Compound ID | 792

Update compound information

MC-352

Synonym(s): YM 17K  |  3,4'-dideoxy-5-O-mycaminosyltylonolide

Class: Macrolide

Agent Type: Small molecule; Direct acting;
Spectrum of activity: Gram-positive & Gram-negative
Mechanism of action: Protein synthesis inhibitor
Target Pathogen: Broad spectrum activity
Institute where first reported: Yamanouchi
Year first mentioned: 1991
Highest development stage: Phase 2
Development status: Inactive
Chemical structure(s):
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Molecular weight: 565.74
Iso. SMILES: CC[C@@H]1[C@H](/C=C(/C=C/C(=O)[C@@H](C[C@@H]([C@@H]([C@H](CCC(=O)O1)C)O[C@H]2[C@@H]([C@H](C[C@H](O2)C)N(C)C)O)CC=O)C)\C)CO
InChI Key: IBYMOKAONAMZRG-AAUSAPTBSA-N
Can. SMILES: CC[C@@H]1[C@H](/C=C(\C)/C=C/C(=O)[C@H](C)C[C@H](CC=O)[C@@H]([C@@H](C)CCC(=O)O1)O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)N(C)C)O)CO
InChI: InChI=1S/C31H51NO8/c1-8-27-24(18-34)15-19(2)9-11-26(35)21(4)16-23(13-14-33)30(20(3)10-12-28(36)39-27)40-31-29(37)25(32(6)7)17-22(5)38-31/h9,11,14-15,20-25,27,29-31,34,37H,8,10,12-13,16-18H2,1-7H3/b11-9+,19-15+/t20-,21+,22+,23-,24+,25-,27+,29+,30+,31-/m0/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/6449941
Citation: https://doi.org/10.1128/aac.36.8.1699

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