Chemical Formula: C11H18N2O2

Chemical Formula C11H18N2O2

Found 60 metabolite its formula value is C11H18N2O2

L,L-Cyclo(leucylprolyl)

(3S,8aS)-1-hydroxy-3-(2-methylpropyl)-3H,4H,6H,7H,8H,8aH-pyrrolo[1,2-a]pyrazin-4-one

C11H18N2O2 (210.1368208)


L,L-Cyclo(leucylprolyl) is found in alcoholic beverages. L,L-Cyclo(leucylprolyl) is produced by microorganisms and is a bitter component of sake and contributes to the flavour of beer. L,L-Cyclo(leucylprolyl), also known as cyclo(leu-pro) or cyclo(L-prolyl-L-leucyl), belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof. L,L-Cyclo(leucylprolyl) is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. Based on a literature review a significant number of articles have been published on L,L-Cyclo(leucylprolyl). L-Leucyl-L-proline lactam. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=2873-36-1 (retrieved 2024-07-10) (CAS RN: 2873-36-1). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Cyclo(L-Leu-L-Pro) is an inhibitory substance targeting to production of norsolorinic acid (NA,a precursor of aflatoxin),which can be isolated from A. xylosoxidans NFRI-A1. Cyclo(L-Leu-L-Pro) inhibits accumulation of NA by A. parasiticus NFRI-95 and inhibits spore formation. Cyclo(L-Leu-L-Pro) inhibits aflatoxin production with an IC50 of 0.2 mg/mL in A. parasiticus SYS-4[1].

   

Cyclo-Ile-Pro-diketopiperazine

Cyclo-Ile-Pro-diketopiperazine

C11H18N2O2 (210.1368208)


   

cis-3-isobutyl-tetrahydroimidazo[1,2-a]pyridine-2,5-dione

cis-3-isobutyl-tetrahydroimidazo[1,2-a]pyridine-2,5-dione

C11H18N2O2 (210.1368208)


   

L-Prolyl-L-valine anhydride

L-Prolyl-L-valine anhydride

C11H18N2O2 (210.1368208)


   

(3S,7xi,8aR)-Cyclo(4-methylprolylnorvalyl)

(3S,7xi,8aR)-Cyclo(4-methylprolylnorvalyl)

C11H18N2O2 (210.1368208)


   
   
   

3-(2-methylpropyl)-2,3,6,7,8,8a-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione

NCGC00169428-02!3-(2-methylpropyl)-2,3,6,7,8,8a-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione

C11H18N2O2 (210.1368208)


   

3-butan-2-yl-2,3,6,7,8,8a-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione

NCGC00380278-02!3-butan-2-yl-2,3,6,7,8,8a-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione

C11H18N2O2 (210.1368208)


   

3-(2-methylpropyl)-2,3,6,7,8,8a-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione

NCGC00169428-03!3-(2-methylpropyl)-2,3,6,7,8,8a-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione

C11H18N2O2 (210.1368208)


   

Cyclo(pro-leu)

Cyclo(-leu-pro)

C11H18N2O2 (210.1368208)


Cyclo(L-Leu-L-Pro) is an inhibitory substance targeting to production of norsolorinic acid (NA,a precursor of aflatoxin),which can be isolated from A. xylosoxidans NFRI-A1. Cyclo(L-Leu-L-Pro) inhibits accumulation of NA by A. parasiticus NFRI-95 and inhibits spore formation. Cyclo(L-Leu-L-Pro) inhibits aflatoxin production with an IC50 of 0.2 mg/mL in A. parasiticus SYS-4[1].

   
   

Cyclo(-leu-pro)

L,L-Cyclo(leucylprolyl)

C11H18N2O2 (210.1368208)


Production by microorganisms. Bitter component of sake and contributes to the flavour of beer. L,L-Cyclo(leucylprolyl) is found in alcoholic beverages. Cyclo(L-Leu-L-Pro) is an inhibitory substance targeting to production of norsolorinic acid (NA,a precursor of aflatoxin),which can be isolated from A. xylosoxidans NFRI-A1. Cyclo(L-Leu-L-Pro) inhibits accumulation of NA by A. parasiticus NFRI-95 and inhibits spore formation. Cyclo(L-Leu-L-Pro) inhibits aflatoxin production with an IC50 of 0.2 mg/mL in A. parasiticus SYS-4[1].

   

Cyclo(proline-leucine)

Cyclo(proline-leucine)

C11H18N2O2 (210.1368208)


   

Cyclo(leucylprolyl)

Cyclo(leucylprolyl)

C11H18N2O2 (210.1368208)


Annotation level-1

   

Gancidin W

3-(2-methylpropyl)-octahydropyrrolo[1,2-a]piperazine-1,4-dione

C11H18N2O2 (210.1368208)


Cyclo(L-Leu-L-Pro) is an inhibitory substance targeting to production of norsolorinic acid (NA,a precursor of aflatoxin),which can be isolated from A. xylosoxidans NFRI-A1. Cyclo(L-Leu-L-Pro) inhibits accumulation of NA by A. parasiticus NFRI-95 and inhibits spore formation. Cyclo(L-Leu-L-Pro) inhibits aflatoxin production with an IC50 of 0.2 mg/mL in A. parasiticus SYS-4[1].

   

2-METHYL-2-PROPANYL 3,4,5,6-TETRAHYDROPYRROLO[3,4-C]PYRROLE-2(1H)-CARBOXYLATE

2-METHYL-2-PROPANYL 3,4,5,6-TETRAHYDROPYRROLO[3,4-C]PYRROLE-2(1H)-CARBOXYLATE

C11H18N2O2 (210.1368208)


   

Pyrrole-2-carboxylic acid, 4-amino-1-hexyl- (6CI)

Pyrrole-2-carboxylic acid, 4-amino-1-hexyl- (6CI)

C11H18N2O2 (210.1368208)


   

(S)-N-BOC-2-Furylalanine tert-butylamine

(S)-N-BOC-2-Furylalanine tert-butylamine

C11H18N2O2 (210.1368208)


   

(S)-TERT-BUTYL 2-(CYANOMETHYL)PYRROLIDINE-1-CARBOXYLATE

(S)-TERT-BUTYL 2-(CYANOMETHYL)PYRROLIDINE-1-CARBOXYLATE

C11H18N2O2 (210.1368208)


   

N-methyl-{[5-(morpholinomethyl)-2-furyl]methyl}amine

N-methyl-{[5-(morpholinomethyl)-2-furyl]methyl}amine

C11H18N2O2 (210.1368208)


   

tert-Butyl 2-cyanopiperidine-1-carboxylate

tert-Butyl 2-cyanopiperidine-1-carboxylate

C11H18N2O2 (210.1368208)


   

(3,3-DIMETHOXY-PROPYL)-(4-METHYL-PYRIDIN-2-YL)-AMINE

(3,3-DIMETHOXY-PROPYL)-(4-METHYL-PYRIDIN-2-YL)-AMINE

C11H18N2O2 (210.1368208)


   

tert-Butyl-2-cyanpiperidin-4-carboxylat

tert-Butyl-2-cyanpiperidin-4-carboxylat

C11H18N2O2 (210.1368208)


   

4-Pyridineethanamine, b,b-diethoxy-

4-Pyridineethanamine, b,b-diethoxy-

C11H18N2O2 (210.1368208)


   

(R)-TERT-BUTYL 2-(CYANOMETHYL)PYRROLIDINE-1-CARBOXYLATE

(R)-TERT-BUTYL 2-(CYANOMETHYL)PYRROLIDINE-1-CARBOXYLATE

C11H18N2O2 (210.1368208)


   

(1-BROMO-NAPHTHALEN-2-YLOXY)-ACETICACID

(1-BROMO-NAPHTHALEN-2-YLOXY)-ACETICACID

C11H18N2O2 (210.1368208)


   

1-Boc-4-Cyanopiperidine

1-Boc-4-Cyanopiperidine

C11H18N2O2 (210.1368208)


   

1-(7-CARBOXYHEPTYL)IMIDAZOLE

1-(7-CARBOXYHEPTYL)IMIDAZOLE

C11H18N2O2 (210.1368208)


   

Bis-2,6-N,N-(2-hydroxyethyl)diaminotoluene

Bis-2,6-N,N-(2-hydroxyethyl)diaminotoluene

C11H18N2O2 (210.1368208)


   

1-ethyl-3-propyl-1h-pyrazole-5-carboxylic acid ethyl ester

1-ethyl-3-propyl-1h-pyrazole-5-carboxylic acid ethyl ester

C11H18N2O2 (210.1368208)


   

tert-Butyl-3-(cyanmethyl)pyrrolidin-1-carboxylat

tert-Butyl-3-(cyanmethyl)pyrrolidin-1-carboxylat

C11H18N2O2 (210.1368208)


   

(S)-1-N-Boc-3-Cyanopiperidine

(S)-1-N-Boc-3-Cyanopiperidine

C11H18N2O2 (210.1368208)


   

tert-butyl (3R)-3-cyanopiperidine-1-carboxylate

tert-butyl (3R)-3-cyanopiperidine-1-carboxylate

C11H18N2O2 (210.1368208)


   

(R)-1-BOC-2-CYANOPIPERIDINE

(R)-1-BOC-2-CYANOPIPERIDINE

C11H18N2O2 (210.1368208)


   

Bicyclo[2.2.1]heptane-1-carboxylic acid, 3-hydrazono-4,7,7-trimethyl- (9CI)

Bicyclo[2.2.1]heptane-1-carboxylic acid, 3-hydrazono-4,7,7-trimethyl- (9CI)

C11H18N2O2 (210.1368208)


   
   

1,3-DI-PYRROLIDIN-1-YL-PROPANE-1,3-DIONE

1,3-DI-PYRROLIDIN-1-YL-PROPANE-1,3-DIONE

C11H18N2O2 (210.1368208)


   

1-Boc-2-(cyanomethyl)pyrrolidine

1-Boc-2-(cyanomethyl)pyrrolidine

C11H18N2O2 (210.1368208)


   

2,8-Diazaspiro[4.5]decane-1,3-dione,2-ethyl-8-methyl-

2,8-Diazaspiro[4.5]decane-1,3-dione,2-ethyl-8-methyl-

C11H18N2O2 (210.1368208)


   

(S)-3-CYANOMETHYL-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

(S)-3-CYANOMETHYL-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

C11H18N2O2 (210.1368208)


   

Ethyl 3-(Tert-Butyl)-1-Methyl-1h-Pyrazole-5-Carboxylate

Ethyl 3-(Tert-Butyl)-1-Methyl-1h-Pyrazole-5-Carboxylate

C11H18N2O2 (210.1368208)


   

2-(5-METHYL-2-FURYL)-2-MORPHOLIN-4-YLETHANAMINE

2-(5-METHYL-2-FURYL)-2-MORPHOLIN-4-YLETHANAMINE

C11H18N2O2 (210.1368208)


   

(R)-TERT-BUTYL 3-(CYANOMETHYL)PYRROLIDINE-1-CARBOXYLATE

(R)-TERT-BUTYL 3-(CYANOMETHYL)PYRROLIDINE-1-CARBOXYLATE

C11H18N2O2 (210.1368208)


   

1H-Pyrrole-2-carboxylicacid,3-amino-5-(1,1-dimethylethyl)-,ethylester(9CI)

1H-Pyrrole-2-carboxylicacid,3-amino-5-(1,1-dimethylethyl)-,ethylester(9CI)

C11H18N2O2 (210.1368208)


   

(S)-(-)-N-BENZYL-1-PHENYLETHYLAMINE

(S)-(-)-N-BENZYL-1-PHENYLETHYLAMINE

C11H18N2O2 (210.1368208)


   

TRIMETHYL-1 6-DIISOCYANATOHEXANE

TRIMETHYL-1 6-DIISOCYANATOHEXANE

C11H18N2O2 (210.1368208)


   

N-Boc-3-Cyanopiperidine

N-Boc-3-Cyanopiperidine

C11H18N2O2 (210.1368208)


   

1-METHYL-3-(2-METHYLPROPYL)-1H-PYRAZOLE-5-CARBOXYLIC ACID ETHYL ESTER

1-METHYL-3-(2-METHYLPROPYL)-1H-PYRAZOLE-5-CARBOXYLIC ACID ETHYL ESTER

C11H18N2O2 (210.1368208)


   

7,7,9-TRIMETHYL-1,3-DIAZA-SPIRO[4.5]DECANE-2,4-DIONE

7,7,9-TRIMETHYL-1,3-DIAZA-SPIRO[4.5]DECANE-2,4-DIONE

C11H18N2O2 (210.1368208)


   

3,9-Diazaspiro[5.5]undecan-2-one, 9-acetyl

3,9-Diazaspiro[5.5]undecan-2-one, 9-acetyl

C11H18N2O2 (210.1368208)


   

1,6-diisocyanato-2,4,4-trimethylhexane

1,6-diisocyanato-2,4,4-trimethylhexane

C11H18N2O2 (210.1368208)


   

(S)-TERT-BUTYL 2-CYANOPIPERIDINE-1-CARBOXYLATE

(S)-TERT-BUTYL 2-CYANOPIPERIDINE-1-CARBOXYLATE

C11H18N2O2 (210.1368208)


   

4-(2,5-Diamino-5-hydroxy-pentyl)-phenol

4-(2,5-Diamino-5-hydroxy-pentyl)-phenol

C11H18N2O2 (210.1368208)


   
   

N-(Cyclohexylcarbamoyl)-2-ryrrolidone

N-(Cyclohexylcarbamoyl)-2-ryrrolidone

C11H18N2O2 (210.1368208)


   

3-Dimethylaminomethyl-4-(1-pyrrolidinyl)-2(5H)-furanone

3-Dimethylaminomethyl-4-(1-pyrrolidinyl)-2(5H)-furanone

C11H18N2O2 (210.1368208)


   

Cyclo(L-leu-L-pro)

Cyclo(L-leu-L-pro)

C11H18N2O2 (210.1368208)


A homodetic cyclic peptide composed from leucyl and prolyl residues.

   
   

Cyclo(D-Leu-D-Pro)

Cyclo(D-Leu-D-Pro)

C11H18N2O2 (210.1368208)


Cyclo(D-Leu-D-Pro) is a polypeptide that can be found by peptide screening. Peptide screening is a research tool that pools active peptides primarily by immunoassay. Peptide screening can be used for protein interaction, functional analysis, epitope screening, especially in the field of agent research and development[1].