β-Amyrin

Inquiry

For Research Use Only.

Category

Terpenes

Cat.No.

NP6299

CAS

559-70-6

Product Name

β-Amyrin

Structure

Product Details

Description

β-Amyrin isolated from the stem bark of Alstonia boonei. It can enhance the total sleeping behavior in pentobarbital-induced sleeping model via the activating of GABAergic neurotransmitter system GABA content in the brain.

Synonyms

OLEAN-12-EN-3BETA-OL;OLEAN-12-EN-3B-OL

IUPAC Name

(3S,4aR,6aR,6bS,8aR,12aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol

Molecular Weight

426.7

Molecular Formula

C30H50O

Canonical SMILES

CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C

InChI

InChI=1S/C30H50O/c1-25(2)15-16-27(5)17-18-29(7)20(21(27)19-25)9-10-23-28(6)13-12-24(31)26(3,4)22(28)11-14-30(23,29)8/h9,21-24,31H,10-19H2,1-8H3/t21-,22-,23+,24-,27+,28-,29+,30+/m0/s1

InChIKey

JFSHUTJDVKUMTJ-QHPUVITPSA-N

Boiling Point

260 °C

Melting Point

187-190°C

Purity

0.96

Density

1.01g/cm3

Solubility

Chloroform (Slightly), methanol (Slightly, Heated)

Appearance

Powder

Application

anti-inflammatory activity

Storage

Refrigerator

Alpha

D19 +99.8° (c = 1.3 in benzene)

BRN

2063468

Color

White to Off-White

Definition

ChEBI: A pentacyclic triterpenoid that is oleanane substituted at the 3beta-position by a hydroxy group and containing a double bond between positions 12 and 13. It is one of the most commonly occurring triterpenoids in higher plants.

EINECS

209-204-6

10-23

Form

Solid

Hazard Class

pKa

15.18±0.70(Predicted)

Refractive Index

1.4910 (estimate)

Risk Statements

Safety Statements

22-45

Uses

Nociceptive

WGK Germany

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