Payload Information
General Information of This Payload
Payload ID | PAY0IJDKT |
|||||
---|---|---|---|---|---|---|
Name | Tubulysin 7 |
|||||
Synonyms |
Tubulysin G; 799822-08-5; EX-A5466G; HY-N7050; AKOS040740945; CS-0101873
Click to Show/Hide
|
|||||
Target(s) | Microtubule (MT) | |||||
Structure | ||||||
Formula | C43H63N5O10S |
|||||
Isosmiles | CC[C@H](C)[C@@H](C(=O)N(COC(=O)C=C(C)C)[C@H](C[C@H](C1=NC(=CS1)C(=O)N[C@@H](CC2=CC=C(C=C2)O)C[C@H](C)C(=O)O)OC(=O)C)C(C)C)NC(=O)[C@H]3CCCCN3C |
|||||
PubChem CID | ||||||
InChI |
InChI=1S/C43H63N5O10S/c1-10-27(6)38(46-40(53)34-13-11-12-18-47(34)9)42(54)48(24-57-37(51)19-25(2)3)35(26(4)5)22-36(58-29(8)49)41-45-33(23-59-41)39(52)44-31(20-28(7)43(55)56)21-30-14-16-32(50)17-15-30/h14-17,19,23,26-28,31,34-36,38,50H,10-13,18,20-22,24H2,1-9H3,(H,44,52)(H,46,53)(H,55,56)/t27-,28-,31+,34+,35+,36+,38-/m0/s1
|
|||||
InChIKey |
QRLSJCMHFBSSJW-OEJISELMSA-N
|
|||||
IUPAC Name |
(2S,4R)-4-[[2-[(1R,3R)-1-acetyloxy-4-methyl-3-[3-methylbut-2-enoyloxymethyl-[(2S,3S)-3-methyl-2-[[(2R)-1-methylpiperidine-2-carbonyl]amino]pentanoyl]amino]pentyl]-1,3-thiazole-4-carbonyl]amino]-5-(4-hydroxyphenyl)-2-methylpentanoic acid
|
|||||
Pharmaceutical Properties | Molecule Weight |
842.1 |
Polar area |
233 |
||
Complexity |
1450 |
xlogp Value |
4.8 |
|||
Heavy Count |
59 |
Rot Bonds |
23 |
|||
Hbond acc |
13 |
Hbond Donor |
4 |
Each Antibody-drug Conjugate Related to This Payload
Full Information of The Activity Data of The ADC(s) Related to This Payload
Alpha-CD30-7 [Investigative]
Discovered Using Cell Line-derived Xenograft Model
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 93.10% (Day 28) | Positive CD30 expression (CD30+++/++) | ||
Method Description |
Alpha-CD30-7 (0.3 m ug/kg, every seven days x3) induces efficient tumor cell killing in cell line-derived models of CD30+, MDR-L540cy HL cells with CD30 expression with high expression.
|
||||
In Vivo Model | L540cy CDX model | ||||
In Vitro Model | Hodgkin's disease | L540cy cells | Homo sapiens | ||
Experiment 2 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 100.00% (Day 16) | Positive CD30 expression (CD30+++/++) | ||
Method Description |
Alpha-CD30-7 (1 m ug/kg, every seven days x3) induces efficient tumor cell killing in cell line-derived models of CD30+, MDR+ DEL/BVR ALCL cells with CD30 expression with high expression.
|
||||
In Vivo Model | DEL/BVR CDX model | ||||
In Vitro Model | Anaplastic large cell lymphoma | DEL/BVR cells | CVCL_1170 |
References
If you find any error in data or bug in web service, please kindly report it to Dr. Shen et al.