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03. Biological Effects of Specific Chemicals
03. Biological Effects of Specific Chemicals
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
05. Industrial Uses
05. Industrial Uses
TMC-135A [CHEBI:66232] (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-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
TMC-135A [CHEBI:66232] (1)
ChEBI Compound Accession Identifier :
[CHEBI:66232]
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 17, which is obtained from Streptomyces sp. TC-1190. It exhibits growth inhibitory effects on a series of human tumour cell lines.
ChEBI Compound Identification Number :
66232
ChEBI InChI Value :
InChI=1S/C39H49N3O8S/c1-24-13-12-16-27-21-29-36(51-23-32(44)40-29)33(35(27)46)41-31(43)22-28(49-3)17-10-5-4-6-11-18-30(25(2)34(24)45)50-38(48)39(19-20-39)42-37(47)26-14-8-7-9-15-26/h4-6,10-11,13-14,17,21,25,28,30,34,45-46H,7-9,12,15-16,18-20,22-23H2,1-3H3,(H,40,44)(H,41,43)(H,42,47)/b5-4+,11-6+,17-10+,24-13-
ChEBI InChIKey Value :
DLJPEMIJOQUTRD-KLLBSFIHSA-N
ChEBI Compound Name :
TMC-135A
ChEBI SMILES Value :
COC1CC(=O)Nc2c(O)c(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)cc1NC(=O)CSc21
ChEBI Substance ID :
160645277
ChEBI URL :
ChEBI:66232
ChemSpider ID :
28533021
Ontomatica Chemical Accession Key (OnChAKey) :
DLJPEMIJOQUTRD_KLLBSFIHSA_N_000_000000
PubChem Compound ID :
10439859