Isocupressic acid

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For Research Use Only.

Size	Price	Stock	Quantity
1 mg	$439	In stock

Category

Terpenes

Cat.No.

NP1377

CAS

1909-91-7

Product Name

Isocupressic acid

Structure

Product Details

Description

Isocupressic acid isolated from the barks of Araucaria cunninghami. It decrease affects the angiogenesis of the female reproductive system, the decrease in blood flow and apoptosis of corpus luteum-derived endothelial cells of the uterine tissue results in abortion.

Synonyms

(13E)-15-Hydroxy-8(17),13-labdadiene-19-oic acid; (15-hydroxy-8(17),13E-labdadien-19-oic acid; (1S,4aR,5S,8aR)-5-[(E)-5-hydroxy-3-methylpent-3-enyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid

Molecular Weight

320.5

Molecular Formula

C20H32O3

Canonical SMILES

CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C

InChI

1S/C20H32O3/c1-14(10-13-21)6-8-16-15(2)7-9-17-19(16,3)11-5-12-20(17,4)18(22)23/h10,16-17,21H,2,5-9,11-13H2,1,3-4H3,(H,22,23)/b14-10+/t16-,17+,19+,20-/m0/s1

InChIKey

DOYKMKZYLAAOGH-DOEMEAPXSA-N

Boiling Point

454.2±38.0 °C(Predicted)

Melting Point

109-110 °C

Flash Point

242.6°C

Purity

0.965

Density

1.06g/cm3

Appearance

Powder

Form

Powder

Packaging

1 mg

pKa

4.68±0.60(Predicted)

Refractive Index

1.527

Uses

Isocupressic Acid inhibits proliferation and induces cell cycle arrest and apoptosis in ovarian cancer cells. It is also associated with spontaneous abortion in cattle after consumption of conifer needles.

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