Showing metabocard for N-Nitrosoproline (BMDB0096148)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2020-03-10 17:01:59 UTC
Update Date2020-04-22 18:56:21 UTC
BMDB IDBMDB0096148
Secondary Accession Numbers
  • BMDB96148
Metabolite Identification
Common NameN-Nitrosoproline
DescriptionN-Nitrosoproline, also known as NO-pro, belongs to the class of organic compounds known as proline and derivatives. Proline and derivatives are compounds containing proline or a derivative thereof resulting from reaction of proline at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. Based on a literature review very few articles have been published on N-Nitrosoproline.
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
1-Nitroso-L-prolineHMDB
1-Nitrosoproline (acd/name 4.0)HMDB
N-Nitroso-L-prolineHMDB
Nitroso-L-prolineHMDB
NitrosoprolineHMDB
NO-ProHMDB
NPROHMDB
Nitrosoproline, (cis)-isomerHMDB
Nitrosoproline, (trans)-isomerHMDB
Nitrosoproline, 14C-labeled CPDHMDB
Nitrosoproline, (D,L)-isomerHMDB
Nitrosoproline, (D)-isomerHMDB
1-Nitrosopyrrolidine-2-carboxylateHMDB
N-NitrosoprolineMeSH
Chemical FormulaC5H8N2O3
Average Molecular Weight144.1286
Monoisotopic Molecular Weight144.053492132
IUPAC Name1-nitrosopyrrolidine-2-carboxylic acid
Traditional Namenitrosoproline
CAS Registry NumberNot Available
SMILES
OC(=O)C1CCCN1N=O
InChI Identifier
InChI=1S/C5H8N2O3/c8-5(9)4-2-1-3-7(4)6-10/h4H,1-3H2,(H,8,9)
InChI KeyWLKPHJWEIIAIFW-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as proline and derivatives. Proline and derivatives are compounds containing proline or a derivative thereof resulting from reaction of proline at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassAmino acids, peptides, and analogues
Direct ParentProline and derivatives
Alternative Parents
Substituents
  • Proline or derivatives
  • Pyrrolidine carboxylic acid
  • Pyrrolidine carboxylic acid or derivatives
  • Pyrrolidine
  • Organic n-nitroso compound
  • Organic nitroso compound
  • Carboxylic acid
  • Monocarboxylic acid or derivatives
  • Azacycle
  • Organoheterocyclic compound
  • Carbonyl group
  • Hydrocarbon derivative
  • Organic oxide
  • Organopnictogen compound
  • Organooxygen compound
  • Organonitrogen compound
  • Organic oxygen compound
  • Organic nitrogen compound
  • Aliphatic heteromonocyclic compound
Molecular FrameworkAliphatic heteromonocyclic compounds
External DescriptorsNot Available
Ontology
StatusExpected but not Quantified
Origin
  • Endogenous
BiofunctionNot Available
ApplicationNot Available
Cellular locationsNot Available
Physical Properties
StateNot Available
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP-0.19ALOGPS
logP0.013ChemAxon
logS-0.52ALOGPS
pKa (Strongest Acidic)3.73ChemAxon
pKa (Strongest Basic)2.78ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area69.97 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity33.42 m³·mol⁻¹ChemAxon
Polarizability12.92 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
Spectra
Biological Properties
Cellular LocationsNot Available
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0041946
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB111682
KNApSAcK IDNot Available
Chemspider ID22565
KEGG Compound IDC19485
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNitrosoproline
METLIN IDNot Available
PubChem Compound24141
PDB IDNot Available
ChEBI IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available