1191255-15-8

Basic information

• Product Name: GanoMycin I
• Synonyms: GanoMycin I
• CAS NO: 1191255-15-8
• Molecular Formula: C₂₁H₂₆O₄
• Molecular Weight: 342.43
• Mol File: 1191255-15-8.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 521.5±50.0 °C(Predicted)
• Appearance: /
• Density: 1.135±0.06 g/cm3(Predicted)
• PKA: 9.68±0.48(Predicted)
• CAS DataBase Reference: GanoMycin I(CAS DataBase Reference)
• NIST Chemistry Reference: GanoMycin I(1191255-15-8)
• EPA Substance Registry System: GanoMycin I(1191255-15-8)

Safety Data

• Hazardous Substances Data: 1191255-15-8(Hazardous Substances Data)

Upstream product

• 1580541-78-1 (5R,3''E)-5-[2',5'-bis(methoxymethoxyphenyl)]-3-(4'',8''-dimethylnona-3'',7''-dien-1''-yl)-2(5H)-furanone 
• 1580541-77-0 (1'R,5E)-1'-[2'',5''-bis(methoxymethoxy)phenyl]prop-2-en-1-yl-6,10-dimethyl-2-methylideneundeca-5,9-dienoate 
• 1580541-76-9 (E)-6,9-dimethyl-2-methylideneundeca-5,9-dienoic acid 
• 1580541-75-8 (E)-6,10-dimethyl-2-methyleneundeca-5,9-dienal 
• 69369-93-3 (E)-6,10-dimethyl-2-methylene-5,9-undecadien-1-ol 
• 5389-87-7 1-chloro-3,7-dimethylocta-2,6-diene 
• 106-24-1 Geraniol 
• 1580541-74-7 (R)-1-[2',5'-bis(methoxymethoxy)phenyl]prop-2-en-1-ol 
• 1580541-73-6 (2'R,3'S)-2-{3'-[2'',5''-bis(methoxymethoxy)phenyl]-2',3'-dihydroxyprop-2-enylsulfonyl}-1,3-benzothiazole 
• 1580541-72-5 (2'R,3'S)-2-{3'-[2'',5''-bis(methoxymethoxy)phenyl]-2',3'-dihydroxyprop-2-enylthio}-1,3-benzothiazole 
• 1580541-71-4 (E)-2-{3'-[2'',5''-bis(methoxymethoxy)phenyl]prop-2-enylthio}-1,3-benzothiazole 
• 1580541-70-3 (E)-3-[2,5-bis(methoxymethoxy)phenyl]prop-2-en-1-ol 
• 40931-14-4 ethyl (E)-3-[2,5-bis(methoxymethoxy)phenyl]prop-2-enoate 
• 13709-07-4 2,5-bis(methoxymethoxy)benzaldehyde 

Relevant articles and documents

Concise syntheses and biological activities of ganomycin I and fornicin A

The first enantioselective syntheses of ganomycin I, a meroterpenoid isolated from the Vietnamese mushroom Ganoderma colossum, and the related meroterpenoid fornicin A were accomplished. Our methodology for the total syntheses of these compounds featured the construction of the butenolide moiety by asymmetric dihydroxylation followed by Julia-Kocienski type olefin formation and ring-closing metathesis reactions. The absolute configurations of the two natural products were determined by comparisons of specific rotation. A cell-based assay of the synthetic compounds with transfected human embryonic kidney 293 tetoff (E-PR293) cells indicated that ganomycin I possesses cytotoxicity and fornicin A possesses weak anti-HIV-1 protease activity without cytotoxicity.