Compound ID | 925

Update compound information

Tripropeptin Z

Class: Natural product antibiotic

Agent Type: Natural product; Direct acting;
Spectrum of activity: Gram-positive
Mechanism of action: Cell wall synthesis inhibitor. Binds to undecaprenyl pyrophosphate
Target Pathogen: Active against methicillin-resistant Staphylococcus aureus, penicillin-resistant Streptococcus sp., and vancomycin-resistant Enterococcus sp.
Institute where first reported: Microbial Chemistry Research Centre, Japan
Year first mentioned: 2005
Development status: Experimental
Chemical structure(s):
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Molecular weight: 1112.19
Iso. SMILES: CC(C)CCCCCCC1CC(=O)NC(C(=O)N2CCCC2C(=O)N3CCCC3C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N4CCC(C4C(=O)NC(C(=O)O1)C(C(=O)O)O)O)CO)C(C(=O)O)O)CCCN=C(N)N)C(C)O
InChI Key: CDGPSUVNLUGBRV-UHFFFAOYSA-N
Can. SMILES: CC(C)CCCCCCC1CC(=O)NC(C(C)O)C(=O)N2CCCC2C(=O)N3CCCC3C(=O)NC(CCCN=C(N)N)C(=O)NC(C(C(=O)O)O)C(=O)NC(CO)C(=O)N4CCC(C4C(=O)NC(C(C(=O)O)O)C(=O)O1)O
InChI: InChI=1S/C48H77N11O19/c1-23(2)11-6-4-5-7-12-25-21-31(63)54-32(24(3)61)44(72)58-19-10-15-29(58)43(71)57-18-9-14-28(57)39(67)52-26(13-8-17-51-48(49)50)38(66)55-33(36(64)45(73)74)40(68)53-27(22-60)42(70)59-20-16-30(62)35(59)41(69)56-34(47(77)78-25)37(65)46(75)76/h23-30,32-37,60-62,64-65H,4-22H2,1-3H3,(H,52,67)(H,53,68)(H,54,63)(H,55,66)(H,56,69)(H,73,74)(H,75,76)(H4,49,50,51)
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/58960775

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