Exact Mass: 101.0841

Exact Mass Matches: 101.0841

Found 110 metabolites which its exact mass value is equals to given mass value 101.0841, within given mass tolerance error 0.001 dalton. Try search metabolite list with more accurate mass tolerance error 0.0002 dalton.

Isovaleramide

TRIMETHYLENEDI(THIOTOSYLATE)

C5H11NO (101.0841)


Isovaleramide is a natural product found in Rhizoclonium hieroglyphicum with data available. C78272 - Agent Affecting Nervous System > C28197 - Antianxiety Agent Isovaleramide is an anticonvulsant that modulates central nervous system activity.

   

Pentanamide

pentanimidic acid

C5H11NO (101.0841)


   

SCHEMBL534447

Isobutyraldoxime O-methyl ether

C5H11NO (101.0841)


   

4-Methylaminobutanal

4-(Methylamino)butanal

C5H11NO (101.0841)


   

5-Aminopentanal

5-Amino-pentanal

C5H11NO (101.0841)


The aminoaldehydes 5-aminopentanal, derived from the oxidation of the diamines putrescine and cadaverine,is produced utilizing a copper amine oxidase (CAO) from Euphorbia characias latex and tested with in vitro cultivation of Leishmania infantum promastigotes.Whereas the aminoaldehydes derived from the oxidation of the diamines were stimulating factors for growth of Leishmania infantum promastigotes, the aldehydes derived from polyamines oxidation had a drastic inhibitory effect on the vitality and growth of these parasites. Thus, a double scenario arises, showing the use of aldehydes from diamines to obtain a large number of organisms of Leishmania infantum promastigotes to use in serological studies, whereas the aldehydes derived from polyamines could be used as a new strategy for therapeutic treatment against these parasites. [HMDB]. 5-Aminopentanal is found in many foods, some of which are watermelon, sorrel, medlar, and cornmint. The aminoaldehydes 5-aminopentanal, derived from the oxidation of the diamines putrescine and cadaverine,is produced utilizing a copper amine oxidase (CAO) from Euphorbia characias latex and tested with in vitro cultivation of Leishmania infantum promastigotes.Whereas the aminoaldehydes derived from the oxidation of the diamines were stimulating factors for growth of Leishmania infantum promastigotes, the aldehydes derived from polyamines oxidation had a drastic inhibitory effect on the vitality and growth of these parasites. Thus, a double scenario arises, showing the use of aldehydes from diamines to obtain a large number of organisms of Leishmania infantum promastigotes to use in serological studies, whereas the aldehydes derived from polyamines could be used as a new strategy for therapeutic treatment against these parasites.

   

3-Methylbutyraldehyde oxime

3-Methylbutyraldehyde oxime

C5H11NO (101.0841)


   

2-methylbutanal oxime

(1E,2S)-2-methylbutanal oxime

C5H11NO (101.0841)


   

(1Z,2S)-2-methylbutanal oxime

(1Z,2S)-2-methylbutanal oxime

C5H11NO (101.0841)


   

N-butylformamide

N-butylmethanimidic acid

C5H11NO (101.0841)


N-butylformamide is classified as a member of the Secondary carboxylic acid amides. Secondary carboxylic acid amides are compounds containing a secondary carboxylic acid amide functional group, with the general structure RC(=O)N(R)H (R,R=alkyl, aryl). N-butylformamide is considered to be slightly soluble (in water) and acidic

   

N-Ethylpropionamide

N-ethylpropanimidic acid

C5H11NO (101.0841)


N-ethylpropionamide is a member of the class of compounds known as secondary carboxylic acid amides. Secondary carboxylic acid amides are compounds containing a secondary carboxylic acid amide functional group, with the general structure RC(=O)N(R)H (R,R=alkyl, aryl). N-ethylpropionamide is soluble (in water) and a very weakly acidic compound (based on its pKa). N-ethylpropionamide can be found in tea, which makes N-ethylpropionamide a potential biomarker for the consumption of this food product.

   

2-Methylbutyramide

2-Methylbutyramide

C5H11NO (101.0841)


   

N,N-Dimethylpropionamide

N,N-Dimethylpropionamide

C5H11NO (101.0841)


   

4-Methylmorpholine

4-Methylmorpholine

C5H11NO (101.0841)


   

(E)-2-Pentanone oxime

(E)-2-Pentanone oxime

C5H11NO (101.0841)


   

N-Pentylidenehydroxylamine

N-Pentylidenehydroxylamine

C5H11NO (101.0841)


   

N-PROPYLACETAMIDE

Acetamide, N-propyl-

C5H11NO (101.0841)


   

Pentaldehyde oxime

Pentaldehyde oxime

C5H11NO (101.0841)


   

2-Methylbutanamide

2-Methylbutanamide

C5H11NO (101.0841)


   

2-aminopentan-3-one

2-aminopentan-3-one

C5H11NO (101.0841)


   

Valeramide

Valeramide

C5H11NO (101.0841)


   

betaine aldehyde

betaine aldehyde

C5H11NO (101.0841)


   

Pentanamide

Pentanamide

C5H11NO (101.0841)


   

(1-Aminocyclobutyl)methanol

(1-Aminocyclobutyl)methanol

C5H11NO (101.0841)


   

1-methylpyrrolidin-3-ol

1-methylpyrrolidin-3-ol

C5H11NO (101.0841)


   

3-ethoxyazetidine

3-ethoxyazetidine

C5H11NO (101.0841)


   

N-Hydroxypiperidine

N-Hydroxypiperidine

C5H11NO (101.0841)


   

3-Hydroxypiperidine

3-Hydroxypiperidine

C5H11NO (101.0841)


   

3-(Aminomethyl)cyclobutanol

3-(Aminomethyl)cyclobutanol

C5H11NO (101.0841)


   

3-Aminocyclopentanol

3-Aminocyclopentanol

C5H11NO (101.0841)


   

Cyclobutanemethanol,3-amino-,cis-(9CI)

Cyclobutanemethanol,3-amino-,cis-(9CI)

C5H11NO (101.0841)


   

[(1S,2S)-2-(Aminomethyl)cyclopropyl]methanol

[(1S,2S)-2-(Aminomethyl)cyclopropyl]methanol

C5H11NO (101.0841)


   

(S)-3-methylmorpholine

(S)-3-methylmorpholine

C5H11NO (101.0841)


   

(3R)-3-Piperidinol

(3R)-3-Piperidinol

C5H11NO (101.0841)


   

(Tetrahydrofuran-3-yl)methylamine

(Tetrahydrofuran-3-yl)methylamine

C5H11NO (101.0841)


   

2,2-Dimethylpropanamide

2,2-Dimethylpropanamide

C5H11NO (101.0841)


   

Diethylformamide

N,N-Diethylformamide

C5H11NO (101.0841)


   

N,N-Dimethylpropanamide

N,N-Dimethylpropanamide

C5H11NO (101.0841)


   

3-(Dimethylamino)propanal

3-(Dimethylamino)propanal

C5H11NO (101.0841)


   

L-(+)-Prolinol

Pyrrolidin-2-ylmethanol

C5H11NO (101.0841)


   

Pivalaldehyde oxime

Pivalaldehyde oxime

C5H11NO (101.0841)


   

2-methylmorpholine

2-methylmorpholine

C5H11NO (101.0841)


   

TRANS-3-AMINO-1-METHYLCYCLOBUTANOL

TRANS-3-AMINO-1-METHYLCYCLOBUTANOL

C5H11NO (101.0841)


   

4-aminopentan-2-one

4-aminopentan-2-one

C5H11NO (101.0841)


   

1-Amino-2-hydroxycyclopentane

1-Amino-2-hydroxycyclopentane

C5H11NO (101.0841)


   

Formamide,N-(1,1-dimethylethyl)-

Formamide,N-(1,1-dimethylethyl)-

C5H11NO (101.0841)


   

3-Methylmorpholine

3-Methylmorpholine

C5H11NO (101.0841)


   

(R)-3-METHOXYPYRROLIDINE

(R)-3-METHOXYPYRROLIDINE

C5H11NO (101.0841)


   

(S)-3-METHOXYPYRROLIDINE

(S)-3-METHOXYPYRROLIDINE

C5H11NO (101.0841)


   

UNII:CGW2AL7PQ7

UNII:CGW2AL7PQ7

C5H11NO (101.0841)


   

3-Methoxycyclobutanamine

3-Methoxycyclobutanamine

C5H11NO (101.0841)


   

cis 3-(Aminomethyl)cyclobutanol

cis 3-(Aminomethyl)cyclobutanol

C5H11NO (101.0841)


   

trans-3-(Aminomethyl)cyclobutanol

trans-3-(Aminomethyl)cyclobutanol

C5H11NO (101.0841)


   

(3S,4S)-4-Methyloxolan-3-amine

(3S,4S)-4-Methyloxolan-3-amine

C5H11NO (101.0841)


   

(3-methyloxetan-3-yl)methanamine

(3-methyloxetan-3-yl)methanamine

C5H11NO (101.0841)


   

(S)-Pyrrolidin-3-ylmethanol

(S)-Pyrrolidin-3-ylmethanol

C5H11NO (101.0841)


   

3-Pyrrolidinylmethanol

3-Pyrrolidinylmethanol

C5H11NO (101.0841)


   

(R)-2-methylmorpholine hydrochloride

(R)-2-methylmorpholine hydrochloride

C5H11NO (101.0841)


   

4,4-DIMETHYLOXAZOLIDINE

4,4-DIMETHYLOXAZOLIDINE

C5H11NO (101.0841)


   

1-(Aminomethyl)cyclobutanol

1-(Aminomethyl)cyclobutanol

C5H11NO (101.0841)


   

N-Isopropylacetamide

N-Isopropylacetamide

C5H11NO (101.0841)


   

Tetrahydrofurfurylamine

Tetrahydrofurfurylamine

C5H11NO (101.0841)


   

3-AMINO-5-HYDROXY-PENTEN-1

3-AMINO-5-HYDROXY-PENTEN-1

C5H11NO (101.0841)


   

2-(azetidin-1-yl)ethanol

2-(azetidin-1-yl)ethanol

C5H11NO (101.0841)


   

a-(Aminomethyl)-cyclopropanemethanol HCl

a-(Aminomethyl)-cyclopropanemethanol HCl

C5H11NO (101.0841)


   

(1R,3R)-3-aminocyclopentan-1-ol hydrochloride

(1R,3R)-3-aminocyclopentan-1-ol hydrochloride

C5H11NO (101.0841)


   

1,4-oxazepane

1,4-oxazepane

C5H11NO (101.0841)


   

3-(Methoxymethyl)azetidine

3-(Methoxymethyl)azetidine

C5H11NO (101.0841)


   

2-(oxetan-3-yl)ethanamine

2-(oxetan-3-yl)ethanamine

C5H11NO (101.0841)


   

4-(methylamino)but-2-en-1-ol

4-(methylamino)but-2-en-1-ol

C5H11NO (101.0841)


   

Tetrahydro-2H-pyran-3-amine

Tetrahydro-2H-pyran-3-amine

C5H11NO (101.0841)


   

[1-(Aminomethyl)cyclopropyl]methanol

[1-(Aminomethyl)cyclopropyl]methanol

C5H11NO (101.0841)


   

3-Amino-cyclobutanemethanol

3-Amino-cyclobutanemethanol

C5H11NO (101.0841)


   

4-Aminotetrahydropyran

4-Aminotetrahydropyran

C5H11NO (101.0841)


   

4-Piperidinol

4-Piperidinol

C5H11NO (101.0841)


   

3-Methoxypyrrolidine

3-Methoxypyrrolidine

C5H11NO (101.0841)


   

Tetrahydro-N-methyl-3-furanamine

Tetrahydro-N-methyl-3-furanamine

C5H11NO (101.0841)


   

2-(Cyclopropylamino)ethanol

2-(Cyclopropylamino)ethanol

C5H11NO (101.0841)


   

(R)-2-Methylmorpholine

(R)-2-Methylmorpholine

C5H11NO (101.0841)


   

1-(Dimethylamino)-2-propanone

1-(Dimethylamino)-2-propanone

C5H11NO (101.0841)


   

Cyclopentanol,2-amino-,(1R,2S)-(9CI)

Cyclopentanol,2-amino-,(1R,2S)-(9CI)

C5H11NO (101.0841)


   

(2R)-2-(Methoxymethyl)azetidine

(2R)-2-(Methoxymethyl)azetidine

C5H11NO (101.0841)


   

4-amino-3-hydroxy-3-methyl-1-butene

4-amino-3-hydroxy-3-methyl-1-butene

C5H11NO (101.0841)


   

(R)-(−)-Tetrahydrofurfurylamine

(R)-(−)-Tetrahydrofurfurylamine

C5H11NO (101.0841)


   

((1R2R)-2-(aminomethyl)cyclopropyl)methanol

((1R2R)-2-(aminomethyl)cyclopropyl)methanol

C5H11NO (101.0841)


   

(1s,3s)-3-Methoxycyclobutan-1-aMine

(1s,3s)-3-Methoxycyclobutan-1-aMine

C5H11NO (101.0841)


   
   

D-prolinol

D-prolinol

C5H11NO (101.0841)


The D-enantiomer of prolinol. Metabolite observed in cancer metabolism.

   

Methylmorpholine

Methylmorpholine

C5H11NO (101.0841)


   

(R)-3-methylmorpholine

(R)-3-methylmorpholine

C5H11NO (101.0841)


   

(2S)-2-(Methoxymethyl)azetidine

(2S)-2-(Methoxymethyl)azetidine

C5H11NO (101.0841)


   

2-Piperidinol

2-Piperidinol

C5H11NO (101.0841)


   

5-aminopent-1-en-3-ol

5-aminopent-1-en-3-ol

C5H11NO (101.0841)


   

3-Methoxy-3-methylazetidine

3-Methoxy-3-methylazetidine

C5H11NO (101.0841)


   

3-methylpyrrolidin-3-ol

3-methylpyrrolidin-3-ol

C5H11NO (101.0841)


   

3-(VINYLOXY)PROPAN-1-AMINE

3-(VINYLOXY)PROPAN-1-AMINE

C5H11NO (101.0841)


   

Butanal, 3-methyl-, oxime, (Z)-

Butanal, 3-methyl-, oxime, (Z)-

C5H11NO (101.0841)


   

Butanal, 2-methyl-, oxime, (E)-

Butanal, 2-methyl-, oxime, (E)-

C5H11NO (101.0841)


   

(Z)-2-methylbutanal oxime

(Z)-2-methylbutanal oxime

C5H11NO (101.0841)


   

FR-0155

pentanimidic acid

C5H11NO (101.0841)


   

2-Methylpropanal O-methyloxime

2-Methylpropanal O-methyloxime

C5H11NO (101.0841)


   

(1E,2S)-2-methylbutanal oxime

(1E,2S)-2-methylbutanal oxime

C5H11NO (101.0841)


   

4-(Methylamino)butanal

4-(Methylamino)butanal

C5H11NO (101.0841)


   

N-butylformamide

N-butylformamide

C5H11NO (101.0841)


A member of the class of formamides that is formamide substituted by a butyl group at the N atom.

   

5-Aminopentanal

5-Aminopentanal

C5H11NO (101.0841)


An omega-aminoaldehyde that is pentanal which is substituted at position 5 by an amino group. It is an intermediate in the biosynthesis of L-lysine derived alkaloids.

   

Aminopentanal

Aminopentanal

C5H11NO (101.0841)


   

Methylaminobutanal

Methylaminobutanal

C5H11NO (101.0841)


   

(2s)-2-methylbutanimidic acid

(2s)-2-methylbutanimidic acid

C5H11NO (101.0841)


   

(2r)-2-methylbutanimidic acid

(2r)-2-methylbutanimidic acid

C5H11NO (101.0841)


   

n-(2-methylpropyl)methanimidic acid

n-(2-methylpropyl)methanimidic acid

C5H11NO (101.0841)


   

2-methylbutanimidic acid

2-methylbutanimidic acid

C5H11NO (101.0841)