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03. Biological Effects of Specific Chemicals
03. Biological Effects of Specific Chemicals
cilofungin [CHEBI:315019] (1)
05. Industrial Uses
05. Industrial Uses
cilofungin [CHEBI:315019] (1)
08. Chemical Category
08. Chemical Category
cilofungin [CHEBI:315019] (1)
cilofungin [CHEBI:315019] (1)
cilofungin [CHEBI:315019] (1)
cilofungin [CHEBI:315019] (1)
cilofungin [CHEBI:315019] (1)
cilofungin [CHEBI:315019] (1)
cilofungin [CHEBI:315019] (1)
cilofungin [CHEBI:315019] (1)
cilofungin [CHEBI:315019] (1)
cilofungin [CHEBI:315019] (1)
ChEBI Compound Accession Identifier :
[CHEBI:315019]
ChEBI Compound Description :
A cyclic hexapeptide echinocandin antibiotic isolated from Aspergillus spp. By inhibiting the conversion of lanosterol to ergosterol, it invades a fungus' ability to synthesize cell walls. A modified form of echinocandin B, it is an antimycotic agent against Candida albicans.
ChEBI Compound Identification Number :
315019
ChEBI InChI Value :
InChI=1S/C49H71N7O17/c1-5-6-7-8-9-10-19-73-31-17-13-28(14-18-31)42(65)50-32-21-34(61)45(68)54-47(70)38-39(62)24(2)22-56(38)49(72)36(26(4)58)52-46(69)37(41(64)40(63)27-11-15-29(59)16-12-27)53-44(67)33-20-30(60)23-55(33)48(71)35(25(3)57)51-43(32)66/h11-18,24-26,30,32-41,45,57-64,68H,5-10,19-23H2,1-4H3,(H,50,65)(H,51,66)(H,52,69)(H,53,67)(H,54,70)/t24-,25+,26+,30+,32-,33-,34+,35-,36-,37-,38-,39-,40-,41-,45+/m0/s1
ChEBI InChIKey Value :
ZKZKCEAHVFVZDJ-MTUMARHDSA-N
ChEBI Compound Name :
cilofungin
ChEBI SMILES Value :
CCCCCCCCOc1ccc(cc1)C(=O)N[C@H]1C[C@@H](O)[C@@H](O)NC(=O)[C@@H]2[C@@H](O)[C@@H](C)CN2C(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H]2C[C@@H](O)CN2C(=O)[C@@H](NC1=O)[C@@H](C)O)[C@H](O)[C@@H](O)c1ccc(O)cc1)[C@@H](C)O
ChEBI Substance ID :
85507136
ChEBI URL :
ChEBI:315019
ChemSpider ID :
NS
Ontomatica Chemical Accession Key (OnChAKey) :
ZKZKCEAHVFVZDJ_MTUMARHDSA_N_000_000000
PubChem Compound ID :
6918120