| Weight | 415.511 g/mol |
|---|---|
| Formula | C22H25NO5S |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 5 |
Thiocolchicine (2730-71-4)
thiocholchicine
Score:
#47 in Medicinal chemistry
,
#2195 in Physics
,
#2743 in Biochemistry
,
#6783 in Chemistry
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- N-acetylcolchinol O-methyl ether and thiocolchicine, potent analogs of colchicine modified in the C ring. Evaluation of the mechanistic basis for their enhanced biological properties. (Journal of Biological Chemistry, 1990)
- Antitubulin effects of derivatives of 3-demethylthiocolchicine, methylthio ethers of natural colchicinoids, and thioketones derived from thiocolchicine. Comparison with colchicinoids (Journal of Medicinal Chemistry, 1990)
- Inhibitors of tubulin polymerization: synthesis and biological evaluation of hybrids of vindoline, anhydrovinblastine and vinorelbine with thiocolchicine, podophyllotoxin and baccatin III. (Bioorganic & Medicinal Chemistry, 2008)
- Thiocolchicine-podophyllotoxin conjugates: dynamic libraries based on disulfide exchange reaction. (Journal of Organic Chemistry, 2006)
- Synthesis and biological evaluation of novel thiocolchicinepodophyllotoxin conjugates (European Journal of Medicinal Chemistry, 2010)
- Antitumor agents. 139. Synthesis and biological evaluation of thiocolchicine analogs 5,6-dihydro-6(S)-(acyloxy)- and 5,6-dihydro-6(S)-[(aroyloxy)methyl]-1,2,3-trimethoxy-9-(methylthio)-8H- cyclohepta[a]naphthalen-8-ones as novel cytotoxic and antimitotic agents. (Journal of Medicinal Chemistry, 1993)
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SMILESCC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)SC)OC)OC)OC
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InChIKeyCMEGANPVAXDBPL-UHFFFAOYSA-N
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