Obtusin - Moligand™,≥98% , CAS No.70588-05-5

CAS: 70588-05-5 Cat. No.: O649260 Formula: C₁₈H₁₆O₇ Peso molecolare: 344.32

QUALITÀ & PUREZZA Moligand™, ≥98%

Synonyms

1,7-Dihydroxy-2,3,8-trimethoxy-6-methylanthracene-9,10-dioneObtusin|9,10-Anthracenedione, 1,7-dihydroxy-2,3,8-trimethoxy-6-methyl-|1,7-dihydroxy-2,3,8-trimethoxy-6-methylanthracene-9,10-dione|Obtusin|1,7-Dihydroxy-2,3,8-trimethoxy-6-methylanthracene-9,10-dion|1,7-dihydroxy-2,3,8-trimethoxy-6-methylanthraquinone

Storage

Protected from light,Store at -20°C

Shipped In

Ice chest + Ice pads

Panoramica

Obtusin, isolated from Cassia obtusifolia Linn seed, is a highly selective and competitive human monoamine oxidase-A (hMAO-A) inhibitor with an IC 50 of 11.12 μM and a K i of 6.15 μM. Obtusin plays a preventive role in neurodegenerative diseases, especially anxiety and depression

Form:Solid

IC50& Target:IC50: 11.12 μM (hMAO-A), Ki: 6.15 (hMAO-A)

Specifiche

Sinonimi

1,7-Dihydroxy-2,3,8-trimethoxy-6-methylanthracene-9,10-dioneObtusin | 9,10-Anthracenedione, 1,7-dihydroxy-2,3,8-trimethoxy-6-methyl- | 1,7-dihydroxy-2,3,8-trimethoxy-6-methylanthracene-9,10-dione | Obtusin | 1,7-Dihydroxy-2,3,8-trimethoxy-6-methylanthracene-9,10-dion | 1,7-dihydroxy-2,3,8-trimethoxy-6-methylanthraquinone

Specifiche e purezza

Moligand™,≥98%

Meccanismi biochimici e fisiologici

Obtusin, isolated from Cassia obtusifolia Linn seed, is a highly selective and competitive human monoamine oxidase-A (hMAO-A) inhibitor with an IC 50 of 11.12 μM and a K i of 6.15 μM. Obtusin plays a preventive role in neurodegenerative diseases, especial

Condizioni di conservazione di stoccaggio

Protected from light,Store at -20°C

Spedito in

Ice chest + Ice pads

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

Grado

Moligand™

Tipo di azione

INHIBITOR

Purezza

≥98%

Nomi e identificatori

Pubchem Sid

528770119

Sorrisi canonici

CC1=CC2=C(C(=C1O)OC)C(=O)C3=C(C(=C(C=C3C2=O)OC)OC)O

IUPAC Name

1,7-dihydroxy-2,3,8-trimethoxy-6-methylanthracene-9,10-dione

InChIKey

CFLNHFUPWNRWJA-UHFFFAOYSA-N

INCHI

1S/C18H16O7/c1-7-5-8-12(18(25-4)13(7)19)15(21)11-9(14(8)20)6-10(23-2)17(24-3)16(11)22/h5-6,19,22H,1-4H3

Isomeri SMILES

CC1=CC2=C(C(=C1O)OC)C(=O)C3=C(C(=C(C=C3C2=O)OC)OC)O

CAS alternativo

70588-05-5

Peso molecolare

344.32

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Anthracenes
      • Subclass Anthraquinones

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Anthracenes
• Subclass: Anthraquinones
• Intermediate Tree Nodes: Not available
• Direct Parent: Hydroxyanthraquinones
• Alternative Parents: Aryl ketones Anisoles Alkyl aryl ethers 1-hydroxy-4-unsubstituted benzenoids Vinylogous acids Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: Hydroxyanthraquinone - Aryl ketone - Anisole - 1-hydroxy-4-unsubstituted benzenoid - Alkyl aryl ether - Vinylogous acid - Ketone - Ether - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as hydroxyanthraquinones. These are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group.
• External Descriptors: Anthraquinone type

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)

EPHX2 Tchem Epoxide hydratase (3844 Activities)

Discover Target: EPHX2

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: DMSO : 5 mg/mL (14.52 mM; ultrasonic and warming and heat to 60°C)
• Sensibilità: light sensitive
• Punto di fusione (°C): 244.5-246.0°C
• Peso molecolare: 344.300 g/mol
• XLogP3: 3.000
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 3
• Exact Mass: 344.09 Da
• Monoisotopic Mass: 344.09 Da
• Topological Polar Surface Area: 102.000 Ų
• Heavy Atom Count: 25
• Formal Charge: 0
• Complexity: 536.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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