Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C20H24NO8P |
Molecular Weight | 437.3802 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C(OC)C(OC)=C2C(CC[C@H](NC(C)=O)C3=CC(OP(O)(O)=O)=CC=C23)=C1
InChI
InChIKey=UGBMEXLBFDAOGL-INIZCTEOSA-N
InChI=1S/C20H24NO8P/c1-11(22)21-16-8-5-12-9-17(26-2)19(27-3)20(28-4)18(12)14-7-6-13(10-15(14)16)29-30(23,24)25/h6-7,9-10,16H,5,8H2,1-4H3,(H,21,22)(H2,23,24,25)/t16-/m0/s1
ZD-6126 (previously known as ANG-453) is a vascular-targeting agent in clinical development for the treatment of solid tumors. ZD-6126 binds to and inhibits tubulin. ZD6126 completed phase I clinical trial in 2008, where was found significant cardiotoxicities. The further development of this drug was terminated.
Originator
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
ZD6126: a novel vascular-targeting agent that causes selective destruction of tumor vasculature. | 2002 Dec 15 |
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ZD-6126 AstraZeneca. | 2004 Apr |
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Novel analogue of colchicine induces selective pro-death autophagy and necrosis in human cancer cells. | 2014 |
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New vascular disrupting agents in upper gastrointestinal malignancies. | 2014 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/18219445
Forty-four patients received ZD6126 (5-112 mg/m2 in the 21-day schedule, n=35; 40-80 mg/m2 in the 14-day schedule, n=9).
Route of Administration:
Intravenous
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DTXSID20944593
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ZD6126
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100000174985
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C2736
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GBO3S6M9W7
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9896434
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DB11872
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219923-05-4
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METABOLITE ACTIVE (PRODRUG)
SUBSTANCE RECORD