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Ganoderic acid Y - 99%, high purity , CAS No.86377-52-8

≥99%

CAS#: 86377-52-8
Formula: C₃₀H₄₆O₃
Molecular Weight: 454.68
PubChem CID: 57397445

Item Number

G647656

Grouped product items
SKU	Size	Availability	Price	Qty
G647656-1mg	1mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$600.90

Terpenoids Triterpenes

View related series

Anti-infection Enterovirus Glucosidase Metabolic Enzyme/Protease Terpenoids Triterpenes

Basic Description

Synonyms	Ganoderic Acid Y\|86377-52-8\|CHEMBL1915760\|Lanosta-7,9(11),24-trien-26-oic acid, 3-hydroxy-, (3beta,24E)-\|CHEBI:172035\|DTXSID501316796\|BDBM50356919\|AKOS040760414\|MS-28287\|HY-125713\|CS-0093392\|(E,6R)-6-[(3S,5R,10S,13R,14R,17R)-3-hydroxy-4,4,10,13,14-pentame
Specifications & Purity	≥99%
Biochemical and Physiological Mechanisms	Ganoderic acid Y is a α-glucosidase inhibitor with an IC 50 of 170 μM for yeast α-glucosidase. Ganoderic acid Y inhibits enterovirus 71 (EV71) replication through blocking EV71 uncoating.
Storage Temp	Protected from light,Store at -80°C
Shipped In	Ice chest + Ice pads
Product Description	Ganoderic acid Y is a α-glucosidase inhibitor with an IC 50 of 170 μM for yeast α-glucosidase. Ganoderic acid Y inhibits enterovirus 71 (EV71) replication through blocking EV71 uncoating. In Vitro Ganoderic acid Y significantly inhibits the replication of the viral RNA (vRNA) of EV71. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Form:Solid

Associated Targets

HMGCR Tclin 3-hydroxy-3-methylglutaryl-coenzyme A reductase 0 Activities

Discover Target: HMGCR

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

GAA Tclin Lysosomal alpha-glucosidase 0 Activities

Discover Target: GAA

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

ACHE Tclin Acetylcholinesterase 0 Activities

Discover Target: ACHE

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SI Tchem Sucrase-isomaltase, intestinal 0 Activities

Discover Target: SI

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

BCHE Tclin Cholinesterase 0 Activities

Discover Target: BCHE

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

Names and Identifiers

IUPAC Name	(E,6R)-6-[(3S,5R,10S,13R,14R,17R)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylhept-2-enoic acid
INCHI	InChI=1S/C30H46O3/c1-19(9-8-10-20(2)26(32)33)21-13-17-30(7)23-11-12-24-27(3,4)25(31)15-16-28(24,5)22(23)14-18-29(21,30)6/h10-11,14,19,21,24-25,31H,8-9,12-13,15-18H2,1-7H3,(H,32,33)/b20-10+/t19-,21-,24+,25+,28-,29-,30+/m1/s1
InChi Key	HUTCYUJPLOTDMX-SPPZYOJVSA-N
Canonical SMILES	CC(CCC=C(C)C(=O)O)C1CCC2(C1(CC=C3C2=CCC4C3(CCC(C4(C)C)O)C)C)C
Isomeric SMILES	C[C@H](CC/C=C(\C)/C(=O)O)[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	86377-52-8
PubChem CID	57397445
MeSH Entry Terms	ganoderic acid Y
Molecular Weight	454.68

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