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ChemicalBook--->CAS DataBase List--->6730-83-2

6730-83-2

6730-83-2 Structure

6730-83-2 Structure
IdentificationBack Directory
[Name]

kaurenoic acid
[CAS]

6730-83-2
[Synonyms]

NSC 339145
Cunabic acid
kaurenoic acid
Kauren-19-oic acid
ent-kaur-16-en-19-oicaci
ent-Kaur-16-en-19-oic acid
(-)-Kaur-16-en-18-oic acid
Kaurane-16-ene-18-oic acid
Kaur-16-en-18-oic acid,(4a)-
ent-Kaur-16(17)-en-19-oic acid
(4R,4aS,6aS,9R,11aR,11bS)-4,11b-dimethyl-8-methylenetetradecahydro-6a,9-methanocyclohepta[a]naphthalene-4-carboxylic acid
[Molecular Formula]

C20H30O2
[MDL Number]

MFCD28978039
[MOL File]

6730-83-2.mol
[Molecular Weight]

302.45
Chemical PropertiesBack Directory
[Melting point ]

171-172 °C
[Boiling point ]

426.6±34.0 °C(Predicted)
[density ]

1.10±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Store in freezer, under -20°C
[solubility ]

DMF: 10 mg/ml; DMSO: 25 mg/ml; DMSO:PBS (pH 7.2) (1:2): 0.3 mg/ml; Ethanol: 10 mg/ml
[form ]

A solid
[pka]

4.70±0.40(Predicted)
[color ]

White to off-white
Safety DataBack Directory
[WGK Germany ]

3
Hazard InformationBack Directory
[Description]

Kaurenoic acid is a diterpene that has been found in C. langsdorffii and has diverse biological activities, including anticancer, antibacterial, antioxidant, and anti-inflammatory properties. It is cytotoxic to 22Rv1 and LNCaP prostate, HT-29, HCT116, SW480, and SW620 colon, and MCF-7 breast cancer cells with IC50 values ranging from 15.03 to 48.87 μg/ml. Kaurenoic acid is active against S. epidermidis, S. capitis, E. faecalis, and S. haemolyticus in vitro (MICs = 6.25-12.5 μg/ml). Kaurenoic acid (50 and 100 mg/kg) reduces colonic myeloperoxidase (MPO) activity and malondialdehyde (MDA) levels in a rat model of acetic acid-induced colitis, as well as colonic tissue damage, leukocytic infiltration, and submucosal edema when administered at a dose of 100 mg/kg.
[Uses]

ent-Kaurenoic Acid can be used in biological study. Kinetic profile of guaco syrup metabolites like coumarin, 7-hydroxycoumarin, o-coumaric acid, kaurenoic acid can be performed for identification of alternative route of coumarin metabolism in human plasma.
[Definition]

ChEBI: An ent-kaurane diterpenoid that is ent-kauran-19-oic acid in which a double bond is present at position 16(17); exhibits anticancer and anti-HIV 1 activity.
Spectrum DetailBack Directory
[Spectrum Detail]

kaurenoic acid(6730-83-2)1HNMR
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