D6388
Dimethyl(2-hydroxy-5-nitrobenzyl)sulfonium bromide
≥95%
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About This Item
Empirical Formula (Hill Notation):
C9H12BrNO3S
CAS Number:
Molecular Weight:
294.17
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
≥95%
form
solid
storage temp.
2-8°C
SMILES string
[Br-].C[S+](C)Cc1cc(ccc1O)[N+]([O-])=O
InChI
1S/C9H11NO3S.BrH/c1-14(2)6-7-5-8(10(12)13)3-4-9(7)11;/h3-5H,6H2,1-2H3;1H
InChI key
VEGVMTIJKACZGO-UHFFFAOYSA-N
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Structure-function relationship in the allosteric L-lactate dehydrogenases from Lactobacillus casei and Lactobacillus curvatus.
U Mayr et al.
European journal of biochemistry, 126(3), 549-558 (1982-09-01)
Y M Peyser et al.
FEBS letters, 259(2), 346-348 (1990-01-01)
Rabbit skeletal muscle myosin subfragment-1 (S-1) was reacted with dimethyl(2-hydroxy-5-nitrobenzyl)sulfonium bromide (DHNBS) resulting in modification of 0.8 tryptophan residues per S-1. In order to assign the most reactive tryptophan of the 5 S-1 tryptophans, antibodies were raised in rabbits against
Inactivation of the nucleoside transporter of the human erythrocyte by dimethyl (2-hydroxy-5-nitrobenzyl) sulphonium bromide.
S D Thorne et al.
Biochemical Society transactions, 19(4), 418S-418S (1991-11-01)
J E McLean et al.
Biochemistry, 40(7), 2194-2200 (2001-05-01)
Brequinar and the active metabolite of leflunomide, A77 1726, have been clearly shown to inhibit human dihydroorotate dehydrogenase (DHODH), but conflicting mechanisms for their inhibition have been reported. DHODH catalyses the conversion of dihydroorotate (DHO) to orotate concurrent with the
C B Peterson et al.
The Journal of biological chemistry, 262(16), 7552-7558 (1987-06-05)
Heparin has been shown to exhibit lower affinity for the antithrombin-thrombin complex than for antithrombin alone (Carlstrom, A.-S., Lieden, K., and Bjork, I. (1977) Thromb. Res. 11, 785-797), suggesting that structural alterations in antithrombin may accompany its reaction with thrombin.
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