3-O-Methyl Estradiol - Moligand™, ≥98% , Channel blocker of TRPML1;Inhibitor of TRPML1;Inhibitor of TRPML2;Inhibitor of TRPML3, CAS No.1035-77-4, Channel blocker of TRPML1;Inhibitor of TRPML1;Inhibitor of TRPML2;Inhibitor of TRPML3

CAS: 1035-77-4 Cat. No.: E610190 Formula: C₁₉H₂₆O₂ Peso molecolare: 286.41 Numero EC: 213-858-8

GRADE & PURITY Moligand™, ≥98%

Synonyms

3-Methoxyoestradiol | NSC 58851 | 3-Methoxyestradiol | 17beta-Estradiol 3-methyl ether | Oestradiol 3-methyl ether | 3-O-Methyl Estradiol | 3-Methoxy-13β-methyl-1,3,5(10)-gonatrien-17β-ol | 17β)-3-Methoxyestra-1,3,5(10)-trien-17-ol | 3-O-Methylestradiol

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Sinonimi

3-Methoxyoestradiol | NSC 58851 | 3-Methoxyestradiol | 17beta-Estradiol 3-methyl ether | Oestradiol 3-methyl ether | 3-O-Methyl Estradiol | 3-Methoxy-13β-methyl-1,3,5(10)-gonatrien-17β-ol | 17β)-3-Methoxyestra-1,3,5(10)-trien-17-ol | 3-O-Methylestradiol

Specifiche e purezza

Moligand™, ≥98%

Condizioni di conservazione di stoccaggio

Store at 2-8°C

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Grado

Moligand™

Tipo di azione

CHANNEL BLOCKER, INHIBITOR

Meccanismo d'azione

Channel blocker of TRPML1;Inhibitor of TRPML1;Inhibitor of TRPML2;Inhibitor of TRPML3

Purezza

≥98%

Nomi e identificatori

• Pubchem Sid: 508817275
• Sorrisi canonici: CC12CCC3C(C1CCC2O)CCC4=C3C=CC(=C4)OC
• IUPAC Name: (8R,9S,13S,14S,17S)-3-methoxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-ol
• InChIKey: ULAADVBNYHGIBP-GFEQUFNTSA-N
• INCHI: 1S/C19H26O2/c1-19-10-9-15-14-6-4-13(21-2)11-12(14)3-5-16(15)17(19)7-8-18(19)20/h4,6,11,15-18,20H,3,5,7-10H2,1-2H3/t15-,16-,17+,18+,19+/m1/s1
• Isomeri SMILES: C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2O)CCC4=C3C=CC(=C4)OC
• WGK Germania: 2
• CAS alternativo: 94535-16-7,1035-77-4
• Numero NSC: 58851
• Termini MeSH: 3-methoxy-17 beta-estradiol;E2 methyl;estradiol-17 beta-3-methyl ether;estradiol-17 beta-3-methyl ether, ((13alpha,17alpha)-(+-))-isomer;estradiol-17 beta-3-methyl ether, ((13alpha,17beta)-(+-))-isomer;estradiol-17 beta-3-methyl ether, ((14beta,17alpha)-(
• Peso molecolare: 286.41
• Reaxy-Rn: 1914697
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1914697&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Classe Steroids and steroid derivatives
      • Subclass Estrane steroids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Classe: Steroids and steroid derivatives
• Subclass: Estrane steroids
• Intermediate Tree Nodes: Not available
• Direct Parent: Estrane steroids
• Alternative Parents: 17-hydroxysteroids Phenanthrenes and derivatives Tetralins Anisoles Alkyl aryl ethers Secondary alcohols Cyclic alcohols and derivatives Hydrocarbon derivatives
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: 17-hydroxysteroid - Estrane-skeleton - Hydroxysteroid - Phenanthrene - Tetralin - Anisole - Alkyl aryl ether - Benzenoid - Cyclic alcohol - Secondary alcohol - Ether - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Aromatic homopolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as estrane steroids. These are steroids with a structure based on the estrane skeleton.
• 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.

DOI: 10.1186/s13321-016-0174-y

Obiettivi associati (umani)

MCOLN2 Tchem Mucolipin-2 (0 Activities)

Discover Target: MCOLN2

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

MCOLN1 Tchem Mucolipin-1 (0 Activities)

Discover Target: MCOLN1

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

MCOLN3 Tchem Mucolipin-3 (0 Activities)

Discover Target: MCOLN3

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

SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)

Discover Target: SLCO1B1

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Punto di infiammabilità (°F): 35.6 °F
• Punto di infiammabilità (°C): 2 °C
• Peso molecolare: 286.400 g/mol
• XLogP3: 3.000
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 286.193 Da
• Monoisotopic Mass: 286.193 Da
• Topological Polar Surface Area: 29.500 Ų
• Heavy Atom Count: 21
• Formal Charge: 0
• Complexity: 395.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 5
• 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