Compound ID | 2650

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Norplicacetin

Class: Natural product antibiotic

Spectrum of activity: Gram-positive
Details of activity: Active against Staphylococcus aureus, Streptococcus pneumoniae, Mycobacterium smegmatis, and Mycobacterium bovis
Description: Natural product from Streptomyces plicatus; amicetin-type
Institute where first reported: Biochemistry Department, Glaxo Research Ltd. Sefton Park, Stoke Poges, Buckinghamshire, England
Year first mentioned: 1977
Development status: Experimental
Chemical structure(s):
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Molecular weight: 503.55
Iso. SMILES: C[C@@H]1[C@H](CC[C@@H](O1)N2C=CC(=NC2=O)NC(=O)C3=CC=C(C=C3)N)O[C@@H]4[C@@H]([C@H]([C@@H]([C@H](O4)C)NC)O)O
InChI Key: HJFXGPLQIPLHSS-UOUGBBRZSA-N
Can. SMILES: C[C@@H]1[C@H](CC[C@H](N2C=CC(=NC2=O)NC(=O)C3=CC=C(C=C3)N)O1)O[C@@H]4[C@@H]([C@H]([C@@H]([C@@H](C)O4)NC)O)O
InChI: InChI=1S/C24H33N5O7/c1-12-16(36-23-21(31)20(30)19(26-3)13(2)35-23)8-9-18(34-12)29-11-10-17(28-24(29)33)27-22(32)14-4-6-15(25)7-5-14/h4-7,10-13,16,18-21,23,26,30-31H,8-9,25H2,1-3H3,(H,27,28,32,33)/t12-,13-,16+,18-,19-,20+,21-,23-/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/101324848
Citation: https://www.jstage.jst.go.jp/article/antibiotics1968/30/7/30_7_604/_pdf/-char/en

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