CAS 114-25-0

Biliverdina

Descripción:

Biliverdina es un pigmento biliar tetrapirrólico verde que es un producto de la degradación del hemo, formado principalmente a partir de la descomposición de la hemoglobina. Se caracteriza por su color verde, que se debe a su sistema de dobles enlaces conjugados, lo que le permite absorber luz en el espectro visible. Biliverdina es soluble en agua y tiene una fórmula molecular de C33H34N4O6, con un peso molecular de aproximadamente 582.6 g/mol. Juega un papel significativo en varios procesos biológicos, incluyendo actuar como un antioxidante y participar en la regulación de funciones celulares. Biliverdina también es un precursor de la bilirrubina, otro pigmento biliar importante. En términos de estabilidad, Biliverdina puede ser sensible a la luz y a los cambios de pH, lo que puede afectar su estructura y reactividad. Su presencia en sistemas biológicos a menudo se asocia con la función hepática y puede ser indicativa de ciertas condiciones médicas cuando se encuentra en concentraciones anormales. En general, Biliverdina es un compuesto importante en bioquímica y medicina, reflejando los complejos procesos del metabolismo del hemo.

Fórmula: C₃₃H₃₄N₄O₆

InChI: InChI=1/C33H34N4O6/c1-7-20-19(6)32(42)37-27(20)14-25-18(5)23(10-12-31(40)41)29(35-25)15-28-22(9-11-30(38)39)17(4)24(34-28)13-26-16(3)21(8-2)33(43)36-26/h7-8,13-15,35H,1-2,9-12H2,3-6H3,(H,36,43)(H,37,42)(H,38,39)(H,40,41)/b26-13-,27-14-,28-15-

Clave InChI: InChIKey=QBUVFDKTZJNUPP-BBROENKCSA-N

SMILES: C(\C1=C(CCC(O)=O)C(C)=C(/C=C\2/C(C=C)=C(C)C(=O)N2)N1)=C3/C(CCC(O)=O)=C(C)C(/C=C\4/C(C)=C(C=C)C(=O)N4)=N3

Sinónimos:

• 21H-Biline-8,12-dipropanoic acid, 3,18-diethenyl-1,19,22,24-tetrahydro-2,7,13,17-tetramethyl-1,19-dioxo-
• 3,18-Diethenyl-1,19,22,24-tetrahydro-2,7,13,17-tetramethyl-1,19-dioxo-21H-biline-8,12-dipropanoic acid
• 3-[(2Z)-2-[[3-(2-carboxyethyl)-4-methyl-5-[(Z)-(4-methyl-5-oxo-3-vinyl-pyrrol-2-ylidene)methyl]-1H-pyrrol-2-yl]methylene]-4-methyl-5-[(Z)-(3-methyl-5-oxo-4-vinyl-pyrrol-2-ylidene)methyl]pyrrol-3-yl]propanoic acid
• 3-[2-[(E)-[(5E)-3-(2-carboxyethyl)-4-methyl-5-[(3-methyl-5-oxo-4-vinyl-pyrrol-2-yl)methylene]pyrrol-2-ylidene]methyl]-4-methyl-5-[(E)-(4-methyl-5-oxo-3-vinyl-pyrrol-2-ylidene)methyl]-1H-pyrrol-3-yl]propanoic acid
• 3-[2-[(Z)-[(5E)-3-(2-carboxyethyl)-4-methyl-5-[(3-methyl-5-oxo-4-vinyl-pyrrol-2-yl)methylene]pyrrol-2-ylidene]methyl]-4-methyl-5-[(Z)-(4-methyl-5-oxo-3-vinyl-pyrrol-2-ylidene)methyl]-1H-pyrrol-3-yl]propanoic acid
• 3-[2-[(Z)-[(5Z)-3-(2-carboxyethyl)-4-methyl-5-[(3-methyl-5-oxo-4-vinyl-pyrrol-2-yl)methylene]pyrrol-2-ylidene]methyl]-4-methyl-5-[(Z)-(4-methyl-5-oxo-3-vinyl-pyrrol-2-ylidene)methyl]-1H-pyrrol-3-yl]propanoic acid
• 3-[2-[[3-(2-carboxyethyl)-4-methyl-5-[(3-methyl-5-oxo-4-vinyl-pyrrol-2-yl)methylene]pyrrol-2-ylidene]methyl]-4-methyl-5-[(4-methyl-5-oxo-3-vinyl-pyrrol-2-ylidene)methyl]-1H-pyrrol-3-yl]propanoic acid
• Biline-8,12-dipropionic acid, 1,19,22,24-tetrahydro-2,7,13,17-tetramethyl-1,19-dioxo-3,18-divinyl-
• Biline-8,12-dipropionic acid, 1,19,22,24-tetrahydro-2,7,13,17-tetramethyl-1,19-dioxo-3,18-divinyl- (8CI)
• Biliverdin IXalpha
• Biliverdin IXα
• Biliverdina
• Biliverdine
• Biliverdine (VAN)
• Biliverdine dihydrochloride
• Dehydrobilirubin
• Nsc 62793
• Oocyan
• Protobiliverdin IXα
• Pyrrole-3-propionic acid, 2-[[3-(2-carboxyethyl)-4-methyl-5-[(3-methyl-5-oxo-4-vinyl-3-pyrrolin-2-ylidene)methyl]-2H-pyrrol-2-ylidene]methyl]-4-methyl-5-[(4-methyl-5-oxo-3-vinyl-3-pyrrolin-2-ylidene)methyl]-
• Uteroverdine
• α-Biliverdin
• Biliverdin
• 3-[2-[(Z)-[(5E)-3-(2-carboxyethyl)-5-[(4-ethenyl-3-methyl-5-oxo-pyrrol-2-yl)methylidene]-4-methyl-pyrrol-2-ylidene]methyl]-5-[(Z)-(3-ethenyl-4-methyl-5-oxo-pyrrol-2-ylidene)methyl]-4-methyl-1H-pyrrol-3-yl]propanoic acid
• 3-[2-[(E)-[(5E)-3-(2-carboxyethyl)-5-[(4-ethenyl-3-methyl-5-oxo-pyrrol-2-yl)methylidene]-4-methyl-pyrrol-2-ylidene]methyl]-5-[(E)-(3-ethenyl-4-methyl-5-oxo-pyrrol-2-ylidene)methyl]-4-methyl-1H-pyrrol-3-yl]propanoic acid
• ocyan
• 3,18-Diethenyl-1,19,22,24-tetrahydro-2,7,13,17-tetrametyl-1,19-dioxo-21H-biline-8,12-dipropanoic Acid

3,18-Diethenyl-1,19,22,24-tetrahydro-2,7,13,17-tetramethyl-1,19-dioxo-21H-biline-8,12-dipropanoic acid

CAS: 114-25-0

Fórmula: C₃₃H₃₄N₄O₆

Pureza: 70%

Forma y color: Solid

Peso molecular: 582.6463

Ref: IN-DA0038B8

Biliverdine

CAS: 114-25-0

Stability Light Sensitive
Applications Biliverdine is a precursor of Bilirubin. Biliverdine is formed in the body from hemoglobin. The bile of amphibians and of birds contains Biliverdine only. It is also an inhibitor for hepatitis C virus.
References Lemberg et al.: Biochem. J., 35, 363 (1941); Gutierrez-Grobe, Y. et al.: Annals. Hepatol., 10, 105 (2011);

Fórmula: C₃₃H₃₄N₄O₆

Forma y color: Dark Green To Black

Peso molecular: 582.65

Ref: TR-B386400

Biliverdine-d4 (Major, may contain up to 3% d0) (Technical Grade)

Producto controlado

CAS: 114-25-0

Applications Labelled Biliverdine is a precursor of Bilirubin. Biliverdine is formed in the body from hemoglobin. The bile of amphibians and of birds contains Biliverdine only. It is also an inhibitor for hepatitis C virus.
References Lemberg et al.: Biochem. J., 35, 363 (1941); Gutierrez-Grobe, Y. et al.: Annals. Hepatol., 10, 105 (2011);

Fórmula: C₃₃H₃₀D₄N₄O₆

Pureza: >90%

Forma y color: Neat

Peso molecular: 586.67

Ref: TR-B386402

Biliverdine

CAS: 114-25-0

Biliverdine is a fluorescent probe that selectively binds to bilirubin and other hydroxycinnamic acids in tissue. Biliverdine can be used to measure the oxidative injury of tissues as well as the activity of enzymes involved in the metabolism of these compounds. The use of biliverdin with other fluorescent probes has been shown to improve the sensitivity and specificity for detecting oxidative injury. Biliverdin has also been shown to have anti-inflammatory properties, which may be due to its ability to inhibit the production of growth factor-β1 and 4-hydroxycinnamic acid.

Fórmula: C₃₃H₃₄N₄O₆

Pureza: Min. 70 Area-%

Forma y color: Green Powder

Peso molecular: 582.65 g/mol

Ref: 3D-FB18596

Biliverdin

CAS: 114-25-0

Biliverdin, produced through the oxidation of bilirubin, can also be synthesized through a non-protoporphyrin pathway in Corynebacterium glutamicum [1].

Fórmula: C₃₃H₃₄N₄O₆

Forma y color: Solid

Peso molecular: 582.65

Ref: TM-T84736