L-Sepiapterin

Suppliers

Names

[ CAS No. ]:
17094-01-8

[ Name ]:
L-Sepiapterin

[Synonym ]:
2-amino-6-(2-hydroxy-propionyl)-7,8-dihydro-3H-pteridin-4-one
MFCD00210214
1-(2-amino-7,8-dihydro-4-hydroxy-6-pteridinyl)-2-hydroxy-1-Propanone
4(3H)-Pteridinone, 2-amino-7,8-dihydro-6-[(2S)-2-hydroxy-1-oxopropyl]-
2-amino-7,8-dihydro-6-[(2S)-2-hydroxy-1-oxopropyl]-4(1H)-Pteridinone
2-amino-7,8-dihydro-6-[(2S)-2-hydroxy-1-oxopropyl]-4(1H)Pteridinone
(S)-2-amino-7,8-dihydro-6-(2-hydroxy-1-oxopropyl)-4(1H)-Pteridinone
Sepiapterine
L-Sepiapterin
Sepiapterin,S-()-2-Amino-7,8-dihydro-6-(2-hydroxy-1-oxopropyl)-4(1H)-pteridinone,L-Sepiapterin
2-Amino-6-[(2S)-2-hydroxypropanoyl]-7,8-dihydro-4(1H)-pteridinone
Sepiapterin
2-Amino-6-L-lactoyl-7,8-dihydro-3H-pteridin-4-on
2-amino-6-(2-hydroxypropanoyl)-7,8-dihydro-1H-pty oeridin-4-one
2-AMINO-7,8-DIHYDRO-6-(2S-HYDROXY-1-OXOPROPYL)-4(1H)-PTERIDINONE
2-amino-6-[(2S)-2-hydroxypropanoyl]-7,8-dihydro-1H-pteridin-4-one
2-Amino-6-[(2S)-2-hydroxypropanoyl]-7,8-dihydropteridin-4(3H)-one
S-(−)-2-Amino-7,8-dihydro-6-(2-hydroxy-1-oxopropyl)-4(1H)-pteridinone
S(-)-2-AMINO-7,8-DIHYDRO-6-(2-HYDROXY-1-OXOPROPYL)-4(1H)-PTERIDINONE
2-amino-6-L-lactoyl-7,8-dihydro-3H-pteridin-4-one

Chemical & Physical Properties

[ Density]:
1.9±0.1 g/cm3

[ Boiling Point ]:
448.1ºC at 760 mmHg

[ Melting Point ]:
> 275 °C (lit.)

[ Molecular Formula ]:
C9H11N5O3

[ Molecular Weight ]:
237.215

[ Flash Point ]:
224.8ºC

[ Exact Mass ]:
237.086182

[ PSA ]:
133.46000

[ LogP ]:
-3.93

[ Vapour Pressure ]:
6.54E-10mmHg at 25°C

[ Index of Refraction ]:
1.822

[ Storage condition ]:
20°C

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Safety Phrases ]:
24/25

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2933990090

Precursor & DownStream

Precursor

DownStream

  • Gentisic acid

Customs

[ HS Code ]: 2933990090

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Bone Morphogenic Protein 4 Mediates NOX1-Dependent eNOS Uncoupling, Endothelial Dysfunction, and COX2 Induction in Type 2 Diabetes Mellitus.

Mol. Endocrinol. 29 , 1123-33, (2015)

We have recently shown that angiotensin II-mediated uncoupling of endothelial nitric oxide synthase (eNOS) contributes to endothelial dysfunction in streptozotocin-induced type 1 diabetes mellitus. Ho...

Sulfa drugs inhibit sepiapterin reduction and chemical redox cycling by sepiapterin reductase.

J. Pharmacol. Exp. Ther. 352(3) , 529-40, (2015)

Sepiapterin reductase (SPR) catalyzes the reduction of sepiapterin to dihydrobiopterin (BH2), the precursor for tetrahydrobiopterin (BH4), a cofactor critical for nitric oxide biosynthesis and alkylgl...

Stromal cell-derived factor 2 is critical for Hsp90-dependent eNOS activation.

Sci. Signal. 8 , ra81, (2015)

Endothelial nitric oxide synthase (eNOS) catalyzes the conversion of l-arginine and molecular oxygen into l-citrulline and nitric oxide (NO), a gaseous second messenger that influences cardiovascular ...


More Articles


Related Compounds

  • L-Asparagine Monohydrate (15N2)
  • L-Uridine
  • L-Proline, 1-cyano-, methyl ester (9CI)
  • L-(3,3-2H2)Leucine
  • L-Arg-D-Ala-OH
  • L-Cytidine
  • 6-Fluoro-2-nitroso-1,2,3,4-tetrahydroisoquinoline-8-carboxylic acid
  • 3-(5-Nitrofuran-2-yl)oxolane-2,5-dione
  • 2,2-Difluoro-2-(4-methyl-3-nitrophenyl)ethan-1-ol
  • 3-[2-(Piperidin-1-yl)pyridin-3-yl]propanoic acid
  • 10-Propyl-6-oxa-9-azaspiro[4.5]decane
  • 2-(1-Amino-3,3-difluorocyclobutyl)-4-chlorophenol
  • 5-(2-Phenylethenyl)benzo[b]thiophene
  • 3-{[5-(Methoxymethyl)furan-2-yl]oxy}-3-methylazetidine
  • 3-[1-[2-[3-(trifluoromethyl)phenyl]acetyl]piperidin-4-yl]-4a,5,6,7,8,8a-hexahydro-1H-quinazoline-2,4-dione
  • 2-Benzoyl-9-oxo-9H-fluorene-1-carboxylic acid
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.