![Benzo[3,4]-18-norandrosta-3,5,15-triene-3(2'H)-carboxylicacid,3',4',5',6'-tetrahydro-3'-hydroxy-15…](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F344809-hyptadienic-acid.webp&w=3840&q=75)
CAS 128397-09-1: Benzo[3,4]-18-norandrosta-3,5,15-triene-3(2'H)-carboxylicacid,3',4',5',6'-tetrahydro-3'-hydroxy-15-(hydroxymethyl)-3',4',9,14,17,17-hexamethyl-,(3b,3'a,4b,4'a,8a,9b,10a,13a,14b)-
Formula:C30H46O4
InChI:InChI=1S/C30H46O4/c1-18-10-13-30(24(32)33)15-14-26(4)20(23(30)29(18,7)34)8-9-22-27(26,5)12-11-21-25(2,3)16-19(17-31)28(21,22)6/h8,16,18,21-23,31,34H,9-15,17H2,1-7H3,(H,32,33)/t18-,21+,22+,23-,26-,27-,28+,29-,30+/m1/s1
InChI key:InChIKey=YFLYOZWZPSYMPX-DCLYBNOZSA-N
SMILES:C[C@]12C([C@]3([C@@](C(O)=O)(CC1)CC[C@@H](C)[C@@]3(C)O)[H])=CC[C@]4([C@@]2(C)CC[C@@]5([C@]4(C)C(CO)=CC5(C)C)[H])[H]
Synonyms:- (+)-Hyptadienic acid
- (3β,3′α,4β,4′α,8α,9β,10α,13α,14β)-3′,4′,5′,6′-Tetrahydro-3′-hydroxy-15-(hydroxymethyl)-3′,4′,9,14,17,17-hexamethylbenzo[3,4]-18-norandrosta-3,5,15-triene-3(2′H)-carboxylic acid
- A(1)-Norursa-2,12-dien-28-oic acid, 19-hydroxy-2-(hydroxymethyl)-
- A(1)-Norursa-2,12-dien-28-oicacid, 19-hydroxy-2-(hydroxymethyl)-
- Benzo[3,4]-18-norandrosta-3,5,15-triene-3(2′H)-carboxylic acid, 3′,4′,5′,6′-tetrahydro-3′-hydroxy-15-(hydroxymethyl)-3′,4′,9,14,17,17-hexamethyl-, (3β,3′α,4β,4′α,8α,9β,10α,13α,14β)-
- Coleonolic acid
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Hyptadienic acid
CAS:Hyptadienic acid: cytotoxic to HepG2 cells, anti-inflammatory, inhibits mouse tumor promotion by DMBA/TPA.Formula:C30H46O4Purity:98%Color and Shape:SolidMolecular weight:470.68Hyptadienic acid
CAS:Controlled ProductHyptadienic acid is a specialized fatty acid, which is derived from the essential oils found in rosemary, a well-known herb in the Lamiaceae family. This compound is notable for its dual mechanism of action, exhibiting both antioxidant and anti-inflammatory properties. As an antioxidant, hyptadienic acid counteracts oxidative stress by neutralizing free radicals, thereby preventing cellular damage. Its anti-inflammatory effects are mediated through the inhibition of key pro-inflammatory mediators, which might be involved in various signaling pathways. Hyptadienic acid is utilized in biomedical research and nutraceutical development due to these bioactive properties. It offers potential applications in the formulation of supplements aimed at enhancing oxidative stress responses and reducing inflammation in chronic conditions. Furthermore, its inclusion in cosmetic formulations is being explored for skin protection and rejuvenation. Scientists are actively investigating its full spectrum of biological activities to better understand its potential benefits and therapeutic applications.Formula:C30H46O4Purity:Min. 95%Molecular weight:470.7 g/mol