Compound ID | 3249

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Crisamicin A

Class: Natural product antibiotic (dimeric pyranonaphthoquinone)

Spectrum of activity: Gram-positive
Details of activity: Active against Staphylococcus aureus
Description: Natural product from Micromonospora purpureochromogenes subsp. halotolerans; contains a dimeric pyranonaphthoquinone scaffold
Year first mentioned: 1986
Development status: Experimental
Chemical structure(s):
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Molecular weight: 598.51
Iso. SMILES: C[C@H]1C2=C([C@H]3[C@@H](O1)CC(=O)O3)C(=O)C4=C(C2=O)C=C(C=C4O)C5=CC6=C(C(=C5)O)C(=O)C7=C(C6=O)[C@@H](O[C@@H]8[C@H]7OC(=O)C8)C
InChI Key: IPAXVRZEFNMCLP-GJPLRXPFSA-N
Can. SMILES: C[C@H]1C2=C(C(=O)C3=C(C=C(C=C3C2=O)C4=CC(=C5C(=C4)C(=O)C6=C(C5=O)[C@H]7[C@H](CC(=O)O7)O[C@H]6C)O)O)[C@H]8[C@H](CC(=O)O8)O1
InChI: InChI=1S/C32H22O12/c1-9-21-25(31-17(41-9)7-19(35)43-31)29(39)23-13(27(21)37)3-11(5-15(23)33)12-4-14-24(16(34)6-12)30(40)26-22(28(14)38)10(2)42-18-8-20(36)44-32(18)26/h3-6,9-10,17-18,31-34H,7-8H2,1-2H3/t9-,10-,17-,18-,31+,32+/m0/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/25023403
Citation: https://www.jstage.jst.go.jp/article/antibiotics1968/39/3/39_3_335/_article

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