Compound ID | 2749

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Steptovirudin

Class: Natural product antibiotic

Agent Type: Natural product; Small molecule; Direct acting;
Spectrum of activity: Gram-positive
Mechanism of action: Cell wall synthesis inhibitor
Target Pathogen: Active against Gram-positives
Description: Natural product from Streptomyces griseoflavus
Year first mentioned: 1975
Development status: Experimental
Chemical structure(s):
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Molecular weight: 720.72
Iso. SMILES: CC(C)C/C=C/C(=O)N[C@@H]1[C@H]([C@H]([C@H](O[C@H]1OC2[C@H]([C@@H]([C@H]([C@@H](O2)CO)O)O)NC(=O)C)CC([C@@H]3[C@H]([C@H]([C@@H](O3)N4CCC(=O)NC4=O)O)O)O)O)O
InChI Key: VFVPUOZOQGGMBI-OJYBKPOHSA-N
Can. SMILES: CC(C)C/C=C/C(=O)N[C@@H]1[C@H]([C@H]([C@@H](CC([C@@H]2[C@H]([C@H]([C@H](N3CCC(=O)NC3=O)O2)O)O)O)O[C@H]1OC4[C@H]([C@@H]([C@H]([C@H](CO)O4)O)O)NC(=O)C)O)O
InChI: InChI=1S/C30H48N4O16/c1-11(2)5-4-6-16(38)32-19-23(43)20(40)14(47-29(19)50-28-18(31-12(3)36)22(42)21(41)15(10-35)48-28)9-13(37)26-24(44)25(45)27(49-26)34-8-7-17(39)33-30(34)46/h4,6,11,13-15,18-29,35,37,40-45H,5,7-10H2,1-3H3,(H,31,36)(H,32,38)(H,33,39,46)/b6-4+/t13?,14-,15+,18+,19-,20+,21+,22+,23-,24+,25-,26-,27-,28?,29+/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/6450317
Citation: https://www.jstage.jst.go.jp/article/antibiotics1968/28/7/28_7_514/_pdf/-char/en

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