Chemical Formula: C11H12N2O3

Chemical Formula C11H12N2O3

Found 121 metabolite its formula value is C11H12N2O3

5-Hydroxy-L-tryptophan

(S)-2-Amino-3-(5-hydroxy-1H-indol-3-yl)propanoic Acid (5-Hydroxytryptophan)

C11H12N2O3 (220.0847882)


5-Hydroxy-L-tryptophan is an aromatic amino acid naturally produced by the body from the essential amino acid L-tryptophan. 5-Hydroxy-L-tryptophan is the immediate precursor of the neurotransmitter serotonin. The conversion to serotonin is catalyzed by the enzyme aromatic L-amino acid decarboxylase (EC 4.1.1.28) (AADC1 also known as DOPA decarboxylase), an essential enzyme in the metabolism of the monoamine neurotransmitters. An accumulation of 5-hydroxy-L-tryptophan in cerebrospinal fluid occurs in aromatic L-amino acid decarboxylase deficiency (AADC deficiency) (OMIM: 608643) accompanied by an increased excretion in the urine of the patients, which are indicative of the disorder but not specific. 5-Hydroxy-L-tryptophan is also increased in other disorders such as in Parkinsons patients with severe postural instability and gait disorders. The amount of endogenous 5-hydroxy-L-tryptophan available for serotonin synthesis depends on the availability of tryptophan and on the activity of various enzymes, especially tryptophan hydroxylase (EC 1.14.16.4), indoleamine 2,3-dioxygenase (EC 1.13.11.52), and tryptophan 2,3-dioxygenase (TDO) (EC 1.13.11.11). 5-Hydroxy-L-tryptophan has been used clinically for over 30 years. In addition to its use in the treatment of depression, the therapeutic administration of 5-hydroxy-L-tryptophan has been shown to be effective in treating a wide variety of conditions, including fibromyalgia, insomnia, binge eating associated with obesity, cerebellar ataxia, and chronic headaches. 5-Hydroxy-L-tryptophan easily crosses the blood-brain barrier and effectively increases central nervous system (CNS) synthesis of serotonin. Supplementation with 5-hydroxy-L-tryptophan is hypothesized to normalize serotonin synthesis, which is putatively related to its antidepressant properties (PMID: 9295177, 17240182, 16023217). When present in sufficiently high levels, 5-hydroxytryptophan can be a neurotoxin and a metabotoxin. A neurotoxin is a compound that disrupts or attacks neural cells or tissue. A metabotoxin is an endogenously produced metabolite that causes adverse health effects at chronically high levels. Signs and symptoms of AADC deficiency generally appear in the first year of life. Affected infants may have severe developmental delay, weak muscle tone (hypotonia), muscle stiffness, difficulty moving, and involuntary writhing movements of the limbs (athetosis). They may be lacking in energy (lethargic), feed poorly, startle easily, and have sleep disturbances. Since 5-hydroxytryptophan is a precursor to serotonin, altered levels of serotonin can accumulate in the brain, which leads to abnormal neural signalling. Infants with AADC deficiency have very low levels of neural signalling molecules while individuals who consume high levels of 5-hydroxytryptophan will have very high levels of neural signalling molecules. Both conditions can lead to vomiting, nausea, extreme drowsiness, and lethargy. 5-Hydroxytryptophan (5-HTP), also known as oxitriptan (INN) is sold over-the-counter in the United Kingdom, the United States, and Canada as a dietary supplement for use as an antidepressant, appetite suppressant, and sleep aid. It is also marketed in many European countries for the indication of major depression under trade names such as Cincofarm, Levothym, Levotonine, Oxyfan, Telesol, Tript-OH, and Triptum. Several double-blind placebo-controlled clinical trials have demonstrated the effectiveness of 5-HTP in the treatment of depression, though a lack of high-quality studies has been noted. More and larger studies are needed to determine if 5-HTP is truly effective in treating depression. 5-hydroxy-L-tryptophan is the L-enantiomer of 5-hydroxytryptophan. It has a role as a human metabolite, a plant metabolite and a mouse metabolite. It is a 5-hydroxytryptophan, a hydroxy-L-tryptophan and a non-proteinogenic L-alpha-amino acid. It is an enantiomer of a 5-hydroxy-D-tryptophan. It is a tautomer of a 5-hydroxy-L-tryptophan zwitterion. 5-Hydroxytryptophan (5-HTP), also known as oxitriptan (INN), is a naturally occurring amino acid and metabolic intermediate in the synthesis of serotonin and melatonin. 5-HTP is sold over-the-counter in the United Kingdom, United States and Canada as a dietary supplement for use as an antidepressant, appetite suppressant, and sleep aid, and is also marketed in many European countries for the indication of major depression under trade names like Cincofarm, Levothym, Levotonine, Oxyfan, Telesol, Tript-OH, and Triptum. Several double-blind placebo-controlled clinical trials have demonstrated the effectiveness of 5-HTP in the treatment of depression, though a lack of high quality studies has been noted. More study is needed to determine efficacy in treating depression. Oxitriptan is an aromatic amino acid with antidepressant activity. In vivo, oxitriptan (or 5-hydroxytryptophan) is converted into 5-hydroxytryptamine (5-HT or serotonin) as well as other neurotransmitters. Oxitriptan may exert its antidepressant activity via conversion to serotonin or directly by binding to serotonin (5-HT) receptors within the central nervous system (CNS). Endogenous oxitriptan is produced from the essential amino acid L-tryptophan. The exogenous therapeutic form is isolated from the seeds of the African plant Griffonia simplicifolia. The immediate precursor in the biosynthesis of SEROTONIN from tryptophan. It is used as an antiepileptic and antidepressant. See also: ... View More ... 5-Hydroxytryptophan (5-HTP), also known as oxitriptan (INN), is a naturally-occurring amino acid and chemical precursor as well as metabolic intermediate in the biosynthesis of the neurotransmitters serotonin and melatonin from tryptophan. 5-Hydroxy-L-tryptophan is found in french plantain. 5-Hydroxy-L-tryptophan. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=4350-09-8 (retrieved 2024-07-02) (CAS RN: 4350-09-8). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). L-5-Hydroxytryptophan (L-5-HTP), a naturally occurring amino acid and a dietary supplement for use as an antidepressant, appetite suppressant, and sleep aid, is the immediate precursor of the neurotransmitter serotonin and a reserpine antagonist[1]. L-5-Hydroxytryptophan (L-5-HTP) is used to treat fibromyalgia, myoclonus, migraine, and cerebellar ataxia[2][3][4][5].

   

5-Hydroxytryptophan

(S)-2-Amino-3-(5-hydroxy-1H-indol-3-yl)-propionic acid;C5-Hydroxy-L-tryptophan;5-HTP;Oxitriptan

C11H12N2O3 (220.0847882)


5-hydroxytryptophan is a tryptophan derivative that is tryptophan substituted by a hydroxy group at position 5. It has a role as a human metabolite and a neurotransmitter. 5-Hydroxytryptophan, DL- is a racemic mixture of 5-hydroxytryptophan (5-HTP), a precursor to the neurotransmitter serotonin with anti-depressant, analgesic and appetite-suppressant activities. DL-5-HTP is decarboxylated to serotonin by aromatic-L-amino-acid decarboxylase, and results in increased serotonin levels within the brain. Mediated through serotonin receptors, elevated levels of serotonin causes increased serotonin neurotransmissions, hence leading to release of depression, pain and appetite. 5-Hydroxy-L-tryptophan is an aromatic amino acid naturally produced by the body from the essential amino acid l-tryptophan. 5-Hydroxy-L-tryptophan is the immediate precursor of the neurotransmitter serotonin. The conversion to serotonin is catalyzed by the enzyme aromatic l-amino acid decarboxylase (EC 4.1.1.28, AADC1 also known as dopa decarboxylase), an essential enzyme in the metabolism of the monoamine neurotransmitters. An accumulation of 5-Hydroxy-L-tryptophan in cerebrospinal fluid occurs in Aromatic l-amino acid decarboxylase deficiency (OMIM 608643), accompanied by an increased excretion in the urine of the patients, which are indicative of the disorder but not specific 5-Hydroxy-L-tryptophan is also increased in other disorders such as in Parkinsons patients with severe postural instability and gait disorders. Confirmation of the diagnosis AADC deficiency is then required by enzyme activity measurement or genetic analysis. The amount of endogenous 5-Hydroxy-L-tryptophan available for serotonin synthesis depends on the availability of tryptophan and on the activity of various enzymes, especially tryptophan hydroxylase (EC 1.14.16.4), indoleamine 2,3-dioxygenase (EC 1.13.11.52), and tryptophan 2,3-dioxygenase. (EC 1.13.11.11, TDO). 5-Hydroxy-L-tryptophan has been used clinically for over 30 years. In addition to depression, the therapeutic administration of 5-Hydroxy-L-tryptophan has been shown to be effective in treating a wide variety of conditions, including fibromyalgia, insomnia, binge eating associated with obesity, cerebellar ataxia, and chronic headaches. 5-Hydroxy-L-tryptophan easily crosses the blood-brain barrier and effectively increases central nervous system (CNS) synthesis of serotonin. Supplementation with 5-Hydroxy-L-tryptophan is hypothesized to normalize serotonin synthesis, which is putatively related to its antidepressant properties. (A3384, A3385, A3386). The immediate precursor in the biosynthesis of SEROTONIN from tryptophan. It is used as an antiepileptic and antidepressant. D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D000928 - Antidepressive Agents A tryptophan derivative that is tryptophan substituted by a hydroxy group at position 5. 5-Hydroxytryptophan, a tryptophan metabolite, is a direct 5-hydroxytryptamine (5-HT) precursor and an L-aromatic amino acid decarboxylase substrate. [1][2][3]. 5-Hydroxytryptophan, a tryptophan metabolite, is a direct 5-hydroxytryptamine (5-HT) precursor and an L-aromatic amino acid decarboxylase substrate. [1][2][3].

   

N-Hydroxy-L-tryptophan

N-Hydroxy-L-tryptophan

C11H12N2O3 (220.0847882)


   

Jasminine

SCHEMBL4951194

C11H12N2O3 (220.0847882)


   

4-Hydroxy-l-tryptophan

2-amino-3-(4-hydroxy-1H-indol-3-yl)propanoic acid

C11H12N2O3 (220.0847882)


An optically active form of 4-hydroxytryptophan having L-configuration.

   

p-Hydroxyl-ethotoin

3-ethyl-5-(4-hydroxyphenyl)imidazolidine-2,4-dione

C11H12N2O3 (220.0847882)


p-Hydroxyl-ethotoin is a metabolite of ethotoin. Ethotoin (marketed as Peganone by Ovation) is an anticonvulsant drug used in the treatment of epilepsy. It is a hydantoin, similar to phenytoin. Ethotoin lacks phenytoins side effects of gingival hyperplasia and hirsutism, however it is less effective. This, combined with the need for frequent dosing has limited its usefulness. Ethotoin is no longer widely used. (Wikipedia)

   

4,4'-Dihydroxyantipyrine

4-hydroxy-2-(4-hydroxyphenyl)-1,5-dimethyl-2,3-dihydro-1H-pyrazol-3-one

C11H12N2O3 (220.0847882)


   

N-hydroxy-L-tryptophan

2-(N-hydroxyamino)-3-(1H-indol-3-yl)propanoic acid

C11H12N2O3 (220.0847882)


   

4-amino-6,7-dimethoxy-3-quinolinol hydrochloride hydrate

4-amino-6,7-dimethoxy-3-quinolinol hydrochloride hydrate

C11H12N2O3 (220.0847882)


   

2-amino-3-(6-hydroxy-1H-indol-3-yl)propanoic Acid

2-amino-3-(6-hydroxy-1H-indol-3-yl)propanoic Acid

C11H12N2O3 (220.0847882)


   
   

2-amino-3-(2-oxoindolin-3-yl)propanoic acid

2-amino-3-(2-oxoindolin-3-yl)propanoic acid

C11H12N2O3 (220.0847882)


   

Oxitriptan

L-5-Hydroxytryptophan

C11H12N2O3 (220.0847882)


D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D000928 - Antidepressive Agents relative retention time with respect to 9-anthracene Carboxylic Acid is 0.053 N - Nervous system > N06 - Psychoanaleptics > N06A - Antidepressants relative retention time with respect to 9-anthracene Carboxylic Acid is 0.054 L-5-Hydroxytryptophan (L-5-HTP), a naturally occurring amino acid and a dietary supplement for use as an antidepressant, appetite suppressant, and sleep aid, is the immediate precursor of the neurotransmitter serotonin and a reserpine antagonist[1]. L-5-Hydroxytryptophan (L-5-HTP) is used to treat fibromyalgia, myoclonus, migraine, and cerebellar ataxia[2][3][4][5].

   

5-hydroxy-L-tryptophan

5-hydroxy-L-tryptophan

C11H12N2O3 (220.0847882)


   

5-hydroxytryptophan

5-Hydroxy-DL-tryptophan

C11H12N2O3 (220.0847882)


5-Hydroxytryptophan, a tryptophan metabolite, is a direct 5-hydroxytryptamine (5-HT) precursor and an L-aromatic amino acid decarboxylase substrate. [1][2][3]. 5-Hydroxytryptophan, a tryptophan metabolite, is a direct 5-hydroxytryptamine (5-HT) precursor and an L-aromatic amino acid decarboxylase substrate. [1][2][3].

   

L-5-Hydroxytryptophan

5-hydroxy-L-tryptophan

C11H12N2O3 (220.0847882)


L-5-Hydroxytryptophan (L-5-HTP), a naturally occurring amino acid and a dietary supplement for use as an antidepressant, appetite suppressant, and sleep aid, is the immediate precursor of the neurotransmitter serotonin and a reserpine antagonist[1]. L-5-Hydroxytryptophan (L-5-HTP) is used to treat fibromyalgia, myoclonus, migraine, and cerebellar ataxia[2][3][4][5].

   

1-(2,4-dimethoxyphenyl)-1H-pyrazol-3-ol

1-(2,4-dimethoxyphenyl)-1H-pyrazol-3-ol

C11H12N2O3 (220.0847882)


   

5-Hydroxy-tryptophan; LC-tDDA; CE10

5-Hydroxy-tryptophan; LC-tDDA; CE10

C11H12N2O3 (220.0847882)


   

5-Hydroxy-tryptophan; LC-tDDA; CE20

5-Hydroxy-tryptophan; LC-tDDA; CE20

C11H12N2O3 (220.0847882)


   

5-Hydroxy-tryptophan; LC-tDDA; CE30

5-Hydroxy-tryptophan; LC-tDDA; CE30

C11H12N2O3 (220.0847882)


   

5-Hydroxy-tryptophan; LC-tDDA; CE40

5-Hydroxy-tryptophan; LC-tDDA; CE40

C11H12N2O3 (220.0847882)


   

5-Hydroxy-tryptophan; AIF; CE0; CorrDec

5-Hydroxy-tryptophan; AIF; CE0; CorrDec

C11H12N2O3 (220.0847882)


   

5-Hydroxy-tryptophan; AIF; CE10; CorrDec

5-Hydroxy-tryptophan; AIF; CE10; CorrDec

C11H12N2O3 (220.0847882)


   

5-Hydroxy-tryptophan; AIF; CE30; CorrDec

5-Hydroxy-tryptophan; AIF; CE30; CorrDec

C11H12N2O3 (220.0847882)


   

5-Hydroxy-tryptophan; AIF; CE0; MS2Dec

5-Hydroxy-tryptophan; AIF; CE0; MS2Dec

C11H12N2O3 (220.0847882)


   

5-Hydroxy-tryptophan; AIF; CE10; MS2Dec

5-Hydroxy-tryptophan; AIF; CE10; MS2Dec

C11H12N2O3 (220.0847882)


   

5-Hydroxy-tryptophan; AIF; CE30; MS2Dec

5-Hydroxy-tryptophan; AIF; CE30; MS2Dec

C11H12N2O3 (220.0847882)


   
   

trans-1-methyl-4-carboxy-5-(3-pyridyl)-2-pyrrolidinone

trans-1-methyl-4-carboxy-5-(3-pyridyl)-2-pyrrolidinone

C11H12N2O3 (220.0847882)


   

3-(3,4-DIMETHOXY-PHENYL)-ISOXAZOL-5-YLAMINE

3-(3,4-DIMETHOXY-PHENYL)-ISOXAZOL-5-YLAMINE

C11H12N2O3 (220.0847882)


   
   
   
   

ETHYL 5-METHOXY-1H-PYRROLO[2, 3-C]PYRIDINE-2-CARBOXYLATE

ETHYL 5-METHOXY-1H-PYRROLO[2, 3-C]PYRIDINE-2-CARBOXYLATE

C11H12N2O3 (220.0847882)


   
   

3-(Dimethylamino)-1-(4-nitrophenyl)prop-2-en-1-one

3-(Dimethylamino)-1-(4-nitrophenyl)prop-2-en-1-one

C11H12N2O3 (220.0847882)


   

Methyl-2-ethoxybenzimidazole-7-carboxylate

Methyl-2-ethoxybenzimidazole-7-carboxylate

C11H12N2O3 (220.0847882)


   

2,4-DIHYDRO-5-(3,4-DIMETHOXYPHENYL)-3H-PYRAZOL-3-ONE

2,4-DIHYDRO-5-(3,4-DIMETHOXYPHENYL)-3H-PYRAZOL-3-ONE

C11H12N2O3 (220.0847882)


   

5-(4’-Hydroxyphenyl)-5-ethylhydantion

5-(4’-Hydroxyphenyl)-5-ethylhydantion

C11H12N2O3 (220.0847882)


   

4,6-dimethyl-2-oxo-3H-pyrido[1,2-a]pyrimidine-4-carboxylic acid

4,6-dimethyl-2-oxo-3H-pyrido[1,2-a]pyrimidine-4-carboxylic acid

C11H12N2O3 (220.0847882)


   

(4-NITROPHENYL)(PYRROLIDIN-1-YL)METHANONE

(4-NITROPHENYL)(PYRROLIDIN-1-YL)METHANONE

C11H12N2O3 (220.0847882)


   

1-(4-FLUOROPHENYL)-5-METHYLTHIO-3-PHENYL-1H-PYRAZOLE

1-(4-FLUOROPHENYL)-5-METHYLTHIO-3-PHENYL-1H-PYRAZOLE

C11H12N2O3 (220.0847882)


   

2-Oxo-1-benzimidazolinebutyric Acid

2-Oxo-1-benzimidazolinebutyric Acid

C11H12N2O3 (220.0847882)


   

2-(4-(2-OXOIMIDAZOLIDIN-1-YL)PHENYL)ACETIC ACID

2-(4-(2-OXOIMIDAZOLIDIN-1-YL)PHENYL)ACETIC ACID

C11H12N2O3 (220.0847882)


   
   

ethyl 3-(hydroxymethyl)imidazo[1,2-a]pyridine-8-carboxylate

ethyl 3-(hydroxymethyl)imidazo[1,2-a]pyridine-8-carboxylate

C11H12N2O3 (220.0847882)


   

5-oxo-1-(pyridin-2-ylmethyl)pyrrolidine-3-carboxylic acid

5-oxo-1-(pyridin-2-ylmethyl)pyrrolidine-3-carboxylic acid

C11H12N2O3 (220.0847882)


   

ETHYL 3-(2-FURYL)-1-METHYL-1H-PYRAZOLE-5-CARBOXYLATE

ETHYL 3-(2-FURYL)-1-METHYL-1H-PYRAZOLE-5-CARBOXYLATE

C11H12N2O3 (220.0847882)


   

3-(2-HYDROXYMETHYL-BENZOIMIDAZOL-1-YL)-PROPIONIC ACID

3-(2-HYDROXYMETHYL-BENZOIMIDAZOL-1-YL)-PROPIONIC ACID

C11H12N2O3 (220.0847882)


   

ethyl 5-cyano-2-ethyl-1,6-dihydro-6-oxo-3-pyridinecarboxylate

ethyl 5-cyano-2-ethyl-1,6-dihydro-6-oxo-3-pyridinecarboxylate

C11H12N2O3 (220.0847882)


   

Ethyl 5-methoxy-1H-pyrrolo[3,2-b]pyridine-2-carboxylate

Ethyl 5-methoxy-1H-pyrrolo[3,2-b]pyridine-2-carboxylate

C11H12N2O3 (220.0847882)


   

ethyl 4-amino-7-hydroxy-1H-indole-2-carboxylate

ethyl 4-amino-7-hydroxy-1H-indole-2-carboxylate

C11H12N2O3 (220.0847882)


   

1-(4-FLUOROPHENYL)-5-METHYL-1H-PYRAZOLE-4-CARBOXYLICACID

1-(4-FLUOROPHENYL)-5-METHYL-1H-PYRAZOLE-4-CARBOXYLICACID

C11H12N2O3 (220.0847882)


   

ETHYL 5-(2-FURYL)-1-METHYL-1H-PYRAZOLE-3-CARBOXYLATE

ETHYL 5-(2-FURYL)-1-METHYL-1H-PYRAZOLE-3-CARBOXYLATE

C11H12N2O3 (220.0847882)


   

ETHYL 7-METHOXY-1H-INDAZOLE-3-CARBOXYLATE

ETHYL 7-METHOXY-1H-INDAZOLE-3-CARBOXYLATE

C11H12N2O3 (220.0847882)


   

ethyl 4-methoxy-1h-indazole-3-carboxylate

ethyl 4-methoxy-1h-indazole-3-carboxylate

C11H12N2O3 (220.0847882)


   

7-HYDROXY-DL-TRYPTOPHAN

7-HYDROXY-DL-TRYPTOPHAN

C11H12N2O3 (220.0847882)


   

(3S)-(-)-3-(TRIFLUOROACETAMIDO)PYRROLIDINEHYDROCHLORIDE

(3S)-(-)-3-(TRIFLUOROACETAMIDO)PYRROLIDINEHYDROCHLORIDE

C11H12N2O3 (220.0847882)


   

methyl 5-cyano-6-propan-2-yloxypyridine-3-carboxylate

methyl 5-cyano-6-propan-2-yloxypyridine-3-carboxylate

C11H12N2O3 (220.0847882)


   

3-(2,4-DIMETHOXY-PHENYL)-ISOXAZOL-5-YLAMINE

3-(2,4-DIMETHOXY-PHENYL)-ISOXAZOL-5-YLAMINE

C11H12N2O3 (220.0847882)


   

N-cyclopropyl-4-methyl-3-nitrobenzamide

N-cyclopropyl-4-methyl-3-nitrobenzamide

C11H12N2O3 (220.0847882)


   

1-(4-aminophenyl)-5-oxopyrrolidine-3-carboxylic acid

1-(4-aminophenyl)-5-oxopyrrolidine-3-carboxylic acid

C11H12N2O3 (220.0847882)


   

6-METHOXY-1H-INDAZOLE-3-CARBOXYLIC ACID ETHYL ESTER

6-METHOXY-1H-INDAZOLE-3-CARBOXYLIC ACID ETHYL ESTER

C11H12N2O3 (220.0847882)


   

5-METHOXY-1H-INDAZOLE-3-CARBOXYLIC ACID ETHYL ESTER

5-METHOXY-1H-INDAZOLE-3-CARBOXYLIC ACID ETHYL ESTER

C11H12N2O3 (220.0847882)


   

1-Isopropyl-7-methyl-1H-pyrido[2,3-d][1,3]oxazine-2,4-dione

1-Isopropyl-7-methyl-1H-pyrido[2,3-d][1,3]oxazine-2,4-dione

C11H12N2O3 (220.0847882)


   

7-Methyl-1-propyl-1H-pyrido[2,3-d][1,3]oxazine-2,4-dione

7-Methyl-1-propyl-1H-pyrido[2,3-d][1,3]oxazine-2,4-dione

C11H12N2O3 (220.0847882)


   

2-ETHYL-3-METHOXY-2H-INDAZOLE-6-CARBOXYLIC ACID

2-ETHYL-3-METHOXY-2H-INDAZOLE-6-CARBOXYLIC ACID

C11H12N2O3 (220.0847882)


   

5-isocyanato-2-(oxan-4-yloxy)pyridine

5-isocyanato-2-(oxan-4-yloxy)pyridine

C11H12N2O3 (220.0847882)


   

5-(3,5-DIMETHYL-PYRAZOL-1-YLMETHYL)-FURAN-2-CARBOXYLIC ACID

5-(3,5-DIMETHYL-PYRAZOL-1-YLMETHYL)-FURAN-2-CARBOXYLIC ACID

C11H12N2O3 (220.0847882)


   

5-Methoxy-pyrazolo[1,5-a]pyridine-3-carboxylic acid ethyl ester

5-Methoxy-pyrazolo[1,5-a]pyridine-3-carboxylic acid ethyl ester

C11H12N2O3 (220.0847882)


   

Ethyl 6-methoxyh-pyrazolo[1,5-a]pyridine-3-carboxylate

Ethyl 6-methoxyh-pyrazolo[1,5-a]pyridine-3-carboxylate

C11H12N2O3 (220.0847882)


   

7-(3-Hydroxypropoxy)-4(1H)-quinazolinone

7-(3-Hydroxypropoxy)-4(1H)-quinazolinone

C11H12N2O3 (220.0847882)


   

4-Carbamonyl-N-Acetoacetanilide

4-Carbamonyl-N-Acetoacetanilide

C11H12N2O3 (220.0847882)


   

Ethyl 4-amino-5-cyano-2-hydroxy-3-methylbenzoate

Ethyl 4-amino-5-cyano-2-hydroxy-3-methylbenzoate

C11H12N2O3 (220.0847882)


   

1-(4-Nitrophenyl)-2-piperidinone

1-(4-Nitrophenyl)-2-piperidinone

C11H12N2O3 (220.0847882)


   

Ethyl 4-methoxy-1H-pyrrolo[2,3-b]pyridine-2-carboxylate

Ethyl 4-methoxy-1H-pyrrolo[2,3-b]pyridine-2-carboxylate

C11H12N2O3 (220.0847882)


   

4,4-dimethyl-7-nitro-2,3-dihydroisoquinolin-1-one

4,4-dimethyl-7-nitro-2,3-dihydroisoquinolin-1-one

C11H12N2O3 (220.0847882)


   

N-(Pyridine-2-carbonyl)-L-proline

N-(Pyridine-2-carbonyl)-L-proline

C11H12N2O3 (220.0847882)


   

6-Ethoxy-7-Methoxyquinazoline-4-One

6-Ethoxy-7-Methoxyquinazoline-4-One

C11H12N2O3 (220.0847882)


   

4-Hydroxytryptophan

2-amino-3-(4-hydroxy-1H-indol-3-yl)propanoic acid

C11H12N2O3 (220.0847882)


A hydroxytryptophan substituted by a hydroxy group at position 4 on the indole ring.

   

methyl 4-(2-oxoimidazolidin-1-yl)benzoate

methyl 4-(2-oxoimidazolidin-1-yl)benzoate

C11H12N2O3 (220.0847882)


   

3-(DIMETHYLAMINO)-2-(2-NITROPHENYL)ACRYLALDEHYDE

3-(DIMETHYLAMINO)-2-(2-NITROPHENYL)ACRYLALDEHYDE

C11H12N2O3 (220.0847882)


   

2-(2-oxo-3-phenylimidazolidin-1-yl)acetic acid

2-(2-oxo-3-phenylimidazolidin-1-yl)acetic acid

C11H12N2O3 (220.0847882)


   

5-(p-methoxyphenyl)-5-methyl-hydantoi

5-(p-methoxyphenyl)-5-methyl-hydantoi

C11H12N2O3 (220.0847882)


   

5-oxo-1-(pyridin-4-ylmethyl)pyrrolidine-3-carboxylic acid

5-oxo-1-(pyridin-4-ylmethyl)pyrrolidine-3-carboxylic acid

C11H12N2O3 (220.0847882)


   

(1,1-Dioxo-1,4-dihydrobenzo[1,2,4]thiadiazin-3-yl)acetic acid ethyl ester

(1,1-Dioxo-1,4-dihydrobenzo[1,2,4]thiadiazin-3-yl)acetic acid ethyl ester

C11H12N2O3 (220.0847882)


   

5-Hydroxy-D-tryptophan

(R)-2-AMINO-3-(5-HYDROXY-1H-INDOL-3-YL)PROPANOIC ACID

C11H12N2O3 (220.0847882)


The D-enantiomer of 5-hydroxytryptophan.

   

4(1H)-Quinazolinone,7-(2-hydroxyethoxy)-

4(1H)-Quinazolinone,7-(2-hydroxyethoxy)-

C11H12N2O3 (220.0847882)


   

6-hydroxy-L-tryptophan

6-hydroxy-L-tryptophan

C11H12N2O3 (220.0847882)


   

5-oxo-1-(pyridin-3-ylmethyl)pyrrolidine-3-carboxylic acid

5-oxo-1-(pyridin-3-ylmethyl)pyrrolidine-3-carboxylic acid

C11H12N2O3 (220.0847882)


   

Ethyl 3-amino-5-(furan-2-yl)-1H-pyrrole-2-carboxylate

Ethyl 3-amino-5-(furan-2-yl)-1H-pyrrole-2-carboxylate

C11H12N2O3 (220.0847882)


   

2-[(4-methyl-1H-benzimidazol-2-yl)methoxy]acetic acid

2-[(4-methyl-1H-benzimidazol-2-yl)methoxy]acetic acid

C11H12N2O3 (220.0847882)


   

6,7-dimethoxy-2-methylquinazolin-4-ol

6,7-dimethoxy-2-methylquinazolin-4-ol

C11H12N2O3 (220.0847882)


   

ETHYL3-HYDROXY-1,2-DIHYDROQUINOXALINE-2-CARBOXYLATE

ETHYL3-HYDROXY-1,2-DIHYDROQUINOXALINE-2-CARBOXYLATE

C11H12N2O3 (220.0847882)


   

2-Hydroxy-L-tryptophan

2-Hydroxy-L-tryptophan

C11H12N2O3 (220.0847882)


An optically active form of 2-hydroxytryptophan having L-configuration.

   

7-hydroxy-L-tryptophan

7-hydroxy-L-tryptophan

C11H12N2O3 (220.0847882)


An optically active form of 7-hydroxytryptophan having L-configuration.

   

2-Hydroxytryptophan

2-Hydroxytryptophan

C11H12N2O3 (220.0847882)


A hydroxytryptophan that is tryptophan substituted by a hydroxy group at position 2 on the indole ring.

   

(S)-5-(4-Hydroxyphenyl)-5-ethylhydantoin

(S)-5-(4-Hydroxyphenyl)-5-ethylhydantoin

C11H12N2O3 (220.0847882)


   

6-Methoxy-2,3-dimethyl-5-nitro-1H-indole

6-Methoxy-2,3-dimethyl-5-nitro-1H-indole

C11H12N2O3 (220.0847882)


   

6-Methoxy-2,3-dimethyl-7-nitro-1H-indole

6-Methoxy-2,3-dimethyl-7-nitro-1H-indole

C11H12N2O3 (220.0847882)


   

5-Methoxy-2,3-dimethyl-6-nitro-1H-indole

5-Methoxy-2,3-dimethyl-6-nitro-1H-indole

C11H12N2O3 (220.0847882)


   

6-Nitro-5-methoxy-1,2-dimethylindole

6-Nitro-5-methoxy-1,2-dimethylindole

C11H12N2O3 (220.0847882)


   

6-Nitro-7-methoxy-2,3-dimethylindole

6-Nitro-7-methoxy-2,3-dimethylindole

C11H12N2O3 (220.0847882)


   

Beta-Hydroxytryptophane

Beta-Hydroxytryptophane

C11H12N2O3 (220.0847882)


   

(2S)-2-ammonio-3-(5-hydroxy-1H-indol-3-yl)propanoate

(2S)-2-ammonio-3-(5-hydroxy-1H-indol-3-yl)propanoate

C11H12N2O3 (220.0847882)


   
   

(2S)-2-azaniumyl-3-(4-hydroxy-1H-indol-3-yl)propanoate

(2S)-2-azaniumyl-3-(4-hydroxy-1H-indol-3-yl)propanoate

C11H12N2O3 (220.0847882)


   

9-N-hydroxy-L-tryptophan

9-N-hydroxy-L-tryptophan

C11H12N2O3 (220.0847882)


   

(S)-beta-hydroxy-L-tryptophan

(S)-beta-hydroxy-L-tryptophan

C11H12N2O3 (220.0847882)


   

threo-beta-hydroxy-L-tryptophan

threo-beta-hydroxy-L-tryptophan

C11H12N2O3 (220.0847882)


   

(2~{S},3~{R})-2-azanyl-3-(1~{H}-indol-3-yl)-3-oxidanyl-propanoic acid

(2~{S},3~{R})-2-azanyl-3-(1~{H}-indol-3-yl)-3-oxidanyl-propanoic acid

C11H12N2O3 (220.0847882)


   

Glycyldehydrophenylalanine

Glycyldehydrophenylalanine

C11H12N2O3 (220.0847882)


   

beta-Hydroxy-L-tryptophan

beta-Hydroxy-L-tryptophan

C11H12N2O3 (220.0847882)


   

N-(2-hydroxy-5-methoxy-1H-indol-3-yl)acetamide

N-(2-hydroxy-5-methoxy-1H-indol-3-yl)acetamide

C11H12N2O3 (220.0847882)


   

2-[(2-Aminoacetyl)amino]-3-phenylprop-2-enoic acid

2-[(2-Aminoacetyl)amino]-3-phenylprop-2-enoic acid

C11H12N2O3 (220.0847882)


   

2,3-Dimethyl-6-nitro-5-trideuteromethoxyindole

2,3-Dimethyl-6-nitro-5-trideuteromethoxyindole

C11H12N2O3 (220.0847882)


   

5-hydroxy-L-tryptophan zwitterion

5-hydroxy-L-tryptophan zwitterion

C11H12N2O3 (220.0847882)


An amino acid zwitterion arising from transfer of a proton from the carboxy to the amino group of 5-hydroxy-L-tryptophan; major species at pH 7.3.

   

3-ethyl-5-(4-hydroxyphenyl)imidazolidine-2,4-dione

3-ethyl-5-(4-hydroxyphenyl)imidazolidine-2,4-dione

C11H12N2O3 (220.0847882)


   

3-hydroxy-L-tryptophan

3-hydroxy-L-tryptophan

C11H12N2O3 (220.0847882)


A hydroxy-L-tryptophan which carries a hydroxy group at position 3.

   

7-hydroxytryptophan

7-hydroxytryptophan

C11H12N2O3 (220.0847882)


A hydroxytryptophan substituted by a hydroxy group at position 7 on the indole ring.