(±)-Equol - Moligand™, 10mM in DMSO , Agonist of TAS2R14;Agonist of TAS2R39, CAS No.94105-90-5, Agonist of TAS2R14;Agonist of TAS2R39

CAS: 94105-90-5 Cat. No.: E427011 Formule: C₁₅H₁₄O₃ Poids moléculaire: 242.27 Numéro CE: 618-999-2

GRADE & PURITY Moligand™, 10mM in DMSO

Synonyms

(plusmn)-Equol | Rac-Equol | SR-01000946366 | 2RZ8A7D0E8 | (-)-Cotinine;(S)-Cotinine;NIH-10498 | AUS-131 | MFCD00016662 | (+/-)Equol | (+/-)-Equol | A859575 | Q27255516 | SCHEMBL949461 | Equol, (+/-)- | 3-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-7-ol | 3,

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Specifications

Synonymes

(plusmn)-Equol | Rac-Equol | SR-01000946366 | 2RZ8A7D0E8 | (-)-Cotinine;(S)-Cotinine;NIH-10498 | AUS-131 | MFCD00016662 | (+/-)Equol | (+/-)-Equol | A859575 | Q27255516 | SCHEMBL949461 | Equol, (+/-)- | 3-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-7-ol | 3,

Spécifications et pureté

Moligand™, 10mM in DMSO

Mécanismes biochimiques et physiologiques

Metabolite of daidzein. Weak estrogenic agonist, and competitive inhibitor of 17β-estradiol at the estradiol receptor.

Conditions de stockage de stockage

Store at -80°C

Expédié en

Dry ice packs + Cold packs

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Grade

Moligand™

Type d'action

AGONIST

Mécanisme d'action

Agonist of TAS2R14;Agonist of TAS2R39

Noms et identifiants

• Pubchem Sid: 528753464
• Sourires canoniques: C1C(COC2=C1C=CC(=C2)O)C3=CC=C(C=C3)O
• IUPAC Name: 3-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-7-ol
• InChIKey: ADFCQWZHKCXPAJ-UHFFFAOYSA-N
• INCHI: 1S/C15H14O3/c16-13-4-1-10(2-5-13)12-7-11-3-6-14(17)8-15(11)18-9-12/h1-6,8,12,16-17H,7,9H2
• Isomères SMILES: C1C(COC2=C1C=CC(=C2)O)C3=CC=C(C=C3)O
• CAS alternatif: 94105-90-5；66036-38-2
• Numéro NSC: 670882
• Termes d'entrée MeSH: (+-)-isomer of equol;3' Hydroxy Equol;3'-hydroxy-equol;4' methoxy 7 isoflavanol;4' O Methyl Equol;4'-methoxy-7-isoflavanol;4'-O-methyl equol;6' Hydroxy Equol;6'-hydroxy-equol;equol;Equol, 4'-O-Methyl
• Poids moléculaire: 242.27
• Reaxy-Rn: 87753
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=87753&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Phenylpropanoids and polyketides
    • Classe Isoflavonoids
      • Subclass Isoflavans

• Kingdom: Organic compounds
• Superclass: Phenylpropanoids and polyketides
• Classe: Isoflavonoids
• Subclass: Isoflavans
• Intermediate Tree Nodes: Not available
• Direct Parent: Isoflavanols
• Alternative Parents: Hydroxyisoflavonoids 1-benzopyrans Alkyl aryl ethers 1-hydroxy-2-unsubstituted benzenoids Benzene and substituted derivatives Oxacyclic compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Hydroxyisoflavonoid - Isoflavanol - Chromane - Benzopyran - 1-benzopyran - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Monocyclic benzene moiety - Benzenoid - Ether - Oxacycle - Organoheterocyclic compound - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as isoflavanols. These are polycyclic compounds containing a hydroxylated isoflavan skeleton.
• External Descriptors: Isoflavans

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.

DOI: 10.1186/s13321-016-0174-y

Cibles associées (humaines)

TAS2R39 Tchem Taste receptor type 2 member 39 (0 Activities)

Discover Target: TAS2R39

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

TAS2R14 Tchem Taste receptor type 2 member 14 (0 Activities)

Discover Target: TAS2R14

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

ESR1 Tclin Estrogen receptor alpha (17718 Activities)

Discover Target: ESR1

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

MCF7 (126967 Activities)

Explore this target

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

Cibles associées (non humaines)

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

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

Aorta (2975 Activities)

Explore this target

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

ureB Urease subunit alpha/Urease subunit beta (701 Activities)

Discover Target: ureB

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

Mécanismes d'action

Propriétés chimiques et physiques

• Sensibilité: Moisture sensitive.
• Point de fusion (°C): 175℃
• Poids moléculaire: 242.270 g/mol
• XLogP3: 3.000
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 242.094 Da
• Monoisotopic Mass: 242.094 Da
• Topological Polar Surface Area: 49.700 Ų
• Heavy Atom Count: 18
• Formal Charge: 0
• Complexity: 273.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Références

1. Liu Xiao-Mei, Wang Zi-Hao, Wei Qian-Xue, Song Yang, Ma Xiao-Xin.  (2024)  Equol exerts anti-tumor effects on choriocarcinoma cells by promoting TRIM21-mediated ubiquitination of ANXA2.  Biology Direct,  19  (1): (1-18).  [PMID:39242533] [10.1186/s13062-024-00519-5]

2. Kemin Mao, Xianghong Wang, Yakun Hou, Xiaowei He, Shuo Geng, Faizan Ahmed Sadiq, Yunhe Lian, Yaxin Sang.  (2024)  Integrated network pharmacology and transcriptomic approach reveal the role of equol in reducing colorectal cancer via regulating multiple cell cycle genes in HCT116 cells.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:39461627] [10.1016/j.ijbiomac.2024.136832]