Chemical Formula: C11H11BrN2O2

Chemical Formula C11H11BrN2O2

Found 28 metabolite its formula value is C11H11BrN2O2

5-Bromotryptophan

(2S)-2-Amino-3-(5-bromo-1H-indol-3-yl)propanoic acid

C11H11BrN2O2 (282.00038459999996)


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

(2S)-2-amino-3-(6-bromo-1H-indol-3-yl)propanoic acid

C11H11BrN2O2 (282.00038459999996)


   

ethyl 2-(5-bromoimidazo[1,2-a]pyridin-2-yl)acetate

ethyl 2-(5-bromoimidazo[1,2-a]pyridin-2-yl)acetate

C11H11BrN2O2 (282.00038459999996)


   

6-(bromomethyl)-2,3-dimethoxyquinoxaline

6-(bromomethyl)-2,3-dimethoxyquinoxaline

C11H11BrN2O2 (282.00038459999996)


   
   

6-BROMO-2-METHYL-IMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER

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

Ethyl (6-bromoimidazo[1,2-a]pyridin-3-yl)acetate

C11H11BrN2O2 (282.00038459999996)


   

Ethyl 6-bromo-7-methylimidazo[1,2-a]pyridine-2-carboxylate

Ethyl 6-bromo-7-methylimidazo[1,2-a]pyridine-2-carboxylate

C11H11BrN2O2 (282.00038459999996)


   

Ethyl (6-bromoimidazo[1,2-a]pyridin-2-yl)acetate

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

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

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

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

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

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

(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

2-azaniumyl-3-(5-bromo-1H-indol-3-yl)propanoate

C11H11BrN2O2 (282.00038459999996)


   

(2S)-2-ammonio-3-(6-bromo-1H-indol-3-yl)propanoate

(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

(2R)-2-azaniumyl-3-(6-bromo-1H-indol-3-yl)propanoate

C11H11BrN2O2 (282.00038459999996)


   
   

L-6-bromotryptophan zwitterion

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

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.