CAS 4651-67-6
:Ácido 7-cetolitocólico
Descripción:
Ácido 7-cetolitocólico es un derivado de ácido biliar que juega un papel en el metabolismo de lípidos y la regulación de los niveles de colesterol en el cuerpo. Se caracteriza por su grupo funcional cetona en la posición C7 del núcleo esteroide, lo que lo distingue de otros ácidos biliares. Este compuesto se encuentra típicamente en la bilis de ciertos animales y está involucrado en la emulsificación de grasas dietéticas, facilitando su absorción en los intestinos. Su estructura incluye un esqueleto esteroide hidrofóbico, que contribuye a su naturaleza anfipática, permitiéndole interactuar tanto con lípidos como con agua. Ácido 7-cetolitocólico también puede exhibir actividades biológicas, incluidos efectos potenciales en el metabolismo de lípidos y la microbiota intestinal. Como ácido biliar, está sujeto a circulación enterohepática, influyendo en su concentración y actividad en el tracto gastrointestinal. Comprender sus propiedades y funciones es importante para la investigación en salud gastrointestinal y trastornos 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
Clave 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 (%)
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100
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50
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90
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95
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100
Encontrado 12 productos.
3α-Hydroxy-7-oxo-5β-cholanic Acid
CAS:Fórmula:C24H38O4Pureza:>97.0%(T)Forma y color:White to Almost white powder to crystalPeso molecular:390.56Ursodeoxycholic Acid EP Impurity F
CAS:Fórmula:C24H38O4Forma y color: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/mol3a-Hydroxy-7-oxo-5b-cholanic acid
CAS:Pureza:95.0%Forma y color:SolidPeso molecular:390.5639953613281Nutriacholic 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:C24H38O4Forma y color:White To Off-WhitePeso molecular:390.56Nutriacholic Acid-d5
CAS:Producto controladoFórmula:C24D5H33O4Forma y color:NeatPeso molecular:395.5873a-Hydroxy-7-oxo-5b-cholanic acid
CAS:Producto 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%Forma y color:White - Almost White Solid PowderPeso molecular:390.56









