20108-30-9

Basic information

• Product Name: FUSICOCCIN
• Synonyms: FUSICOCCIN;fusicoccin from fusicoccum amygdali;3-[2-(Acetyloxy)-1-methylethyl]-1,2,4,5,6,6a,7,8,9,10a-decahydro-1,5-dihydroxy-9-(methoxymethyl)-6,10a-dimethylcyclopenta[a,d]-dicylo coten-4-yl-6;.alpha.-D-Glucopyranoside, 3-[2-(acetyloxy)-1-methylethyl]-1,2,4,5,6,6A,7,8,9,10A-decahydro-1,5-dihydroxy-9-(methoxymethyl)-6,10A-dimethyldicyclopenta[A,D]cycloocten-4-yl 6-o-(1,1-dimethyl-2-propenyl)-, 3-acetate, [1S-[1.alpha.,3(R*),4.alpha.,5.beta.,6.beta.,6A.alpha.,9.beta.,10A.beta.]]-;Fucicoccin;Fusicoccin a;Nsc113500
• CAS NO: 20108-30-9
• Molecular Formula: C₃₆H₅₆O₁₂
• Molecular Weight: 680.82
• Product Categories: Carbohydrates;Carbohydrates A to;Carbohydrates D-FBiochemicals and Reagents;Monosaccharide
• Mol File: 20108-30-9.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 760.2°Cat760mmHg
• Flash Point: 227°C
• Appearance: /
• Density: 1.24g/cm³
• Vapor Pressure: 1.12E-26mmHg at 25°C
• Refractive Index: 1.555
• Storage Temp.: −20°C
• CAS DataBase Reference: FUSICOCCIN(CAS DataBase Reference)
• NIST Chemistry Reference: FUSICOCCIN(20108-30-9)
• EPA Substance Registry System: FUSICOCCIN(20108-30-9)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 20108-30-9(Hazardous Substances Data)

Usage

Uses

Fusicoccin is a 14-3-3-dependent activator of H+-ATPase.

InChI:InChI=1/C36H56O12/c1-10-35(6,7)45-17-26-30(41)33(46-21(5)38)31(42)34(47-26)48-32-28-24(18(2)15-44-20(4)37)13-27(39)36(28,8)14-25-22(16-43-9)11-12-23(25)19(3)29(32)40/h10,14,18-19,22-23,26-27,29-34,39-42H,1,11-13,15-17H2,2-9H3/b25-14-/t18-,19-,22-,23+,26-,27+,29-,30-,31-,32-,33+,34-,36+/m1/s1

Upstream product

• 2280-44-6 D-Glucose 
• 214356-01-1 (+)-fusicocca-2,10⁽¹⁴⁾-diene 

Relevant articles and documents

Conversion of [19-2H2]fusicocca-2,10(14)-diene into its 8β-ol and fusicoccins by Phomopsis (Fusicoccum) amygdali

Feeding experiments of (+)-[19-2H2]fusicocca-2,10(14)-diene, a deuterated derivative of a new candidate for the initially-forming fusicoccane-hydrocarbon in the fusicoccin biosynthesis, with the fusicoccin- producing fungus Phomopsis (Fusicoccum) amygdali have revealed its incorporation into fusicoccins J and A through (+)-fusicocca-2,10(14)-dien- 8β-ol, whose occurrence in the mycelial extract has been confirmed by direct comparison of its 1H NMR and GC-MS data with those of the synthetic sample, proving the early biosynthetic route leading to the aglycons of fusicoccins. (C) 2000 Elsevier Science Ltd.