Phloracetophenone - 10mM in DMSO , CAS No.480-66-0

CAS: 480-66-0 Cat. No.: P424177 Fórmula: C₈H₈O₄ Peso molecular: 168.15 Beilstein Registry Number: 1911197 Número CE: 207-556-5 PubChem CID: 68073

GRAU & PUREZA 10mM in DMSO

Synonyms

BDBM50249070 | 2-Acetylphloroglucinol | CK2566 | NSC 54927 | SCHEMBL105416 | Acetophenone, 2',4',6'-trihydroxy- (8CI) | InChI=1/C8H8O4/c1-4(9)8-6(11)2-5(10)3-7(8)12/h2-3,10-12H,1H | BRD-K64824948-001-02-2 | Phloracetophenone | 2',6'-Trihydroxyacetophenone

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Visão geral

Information

Phloracetophenone Phloracetophenone, or 2,4,6-trihydroxyacetophenone (THA), the aglycone component of phloracetophenone glucoside, is a naturally occurring compound obtained from the rhizome of Curcuma comosa (Family Zingiberaceae). Phloracetophenone can stimulate CYP7A1 activity. Phloracetophenone induces cholestasis in rats mediated through Mrp2.

Especificações

Sinónimos

BDBM50249070 | 2-Acetylphloroglucinol | CK2566 | NSC 54927 | SCHEMBL105416 | Acetophenone, 2',4',6'-trihydroxy- (8CI) | InChI=1/C8H8O4/c1-4(9)8-6(11)2-5(10)3-7(8)12/h2-3,10-12H,1H | BRD-K64824948-001-02-2 | Phloracetophenone | 2',6'-Trihydroxyacetophenone

Especificações e pureza

10mM in DMSO

Mecanismos bioquímicos e fisiológicos

Phloracetophenone, or 2,4,6-trihydroxyacetophenone (THA), the aglycone component of phloracetophenone glucoside, is a naturally occurring compound obtained from the rhizome of Curcuma comosa (Family Zingiberaceae). Phloracetophenone can stimulate CYP7A1 a

Condições de armazenamento de armazenamento

Store at -80°C

Enviado em

Dry ice packs + Cold packs

Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.

Nomes e identificadores

Pubchem Sid

528775438

Sorrisos canónicos

CC(=O)C1=C(C=C(C=C1O)O)O

IUPAC Name

1-(2,4,6-trihydroxyphenyl)ethanone

InChIKey

XLEYFDVVXLMULC-UHFFFAOYSA-N

INCHI

1S/C8H8O4/c1-4(9)8-6(11)2-5(10)3-7(8)12/h2-3,10-12H,1H3

SMILES isoméricas

CC(=O)C1=C(C=C(C=C1O)O)O

WGK Alemanha

3

RTECS

AN0528000

CAS alternativo

249278-28-2

PubChem CID

68073

Peso molecular

168.15

Beilstein

1911197

Reaxy-Rn

1911197

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Carbonyl compounds
        • Level5 Ketones
          • Level6 Aryl ketones
            • Level7 Phenylketones
              • Level8 Alkyl-phenylketones

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Carbonyl compounds
• Intermediate Tree Nodes: Ketones - Aryl ketones - Phenylketones
• Direct Parent: Alkyl-phenylketones
• Alternative Parents: Acylphloroglucinols and derivatives Acetophenones Benzoyl derivatives Aryl alkyl ketones 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Vinylogous acids Polyols Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Alkyl-phenylketone - Acylphloroglucinol derivative - Acetophenone - Phloroglucinol derivative - Benzenetriol - Aryl alkyl ketone - Benzoyl - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Benzenoid - Monocyclic benzene moiety - Vinylogous acid - Polyol - Hydrocarbon derivative - Organic oxide - Aromatic homomonocyclic compound
• Descrição: This compound belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.
• External Descriptors: methyl ketone - aromatic ketone - benzenetriol

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

Alvos associados (humanos)

SRC Tclin Tyrosine-protein kinase SRC (10310 Activities)

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CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

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HL-60 (67320 Activities)

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HT-29 (80576 Activities)

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LoVo (4724 Activities)

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PC-3 (62116 Activities)

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SK-MEL-28 (48833 Activities)

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U-937 (7138 Activities)

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A549 (127892 Activities)

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MIA PaCa-2 (5949 Activities)

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HCT-116 (91556 Activities)

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HeLa (62764 Activities)

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SLC28A3 Tchem Solute carrier family 28 member 3 (29 Activities)

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HPGD Tchem 15-hydroxyprostaglandin dehydrogenase [NAD+] (24926 Activities)

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

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SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)

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USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)

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MEN1 Tchem Menin/Histone-lysine N-methyltransferase MLL (48157 Activities)

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Alvos associados (não humanos)

Plasmodium falciparum (966862 Activities)

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Crotalus adamanteus (3 Activities)

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Mecanismos de ação

Propriedades químicas e físicas

• Ponto de fusão (°C): 218-222°C
• Peso molecular: 168.150 g/mol
• XLogP3: 1.100
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• Exact Mass: 168.042 Da
• Monoisotopic Mass: 168.042 Da
• Topological Polar Surface Area: 77.800 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 168.000
• 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