Oleanolic acid - Moligand™, analytical standard, ≥98% , CAS No.508-02-1

CAS: 508-02-1 Cat. No.: O110087 Formule: C30H48O3 Poids moléculaire: 456.7 Beilstein Registry Number: 10(4)1164 Numéro CE: 208-081-6
DISPONIBLE À COMMANDE
QUALITÉ & PURETÉ Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods. Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98%
Synonyms
Caryophyllin | OLEANOLIC_ACID | SMR000445561 | Oleanolic acid, analytical standard | OLEANOLIC ACID (CONSTITUENT OF HOLY BASIL LEAF) [DSC] | (4aS,5S,6aS,6bR,8R,8aR,10S,12aR,12bR,14bS)-10-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,6b,7,8,8a,9,10,11
Storage
Store at 2-8°C
Shipped In
Wet ice
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Taille
USA
Allemagne (EU)*
Prix
Qté
20mg
O110087-20mg
5 En stock
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16,90$US
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Pourquoi cette qualité

Moligand™, analytical standard, ≥98% Analytical standard,Moligand™ pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.

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Stockage & expédition

Store at 2-8°C Expédition Wet ice. Consultez le COA spécifique au lot pour les spécifications exactes.

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Documents qualité

SDS, COA, fiche technique et fiche de spécifications disponibles au téléchargement. COA spécifique au lot accessible via la recherche par numéro de lot.

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Preuve documentaire

Cité dans 42 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Vue d’ensemble

Oleanolic acid is a hydroxyl pentacyclic triterpenoic acid (HPTA), which exhibits antibacterial, antitumor and antileishmanial activity.

Spécifications

Synonymes
Caryophyllin | OLEANOLIC_ACID | SMR000445561 | Oleanolic acid, analytical standard | OLEANOLIC ACID (CONSTITUENT OF HOLY BASIL LEAF) [DSC] | (4aS,5S,6aS,6bR,8R,8aR,10S,12aR,12bR,14bS)-10-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,6b,7,8,8a,9,10,11
Spécifications et pureté
Moligand™, analytical standard, ≥98%
Mécanismes biochimiques et physiologiques
Natural triterpenoid. Various pharmacological attributes. Antiviral, anti-inflammatory, antiangiogenic, antiapoptotic and antitumor activities in vitro and in vivo .
Conditions de stockage de stockage
Store at 2-8°C
Expédié en
Wet ice
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Grade
Analytical standard, Moligand™
Note
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Pureté
≥98%
Noms et identifiants
Pubchem Sid
Sourires canoniques
CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C
IUPAC Name
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid
InChIKey
MIJYXULNPSFWEK-GTOFXWBISA-N
INCHI
1S/C30H48O3/c1-25(2)14-16-30(24(32)33)17-15-28(6)19(20(30)18-25)8-9-22-27(5)12-11-23(31)26(3,4)21(27)10-13-29(22,28)7/h8,20-23,31H,9-18H2,1-7H3,(H,32,33)/t20-,21-,22+,23-,27-,28+,29+,30-/m0/s1
Isomères SMILES
C[C@]12CC[C@@H](C([C@@H]1CC[C@@]3([C@@H]2CC=C4[C@]3(CC[C@@]5([C@H]4CC(CC5)(C)C)C(=O)O)C)C)(C)C)O
WGK Allemagne
2
RTECS
RK0177965
Poids moléculaire
456.7
Beilstein
10(4)1164
Reaxy-Rn
2228564
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2228564&ln=

Documentation

📋 Fiche de données de sécurité (FDS)

Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.

<<<<<<< HEAD Télécharger la SDS → ======= Télécharger la SDS → >>>>>>> release248-p3

✅ Certificat d'analyse (COA)

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📊 Fiche technique

Résumé de référence rapide des spécifications et applications du produit.

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🔬 Fiche de spécifications

Attributs de qualité complets et critères d'acceptation pour cette qualité.

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Données avancées

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
ClassePrenol lipids
SubclassTriterpenoids
Intermediate Tree Nodes Not available
Direct ParentTriterpenoids
Alternative Parents Secondary alcohols  Cyclic alcohols and derivatives  Monocarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic homopolycyclic compounds
Substituents Triterpenoid - Cyclic alcohol - Secondary alcohol - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic homopolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.
External Descriptors Oleanane triterpenoids
Structure 3D
Modèle de structure chimique interactif





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CES1 Tchem Liver carboxylesterase 1 (1 Activities)
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PTPN1 Tchem Tyrosine-protein phosphatase non-receptor type 1 (4 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PTPRC Tchem Receptor-type tyrosine-protein phosphatase C (1 Activities)
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F3 Tclin Tissue factor (1 Activities)
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AKR1B10 Tchem Aldo-keto reductase family 1 member B10 (5 Activities)
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GPBAR1 Tchem G-protein coupled bile acid receptor 1 (1 Activities)
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CDC25B Tchem M-phase inducer phosphatase 2 (1 Activities)
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EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)
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TOP1 Tclin DNA topoisomerase I (7553 Activities)
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TOP2A Tclin DNA topoisomerase II alpha (6317 Activities)
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ACHE Tclin Acetylcholinesterase (18204 Activities)
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PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
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PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)
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PTPN2 Tchem T-cell protein-tyrosine phosphatase (1317 Activities)
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PLK1 Tchem Serine/threonine-protein kinase PLK1 (28605 Activities)
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Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

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8 results found

Lot NumberCertificate TypeDateArticle
G2403647G2403647Certificate of AnalysisApr 02, 2026 O110087
L2525623L2525623Certificate of AnalysisDec 15, 2025 O110087
I2508463I2508463Certificate of AnalysisJul 12, 2025 O110087
G2403645G2403645Certificate of AnalysisMay 23, 2024 O110087
G2403646G2403646Certificate of AnalysisMay 23, 2024 O110087
G2403648G2403648Certificate of AnalysisMay 23, 2024 O110087
I2304093I2304093Certificate of AnalysisSep 11, 2023 O110087
G2214309G2214309Certificate of AnalysisJun 10, 2022 O110087
Propriétés chimiques et physiques
Rotation spécifique [α]76 ° (C=1, CHCl3)
Point de fusion (°C)300°C
Poids moléculaire456.700 g/mol
XLogP37.500
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass456.36 Da
Monoisotopic Mass456.36 Da
Topological Polar Surface Area57.500 Ų
Heavy Atom Count33
Formal Charge0
Complexity885.000
Isotope Atom Count0
Defined Atom Stereocenter Count8
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
FAQ et articles
Citations of This Product
Calculateurs de solution
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