan 1;19(1):295-305. doi: 10.1016/j.bmc.2010.11.024. Epub 2010 Nov 11.
Ref 14 Phosphoramidate protides of five flavones and their antiproliferative activity against HepG2 and L-O2 cell lines. Eur J Med Chem. 2016 Apr 13;112:196-208. doi: 10.1016/j.ejmech.2016.02.012. Epub 2016 Feb 18.
Ref 15 A new class of hybrid anticancer agents inspired by the synergistic effects of curcumin and genistein: Design, synthesis, and anti-proliferative evaluation. Bioorg Med Chem Lett. 2015 Oct 15;25(20):4553-6. doi: 10.1016/j.bmcl.2015.08.064. Epub 2015 Aug 24.
Ref 16 Discovery of (E)-5-(benzylideneamino)-1H-benzo[d]imidazol-2(3H)-one derivatives as inhibitors for PTK6. Bioorg Med Chem Lett. 2014 Oct 1;24(19):4659-4663. doi: 10.1016/j.bmcl.2014.08.036. Epub 2014 Aug 23.
Ref 17 Targeting DNA methylation with small molecules: what's next?. J Med Chem. 2015 Mar 26;58(6):2569-83. doi: 10.1021/jm500843d. Epub 2014 Dec 4.
Ref 18 DrugMatrix in vitro pharmacology data.
Ref 19 Epigallocatechin 3-O-gallate induces 67 kDa laminin receptor-mediated cell death accompanied by downregulation of ErbB proteins and altered lipid raft clustering in mammary and epidermoid carcinoma cells. J Nat Prod. 2014 Feb 28;77(2):250-7. doi: 10.1021/np4007712. Epub 2014 Jan 23.
Ref 20 Novel 5-aminoflavone derivatives as specific antitumor agents in breast cancer. J Med Chem. 1996 Aug 30;39(18):3461-9. doi: 10.1021/jm950938g.
Ref 21 Predictive model for L-type channel inhibition: multichannel block in QT prolongation risk assessment. J Appl Toxicol. 2012 Oct;32(10):858-66. doi: 10.1002/jat.2784. Epub 2012 Jul 3.
Ref 22 IC50 data for the L-type calcium channel extracted from a set of literature articles.
Ref 23 Anti-inflammatory principles from Lindera aggregata. Bioorg Med Chem Lett. 2020 Jul 1;30(13):127224. doi: 10.1016/j.bmcl.2020.127224. Epub 2020 Apr 27.
Ref 24 Anti-inflammatory and Antiosteoporosis Flavonoids from the Rhizomes of Helminthostachys zeylanica. J Nat Prod. 2017 Feb 24;80(2):246-253. doi: 10.1021/acs.jnatprod.5b01164. Epub 2017 Feb 7.
Ref 25 Effect of flavonoids on androgen and glucocorticoid receptors based on in vitro reporter gene assay. Bioorg Med Chem Lett. 2009 Aug 15;19(16):4706-10. doi: 10.1016/j.bmcl.2009.06.073. Epub 2009 Jun 23.
Ref 26 Discovery of Icenticaftor (QBW251), a Cystic Fibrosis Transmembrane Conductance Regulator Potentiator with Clinical Efficacy in Cystic Fibrosis and Chronic Obstructive Pulmonary Disease. J Med Chem. 2021 Jun 10;64(11):7241-7260. doi: 10.1021/acs.jmedchem.1c00343. Epub 2021 May 24.
Ref 27 Discovery of flavonoid derivatives as anti-HCV agents via pharmacophore search combining molecular docking strategy. Eur J Med Chem. 2012 Jun;52:33-43. doi: 10.1016/j.ejmech.2012.03.002. Epub 2012 Mar 8.
Ref 28 Structural studies on bioactive compounds. 23. Synthesis of polyhydroxylated 2-phenylbenzothiazoles and a comparison of their cytotoxicities and pharmacological properties with genistein and quercetin. J Med Chem. 1994 May 27;37(11):1689-95. doi: 10.1021/jm00037a020.
Ref 29 (S)-Erypoegin K, an isoflavone isolated from Erythrina poeppigiana, is a novel inhibitor of topoisomerase II: Induction of G2 phase arrest in human gastric cancer cells. Bioorg Med Chem. 2021 Jan 15;30:115904. doi: 10.1016/j.bmc.2020.115904. Epub 2020 Dec 5.
Ref 30 Discovery of nonsteroidal 17beta-hydroxysteroid dehydrogenase 1 inhibitors by pharmacophore-based screening of virtual compound libraries. J Med Chem. 2008 Jul 24;51(14):4188-99. doi: 10.1021/jm800054h. Epub 2008 Jun 6.
Ref 31 Biomimetic syntheses and antiproliferative activities of racemic, natural (-), and unnnatural (+) glyceollin I. J Med Chem. 2011 May 26;54(10):3506-23. doi: 10.1021/jm101619e. Epub 2011 Apr 22.
Ref 32 Cells lacking DNA topoisomerase II beta are resistant to genistein. J Nat Prod. 2007 May;70(5):763-7. doi: 10.1021/np060609z. Epub 2007 Apr 6.
Ref 33 Synthetic 2',5'-dimethoxychalcones as G(2)/M arrest-mediated apoptosis-inducing agents and inhibitors of nitric oxide production in rat macrophages. Eur J Med Chem. 2007 May;42(5):660-8. doi: 10.1016/j.ejmech.2006.12.009. Epub 2007 Jan 9.
Ref 34 Activities of plant-derived phenols in a fibroblast cell culture model. J Nat Prod. 1999 Mar;62(3):481-3. doi: 10.1021/np9801559.
Ref 35 The A-CD analogue of 16 beta,17 alpha-estriol is a potent and highly selective estrogen receptor beta agonist. Medchemcomm. 2013;4(11):1439-1442.
Ref 36 Chisopanins A-K, 11 new protolimonoids from Chisocheton paniculatus and their anti-inflammatory activities. Bioorg Med Chem. 2011 Feb 15;19(4):1409-17. doi: 10.1016/j.bmc.2011.01.007. Epub 2011 Jan 11.
Ref 37 Screening of ~5500 FDA-approved drugs and clinical candidates for anti-SARS-CoV-2 activity.
Ref 38 Flavones as isosteres of 4(1H)-quinolones: discovery of ligand efficient and dual stage antimalarial lead compounds. Eur J Med Chem. 2013 Nov;69:872-80. doi: 10.1016/j.ejmech.2013.09.008. Epub 2013 Sep 20.
Ref 39 Co-existence of alpha-glucosidase-inhibitory and liver X receptor-regulatory activities and their separation by structural development. Bioorg Med Chem. 2008 Apr 15;16(8):4272-85. doi: 10.1016/j.bmc.2008.02.078. Epub 2008 Feb 29.
Ref 40 Estrogen Receptor (ER) Subtype Selectivity Identifies 8-Prenylapigenin as an ER Agonist from Glycyrrhiza inflata and Highlights the Importance of Chemical and Biological Authentication. J Nat Prod. 2018 Apr 27;81(4):966-975. doi: 10.1021/acs.jnatprod.7b01070. Epub 2018 Apr 11.
Ref 41 Cornusides A-O, Bioactive Iridoid Glucoside Dimers from the Fruit of Cornus officinalis. J Nat Prod. 2017 Dec 22;80(12):3103-3111. doi: 10.1021/acs.jnatprod.6b01127. Epub 2017 Nov 15.
Ref 42 New bioactive flavonoids and stilbenes in cub resin insecticide. J Nat Prod. 1999 Feb;62(2):205-10. doi: 10.1021/np980119+.
Ref 43 Synthesis of a novel series of diphenolic chromone derivatives as inhibitors of NO production in LPS-activated RAW264.7 macrophages. Bioorg Med Chem. 2010 Apr 15;18(8):2864-71. doi: 10.1016/j.bmc.2010.03.020. Epub 2010 Mar 12.
Ref 44 Synthesis, anti-inflammatory, and antioxidant activities of 18beta-glycyrrhetinic acid derivatives as chemical mediators and xanthine oxidase inhibitors. Bioorg Med Chem. 2009 Apr 1;17(7):2785-92. doi: 10.1016/j.bmc.2009.02.025. Epub 2009 Feb 21.
Ref 45 Anti-inflammatory isoflavones and isoflavanones from the roots of Pongamia pinnata (L.) Pierre. Bioorg Med Chem Lett. 2018 Apr 1;28(6):1050-1055. doi: 10.1016/j.bmcl.2018.02.026. Epub 2018 Feb 15.
Ref 46 Melanin synthesis inhibitors from Lespedeza floribunda. J Nat Prod. 2009 Feb 27;72(2):194-203. doi: 10.1021/np800395j.
Ref 47 Synthesis, molecular characterization, and biological activity of novel synthetic derivatives of chromen-4-one in human cancer cells. J Med Chem. 2006 Jun 29;49(13):3800-8. doi: 10.1021/jm051068y.
Ref 48 Isoflavonoids and other compounds from Psorothamnus arborescens with antiprotozoal activities. J Nat Prod. 2006 Jan;69(1):43-9. doi: 10.1021/np0502600.
Ref 49 Novel vitexin-inspired scaffold against leukemia. Eur J Med Chem. 2018 Feb 25;146:501-510. doi: 10.1016/j.ejmech.2018.01.004. Epub 2018 Jan 31.
Ref 50 Polyphenolic Phytochemicals in Cancer Prevention and Therapy: Bioavailability versus Bioefficacy. J Med Chem. 2017 Dec 14;60(23):9413-9436. doi: 10.1021/acs.jmedchem.6b01026. Epub 2017 Jul 11.
Ref 51 Structure-based identification of OATP1B1/3 inhibitors. Mol Pharmacol. 2013 Jun;83(6):1257-67. doi: 10.1124/mol.112.084152. Epub 2013 Apr 9.
Ref 52 Activation of CFTR by UCCF-029 and genistein. Bioorg Med Chem Lett. 2008 Jul 15;18(14):3874-7. doi: 10.1016/j.bmcl.2008.06.051. Epub 2008 Jun 19.
Ref 53 Potential cncer chemopreventive flavonoids from the stems of Tephrosia toxicaria. J Nat Prod. 2003 Sep;66(9):1166-70. doi: 10.1021/np0302100.
Ref 54 Inhibitory constituents of Sophora tonkinensis on nitric oxide production in RAW 264.7 macrophages. Bioorg Med Chem Lett. 2015 Feb 15;25(4):960-2. doi: 10.1016/j.bmcl.2014.12.012. Epub 2014 Dec 13.
Ref 55 Natural ortho-dihydroxyisoflavone derivatives from aged Korean fermented soybean paste as potent tyrosinase and melanin formation inhibitors. Bioorg Med Chem Lett. 2010 Feb 1;20(3):1162-4. doi: 10.1016/j.bmcl.2009.12.021. Epub 2009 Dec 6.
Ref 56 Isolation and structure elucidation of an isoflavone and a sesterterpenoic acid from Henriettella fascicularis. J Nat Prod. 2002 Dec;65(12):1749-53. doi: 10.1021/np0201164.
Ref 57 Another look at phenolic compounds in cancer therapy the effect of polyphenols on ubiquitin-proteasome system. Eur J Med Chem. 2019 Apr 1;167:291-311. doi: 10.1016/j.ejmech.2019.01.044. Epub 2019 Jan 30.
Ref 58 Suberoylanilide hydroxamic acid, a histone deacetylase inhibitor, induces the production of anti-inflammatory cyclodepsipeptides from Beauveria felina. J Nat Prod. 2013 Jul 26;76(7):1260-6. doi: 10.1021/np400143j. Epub 2013 Jul 3.
Ref 59 Structure-activity relationships of flavonoids as inhibitors of breast cancer resistance protein (BCRP). Bioorg Med Chem. 2011 Mar 15;19(6):2090-102. doi: 10.1016/j.bmc.2010.12.043. Epub 2010 Dec 30.
Ref 60 Fluorinated F508-CFTR correctors and potentiators for PET imaging. Bioorg Med Chem Lett. 2012 Feb 15;22(4):1602-5. doi: 10.1016/j.bmcl.2011.12.128. Epub 2012 Jan 3.
Ref 61 Synthesis and characterization of 3-arylquinazolinone and 3-arylquinazolinethione derivatives as selective estrogen receptor beta modulators. J Med Chem. 2006 Apr 20;49(8):2440-55. doi: 10.1021/jm0509389.
Ref 62 In-silico fragment-based identification of novel angiogenesis inhibitors. Bioorg Med Chem Lett. 2007 Aug 15;17(16):4551-6. doi: 10.1016/j.bmcl.2007.05.104. Epub 2007 Jun 15.
Ref 63 [(Alkylamino)methyl]acrylophenones: potent and selective inhibitors of the epidermal growth factor receptor protein tyrosine kinase. J Med Chem. 1995 Jun 23;38(13):2441-8. doi: 10.1021/jm00013a020.

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