Tripterifordin

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For Research Use Only.

Size	Price	Stock	Quantity
1 mg	$439	In stock

Category

Diterpenoids

Cat.No.

NP1271

CAS

139122-81-9

Product Name

Tripterifordin

Structure

Product Details

Description

Tripterifordin is isolated from the roots of Tripterygium wilfordii.

Synonyms

Tripterifordin; 139122-81-9; Hypodiolide A; (1R,2R,5R,6R,8S,11S,12R)-6-hydroxy-6,12-dimethyl-14-oxapentacyclo[10.3.3.15,8.01,11.02,8]nonadecan-13-oneKauran-18-oic acid, 16,20-dihydroxy-, delta-lactone, (4alpha)-

IUPAC Name

(1R,2R,5R,6R,8S,11S,12R)-6-hydroxy-6,12-dimethyl-14-oxapentacyclo[10.3.3.15,8.01,11.02,8]nonadecan-13-one

Molecular Weight

318.5

Molecular Formula

C20H30O3

Canonical SMILES

CC12CCCC3(C1CCC45C3CCC(C4)C(C5)(C)O)COC2=O

InChI

InChI=1S/C20H30O3/c1-17-7-3-8-20(12-23-16(17)21)14(17)6-9-19-10-13(4-5-15(19)20)18(2,22)11-19/h13-15,22H,3-12H2,1-2H3/t13-,14-,15-,17-,18-,19+,20+/m1/s1

InChIKey

KLMZPLYXGZZBCX-CJSYXLNHSA-N

Boiling Point

485.1±45.0 °C at 760 mmHg

Flash Point

198.6±21.5 °C

Purity

> 95%

Density

1.2±0.1 g/cm3

Solubility

In vitro:
10 mM in DMSO

Appearance

Powder

Application

anti-HIV;

Storage

Store at -20°C

Definition

ChEBI: A kaurane diterpenoid that is (5beta,8alpha,13alpha)-18,20-epoxykauran-18-one substituted by a hydroxy group at position 16. Isolated from the roots of Tripterygium wilfordii, it exhibits anti
HIV activity.

Form

Powder

Packaging

1 mg

pKa

15.24±0.40(Predicted)

Vapor Pressure

0.0±2.8 mmHg at 25°C

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