Gypenoside XLIX - 10mM in DMSO , CAS No.94987-08-3

CAS: 94987-08-3 Cat. No.: G580410 Peso molecular: 1047.23 PubChem CID: 16007240
Disponible para pedir
GRADE & PURITY 10mM in DMSO
Synonyms
Dammar-​24-​en-​19-​al,3-​[(O-​6-​deoxy-​α-​L-​mannopyranosyl-​(1→2)​-​O-​[β-​D-​xylopyranosyl-​(1→3)​]​-​α-​L-​arabinopyranosyl)​oxy]​-​21-​(β-​D-​glucopyranosyloxy)​-​20-​hydroxy-​,(3β)​-
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1ml
G580410-1ml
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
189,90US$
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Information

Gypenoside XLIX Gypenoside XLIX, a naturally occurring gynosaponin, is a selective peroxisome proliferator-activated receptor (PPAR)-alpha activator.

Specifications

Sinónimos
Dammar-​24-​en-​19-​al, 3-​[(O-​6-​deoxy-​α-​L-​mannopyranosyl-​(1→2)​-​O-​[β-​D-​xylopyranosyl-​(1→3)​]​-​α-​L-​arabinopyranosyl)​oxy]​-​21-​(β-​D-​glucopyranosyloxy)​-​20-​hydroxy-​, (3β)​-
Especificaciones y pureza
10mM in DMSO
Mecanismos bioquímicos y fisiológicos
Gypenoside XLIX, a naturally occurring gynosaponin, is a selective peroxisome proliferator-activated receptor (PPAR)-alpha activator.
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores
Sonrisas canónicasCC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C5CCC6C(CCC6(C5(CCC4C3(C)C)C)C)C(CCC=C(C)C)(COC7C(C(C(C(O7)CO)O)O)O)O)C=O)O)OC8C(C(C(CO8)O)O)O)O)O)O
IUPAC Name(3S,5S,8R,9S,10S,13R,14R,17S)-17-[(2S)-2-hydroxy-6-methyl-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhept-5-en-2-yl]-3-[(2S,3R,4S,5S)-5-hydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,4,8,14-tetramethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde
InChIKeyAFEVCSJFNQWWDF-AZFNEDKCSA-N
INCHI1S/C52H86O21/c1-24(2)9-8-15-52(65,23-68-45-40(63)38(61)36(59)30(19-53)70-45)27-12-16-49(6)26(27)10-11-32-50(49,7)17-13-31-48(4,5)33(14-18-51(31,32)22-54)71-47-43(73-46-41(64)37(60)34(57)25(3)69-46)42(29(56)21-67-47)72-44-39(62)35(58)28(55)20-66-44/h9,22,25-47,53,55-65H,8,10-21,23H2,1-7H3/t25-,26+,27-,28+,29-,30+,31-,32-,33-,34-,35-,36+,37+,38-,39+,40+,41+,42-,43+,44-,45+,46-,47-,49+,50+,51+,52+/m0/s1
Isómeros SMILES C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@@H]2[C@H]([C@H](CO[C@H]2O[C@H]3CC[C@@]4([C@H]5CC[C@@H]6[C@H](CC[C@]6([C@@]5(CC[C@H]4C3(C)C)C)C)[C@@](CCC=C(C)C)(CO[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)CO)O)O)O)O)C=O)O)O[C@H]8[C@@H]([C@H]([C@@H](CO8)O)O)O)O)O)O
PubChem CID 16007240
Peso molecular 1047.23

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
ClasePrenol lipids
SubclassTerpene glycosides
Intermediate Tree Nodes Triterpene glycosides
Direct ParentTriterpene saponins
Alternative Parents Triterpenoids  Steroidal glycosides  19-oxosteroids  14-alpha-methylsteroids  Hydroxysteroids  Fatty acyl glycosides of mono- and disaccharides  Alkyl glycosides  Disaccharides  O-glycosyl compounds  Oxanes  Tertiary alcohols  Secondary alcohols  Polyols  Acetals  Oxacyclic compounds  Hydrocarbon derivatives  Primary alcohols  Aldehydes  Organic oxides  
Molecular FrameworkAliphatic heteropolycyclic compounds
Substituents Triterpene saponin - Triterpenoid - Steroidal glycoside - 20-hydroxysteroid - 19-oxosteroid - Hydroxysteroid - 14-alpha-methylsteroid - Oxosteroid - Steroid - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - O-glycosyl compound - Disaccharide - Glycosyl compound - Fatty acyl - Oxane - Tertiary alcohol - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Primary alcohol - Alcohol - Organic oxygen compound - Organic oxide - Carbonyl group - Organooxygen compound - Aldehyde - Hydrocarbon derivative - Aliphatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as triterpene saponins. These are glycosylated derivatives of triterpene sapogenins. The sapogenin moiety backbone is usually based on the oleanane, ursane, taraxastane, bauerane, lanostane, lupeol, lupane, dammarane, cycloartane, friedelane, hopane, 9b,19-cyclo-lanostane, cycloartane, or cycloartanol skeleton.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
SolubilidadSolubility (25°C) In vitro DMSO: 100 mg/mL (95.49 mM);    
Peso molecular1047.200 g/mol
XLogP30.400
Hydrogen Bond Donor Count12
Hydrogen Bond Acceptor Count21
Rotatable Bond Count15
Exact Mass1046.57 Da
Monoisotopic Mass1046.57 Da
Topological Polar Surface Area334.000 Ų
Heavy Atom Count73
Formal Charge0
Complexity1910.000
Isotope Atom Count0
Defined Atom Stereocenter Count27
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Jiayi Gu, Manhui Zhu, Lele Li, Xin Cao, Xiaoli Yu, Xiaobo Huang, Lili Huang, Qi Cai, Yan Zhu, Wendie Li, Yong Wang.  (2026)  Gypenoside XLIX ameliorates diabetic retinopathy by downregulating prostaglandin-endoperoxide synthase 2 in retinal pigment epithelium cells to inhibit ferroptosis and preserve tight junction integrity.  Frontiers in Pharmacology,      [PMID:41948729] [10.3389/fphar.2026.1777313]
Calculadoras de soluciones
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