Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C18H17BrN4O3 |
Molecular Weight | 417.257 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC(=CC(Br)=C1OC)[C@@H]2C3=CC=C(N)C(N)=C3OC(N)=C2C#N
InChI
InChIKey=JXONINOYTKKXQQ-CQSZACIVSA-N
InChI=1S/C18H17BrN4O3/c1-24-13-6-8(5-11(19)17(13)25-2)14-9-3-4-12(21)15(22)16(9)26-18(23)10(14)7-20/h3-6,14H,21-23H2,1-2H3/t14-/m1/s1
Crolibulin is a tubulin-disrupting agent, interacting at the colchicine-binding site, developed by EpiCept Corporation (which was later acquired by Immune Pharmaceuticals). The compound exhibits anti-cancer effect by vascular disruption and inhibition of apoptosis. In preclinical animal tumor models, combination therapy with crolibulin has demonstrated the synergistic activity with cytotoxic drugs as well as anti-angiogenic drugs, such as Avastin. The drug was investigated in clinical trials for the treatment of anaplastic thyroid cancer and has demonstrated a positive effect.
Approval Year
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NCI_THESAURUS |
C67421
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1000852-17-4
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23649181
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DB12925
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CHEMBL2103852
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DTXSID10142925
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9ENT43KY91
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C66938
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9247
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ACTIVE MOIETY