Chemical Formula: C10H13NO4

Chemical Formula C10H13NO4

Found 108 metabolite its formula value is C10H13NO4

Methyldopa

3-(3,4-Dihydroxyphenyl)-alpha-methyl-L-a lanine

C10H13NO4 (211.0844538)


Methyl dopa appears as colorless or almost colorless crystals or white to yellowish-white fine powder. Almost tasteless. In the sesquihydrate form. pH (saturated aqueous solution) about 5.0. (NTP, 1992) Alpha-methyl-L-dopa is a derivative of L-tyrosine having a methyl group at the alpha-position and an additional hydroxy group at the 3-position on the phenyl ring. It has a role as a hapten, an antihypertensive agent, an alpha-adrenergic agonist, a peripheral nervous system drug and a sympatholytic agent. It is a L-tyrosine derivative and a non-proteinogenic L-alpha-amino acid. Methyldopa, or α-methyldopa, is a centrally acting sympatholytic agent and an antihypertensive agent. It is an analog of DOPA (3,4‐hydroxyphenylanine), and it is a prodrug, meaning that the drug requires biotransformation to an active metabolite for therapeutic effects. Methyldopa works by binding to alpha(α)-2 adrenergic receptors as an agonist, leading to the inhibition of adrenergic neuronal outflow and reduction of vasoconstrictor adrenergic signals. Methyldopa exists in two isomers D-α-methyldopa and L-α-methyldopa, which is the active form. First introduced in 1960 as an antihypertensive agent, methyldopa was considered to be useful in certain patient populations, such as pregnant women and patients with renal insufficiency. Since then, methyldopa was largely replaced by newer, better-tolerated antihypertensive agents; however, it is still used as monotherapy or in combination with [hydrochlorothiazide]. Methyldopa is also available as intravenous injection, which is used to manage hypertension when oral therapy is unfeasible and to treat hypertensive crisis. Methyldopa anhydrous is a Central alpha-2 Adrenergic Agonist. The mechanism of action of methyldopa anhydrous is as an Adrenergic alpha2-Agonist. Methyldopa (alpha-methyldopa or α-methyldopa) is a centrally active sympatholytic agent that has been used for more than 50 years for the treatment of hypertension. Methyldopa has been clearly linked to instances of acute and chronic liver injury that can be severe and even fatal. Methyldopa is a phenylalanine derivative and an aromatic amino acid decarboxylase inhibitor with antihypertensive activity. Methyldopa is a prodrug and is metabolized in the central nervous system. The antihypertensive action of methyldopa seems to be attributable to its conversion into alpha-methylnorepinephrine, which is a potent alpha-2 adrenergic agonist that binds to and stimulates potent central inhibitory alpha-2 adrenergic receptors. This results in a decrease in sympathetic outflow and decreased blood pressure. Methyldopa or alpha-methyldopa (brand names Aldomet, Apo-Methyldopa, Dopamet, Novomedopa) is a centrally-acting adrenergic antihypertensive medication. Its use is now deprecated following introduction of alternative safer classes of agents. However it continues to have a role in otherwise difficult to treat hypertension and gestational hypertension (formerly known as pregnancy-induced hypertension). Methyldopa is an aromatic-amino-acid decarboxylase inhibitor in animals and in man. Only methyldopa, the L-isomer of alpha-methyldopa, has the ability to inhibit dopa decarboxylase and to deplete animal tissues of norepinephrine. In man the antihypertensive activity appears to be due solely to the L-isomer. About twice the dose of the racemate (DL-alpha-methyldopa) is required for equal antihypertensive effect. Methyldopa has no direct effect on cardiac function and usually does not reduce glomerular filtration rate, renal blood flow, or filtration fraction. Cardiac output usually is maintained without cardiac acceleration. In some patients the heart rate is slowed. Normal or elevated plasma renin activity may decrease in the course of methyldopa therapy. Methyldopa reduces both supine and standing blood pressure. Methyldopa usually produces highly effective lowering of the supine pressure with infrequent symptomatic postural hypotension. Exercise hy... Methyldopa or alpha-methyldopa (brand names Aldomet, Apo-Methyldopa, Dopamet, Novomedopa) is a centrally-acting adrenergic antihypertensive medication. Its use is now deprecated following introduction of alternative safer classes of agents. However it continues to have a role in otherwise difficult to treat hypertension and gestational hypertension (formerly known as pregnancy-induced hypertension). Methyldopa is an aromatic-amino-acid decarboxylase inhibitor in animals and in man. Only methyldopa, the L-isomer of alpha-methyldopa, has the ability to inhibit dopa decarboxylase and to deplete animal tissues of norepinephrine. In man the antihypertensive activity appears to be due solely to the L-isomer. About twice the dose of the racemate (DL-alpha-methyldopa) is required for equal antihypertensive effect. Methyldopa has no direct effect on cardiac function and usually does not reduce glomerular filtration rate, renal blood flow, or filtration fraction. Cardiac output usually is maintained without cardiac acceleration. In some patients the heart rate is slowed. Normal or elevated plasma renin activity may decrease in the course of methyldopa therapy. Methyldopa reduces both supine and standing blood pressure. Methyldopa usually produces highly effective lowering of the supine pressure with infrequent symptomatic postural hypotension. Exercise hypotension and diurnal blood pressure variations rarely occur. Methyldopa, in its active metabolite form, is a central alpha-2 receptor agonist. Using methyldopa leads to alpha-2 receptor-negative feedback to sympathetic nervous system (SNS) (centrally and peripherally), allowing peripheral sympathetic nervous system tone to decrease. Such activity leads to a decrease in total peripheral resistance (TPR) and cardiac output. When introduced it was a mainstay of antihypertensive therapy, but its use has declined, with increased use of other safer classes of agents. One of its important present-day uses is in the management of pregnancy-induced hypertension, as it is relatively safe in pregnancy compared to other antihypertensive drugs (Wikipedia). Methyldopa or alpha-methyldopa (brand names Aldomet, Apo-Methyldopa, Dopamet, Novomedopa) is a centrally-acting adrenergic antihypertensive medication. Its use is now deprecated following introduction of alternative safer classes of agents. However it continues to have a role in otherwise difficult to treat hypertension and gestational hypertension (formerly known as pregnancy-induced hypertension).; Methyldopa is an aromatic-amino-acid decarboxylase inhibitor in animals and in man. Only methyldopa, the L-isomer of alpha-methyldopa, has the ability to inhibit dopa decarboxylase and to deplete animal tissues of norepinephrine. In man the antihypertensive activity appears to be due solely to the L-isomer. About twice the dose of the racemate (DL-alpha-methyldopa) is required for equal antihypertensive effect. Methyldopa has no direct effect on cardiac function and usually does not reduce glomerular filtration rate, renal blood flow, or filtration fraction. Cardiac output usually is maintained without cardiac acceleration. In some patients the heart rate is slowed. Normal or elevated plasma renin activity may decrease in the course of methyldopa therapy. Methyldopa reduces both supine and standing blood pressure. Methyldopa usually produces highly effective lowering of the supine pressure with infrequent symptomatic postural hypotension. Exercise hypotension and diurnal blood pressure variations rarely occur.; Methyldopa, in its active metabolite form, is a central alpha-2 receptor agonist. Using methyldopa leads to alpha-2 receptor-negative feedback to sympathetic nervous system (SNS) (centrally and peripherally), allowing peripheral sympathetic nervous system tone to decrease. Such activity leads to a decrease in total peripheral resistance (TPR) and cardiac output.; When introduced it was a mainstay of antihypertensive therapy, but its use has declined, with increased use of other safer classes of agents. One of its important present-day uses is in the management of pregnancy-induced hypertension, as it is relatively safe in pregnancy compared to other antihypertensive drugs. C - Cardiovascular system > C02 - Antihypertensives > C02A - Antiadrenergic agents, centrally acting > C02AB - Methyldopa D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents > D013565 - Sympatholytics D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D000322 - Adrenergic Agonists C78274 - Agent Affecting Cardiovascular System > C270 - Antihypertensive Agent D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents C78272 - Agent Affecting Nervous System > C66884 - Dopamine Agonist Methyldopa (L-(-)-α-Methyldopa), a potent antihyoertensive agent, is an alpha-adrenergic agonist (selective for α2-adrenergic receptors). Methyldopa is a proagent and is metabolized (α-Methylepinephrine) in the central nervous system[1][2].

   

Enicoflavine

3-(Aminomethylene)-alpha-ethenyltetrahydro-4-hydroxy-2-oxo-2H-pyran-4-acetaldehyde

C10H13NO4 (211.0844538)


   

3-Hydroxy-5-methyl-L-tyrosine

3-Hydroxy-5-methyl-L-tyrosine

C10H13NO4 (211.0844538)


   

3-Methoxytyrosine

2-amino-3-(4-hydroxy-3-methoxyphenyl)propanoic acid

C10H13NO4 (211.0844538)


3-Methoxytyrosine, also known as 3-O-methyldopa or vanilalanine, belongs to the class of organic compounds known as tyrosine and derivatives. Tyrosine and derivatives are compounds containing tyrosine or a derivative thereof resulting from reaction of tyrosine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. 3-Methoxytyrosine is one of the main biochemical markers for Aromatic L-amino acid decarboxylase (AADC, EC4.1.1.28) deficiency, an inborn error of metabolism that affects serotonin and dopamine biosynthesis. Chronically high levels of 3-methoxytyrosine are associated with aromatic L-amino acid decarboxylase (AADC, 28) deficiency, an inborn error of metabolism that affects serotonin and dopamine biosynthesis. 3-Methoxytyrosine is a potentially toxic compound. 3-Methoxytyrosine, with regard to humans, has been found to be associated with several diseases such as epilepsy, early-onset, vitamin b6-dependent and pyridoxamine 5-prime-phosphate oxidase deficiency; 3-methoxytyrosine has also been linked to several inborn metabolic disorders including sepiapterin reductase deficiency and aromatic l-amino acid decarboxylase deficiency. 3-Methoxytyrosine is one of the main biochemical markers for Aromatic L-amino acid decarboxylase (AADC, EC 4.1.1.28) deficiency, an inborn error of metabolism that affects serotonin and dopamine biosynthesis. Patients are usually detected in infancy due to developmental delay, hypotonia, and extrapyramidal movements. Diagnosis is based on an abnormal neurotransmitter metabolite profile in CSF and reduced AADC activity in plasma. 3-methoxytyrosine is elevated in CSF, plasma, and urine. (PMID 1357595, 1281049, 16288991) [HMDB] 3-O-Methyldopa (3-Methoxy-L-tyrosine) is a metabolite of L-DOPA which is formed by catechol-O-methyltransferase (COMT). 3-O-Methyldopa competitively inhibits the pharmacodynamics of l-DOPA and dopamine[1]. 3-O-Methyldopa (3-Methoxy-L-tyrosine) is a metabolite of L-DOPA which is formed by catechol-O-methyltransferase (COMT). 3-O-Methyldopa competitively inhibits the pharmacodynamics of l-DOPA and dopamine[1].

   

3-O-Methyl-a-methyldopa

(2S)-2-amino-3-(4-hydroxy-3-methoxyphenyl)propanoic acid

C10H13NO4 (211.0844538)


3-O-Methyl-a-methyldopa is a metabolite of methyldopa. Methyldopa (-α-Methyl-3,4-dihydroxyphenylalanine; Aldomet, Aldoril, Dopamet, Dopegyt, etc. ) is an alpha-adrenergic agonist (selective for α2-adrenergic receptors) psychoactive drug used as a sympatholytic or antihypertensive. Its use is now mostly deprecated following the introduction of alternative safer classes of agents. However, it continues to have a role in otherwise difficult to treat hypertension and gestational hypertension (also known as pregnancy-induced hypertension). (Wikipedia) 3-O-Methyldopa (3-Methoxy-L-tyrosine) is a metabolite of L-DOPA which is formed by catechol-O-methyltransferase (COMT). 3-O-Methyldopa competitively inhibits the pharmacodynamics of l-DOPA and dopamine[1]. 3-O-Methyldopa (3-Methoxy-L-tyrosine) is a metabolite of L-DOPA which is formed by catechol-O-methyltransferase (COMT). 3-O-Methyldopa competitively inhibits the pharmacodynamics of l-DOPA and dopamine[1].

   

3-Hydroxy-alpha-methyl-DL-tyrosine

2-amino-3-(3,4-dihydroxyphenyl)-2-methylpropanoic acid

C10H13NO4 (211.0844538)


C - Cardiovascular system > C02 - Antihypertensives > C02A - Antiadrenergic agents, centrally acting > C02AB - Methyldopa D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents > D013565 - Sympatholytics D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D000322 - Adrenergic Agonists D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents

   

Melevodopa

Levodopa methyl ester hydrochloride, (DL)-isomer

C10H13NO4 (211.0844538)


   

CJ 14877

Methyl 5-(1,2-dihydroxypropyl)-2-pyridinecarboxylate

C10H13NO4 (211.0844538)


   

n-salicyloyl-2-aminopropan-1,3-diol

n-salicyloyl-2-aminopropan-1,3-diol

C10H13NO4 (211.0844538)


   

3,4,5-Trimethoxybenzamide

3,4,5-Trimethoxybenzamide

C10H13NO4 (211.0844538)


   

2-amino-3-(2,4-dihydroxy-6-methylphenyl)propanoic acid

2-amino-3-(2,4-dihydroxy-6-methylphenyl)propanoic acid

C10H13NO4 (211.0844538)


   

DIETHYL 1H-PYRROLE-2,3-DICARBOXYLATE

DIETHYL 1H-PYRROLE-2,3-DICARBOXYLATE

C10H13NO4 (211.0844538)


   

3-(Hydroxymethyl)tyrosine

3-(Hydroxymethyl)tyrosine

C10H13NO4 (211.0844538)


   
   

Bryonamide B

Benzamide, 4-hydroxy-N-(2-hydroxyethyl)-3-methoxy-

C10H13NO4 (211.0844538)


   
   
   

N-[2,5-dihydroxy-4-(methoxymethyl)phenyl]acetamide

N-[2,5-dihydroxy-4-(methoxymethyl)phenyl]acetamide

C10H13NO4 (211.0844538)


   

Methyl 5-(1,2-dihydroxypropyl)pyridine-2-carboxylate

Methyl 5-(1,2-dihydroxypropyl)pyridine-2-carboxylate

C10H13NO4 (211.0844538)


   

methyl-(5-formyl-1H-pyrrole-2-yl)-4-hydroxybutyrate

methyl-(5-formyl-1H-pyrrole-2-yl)-4-hydroxybutyrate

C10H13NO4 (211.0844538)


   

N-[2-(3,4-Dihydroxyphenyl)-2-hydroxyethyl]acetamide

N-[2-(3,4-Dihydroxyphenyl)-2-hydroxyethyl]acetamide

C10H13NO4 (211.0844538)


   

N-[(3,4,5-trimethoxyphenyl)methylidene]hydroxylamine

N-[(3,4,5-trimethoxyphenyl)methylidene]hydroxylamine

C10H13NO4 (211.0844538)


   

6-Maleimidocaproic acid

6-Maleimidocapronic acid

C10H13NO4 (211.0844538)


   

Methyldopa

1H-INDAZOLE-3,6-DICARBOXYLICACID,6-METHYLESTER

C10H13NO4 (211.0844538)


CONFIDENCE standard compound; INTERNAL_ID 1284; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 1003; ORIGINAL_PRECURSOR_SCAN_NO 1001 C - Cardiovascular system > C02 - Antihypertensives > C02A - Antiadrenergic agents, centrally acting > C02AB - Methyldopa D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents > D013565 - Sympatholytics D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D000322 - Adrenergic Agonists C78274 - Agent Affecting Cardiovascular System > C270 - Antihypertensive Agent D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents C78272 - Agent Affecting Nervous System > C66884 - Dopamine Agonist CONFIDENCE standard compound; INTERNAL_ID 1284; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 1000; ORIGINAL_PRECURSOR_SCAN_NO 997 CONFIDENCE standard compound; INTERNAL_ID 1284; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 999; ORIGINAL_PRECURSOR_SCAN_NO 998 CONFIDENCE standard compound; INTERNAL_ID 1284; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 998; ORIGINAL_PRECURSOR_SCAN_NO 996 CONFIDENCE standard compound; INTERNAL_ID 1284; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 1004; ORIGINAL_PRECURSOR_SCAN_NO 1001 CONFIDENCE standard compound; INTERNAL_ID 1284; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 996; ORIGINAL_PRECURSOR_SCAN_NO 994 CONFIDENCE standard compound; INTERNAL_ID 1284; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 1895; ORIGINAL_PRECURSOR_SCAN_NO 1893 CONFIDENCE standard compound; INTERNAL_ID 1284; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 1905; ORIGINAL_PRECURSOR_SCAN_NO 1903 CONFIDENCE standard compound; INTERNAL_ID 1284; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 1906; ORIGINAL_PRECURSOR_SCAN_NO 1904 CONFIDENCE standard compound; INTERNAL_ID 1284; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 1906; ORIGINAL_PRECURSOR_SCAN_NO 1903 Methyldopa (L-(-)-α-Methyldopa), a potent antihyoertensive agent, is an alpha-adrenergic agonist (selective for α2-adrenergic receptors). Methyldopa is a proagent and is metabolized (α-Methylepinephrine) in the central nervous system[1][2].

   

Methoxytyrosine

Methoxytyrosine

C10H13NO4 (211.0844538)


Annotation level-3

   

3-METHOXY-L-TYROSINE

3-METHOXY-L-TYROSINE

C10H13NO4 (211.0844538)


   

3-Methoxytyrosine

(DL)-3-O-Methyldopa

C10H13NO4 (211.0844538)


3-O-Methyldopa (3-Methoxy-L-tyrosine) is a metabolite of L-DOPA which is formed by catechol-O-methyltransferase (COMT). 3-O-Methyldopa competitively inhibits the pharmacodynamics of l-DOPA and dopamine[1]. 3-O-Methyldopa (3-Methoxy-L-tyrosine) is a metabolite of L-DOPA which is formed by catechol-O-methyltransferase (COMT). 3-O-Methyldopa competitively inhibits the pharmacodynamics of l-DOPA and dopamine[1].

   

Vanilalanine

L-4-Hydroxy-3-methoxyphenylalanine

C10H13NO4 (211.0844538)


   

3-O-Methyl-L-DOPA

3-O-Methyl-L-DOPA

C10H13NO4 (211.0844538)


3-O-Methyldopa (3-Methoxy-L-tyrosine) is a metabolite of L-DOPA which is formed by catechol-O-methyltransferase (COMT). 3-O-Methyldopa competitively inhibits the pharmacodynamics of l-DOPA and dopamine[1]. 3-O-Methyldopa (3-Methoxy-L-tyrosine) is a metabolite of L-DOPA which is formed by catechol-O-methyltransferase (COMT). 3-O-Methyldopa competitively inhibits the pharmacodynamics of l-DOPA and dopamine[1].

   

6-HYDROXY-1,2,3,4-TETRAHYDRO-3-ISOQUINOLINECARBOXYLIC ACIDHYDRATE

6-HYDROXY-1,2,3,4-TETRAHYDRO-3-ISOQUINOLINECARBOXYLIC ACIDHYDRATE

C10H13NO4 (211.0844538)


   

5-(4-Morpholinylmethyl)-2-furoic acid

5-(4-Morpholinylmethyl)-2-furoic acid

C10H13NO4 (211.0844538)


   

Methyl 4-amino-2,6-dimethoxybenzoate

Methyl 4-amino-2,6-dimethoxybenzoate

C10H13NO4 (211.0844538)


   

2,2-DIMETHYL-5-(2-TETRAHYDROPYRROLYLIDENE)-1,3-DIOXANE-4,6-DIONE

2,2-DIMETHYL-5-(2-TETRAHYDROPYRROLYLIDENE)-1,3-DIOXANE-4,6-DIONE

C10H13NO4 (211.0844538)


   

3-AMINO-3-(2-HYDROXY-3-METHOXY-PHENYL)-PROPIONIC ACID

3-AMINO-3-(2-HYDROXY-3-METHOXY-PHENYL)-PROPIONIC ACID

C10H13NO4 (211.0844538)


   

N-[(2,3,4-trimethoxyphenyl)methylidene]hydroxylamine

N-[(2,3,4-trimethoxyphenyl)methylidene]hydroxylamine

C10H13NO4 (211.0844538)


   

2-(morpholin-4-ylmethyl)furan-3-carboxylic acid

2-(morpholin-4-ylmethyl)furan-3-carboxylic acid

C10H13NO4 (211.0844538)


   

methyl 3-carboxy-1,4-dimethyl-1H-pyrrole-2-acetate

methyl 3-carboxy-1,4-dimethyl-1H-pyrrole-2-acetate

C10H13NO4 (211.0844538)


   

3-AMINO-3-(2-HYDROXY-4-METHOXY-PHENYL)-PROPIONIC ACID

3-AMINO-3-(2-HYDROXY-4-METHOXY-PHENYL)-PROPIONIC ACID

C10H13NO4 (211.0844538)


   

AMINO-(2,3-DIMETHOXY-PHENYL)-ACETIC ACID

AMINO-(2,3-DIMETHOXY-PHENYL)-ACETIC ACID

C10H13NO4 (211.0844538)


   

Benzene,1,4-diethoxy-2-nitro-

Benzene,1,4-diethoxy-2-nitro-

C10H13NO4 (211.0844538)


   

Melevodopa

(2S)-2-amino-3-(3,4-dihydroxyphenyl)propanoic acid methyl ester

C10H13NO4 (211.0844538)


N - Nervous system > N04 - Anti-parkinson drugs > N04B - Dopaminergic agents > N04BA - Dopa and dopa derivatives D002491 - Central Nervous System Agents > D018726 - Anti-Dyskinesia Agents > D000978 - Antiparkinson Agents C78272 - Agent Affecting Nervous System > C66884 - Dopamine Agonist

   

2-Ethoxycarbonyl-3,5-dimethyl-1H-pyrrole-3-carboxylic acid

2-Ethoxycarbonyl-3,5-dimethyl-1H-pyrrole-3-carboxylic acid

C10H13NO4 (211.0844538)


   

(1,3-BENZOXAZOL-2-YLTHIO)ACETICACID

(1,3-BENZOXAZOL-2-YLTHIO)ACETICACID

C10H13NO4 (211.0844538)


   

Ethyl 2,4-dihydroxy-5,6-dimethylnicotinate

Ethyl 2,4-dihydroxy-5,6-dimethylnicotinate

C10H13NO4 (211.0844538)


   

5-hydroxy-2-(4-morpholinylmethyl)-4H-pyran-4-one(SALTDATA: FREE)

5-hydroxy-2-(4-morpholinylmethyl)-4H-pyran-4-one(SALTDATA: FREE)

C10H13NO4 (211.0844538)


   

(2,2-dimethyl-1,3-dioxolan-4-yl)methyl 2-cyanoprop-2-enoate

(2,2-dimethyl-1,3-dioxolan-4-yl)methyl 2-cyanoprop-2-enoate

C10H13NO4 (211.0844538)


   

5-(morpholin-4-ylmethyl)furan-3-carboxylic acid

5-(morpholin-4-ylmethyl)furan-3-carboxylic acid

C10H13NO4 (211.0844538)


   

(S)-2-TERT-BUTOXYCARBONYLAMINO-3-(3-HYDROXY-PHENYL)-PROPIONICACID

(S)-2-TERT-BUTOXYCARBONYLAMINO-3-(3-HYDROXY-PHENYL)-PROPIONICACID

C10H13NO4 (211.0844538)


   

methyl 5-amino-2,4-dimethoxybenzoate

methyl 5-amino-2,4-dimethoxybenzoate

C10H13NO4 (211.0844538)


   

3-amino-3-(4-hydroxy-3-methoxyphenyl)propanoic acid

3-amino-3-(4-hydroxy-3-methoxyphenyl)propanoic acid

C10H13NO4 (211.0844538)


   

4-(Ethoxycarbonyl)-3,5-dimethyl-1H-pyrrole-2-carboxylic acid

4-(Ethoxycarbonyl)-3,5-dimethyl-1H-pyrrole-2-carboxylic acid

C10H13NO4 (211.0844538)


   

Methyl 2-amino-4,5-dimethoxybenzoate

Methyl 2-amino-4,5-dimethoxybenzoate

C10H13NO4 (211.0844538)


   

3-AMINO-3-(4-HYDROXY-2-METHOXY-PHENYL)-PROPIONIC ACID

3-AMINO-3-(4-HYDROXY-2-METHOXY-PHENYL)-PROPIONIC ACID

C10H13NO4 (211.0844538)


   

(R)-3-(3-Hydroxy-4-methoxyphenyl)-beta-alanine

(R)-3-(3-Hydroxy-4-methoxyphenyl)-beta-alanine

C10H13NO4 (211.0844538)


   

Amino(3,5-dimethoxyphenyl)acetic acid

Amino(3,5-dimethoxyphenyl)acetic acid

C10H13NO4 (211.0844538)


   

Methyl 2-amino-4,6-dimethoxybenzoate

Methyl 2-amino-4,6-dimethoxybenzoate

C10H13NO4 (211.0844538)


   

2-Amino-5-ethoxy-4-methoxybenzoic acid

2-Amino-5-ethoxy-4-methoxybenzoic acid

C10H13NO4 (211.0844538)


   

ethyl 3-methoxy-1-methyl-2-oxo-1,2-dihydropyridine-4-carboxylate

ethyl 3-methoxy-1-methyl-2-oxo-1,2-dihydropyridine-4-carboxylate

C10H13NO4 (211.0844538)


   

(-)-6BETA-HYDROXYMETHYL-7ALPHA-HYDROXY-CIS-2-OXABICYCLO[3.3.0]OCTAN-3-ONE

(-)-6BETA-HYDROXYMETHYL-7ALPHA-HYDROXY-CIS-2-OXABICYCLO[3.3.0]OCTAN-3-ONE

C10H13NO4 (211.0844538)


   

diethyl 1H-pyrrole-3,4-dicarboxylate

diethyl 1H-pyrrole-3,4-dicarboxylate

C10H13NO4 (211.0844538)


   

1-(2,2-Dimethoxyethyl)-2-nitrobenzene

1-(2,2-Dimethoxyethyl)-2-nitrobenzene

C10H13NO4 (211.0844538)


   

4-(2-Aminoethoxy)-3-methoxybenzoic acid

4-(2-Aminoethoxy)-3-methoxybenzoic acid

C10H13NO4 (211.0844538)


   

Ethyl 4-Ethoxy-2-oxo-1,2-dihydropyridine-3-carboxylate

Ethyl 4-Ethoxy-2-oxo-1,2-dihydropyridine-3-carboxylate

C10H13NO4 (211.0844538)


   

Toluene, 5-ethoxy-4-methoxy-2-nitro- (6CI)

Toluene, 5-ethoxy-4-methoxy-2-nitro- (6CI)

C10H13NO4 (211.0844538)


   

Toluene, 4-ethoxy-5-methoxy-2-nitro- (6CI)

Toluene, 4-ethoxy-5-methoxy-2-nitro- (6CI)

C10H13NO4 (211.0844538)


   

Toluene, 3-ethoxy-4-methoxy-5-nitro- (6CI)

Toluene, 3-ethoxy-4-methoxy-5-nitro- (6CI)

C10H13NO4 (211.0844538)


   

3,4,5-TRIMETHOXYBENZALDOXIME

3,4,5-TRIMETHOXYBENZALDOXIME

C10H13NO4 (211.0844538)


   

3-(3-Hydroxy-4-methoxyphenyl)-DL-beta-alanine

3-(3-Hydroxy-4-methoxyphenyl)-DL-beta-alanine

C10H13NO4 (211.0844538)


   

2-[(Furan-2-carbonyl)-amino]-pentanoic acid

2-[(Furan-2-carbonyl)-amino]-pentanoic acid

C10H13NO4 (211.0844538)


   

(2R)-2-amino-3-(3,4-dihydroxyphenyl)-2-methylpropanoic acid

(2R)-2-amino-3-(3,4-dihydroxyphenyl)-2-methylpropanoic acid

C10H13NO4 (211.0844538)


   

Benzamide,3,4,5-trihydroxy-N-propyl- (9CI)

Benzamide,3,4,5-trihydroxy-N-propyl- (9CI)

C10H13NO4 (211.0844538)


   

methyl (E)-3-(5-nitrocyclohex-1-en-1-yl)acrylate

methyl (E)-3-(5-nitrocyclohex-1-en-1-yl)acrylate

C10H13NO4 (211.0844538)


   

Benzene,1,2-diethoxy-4-nitro-

Benzene,1,2-diethoxy-4-nitro-

C10H13NO4 (211.0844538)


   

3-(2,4-DIMETHYL-5-CARBOXY-1H-PYRROLE-3-YL)PROPANOIC ACID

3-(2,4-DIMETHYL-5-CARBOXY-1H-PYRROLE-3-YL)PROPANOIC ACID

C10H13NO4 (211.0844538)


   

Lisadimate

2,3-dihydroxypropyl 4-aminobenzoate

C10H13NO4 (211.0844538)


C1892 - Chemopreventive Agent > C851 - Sunscreen

   

3-AMINO-6-(MORPHOLIN-4-YL)PYRIDAZINE

3-AMINO-6-(MORPHOLIN-4-YL)PYRIDAZINE

C10H13NO4 (211.0844538)


   

(+)-4-FLUOROTARTRANILICACID

(+)-4-FLUOROTARTRANILICACID

C10H13NO4 (211.0844538)


   

AMINO-(4-HYDROXY-3-ETHOXY-PHENYL)-ACETIC ACID

AMINO-(4-HYDROXY-3-ETHOXY-PHENYL)-ACETIC ACID

C10H13NO4 (211.0844538)


   

1-(tert-Butoxycarbonyl)-1H-pyrrole-2-carboxylic acid

1-(tert-Butoxycarbonyl)-1H-pyrrole-2-carboxylic acid

C10H13NO4 (211.0844538)


   

2-amino-3-(2-hydroxy-3-methoxyphenyl)propanoic acid

2-amino-3-(2-hydroxy-3-methoxyphenyl)propanoic acid

C10H13NO4 (211.0844538)


   

Tyrosine, 3-hydroxy-O-methyl-

Tyrosine, 3-hydroxy-O-methyl-

C10H13NO4 (211.0844538)


   

3-Hydroxy-N-methyl-L-tyrosine

3-Hydroxy-N-methyl-L-tyrosine

C10H13NO4 (211.0844538)


   

3-(3,4-Dihydroxyphenyl)-2-(methylamino)propanoic acid

3-(3,4-Dihydroxyphenyl)-2-(methylamino)propanoic acid

C10H13NO4 (211.0844538)


   

L-4-Hydroxy-3-methoxyphenylalanine

L-4-Hydroxy-3-methoxyphenylalanine

C10H13NO4 (211.0844538)


   

(2S)-2-ammonio-3-(3,4-dihydroxy-5-methylphenyl)propanoate

(2S)-2-ammonio-3-(3,4-dihydroxy-5-methylphenyl)propanoate

C10H13NO4 (211.0844538)


   

3-hydroxy-L-homotyrosine

3-hydroxy-L-homotyrosine

C10H13NO4 (211.0844538)


   
   

(2S,3S)-2-amino-3-hydroxy-4-(4-hydroxyphenyl)butanoic acid

(2S,3S)-2-amino-3-hydroxy-4-(4-hydroxyphenyl)butanoic acid

C10H13NO4 (211.0844538)


   

N-methyl-L-dopa zwitterion

N-methyl-L-dopa zwitterion

C10H13NO4 (211.0844538)


   

N-methyl-D-dopa zwitterion

N-methyl-D-dopa zwitterion

C10H13NO4 (211.0844538)


   

3-hydroxy-N-methyl-D-tyrosine

3-hydroxy-N-methyl-D-tyrosine

C10H13NO4 (211.0844538)


   

4-O-methyl-L-dopa zwitterion

4-O-methyl-L-dopa zwitterion

C10H13NO4 (211.0844538)


An aromatic L-alpha-amino acid zwitterion resulting from transfer of a proton from the carboxy to the amino group of 4-O-methyl-L-dopa. Major species at pH 7.3

   

5-hydroxy-3-methyl-L-tyrosine

5-hydroxy-3-methyl-L-tyrosine

C10H13NO4 (211.0844538)


A tyrosine derivative that is L-tyrosine in which the hydrogens at positions 3 and 5 on the phenyl ring are replaced by a methyl and hydroxy groups respectively.

   

3-O-Methyldopa

3-O-Methyldopa

C10H13NO4 (211.0844538)


A L-tyrosine derivative that is the 3-methoxy derivative of L-dopa.

   

L-Methyldopa

3-Hydroxy-alpha-methyl-DL-tyrosine

C10H13NO4 (211.0844538)


C - Cardiovascular system > C02 - Antihypertensives > C02A - Antiadrenergic agents, centrally acting > C02AB - Methyldopa D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents > D013565 - Sympatholytics D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D000322 - Adrenergic Agonists D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents

   

4-O-methyl-L-dopa

4-O-methyl-L-dopa

C10H13NO4 (211.0844538)


An L-dopa in which the hydroxy group at position 4 is replaced by a methoxy group.

   

5-hydroxy-3-methyl-L-tyrosine zwitterion

5-hydroxy-3-methyl-L-tyrosine zwitterion

C10H13NO4 (211.0844538)


An amino acid zwitterion resulting from a transfer of a proton from the carboxy to the amino group of 5-hydroxy-3-methyl-L-tyrosine; major species at pH 7.3.

   

alpha-Methyl-L-dopa

alpha-Methyl-L-dopa

C10H13NO4 (211.0844538)


A derivative of L-tyrosine having a methyl group at the alpha-position and an additional hydroxy group at the 3-position on the phenyl ring.

   

3-O-methyldopa zwitterion

3-O-methyldopa zwitterion

C10H13NO4 (211.0844538)


An aromatic L-alpha-amino acid zwitterion resulting from transfer of a proton from the carboxy to the amino group of 3-O-methyldopa. Major species at pH 7.3

   

(5-formyl-1h-pyrrol-2-yl)methyl 4-hydroxybutanoate

(5-formyl-1h-pyrrol-2-yl)methyl 4-hydroxybutanoate

C10H13NO4 (211.0844538)


   

n-[2,5-dihydroxy-4-(methoxymethyl)phenyl]ethanimidic acid

n-[2,5-dihydroxy-4-(methoxymethyl)phenyl]ethanimidic acid

C10H13NO4 (211.0844538)


   

5,7-dihydroxy-2-(2-hydroxy-2-methylpropyl)azepin-4-one

5,7-dihydroxy-2-(2-hydroxy-2-methylpropyl)azepin-4-one

C10H13NO4 (211.0844538)


   

methyl 2-[2-formyl-5-(hydroxymethyl)pyrrol-1-yl]propanoate

methyl 2-[2-formyl-5-(hydroxymethyl)pyrrol-1-yl]propanoate

C10H13NO4 (211.0844538)


   

[2-(ethoxymethyl)-5-formylpyrrol-1-yl]acetic acid

[2-(ethoxymethyl)-5-formylpyrrol-1-yl]acetic acid

C10H13NO4 (211.0844538)


   

4-[2-formyl-5-(hydroxymethyl)pyrrol-1-yl]butanoic acid

4-[2-formyl-5-(hydroxymethyl)pyrrol-1-yl]butanoic acid

C10H13NO4 (211.0844538)


   

methyl 5-[(1s,2s)-1,2-dihydroxypropyl]pyridine-2-carboxylate

methyl 5-[(1s,2s)-1,2-dihydroxypropyl]pyridine-2-carboxylate

C10H13NO4 (211.0844538)


   

n-(1,3-dihydroxypropan-2-yl)-2-hydroxybenzenecarboximidic acid

n-(1,3-dihydroxypropan-2-yl)-2-hydroxybenzenecarboximidic acid

C10H13NO4 (211.0844538)