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MW 680.8 Da, Purity >90%. H+-ATPase activator. NF-κB activator. 14-3-3 protein binder. Induces H+ extrusion from plant cells. Stimulates cytochrome c release from mitochondria. Reduces cellular H2O2 scavenging capacity. Induces membrane hyperpolarization. Induces seed germination and opening of the stomata in plants and promotes platelet aggregation *in vivo.*.

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Chemical Structure - Fusicoccin, H+-ATPase activator (AB145208), expandable thumbnail

Key facts

CAS number
20108-30-9
Purity
> 90%
Source
Fusicoccum amygdali
Molecular weight
680.8 Da
Molecular formula
C36H56O12
PubChem identifier
46936214
Nature
Native

Target data

Recommended products

MW 680.8 Da, Purity >90%. H+-ATPase activator. NF-κB activator. 14-3-3 protein binder. Induces H+ extrusion from plant cells. Stimulates cytochrome c release from mitochondria. Reduces cellular H2O2 scavenging capacity. Induces membrane hyperpolarization. Induces seed germination and opening of the stomata in plants and promotes platelet aggregation *in vivo.*.

Key facts

Purity
> 90%
Source
Fusicoccum amygdali
PubChem identifier
46936214
Solubility

Soluble in ethanol.

Biochemical name
[(2S)-2-[(1E,3R,4R,8S,9S,10R,11R,14R)-8-[(2S,3S,4R,5S,6S)-4-acetyloxy-3,5-dihydroxy-6-(2-methylbut-3-en-2-yloxymethyl)oxan-2-yl]oxy-4,9-dihydroxy-14-(methoxymethyl)-3,10-dimethyl-6-tricyclo[9.3.0.03,7]tetradeca-1,6-dienyl]propyl] acetate
Biological description

H+-ATPase activator. NF-κB activator. 14-3-3 protein binder. Induces H+ extrusion from plant cells. Stimulates cytochrome c release from mitochondria. Reduces cellular H2O2 scavenging capacity. Induces membrane hyperpolarization. Induces seed germination and opening of the stomata in plants and promotes platelet aggregation *in vivo.*

Canonical SMILES
CC1C2CCC(C2=CC3(C(CC(=C3C(C1O)OC4C(C(C(C(O4)COC(C)(C)C=C)O)OC(=O)C)O)C(C)COC(=O)C)O)C)COC
Isomeric SMILES
C[C@@H]1[C@H]\2CC[C@H](/C2=C/[C@]3([C@@H](CC(=C3[C@@H]([C@H]1O)O[C@@H]4[C@H]([C@@H]([C@H]([C@@H](O4)COC(C)(C)C=C)O)OC(=O)C)O)[C@H](C)COC(=O)C)O)C)COC
InChI
InChI=1S/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
InChIKey
KXTYBXCEQOANSX-MQYZIMMHSA-N
IUPAC name
[(2S)-2-[(1E,3R,4R,8S,9S,10R,11R,14R)-8-[(2S,3S,4R,5S,6S)-4-acetyloxy-3,5-dihydroxy-6-(2-methylbut-3-en-2-yloxymethyl)oxan-2-yl]oxy-4,9-dihydroxy-14-(methoxymethyl)-3,10-dimethyl-6-tricyclo[9.3.0.03,7]tetradeca-1,6-dienyl]propyl] acetate

Storage

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C
Storage information
Store under desiccating conditions, The product can be stored for up to 12 months

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1 product image

  • Chemical Structure - Fusicoccin, H+-ATPase activator (ab145208), expandable thumbnail

    Chemical Structure - Fusicoccin, H+-ATPase activator (ab145208)

    2D chemical structure image of ab145208, Fusicoccin, H+-ATPase activator

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Product protocols

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