General Information of This Payload
Payload ID
PAY0OSSQB
Name
STING agonist of TAK500
Synonyms
STING agonist of TAK500
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Target(s) Stimulator of interferon genes protein (STING1)
Structure
Formula
C30H31F2N9O11P2S2
Isosmiles
CNCc1ccccc1C(=O)Nc1ncnc2c1ncn2[C@@H]1O[C@@H]2CO[P@@](=O)(S)O[C@@H]3[C@H](O)[C@@H](CO[P@@](=O)(S)O[C@H]2[C@H]1F)O[C@H]3n1cc(F)c2c(=O)[nH]cnc21
InChI
InChI=1S/C30H31F2N9O11P2S2/c1-33-6-13-4-2-3-5-14(13)27(43)39-24-20-26(36-10-34-24)41(12-38-20)29-19(32)22-17(50-29)9-48-54(46,56)52-23-21(42)16(8-47-53(45,55)51-22)49-30(23)40-7-15(31)18-25(40)35-11-37-28(18)44/h2-5,7,10-12,16-17,19,21-23,29-30,33,42H,6,8-9H2,1H3,(H,45,55)(H,46,56)(H,35,37,44)(H,34,36,39,43)/t16-,17-,19-,21-,22-,23-,29-,30-,53-,54-/m1/s1
InChIKey
ISJSBNLSDPJHRZ-ZQXNSGKOSA-N
Pharmaceutical Properties
Molecule Weight
857.708
Polar area
245.16
Complexity
857.1027745
xlogp Value
3.0621
Heavy Count
56
Rot Bonds
6
Hbond acc
18
Hbond Donor
6
Each Antibody-drug Conjugate Related to This Payload
Full Information of The Activity Data of The ADC(s) Related to This Payload
TAK-500 [Phase 1/2 (Terminated)]
Identified from the Human Clinical Data
Click To Hide/Show 2 Activity Data Related to This Level
Experiment 1 Reporting the Activity Date of This ADC [1]
Related Clinical Trial
NCT Number NCT04879849  Phase Status Phase 1
Clinical Description
An open-label, phase 1, dose-escalation study to evaluate the safety and preliminary antitumor activity of TAK-676 with pembrolizumab following radiation therapy in the treatment of non-small-cell lung cancer, triple-negative breast cancer, or squamous-cell carcinoma of the head and neck that has progressed on checkpoint inhibitors.
Experiment 2 Reporting the Activity Date of This ADC [2]
Related Clinical Trial
NCT Number NCT04420884  Phase Status Phase 1
Clinical Description
An open-label, dose escalation, phase 1 study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of TAK-676 as a single agent and in combination with pembrolizumab in adult patients with advanced or metastatic solid tumors.
References
Ref 1 An Open-label, Phase 1, Dose-escalation Study to Evaluate the Safety and Preliminary Antitumor Activity of TAK-676 With Pembrolizumab Following Radiation Therapy in the Treatment of Non-small-cell Lung Cancer, Triple-negative Breast Cancer, or Squamous-cell Carcinoma of the Head and Neck That Has Progressed on Checkpoint Inhibitors
Ref 2 An Open-label, Dose Escalation, Phase 1 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of TAK-676 as a Single Agent and in Combination With Pembrolizumab in Adult Patients With Advanced or Metastatic Solid Tumors