537306
D-Hydroorotic acid
98%
동의어(들):
R-2,6-Dioxohexahydro-4-pyrimidinecarboxylic acid, Dihydro-D-orotic acid
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
실험식(Hill 표기법):
C5H6N2O4
CAS 번호:
Molecular Weight:
158.11
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
Assay:
98%
InChI
1S/C5H6N2O4/c8-3-1-2(4(9)10)6-5(11)7-3/h2H,1H2,(H,9,10)(H2,6,7,8,11)/t2-/m1/s1
SMILES string
OC(=O)[C@H]1CC(=O)NC(=O)N1
InChI key
UFIVEPVSAGBUSI-UWTATZPHSA-N
assay
98%
optical activity
[α]20/D −33°, c = 1 in NaHCO3
mp
255 °C (dec.) (lit.)
functional group
carboxylic acid
Quality Level
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
저장 등급
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Mihwa Lee et al.
Journal of molecular biology, 348(3), 523-533 (2005-04-14)
Escherichia coli dihydroorotase has been crystallized in the presence of the product, L-dihydroorotate (L-DHO), and the structure refined at 1.9A resolution. The structure confirms that previously reported (PDB entry 1J79), crystallized in the presence of the substrate N-carbamyl-D,L-aspartate (D, L-CA-asp)
Claudia A McDonald et al.
Biochemistry, 50(14), 2714-2716 (2011-03-16)
Adding the two residues comprising the conserved proton-transfer network of Class 2 dihydroorotate dehydrogenase (DHOD) to the Cys130Ser Class 1A DHOD did not restore the function of the active site base or rapid flavin reduction. Studies of triple, double, and
Rebecca L Fagan et al.
Biochemistry, 45(50), 14926-14932 (2006-12-13)
Dihydroorotate dehydrogenases (DHODs) oxidize dihydroorotate (DHO) to orotate using the FMN prosthetic group to abstract a hydride equivalent from C6 and a protein residue (Ser for Class 2 DHODs) to deprotonate C5. The fundamental question of whether the scission of
Rebecca L Fagan et al.
Biochemistry, 48(30), 7169-7178 (2009-06-18)
Dihydroorotate dehydrogenases (DHODs) catalyze the only redox step in de novo pyrimidine biosynthesis, the oxidation of dihydroorotate (DHO) to orotate (OA). During the reaction, the hydrogen at C6 of DHO is transferred to N5 of the isoalloxazine ring of an
[Development of anti-trypanosome drugs targeting nucleotides biosynthesis and red-ox regulatory pathway].
Kiyoshi Kita et al.
Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme, 54(12 Suppl), 1676-1683 (2009-09-01)
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