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ChemicalBook--->CAS DataBase List--->6779-87-9

6779-87-9

6779-87-9 Structure

6779-87-9 Structure
IdentificationBack Directory
[Name]

7,8-DIHYDRO-L-BIOPTERIN
[CAS]

6779-87-9
[Synonyms]

BH2
DIHYDROBIOPTERIN
7,8-dihydrobiopterin
7,8-DIHYDRO-L-BIOPTERIN
L-erythro-Dihydrobiopterin
L-erythro-7,8-Dihydrobiopterin
2-amino-6-(1,2-dihydroxypropyl)-7,8-dihydro-1H-pteridin-4-one
2-Amino-6-(1,2-dihydroxy-propyl)-7,8-dihydro-3H-pteridin-4-one
2-AMINO-6-(1R,2S-DIHYDROXYPROPYL)-7,8-DIHYDRO-4(1H)-PTERIDINONE
4(1H)-pteridinone, 2-amino-6-(1,2-dihydroxypropyl)-7,8-dihydro-
2-Amino-6-[(1R,2S)-1,2-dihydroxypropyl]-7,8-dihydro-4(3H)-pteridinone
2-aMino-6-((1S,2R)-1,2-dihydroxypropyl)-7,8-dihydropteridin-4(3H)-one
[Molecular Formula]

C9H13N5O3
[MDL Number]

MFCD00049357
[MOL File]

6779-87-9.mol
[Molecular Weight]

239.23
Chemical PropertiesBack Directory
[Appearance]

Yellow Powder
[Melting point ]

>300°C dec.
[Boiling point ]

470.8±55.0 °C(Predicted)
[density ]

1.88
[storage temp. ]

−20°C
[solubility ]

Aqueous Acid (Slightly, Sonicated), Aqueous Base (Slightly), DMSO (Slightly), Me
[form ]

Solid
[pka]

10.47±0.20(Predicted)
[color ]

Pale Yellow to Brown
[BRN ]

536551
[Stability:]

Hygroscopic
[InChIKey]

FEMXZDUTFRTWPE-AWFVSMACSA-N
[CAS DataBase Reference]

6779-87-9
Hazard InformationBack Directory
[Chemical Properties]

Yellow Powder
[Uses]

An oxidation producct of tetrahydrobiopterin, a naturally occurring cofactor of the aromatic amino acid hydroxylase and is involved in the synthesis of tyrosine and the neurotransmitters dopamine and serotonin. It is a noncompetitive inhibitor of G
[Uses]

The reduced form of Biopterin. An oxidation product of tetrahydrobiopterin, a naturally occurring cofactor of the aromatic amino acid hydroxylase and is involved in the synthesis of tyrosine and the neurotransmitters dopamine and serotonin. It is a noncompetitive inhibitor of GTP cyclohydrolase I, with a Ki of 14.4 μM.
[Uses]

BH2 is a precursor of BH4 synthesis. It is a noncompetitive inhibitor of GTP cyclohydrolase I, with a Ki of 14.4 μM.
[Description]

BH2 is a precursor of BH4 synthesis. It is a noncompetitive inhibitor of GTP cyclohydrolase I, with a Ki of 14.4 μM.
[Definition]

ChEBI:L-erythro-7,8-dihydrobiopterin is a 7,8-dihydrobiopterin in which the 1,2-dihydroxypropyl group has (1R,2S)-configuration; naturally occurring form. It is an enantiomer of a D-erythro-7,8-dihydrobiopterin.
[storage]

Store at -20°C
[References]

[1] shen r, alam a, zhang y. inhibition of gtp cyclohydrolase i by pterins[j]. biochimica et biophysica acta (bba)-general subjects, 1988, 965(1): 9-15.
[2] sugiyama t, levy b d, michel t. tetrahydrobiopterin recycling, a key determinant of endothelial nitric-oxide synthase-dependent signaling pathways in cultured vascular endothelial cells[j]. journal of biological chemistry, 2009, 284(19): 12691-12700.
Safety DataBack Directory
[WGK Germany ]

3
[F ]

3-10
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