Basic Description

Synonyms	7-hydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one;hydrate \| MLS002695944 \| CHEBI:73111 \| AKOS025310104 \| Esculetin-6-beta-D-glucopyranoside \| CCG-207863 \| Esculin Sesquihydrate min. 97.5%, DAB, for biochemistry \| M
Specifications & Purity	for microbiology
Storage Temp	Room temperature
Shipped In	Normal
Grade	for microbiology

Associated Targets(Human)

ERAP2 Tchem Endoplasmic reticulum aminopeptidase 2 (387 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ERAP1 Tchem Endoplasmic reticulum aminopeptidase 1 (581 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GMNN Tbio Geminin (128009 Activities)

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ATXN2 Tbio Ataxin-2 (54410 Activities)

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RAN Tchem GTP-binding nuclear protein Ran/Importin subunit beta-1/Snurportin-1 (21853 Activities)

Discover Target: RAN

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)

Discover Target: Txnrd1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Names and Identifiers

IUPAC Name	7-hydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one;hydrate
INCHI	InChI=1S/C15H16O9.H2O/c16-5-10-12(19)13(20)14(21)15(24-10)23-9-3-6-1-2-11(18)22-8(6)4-7(9)17;/h1-4,10,12-17,19-21H,5H2;1H2/t10-,12-,13+,14-,15-;/m1./s1
InChi Key	CQYPGSKIFJFVDQ-QWFKVUSTSA-N
Canonical SMILES	C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O.O
Isomeric SMILES	C1=CC(=O)OC2=CC(=C(C=C21)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)O.O
Alternate CAS	531-75-9
PubChem CID	16211025
Molecular Weight	367.31

Certificates

Certificate of Analysis(COA)

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1 results found

Lot Number	Certificate Type	Date	Item
F2328995	Certificate of Analysis	Jun 15, 2023	E433254

Chemical and Physical Properties

Melt Point(°C)	204-206°C

Citations of This Product

1. Yong-Yu Yang, Jing-Jing Qi, Si-Yi Jiang, Ling Ye. (2023) Esculin ameliorates obesity-induced insulin resistance by improving adipose tissue remodeling and activating the IRS1/PI3K/AKT/GLUT4 pathway. JOURNAL OF ETHNOPHARMACOLOGY, (6): (117251). [PMID:37778516]
2. Jiangwei Ni, Ge Li, Ningfeng Dai, Zijiao Quan, Haibin Tong, Yu Liu. (2023) Esculin alleviates LPS-induced acute lung injury via inhibiting neutrophil recruitment and migration. INTERNATIONAL IMMUNOPHARMACOLOGY, 119 (110177). [PMID:37068336]

References

1. Yong-Yu Yang, Jing-Jing Qi, Si-Yi Jiang, Ling Ye. (2023) Esculin ameliorates obesity-induced insulin resistance by improving adipose tissue remodeling and activating the IRS1/PI3K/AKT/GLUT4 pathway. JOURNAL OF ETHNOPHARMACOLOGY, (6): (117251). [PMID:37778516]
2. Jiangwei Ni, Ge Li, Ningfeng Dai, Zijiao Quan, Haibin Tong, Yu Liu. (2023) Esculin alleviates LPS-induced acute lung injury via inhibiting neutrophil recruitment and migration. INTERNATIONAL IMMUNOPHARMACOLOGY, 119 (110177). [PMID:37068336]

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Esculin - suitable for microbiology, high purity , CAS No.66778-17-4