Chemical Formula: C5H14N2

Chemical Formula C5H14N2

Found 34 metabolite its formula value is C5H14N2

Cadaverine

Pentamethylenediamine dihydrochloride

C5H14N2 (102.1156924)


Cadaverine is a foul-smelling diamine formed by bacterial decarboxylation of lysine that occurs during protein hydrolysis during putrefaction of animal tissue. However, this diamine is not purely associated with putrefaction. It is also produced in small quantities by mammals. In particular, it is partially responsible for the distinctive smell of urine and semen. Elevated levels of cadaverine have been found in the urine of some patients with defects in lysine metabolism. Cadaverine is toxic in large doses. In rats it had a low acute oral toxicity of more than 2000 mg/kg body weight .; Cadaverine is a foul-smelling molecule produced by protein hydrolysis during putrefaction of animal tissue. Cadaverine is a toxic diamine with the formula NH2(CH2)5NH2, which is similar to putrescine. Cadaverine is also known by the names 1,5-pentanediamine and pentamethylenediamine. Cadaverine is a foul-smelling diamine formed by bacterial decarboxylation of lysine that occurs during protein hydrolysis during putrefaction of animal tissue. However, this diamine is not purely associated with putrefaction. Cadaverine is a toxic diamine with the formula NH2(CH2)5NH2, which is similar to putrescines NH2(CH2)4NH2. Cadaverine is also known by the names 1,5-pentanediamine and pentamethylenediamine. It is also produced in small quantities by mammals. In particular, it is partially responsible for the distinctive smell of urine and semen. Elevated levels of cadaverine have been found in the urine of some patients with defects in lysine metabolism. Cadaverine is toxic in large doses. In rats it had a low acute oral toxicity of more than 2000 mg/kg body weight. Cadaverine can be found in Corynebacterium (PMID:27872963). Acquisition and generation of the data is financially supported in part by CREST/JST. C78272 - Agent Affecting Nervous System > C66880 - Anticholinergic Agent KEIO_ID C032

   

N-Methylputrescine

N1-Methyl-1,4-butanediamine

C5H14N2 (102.1156924)


N-Methylputrescine is a byproduct of putrescine (a diamine), via methylation by putrescine N-methyltransferase (PMT; EC 2.1.1.53). N-methylputrescine is able to affect protein synthesis to a small extent in stimulated H-35 hepatoma cells, being an inhibitor of cellular insulin-induced ornithine decarboxylase activity. (PMID: 2051998). Putrescine is related to cadaverine (another polyamine). Both are produced by the breakdown of amino acids in living and dead organisms and both are toxic in large doses. Putrescine and cadaverine are largely responsible for the foul odor of putrefying flesh, but also contribute to the odor of such processes as bad breath and bacterial vaginosis. Putrescine is also found in semen. Putrescine attacks s-adenosyl methionine and converts it to spermidine. Spermidine in turn attacks another s-adenosyl methionine and converts it to spermine. Putrescine is synthesized in small quantities by healthy living cells by the action of ornithine decarboxylase. N-Methylputrescine is a microbial metabolite. N-Methylputrescine is a byproduct of putrescine (a diamine), via methylation by putrescine N-methyltransferase (PMT; EC 2.1.1.53). N-methylputrescine is able to affect protein synthesis to a small extent in stimulated H-35 hepatoma cells, being an inhibitor of cellular insulin-induced ornithine decarboxylase activity. (PMID: 2051998). Putrescine is related to cadaverine (another polyamine). Both are produced by the breakdown of amino acids in living and dead organisms and both are toxic in large doses. Putrescine and cadaverine are largely responsible for the foul odor of putrefying flesh, but also contribute to the odor of such processes as bad breath and bacterial vaginosis. Putrescine is also found in semen. Putrescine attacks s-adenosyl methionine and converts it to spermidine. Spermidine in turn attacks another s-adenosyl methionine and converts it to spermine. Putrescine is synthesized in small quantities by healthy living cells by the action of ornithine decarboxylase. [HMDB]

   

2-isopropylaminoethylamine

(2-aminoethyl)(propan-2-yl)amine

C5H14N2 (102.1156924)


2-isopropylaminoethylamine is classified as a member of the Dialkylamines. Dialkylamines are organic compounds containing a dialkylamine group, characterized by two alkyl groups bonded to the amino nitrogen. 2-isopropylaminoethylamine is considered to be soluble (in water) and basic

   

Cadaverine

Cadaverine

C5H14N2 (102.1156924)


An alkane-alpha,omega-diamine comprising a straight-chain pentane core with amino substitutents at positions 1 and 5. A colourless syrupy liquid diamine with a distinctive unpleasant odour, it is a homologue of putresceine and is formed by the bacterial decarboxylation of lysine that occurs during protein hydrolysis during putrefaction of animal tissue. It is also found in plants such as soyabean. C78272 - Agent Affecting Nervous System > C66880 - Anticholinergic Agent

   

Cadaverine; AIF; CE0; MS2Dec

Cadaverine; AIF; CE0; MS2Dec

C5H14N2 (102.1156924)


   

Cadaverine; AIF; CE10; MS2Dec

Cadaverine; AIF; CE10; MS2Dec

C5H14N2 (102.1156924)


   

Cadaverine; AIF; CE30; MS2Dec

Cadaverine; AIF; CE30; MS2Dec

C5H14N2 (102.1156924)


   

N-(N-PROPYL)ETHYLENEDIAMINE

N-(N-PROPYL)ETHYLENEDIAMINE

C5H14N2 (102.1156924)


   

2-amino-1-dimethylaminopropane

2-amino-1-dimethylaminopropane

C5H14N2 (102.1156924)


   

N-ETHYL-N-METHYLETHYLENEDIAMINE

N-ETHYL-N-METHYLETHYLENEDIAMINE

C5H14N2 (102.1156924)


   

1,3-Diaminopentane

1,3-Diaminopentane

C5H14N2 (102.1156924)


   

3-(Ethylamino)propylamine

3-(Ethylamino)propylamine

C5H14N2 (102.1156924)


   

N,2-Dimethyl-1,3-propanediamine

N,2-Dimethyl-1,3-propanediamine

C5H14N2 (102.1156924)


   

pentane-1,2-diamine

pentane-1,2-diamine

C5H14N2 (102.1156924)


   

pentane-1,4-diamine

pentane-1,4-diamine

C5H14N2 (102.1156924)


   

2,2-Dimethyl-1,3-propanediamine

2,2-Dimethyl-1,3-propanediamine

C5H14N2 (102.1156924)


   

2-Methylbutane-1,4-diamine

2-Methylbutane-1,4-diamine

C5H14N2 (102.1156924)


   

N1,2-Dimethyl-1,2-propanediamine

N1,2-Dimethyl-1,2-propanediamine

C5H14N2 (102.1156924)


   

D-(+)-2-Methylputrescine

D-(+)-2-Methylputrescine

C5H14N2 (102.1156924)


   

N,N-Dimethyl-1,3-propanediamine

N,N-Dimethyl-1,3-propanediamine

C5H14N2 (102.1156924)


   

Bis(dimethylamino)methane

Bis(dimethylamino)methane

C5H14N2 (102.1156924)


   

3-Methyl-1,3-butanediamine

3-Methyl-1,3-butanediamine

C5H14N2 (102.1156924)


   

N,N,N′-trimethylethylenediamine

N,N,N′-trimethylethylenediamine

C5H14N2 (102.1156924)


   

N2,2-Dimethyl-1,2-propanediamine

N2,2-Dimethyl-1,2-propanediamine

C5H14N2 (102.1156924)


   

(±)-N1,N1-dimethylpropane-1,2-diamine

(±)-N1,N1-dimethylpropane-1,2-diamine

C5H14N2 (102.1156924)


   

3-Dimethylaminopropylamine

3-Dimethylaminopropylamine

C5H14N2 (102.1156924)


   

N,N-dimethylpropane-1,2-diamine

N,N-dimethylpropane-1,2-diamine

C5H14N2 (102.1156924)


   

(2-Aminoethyl)(ethyl)methylamine

(2-Aminoethyl)(ethyl)methylamine

C5H14N2 (102.1156924)


   

1-Butyl-1-methylhydrazine

1-Butyl-1-methylhydrazine

C5H14N2 (102.1156924)


   

1,1-Dimethyl-2-n-propylhydrazine

1,1-Dimethyl-2-n-propylhydrazine

C5H14N2 (102.1156924)


   

1-Isobutyl-1-methylhydrazine

1-Isobutyl-1-methylhydrazine

C5H14N2 (102.1156924)


   

N-Isopropylethylenediamine

N-Isopropylethylenediamine

C5H14N2 (102.1156924)


   

N-Methylputrescine

N-Methylputrescine

C5H14N2 (102.1156924)


An N-monosubstituted putrescine where the N-substituent is methyl.

   

2-isopropylaminoethylamine

2-isopropylaminoethylamine

C5H14N2 (102.1156924)


A primary aliphatic amine that is ethane-1,2-diamine substituted by an isopropyl group at the N atom.