CAS 4651-67-6
:Ácido 7-cetolitocólico
Descrição:
Ácido 7-cetolitocólico é um derivado de ácido biliar que desempenha um papel no metabolismo de lipídios e na regulação dos níveis de colesterol no corpo. É caracterizado pelo seu grupo funcional cetona na posição C7 do núcleo esteroide, o que o distingue de outros ácidos biliares. Este composto é tipicamente encontrado na bile de certos animais e está envolvido na emulsificação de gorduras dietéticas, facilitando sua absorção nos intestinos. Sua estrutura inclui uma espinha dorsal esteroide hidrofóbica, que contribui para sua natureza anfipática, permitindo que interaja tanto com lipídios quanto com água. Ácido 7-cetolitocólico também pode exibir atividades biológicas, incluindo efeitos potenciais no metabolismo de lipídios e na microbiota intestinal. Como um ácido biliar, está sujeito à circulação entero-hepática, influenciando sua concentração e atividade no trato gastrointestinal. Compreender suas propriedades e funções é importante para a pesquisa em saúde gastrointestinal e distúrbios metabólicos.
Fórmula:C24H38O4
InChI:InChI=1S/C24H38O4/c1-14(4-7-21(27)28)17-5-6-18-22-19(9-11-24(17,18)3)23(2)10-8-16(25)12-15(23)13-20(22)26/h14-19,22,25H,4-13H2,1-3H3,(H,27,28)/t14-,15+,16-,17-,18+,19+,22+,23+,24-/m1/s1
Chave InChI:InChIKey=DXOCDBGWDZAYRQ-AURDAFMXSA-N
SMILES:C[C@@]12[C@]([C@]3([C@@]([C@]4(C)[C@](CC3=O)(C[C@H](O)CC4)[H])(CC1)[H])[H])(CC[C@@]2([C@@H](CCC(O)=O)C)[H])[H]
Sinónimos:- (3Alpha,5Beta)-3-Hydroxy-7-Oxocholan-24-Oic Acid
- (3Alpha,5Beta,8Xi,9Xi,10Xi,13Xi,14Xi,17Xi,20Xi)-3-Hydroxy-7-Oxocholan-24-Oic Acid
- (3α,5β)-3-Hydroxy-7-oxo-Cholan-24-oic acid
- (3α,5β)-3-Hydroxy-7-oxocholan-24-oic acid
- 3-Hydroxy-7-Oxocholan-24-Oic Acid
- 3Alpha-Hydroxy-7-Oxo-5Beta-Cholanic Acid
- 3alpha-Hydroxy-7-oxo-5-cholanic acid
- 3alpha-Hydroxy-7-oxo-5beta-cholic acid
- 3α-Hydroxy-7-keto-5β-cholan-24-oic acid
- 3α-Hydroxy-7-keto-5β-cholanic acid
- 3α-Hydroxy-7-oxo-5β-cholan-24-oic acid
- 3α-Hydroxy-7-oxo-5β-cholan-24-oicacid
- 3α-Hydroxy-7-oxo-5β-cholanic acid
- 3α-Hydroxy-7-oxo-5β-cholanoic acid
- 3α-Hydroxy-7-oxo-5β-cholic acid
- 5β-Cholan-24-oic acid, 3α-hydroxy-7-oxo-
- 5β-Cholanic acid, 3α-hydroxy-7-oxo-
- 5β-Cholanic acid-3α-ol-7-one
- 7-Ketochenodeoxycholic acid
- 7-Ketolithocholic acid
- 7-Oxo-3α-hydroxycholan-24-oic acid
- 7-Oxolithocholic acid
- 7-keto-Lithocholic acid
- 7K-Lca
- Cholan-24-oic acid, 3-hydroxy-7-oxo-, (3α,5β)-
- Hydroxycholanicacid
- NSC 226118
- Nutriacholic acid
- Obeticholic Acid Intermediate
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Pureza (%)
0
100
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0
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50
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90
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95
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100
12 produtos.
3α-Hydroxy-7-oxo-5β-cholanic Acid
CAS:Fórmula:C24H38O4Pureza:>97.0%(T)Cor e Forma:White to Almost white powder to crystalPeso molecular:390.56Ursodeoxycholic Acid EP Impurity F
CAS:Fórmula:C24H38O4Cor e Forma:White To Off-White SolidPeso molecular:390.563-α-Hydroxy-7-Keto-5β-Cholanic Acid
CAS:3-α-Hydroxy-7-Keto-5β-Cholanic AcidPureza:98%Peso molecular:390.56g/molNutriacholic Acid
CAS:<p>Impurity Ursodeoxycholic Acid EP Impurity F<br>Applications Nutriacholic Acid (Ursodeoxycholic Acid EP Impurity F) is derivative of Lithocholic Acid (L469180), a cholic acid derivative as TGR5 modulator.<br>References Schneider, H., et al.: Bioorg. Med. Chem. Lett., 6, 637 (1996); Takamine, F., et al.: Microbiol. Immunol., 39, 11 (1995); Yamashita, H., et al.: Hepatol., 20, 663 (1994);<br></p>Fórmula:C24H38O4Cor e Forma:White To Off-WhitePeso molecular:390.563a-Hydroxy-7-oxo-5b-cholanic acid
CAS:Produto Controlado<p>3a-Hydroxy-7-oxo-5b-cholanic acid (3OHC) is a metabolite of 7-oxo-5b-cholanate, which is synthesized from cholic acid by the bacterial strain Clostridium species. 3OHC has been shown to be a potent inhibitor of human serum primary sclerosing cholangitis, which is an inflammatory disease of the bile ducts in the liver. It functions by inhibiting the formation of hydroxyl radicals, which are reactive oxygen species that cause tissue injury. The hydroxyl group in 3OHC reacts with the sulfhydryl groups on cysteine residues in proteins and forms sulfenic acids, which react with hydrogen peroxide to form chemically stable products. 3OHC also inhibits bacterial growth by binding to DNA and inhibiting transcription and replication.</p>Fórmula:C24H38O4Pureza:Min. 95%Peso molecular:390.56 g/mol7-Ketolithocholic acid
CAS:7-Ketolithocholic acid absorbs and reduces endogenous bile acid and cholesterol secretion.Fórmula:C24H38O4Pureza:98.68% - 99.9%Cor e Forma:White - Almost White Solid PowderPeso molecular:390.56









