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· · COA & SDS available for every product · Same-day shipping on in-stock items Ganoderol B - ≥97% , CAS No.104700-96-1
Synonyms
(3beta,24E)-Lanosta-7,9(11),24-trien-3,26-diol | HY-N2223 | UNII-Z99BBB5WR6 | (+)-Ganoderol B | (3S,5R,10S,13R,14R,17R)-17-((E,2R)-7-HYDROXY-6-METHYLHEPT-5-EN-2-YL)-4,4,10,13,14-PENTAMETHYL-2,3,5,6,12,15,16,17-OCTAHYDRO-1H-CYCLOPENTA(A)PHENANTHREN-3-OL |
Storage
Protected from light,Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Why this grade ≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Protected from light,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.
Overview Ganoderol B is a potent α-glucosidase inhibitor. Ganoderol B has high α-glucosidase inhibition with an IC 50 of 48.5 μg/mL (119.8 μM).
Form:Solid
Specifications Synonyms
(3beta, 24E)-Lanosta-7, 9(11), 24-trien-3, 26-diol | HY-N2223 | UNII-Z99BBB5WR6 | (+)-Ganoderol B | (3S, 5R, 10S, 13R, 14R, 17R)-17-((E, 2R)-7-HYDROXY-6-METHYLHEPT-5-EN-2-YL)-4, 4, 10, 13, 14-PENTAMETHYL-2, 3, 5, 6, 12, 15, 16, 17-OCTAHYDRO-1H-CYCLOPENTA(A)PHENANTHREN-3-OL |
Specifications & Purity
≥97%
Biochemical and Physiological Mechanisms
Ganoderol B is a potent α-glucosidase inhibitor. Ganoderol B has high α-glucosidase inhibition with an IC 50 of 48.5 μg/mL (119.8 μM).
Storage
Protected from light, Store at -80°C
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(CCC=C(C)CO)C1CCC2(C1(CC=C3C2=CCC4C3(CCC(C4(C)C)O)C)C)C IUPAC Name (3S,5R,10S,13R,14R,17R)-17-[(E,2R)-7-hydroxy-6-methylhept-5-en-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-3-ol InChIKey AOXXVRDKZLRGTJ-AZIDVCJLSA-N INCHI 1S/C30H48O2/c1-20(19-31)9-8-10-21(2)22-13-17-30(7)24-11-12-25-27(3,4)26(32)15-16-28(25,5)23(24)14-18-29(22,30)6/h9,11,14,21-22,25-26,31-32H,8,10,12-13,15-19H2,1-7H3/b20-9+/t21-,22-,25+,26+,28-,29-,30+/m1/s1 Isomeric SMILES C[C@H](CC/C=C(\C)/CO)[C@H]1CC[C@@]2([C@@]1(CC=C3C2=CC[C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)C)C Alternate CAS 104700-96-1 PubChem CID 13934286 MeSH Entry Terms ganoderol B Molecular Weight 440.70
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 Dihydroxy bile acids, alcohols and derivatives 3-hydroxy delta-7-steroids 3-beta-hydroxysteroids 14-alpha-methylsteroids Delta-7-steroids Fatty alcohols Secondary alcohols Cyclic alcohols and derivatives Primary alcohols Hydrocarbon derivatives Molecular Framework Aliphatic homopolycyclic compounds Substituents Triterpenoid - 26-hydroxysteroid - Dihydroxy bile acid, alcohol, or derivatives - Hydroxy bile acid, alcohol, or derivatives - Cholane-skeleton - Bile acid, alcohol, or derivatives - 3-hydroxy-delta-7-steroid - 3-hydroxysteroid - 14-alpha-methylsteroid - Hydroxysteroid - 3-beta-hydroxysteroid - Delta-7-steroid - Steroid - Fatty alcohol - Fatty acyl - Cyclic alcohol - Secondary alcohol - Hydrocarbon derivative - Alcohol - Organooxygen compound - Primary alcohol - Organic oxygen compound - 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 Not available 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 Molecular Weight 440.700 g/mol XLogP3 7.400 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 5 Exact Mass 440.365 Da Monoisotopic Mass 440.365 Da Topological Polar Surface Area 40.500 Ų Heavy Atom Count 32 Formal Charge 0 Complexity 832.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 7 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 1 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 1 Covalently-Bonded Unit Count 1
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