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· · COA & SDS available for every product · Same-day shipping on in-stock items (20S)-Protopanaxatriol - 10mM in DMSO , CAS No.34080-08-5
GRADE & PURITY 10mM in DMSO
Synonyms
(20S)-Protopanaxatriol|34080-08-5|Protopanaxatriol|Protopanaxtriol|20(S)-protopanaxatriol|20S-Protopanaxatriol|g-PPT|ZMK19P3WMP|20(S)-APPT|CHEBI:75951|dammar-24-ene-3beta,6alpha,12beta,20-tetrol|(3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-17-[(2S)-2-hydroxy-6-me
Shipped In
Dry ice packs + Cold packs
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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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
(20S)-Protopanaxatriol | 34080-08-5 | Protopanaxatriol | Protopanaxtriol | 20(S)-protopanaxatriol | 20S-Protopanaxatriol | g-PPT | ZMK19P3WMP | 20(S)-APPT | CHEBI:75951 | dammar-24-ene-3beta, 6alpha, 12beta, 20-tetrol | (3S, 5R, 6S, 8R, 9R, 10R, 12R, 13R, 14R, 17S)-17-[(2S)-2-hydroxy-6-me
Specifications & Purity
10mM in DMSO
Biochemical and Physiological Mechanisms
Ginsenoside Rg1 , Re, Rf and Rg2 analog. Increases intracellular Ca 2+ levels. Induces eNOS activation and NO production. Functional GR and ERβ receptor ligand. Active in vivo.
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Canonical Smiles CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CC(C4C3(CCC(C4(C)C)O)C)O)C)O)C)O)C IUPAC Name (3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-17-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,6,12-triol InChIKey SHCBCKBYTHZQGZ-CJPZEJHVSA-N INCHI 1S/C30H52O4/c1-18(2)10-9-13-30(8,34)19-11-15-28(6)24(19)20(31)16-22-27(5)14-12-23(33)26(3,4)25(27)21(32)17-29(22,28)7/h10,19-25,31-34H,9,11-17H2,1-8H3/t19-,20+,21-,22+,23-,24-,25-,27+,28+,29+,30-/m0/s1 Isomeric SMILES CC(=CCC[C@@](C)([C@H]1CC[C@@]2([C@@H]1[C@@H](C[C@H]3[C@]2(C[C@@H]([C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)O)C)O)C)O)C Molecular Weight 476.73 Reaxy-Rn 48405371 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=48405371&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 Kingdom Organic compounds Superclass Lipids and lipid-like molecules Class Prenol lipids Subclass Triterpenoids Intermediate Tree Nodes Not available Direct Parent Triterpenoids Alternative Parents 6-hydroxysteroids 3-beta-hydroxysteroids 14-alpha-methylsteroids 12-hydroxysteroids Tertiary alcohols Secondary alcohols Cyclic alcohols and derivatives Polyols Hydrocarbon derivatives Molecular Framework Aliphatic homopolycyclic compounds Substituents Triterpenoid - 20-hydroxysteroid - 3-hydroxysteroid - 12-hydroxysteroid - 6-hydroxysteroid - Hydroxysteroid - 14-alpha-methylsteroid - 3-beta-hydroxysteroid - Steroid - Cyclic alcohol - Tertiary alcohol - Secondary alcohol - Polyol - Organooxygen compound - Alcohol - Organic oxygen compound - Hydrocarbon derivative - Aliphatic homopolycyclic compound Description This compound belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. External Descriptors 3beta-hydroxy steroid - 6alpha-hydroxy steroid - tetracyclic triterpenoid - sapogenin - 12beta-hydroxy steroid Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Sensitivity light sensitive Molecular Weight 476.700 g/mol XLogP3 5.900 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 4 Exact Mass 476.387 Da Monoisotopic Mass 476.387 Da Topological Polar Surface Area 80.900 Ų Heavy Atom Count 34 Formal Charge 0 Complexity 817.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 11 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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