Chemical Formula: C11H11BrN2O2
Chemical Formula C11H11BrN2O2
Found 28 metabolite its formula value is C11H11BrN2O2
5-Bromotryptophan
5-Bromotryptophan (CAS: 6548-09-0) belongs to the class of organic compounds known as indolyl carboxylic acids and derivatives. Indolyl carboxylic acids and derivatives are compounds containing a carboxylic acid chain (of at least 2 carbon atoms) linked to an indole ring. 5-Bromotryptophan has been identified in blood (PMID: 31396400). 5-Bromo-L-tryptophan is an α-amino acid derivative that can be found in Semenospongia sp.[1].
6-Bromo-L-tryptophan
C11H11BrN2O2 (282.00038459999996)
ethyl 2-(5-bromoimidazo[1,2-a]pyridin-2-yl)acetate
C11H11BrN2O2 (282.00038459999996)
6-(bromomethyl)-2,3-dimethoxyquinoxaline
C11H11BrN2O2 (282.00038459999996)
6-BROMO-2-METHYL-IMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER
C11H11BrN2O2 (282.00038459999996)
Ethyl (6-bromoimidazo[1,2-a]pyridin-3-yl)acetate
C11H11BrN2O2 (282.00038459999996)
Ethyl 6-bromo-7-methylimidazo[1,2-a]pyridine-2-carboxylate
C11H11BrN2O2 (282.00038459999996)
Ethyl (6-bromoimidazo[1,2-a]pyridin-2-yl)acetate
C11H11BrN2O2 (282.00038459999996)
ethyl 3-bromo-5-methyl-1H-pyrrolo[3,2-b]pyridine-2-carboxylate
C11H11BrN2O2 (282.00038459999996)
Ethyl 8-bromo-6-methylimidazo[1,2-a]pyridine-2-carboxylate
C11H11BrN2O2 (282.00038459999996)
ethyl 6-broMo-2-Methyl-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
C11H11BrN2O2 (282.00038459999996)
ethyl 5-broMo-2-Methyl-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
C11H11BrN2O2 (282.00038459999996)
Ethyl 8-bromo-5-methylimidazo[1,2-a]pyridine-2-carboxylate
C11H11BrN2O2 (282.00038459999996)
(R)-2-Amino-3-(6-bromo-1H-indol-3-yl)propanoic acid
C11H11BrN2O2 (282.00038459999996)
2-azaniumyl-3-(5-bromo-1H-indol-3-yl)propanoate
C11H11BrN2O2 (282.00038459999996)
(2S)-2-ammonio-3-(6-bromo-1H-indol-3-yl)propanoate
C11H11BrN2O2 (282.00038459999996)
(2R)-2-azaniumyl-3-(6-bromo-1H-indol-3-yl)propanoate
C11H11BrN2O2 (282.00038459999996)
L-6-bromotryptophan zwitterion
C11H11BrN2O2 (282.00038459999996)
The L-alpha-amino acid zwitterion that results from the transfer of a proton from the carboxylic acid group to the alpha-amino group of L-6-bromotryptophan. The major species at pH 7.3.
L-6-bromotryptophan
C11H11BrN2O2 (282.00038459999996)
A bromoamino acid that is L-tryptophan in which the hydrogen at position 6 of the indole ring is substituted by bromine.