more general categories
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03. Biological Effects of Specific Chemicals
03. Biological Effects of Specific Chemicals
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
05. Industrial Uses
05. Industrial Uses
TMC-135B [CHEBI:66233] (1)
06. Name of Biological Source of Chemical
06. Name of Biological Source of Chemical
Streptomyces (157)
07. Part of Biological Source of Chemical
07. Part of Biological Source of Chemical
unspecified structure [PO:0000004] (703)
08. Chemical Category
08. Chemical Category
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
TMC-135B [CHEBI:66233] (1)
ChEBI Compound Accession Identifier :
[CHEBI:66233]
ChEBI Compound Description :
An organonitrogen heterocyclic compound that is a 21-membered macrocyclic lactam substituted by a ({1-[(cyclohex-1-en-1-ylcarbonyl)amino]cyclopropyl}carbonyl)oxy group at position 18. It is isolated from Streptomyces sp. TC-1190 and exhibits growth inhibitory effects on a series of human tumour cell lines.
ChEBI Compound Identification Number :
66233
ChEBI InChI Value :
InChI=1S/C39H49N3O8S/c1-24-13-12-17-28-35(46)29(22-30-36(28)51-23-33(44)41-30)40-32(43)21-27(49-3)16-10-5-4-6-11-18-31(25(2)34(24)45)50-38(48)39(19-20-39)42-37(47)26-14-8-7-9-15-26/h4-6,10-11,13-14,16,22,25,27,31,34,45-46H,7-9,12,15,17-21,23H2,1-3H3,(H,40,43)(H,41,44)(H,42,47)/b5-4+,11-6+,16-10+,24-13-
ChEBI InChIKey Value :
YIMYDHUFVYSTEY-WUWQZELJSA-N
ChEBI Compound Name :
TMC-135B
ChEBI SMILES Value :
COC1CC(=O)Nc2cc3NC(=O)CSc3c(CC\C=C(C)/C(O)C(C)C(C\C=C\C=C\C=C\1)OC(=O)C1(CC1)NC(=O)C1=CCCCC1)c2O
ChEBI Substance ID :
160645288
ChEBI URL :
ChEBI:66233
ChemSpider ID :
NS
Ontomatica Chemical Accession Key (OnChAKey) :
YIMYDHUFVYSTEY_WUWQZELJSA_N_000_000000
PubChem Compound ID :
11765429