Cucurbitacin E-2-O-glucoside - ≥95% , CAS No.1398-78-3

CAS: 1398-78-3 Cat. No.: E463787 Formule: C38H54O13 Poids moléculaire: 718.83 Numéro CE: 215-745-9
DISPONIBLE À COMMANDE
GRADE & PURITY ≥95%
Synonyms
alpha-Elaterin 2-D-glucopyranoside | 6984R18595 | COLOCYNTHINUM [HPUS] | Q27137271 | COLOCYNTHINUM | UNII-6984R18595 | [(E,6R)-6-hydroxy-6-[(8S,9R,10R,13R,14S,16R,17R)-16-hydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(h
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
Size
Allemagne (EU)
USA*
Price
Qty
1mg
E463787-1mg
Sur commande · 8–12 semaines

626,42€

732,28€
Enregistrer 105,86 € (14.46%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Vue d’ensemble

Product Application:

Cucurbitacin E 2-O-Glucoside is a metabolite of Cucurbitacin E (C838800), a highly oxidated steroid consisting of a tetracyclic triterpene. Cucurbitacin E is known to possess broad spectrum of potential anti-inflammatory, antitumor andantioxidant effects.

Specifications

Synonymes
alpha-Elaterin 2-D-glucopyranoside | 6984R18595 | COLOCYNTHINUM [HPUS] | Q27137271 | COLOCYNTHINUM | UNII-6984R18595 | [(E,6R)-6-hydroxy-6-[(8S,9R,10R,13R,14S,16R,17R)-16-hydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(h
Spécifications et pureté
≥95%
Conditions de stockage de stockage
Store at -20°C
Expédié en
Ice chest + Ice pads
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Pureté
≥95%
Noms et identifiants
Sourires canoniquesCC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3C=C(C(=O)C4(C)C)OC5C(C(C(C(O5)CO)O)O)O)C)C)C)O)O
IUPAC Name[(E,6R)-6-hydroxy-6-[(8S,9R,10R,13R,14S,16R,17R)-16-hydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-17-yl]-2-methyl-5-oxohept-3-en-2-yl] acetate
InChIKeyQKEJRKXVLGOJMB-YYBMGDPWSA-N
INCHI1S/C38H54O13/c1-18(40)51-33(2,3)13-12-25(42)38(9,48)30-21(41)15-35(6)24-11-10-19-20(37(24,8)26(43)16-36(30,35)7)14-22(31(47)34(19,4)5)49-32-29(46)28(45)27(44)23(17-39)50-32/h10,12-14,20-21,23-24,27-30,32,39,41,44-46,48H,11,15-17H2,1-9H3/b13-12+/t20-,21-,23-,24+,27-,28+,29-,30+,32-,35+,36-,37+,38+/m1/s1
Isomères SMILES CC(=O)OC(C)(C)/C=C/C(=O)[C@@](C)([C@H]1[C@@H](C[C@@]2([C@@]1(CC(=O)[C@@]3([C@H]2CC=C4[C@H]3C=C(C(=O)C4(C)C)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)C)C)C)O)O
Numéro ONU 2811
Poids moléculaire 718.83
Reaxy-Rn 6628057
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6628057&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
ClasseSteroids and steroid derivatives
SubclassSteroidal glycosides
Intermediate Tree Nodes Steroidal saponins
Direct ParentCucurbitacin glycosides
Alternative Parents Triterpenoids  Cucurbitacins  Steroid esters  11-oxosteroids  14-alpha-methylsteroids  16-alpha-hydroxysteroids  3-oxo delta-1-steroids  Delta-1-steroids  Hexoses  O-glycosyl compounds  Cyclohexenones  Oxanes  Acyloins  Tertiary alcohols  Acryloyl compounds  Alpha-hydroxy ketones  Enones  Carboxylic acid esters  Secondary alcohols  Cyclic alcohols and derivatives  Oxacyclic compounds  Acetals  Monocarboxylic acids and derivatives  Polyols  Organic oxides  Primary alcohols  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteropolycyclic compounds
Substituents Cucurbitacin glycoside skeleton - Cucurbitacin skeleton - Triterpenoid - 22-oxosteroid - 21-oxosteroid - Steroid ester - 20-hydroxysteroid - Oxosteroid - 3-oxo-delta-1-steroid - Hydroxysteroid - 16-hydroxysteroid - 16-alpha-hydroxysteroid - 11-oxosteroid - 14-alpha-methylsteroid - 3-oxosteroid - Delta-1-steroid - Hexose monosaccharide - Glycosyl compound - O-glycosyl compound - Cyclohexenone - Oxane - Acyloin - Monosaccharide - Tertiary alcohol - Acryloyl-group - Alpha-hydroxy ketone - Alpha,beta-unsaturated ketone - Enone - Cyclic alcohol - Secondary alcohol - Ketone - Cyclic ketone - Carboxylic acid ester - Polyol - Acetal - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organoheterocyclic compound - Oxacycle - Primary alcohol - Carbonyl group - Organooxygen compound - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Alcohol - Aliphatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as cucurbitacin glycosides. These are polycyclic compounds containing a carbohydrate derivative glycosidically linked to a curcubitane nucleus.
External Descriptors beta-D-glucoside - acetate ester - monosaccharide derivative - triterpenoid saponin - cucurbitacin
Structure 3D
Modèle de structure chimique interactif





Cibles associées (humaines)
HCT-8 (3484 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bel-7402 (4577 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HepG2 (196354 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A2780 (11979 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propriétés chimiques et physiques
Point d'éclair (°F)Not applicable
Point d'éclair (°C)Not applicable
Poids moléculaire718.800 g/mol
XLogP31.400
Hydrogen Bond Donor Count6
Hydrogen Bond Acceptor Count13
Rotatable Bond Count9
Exact Mass718.356 Da
Monoisotopic Mass718.356 Da
Topological Polar Surface Area217.000 Ų
Heavy Atom Count51
Formal Charge0
Complexity1580.000
Isotope Atom Count0
Defined Atom Stereocenter Count13
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds1
Covalently-Bonded Unit Count1
Calculateurs de solution
Avis

Avis des clients

Foire aux questions

What is the purity of this product?
This product is supplied at ≥95% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.
How should this product be stored?
Store at ?20 °C. Freezer storage is required to maintain the specified shelf life.
How is this product shipped?
This product ships in an insulated container with ice pads. Unpack on arrival and transfer it to the storage condition stated above.
What are the CAS number, molecular formula and molecular weight?
The CAS Number is 1398-78-3, the molecular formula is C38H54O13, and the molecular weight is 718.83 g/mol. InChIKey QKEJRKXVLGOJMB-YYBMGDPWSA-N.
What documentation is provided?
Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.