Gypenoside XLIX - ≥95% , CAS No.94987-08-3

CAS: 94987-08-3 Cat. No.: G414354 Peso molecular: 1047.23 PubChem CID: 16007240
Disponible para pedir
GRADE & PURITY ≥95%
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
Protected from light,Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5mg
G414354-5mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
93,90US$
25mg
G414354-25mg
4
359,90US$
50mg
G414354-50mg
2
565,90US$
100mg
G414354-100mg
2
899,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

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

🌡

Storage & shipping

Protected from light,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 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.

Gypenoside XLIX, a dammarane-type glycoside, is a prominent component of G. pentaphyllum. Gypenoside XLIX is a selective peroxisome proliferator-activated receptor (PPAR)-alpha activator and inhibits cytokine-induced vascular cell adhesion molecule-1 (VCAM-1) overexpression and hyperactivity in human endothelial cells


Application
Gypenoside XLIX is a naturally occurring gynosaponin inhibits NF-κB activation via a PPAR-α-dependent pathway.

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
≥95%
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
Protected from light, Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Tipo de acción
ACTIVATOR
Pureza
≥95%
Nombres e identificadores
Pubchem Sid504768005
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504768005
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:

Find and download the COA for your product by matching the lot number on the packaging.

6 results found

Lot NumberCertificate TypeFechaArticulo
F2317030Certificate of AnalysisApr 02, 2026 G414354
F2317034Certificate of AnalysisApr 02, 2026 G414354
F2317035Certificate of AnalysisApr 02, 2026 G414354
F2317036Certificate of AnalysisApr 02, 2026 G414354
F2317131Certificate of AnalysisApr 02, 2026 G414354
F2317154Certificate of AnalysisApr 02, 2026 G414354
Propiedades químicas y físicas
SolubilidadDMSO : 125 mg/mL (119.36 mM; Need ultrasonic)
SensibilidadLight sensitive
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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