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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 17:30:10 UTC

Update Date

2022-03-07 02:52:09 UTC

HMDB ID

HMDB0029396

Secondary Accession Numbers

HMDB29396

Metabolite Identification

Common Name

L-cis-3-Amino-2-pyrrolidinecarboxylic acid

Description

L-cis-3-Amino-2-pyrrolidinecarboxylic acid, also known as L-cis-3-aminoproline or 3-aminopyrrolidine-2-carboxylate, 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 a significant number of articles have been published on L-cis-3-Amino-2-pyrrolidinecarboxylic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
L-cis-3-Amino-2-pyrrolidinecarboxylate	Generator
L-cis-3-Aminoproline	HMDB
3-Aminopyrrolidine-2-carboxylate	HMDB

Chemical Formula

C₅H₁₀N₂O₂

Average Molecular Weight

130.1451

Monoisotopic Molecular Weight

130.074227574

IUPAC Name

3-aminopyrrolidine-2-carboxylic acid

Traditional Name

3-aminopyrrolidine-2-carboxylic acid

CAS Registry Number

25876-88-4

SMILES

NC1CCNC1C(O)=O

InChI Identifier

InChI=1S/C5H10N2O2/c6-3-1-2-7-4(3)5(8)9/h3-4,7H,1-2,6H2,(H,8,9)

InChI Key

VJLXSTXGGXYQCT-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.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Proline and derivatives

Alternative Parents

Substituents

Proline or derivatives
Alpha-amino acid
Pyrrolidine carboxylic acid
Pyrrolidine carboxylic acid or derivatives
Pyrrolidine
Amino acid
Carboxylic acid
Azacycle
Organoheterocyclic compound
Secondary amine
Secondary aliphatic amine
Monocarboxylic acid or derivatives
Organic nitrogen compound
Organic oxygen compound
Primary amine
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Primary aliphatic amine
Organic oxide
Hydrocarbon derivative
Carbonyl group
Amine
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0029396)
Cytoplasm (HMDB: HMDB0029396)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0029396)

Source

Endogenous

Endogenous (HMDB: HMDB0029396)

Plant

Plant (HMDB: HMDB0029396)

Exogenous

Food

Food (HMDB: HMDB0029396)

Vegetable

Mushroom

Exogenous (HMDB: HMDB0029396)

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	215 °C	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	293 g/L	ALOGPS
logP	-3.1	ALOGPS
logP	-3.8	ChemAxon
logS	0.35	ALOGPS
pKa (Strongest Acidic)	1.59	ChemAxon
pKa (Strongest Basic)	10.84	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	75.35 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	31.04 m³·mol⁻¹	ChemAxon
Polarizability	12.69 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	127.506	31661259
DarkChem	[M-H]-	121.042	31661259
DeepCCS	[M+H]+	128.964	30932474
DeepCCS	[M-H]-	126.202	30932474
DeepCCS	[M-2H]-	162.471	30932474
DeepCCS	[M+Na]+	137.33	30932474
AllCCS	[M+H]+	128.8	32859911
AllCCS	[M+H-H2O]+	124.1	32859911
AllCCS	[M+NH4]+	133.1	32859911
AllCCS	[M+Na]+	134.4	32859911
AllCCS	[M-H]-	121.8	32859911
AllCCS	[M+Na-2H]-	123.9	32859911
AllCCS	[M+HCOO]-	126.2	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
L-cis-3-Amino-2-pyrrolidinecarboxylic acid	NC1CCNC1C(O)=O	2400.9	Standard polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid	NC1CCNC1C(O)=O	1266.9	Standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid	NC1CCNC1C(O)=O	1636.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,1TMS,isomer #1	C[Si](C)(C)OC(=O)C1NCCC1N	1362.1	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,1TMS,isomer #2	C[Si](C)(C)NC1CCNC1C(=O)O	1562.3	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,1TMS,isomer #3	C[Si](C)(C)N1CCC(N)C1C(=O)O	1452.9	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,2TMS,isomer #1	C[Si](C)(C)NC1CCNC1C(=O)O[Si](C)(C)C	1527.5	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,2TMS,isomer #1	C[Si](C)(C)NC1CCNC1C(=O)O[Si](C)(C)C	1503.3	Standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,2TMS,isomer #2	C[Si](C)(C)OC(=O)C1C(N)CCN1[Si](C)(C)C	1486.3	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,2TMS,isomer #2	C[Si](C)(C)OC(=O)C1C(N)CCN1[Si](C)(C)C	1457.5	Standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,2TMS,isomer #3	C[Si](C)(C)N(C1CCNC1C(=O)O)[Si](C)(C)C	1698.5	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,2TMS,isomer #3	C[Si](C)(C)N(C1CCNC1C(=O)O)[Si](C)(C)C	1578.3	Standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,2TMS,isomer #4	C[Si](C)(C)NC1CCN([Si](C)(C)C)C1C(=O)O	1601.5	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,2TMS,isomer #4	C[Si](C)(C)NC1CCN([Si](C)(C)C)C1C(=O)O	1524.9	Standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,3TMS,isomer #1	C[Si](C)(C)OC(=O)C1NCCC1N([Si](C)(C)C)[Si](C)(C)C	1713.7	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,3TMS,isomer #1	C[Si](C)(C)OC(=O)C1NCCC1N([Si](C)(C)C)[Si](C)(C)C	1679.8	Standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,3TMS,isomer #2	C[Si](C)(C)NC1CCN([Si](C)(C)C)C1C(=O)O[Si](C)(C)C	1593.9	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,3TMS,isomer #2	C[Si](C)(C)NC1CCN([Si](C)(C)C)C1C(=O)O[Si](C)(C)C	1644.5	Standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,3TMS,isomer #3	C[Si](C)(C)N1CCC(N([Si](C)(C)C)[Si](C)(C)C)C1C(=O)O	1743.8	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,3TMS,isomer #3	C[Si](C)(C)N1CCC(N([Si](C)(C)C)[Si](C)(C)C)C1C(=O)O	1677.7	Standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,4TMS,isomer #1	C[Si](C)(C)OC(=O)C1C(N([Si](C)(C)C)[Si](C)(C)C)CCN1[Si](C)(C)C	1778.7	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,4TMS,isomer #1	C[Si](C)(C)OC(=O)C1C(N([Si](C)(C)C)[Si](C)(C)C)CCN1[Si](C)(C)C	1774.2	Standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C1NCCC1N	1618.4	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1CCNC1C(=O)O	1798.4	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N1CCC(N)C1C(=O)O	1717.6	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1CCNC1C(=O)O[Si](C)(C)C(C)(C)C	1963.7	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1CCNC1C(=O)O[Si](C)(C)C(C)(C)C	1919.3	Standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)C1C(N)CCN1[Si](C)(C)C(C)(C)C	1931.8	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)C1C(N)CCN1[Si](C)(C)C(C)(C)C	1887.4	Standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N(C1CCNC1C(=O)O)[Si](C)(C)C(C)(C)C	2111.2	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N(C1CCNC1C(=O)O)[Si](C)(C)C(C)(C)C	2019.4	Standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC1CCN([Si](C)(C)C(C)(C)C)C1C(=O)O	2069.0	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC1CCN([Si](C)(C)C(C)(C)C)C1C(=O)O	1959.2	Standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C1NCCC1N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2314.7	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C1NCCC1N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2276.7	Standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1CCN([Si](C)(C)C(C)(C)C)C1C(=O)O[Si](C)(C)C(C)(C)C	2251.1	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1CCN([Si](C)(C)C(C)(C)C)C1C(=O)O[Si](C)(C)C(C)(C)C	2252.4	Standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N1CCC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1C(=O)O	2365.8	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N1CCC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1C(=O)O	2310.4	Standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C1C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CCN1[Si](C)(C)C(C)(C)C	2630.3	Semi standard non polar	33892256
L-cis-3-Amino-2-pyrrolidinecarboxylic acid,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C1C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CCN1[Si](C)(C)C(C)(C)C	2547.9	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - L-cis-3-Amino-2-pyrrolidinecarboxylic acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a6u-9000000000-78cb9a1895b79c7b7a4e	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - L-cis-3-Amino-2-pyrrolidinecarboxylic acid GC-MS (1 TMS) - 70eV, Positive	splash10-0abc-9200000000-ef86c69af08195670e4a	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - L-cis-3-Amino-2-pyrrolidinecarboxylic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - L-cis-3-Amino-2-pyrrolidinecarboxylic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - L-cis-3-Amino-2-pyrrolidinecarboxylic acid 10V, Positive-QTOF	splash10-03e9-2900000000-f162b090a7100e2db22a	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - L-cis-3-Amino-2-pyrrolidinecarboxylic acid 20V, Positive-QTOF	splash10-03di-8900000000-867e5b2ec02907a4ba85	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - L-cis-3-Amino-2-pyrrolidinecarboxylic acid 40V, Positive-QTOF	splash10-0gi3-9000000000-ea6428a48213ecbcee5f	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - L-cis-3-Amino-2-pyrrolidinecarboxylic acid 10V, Negative-QTOF	splash10-004r-6900000000-80a0c6a0089a8f650321	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - L-cis-3-Amino-2-pyrrolidinecarboxylic acid 20V, Negative-QTOF	splash10-01ri-9600000000-7e48ee1222177452c968	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - L-cis-3-Amino-2-pyrrolidinecarboxylic acid 40V, Negative-QTOF	splash10-014r-9100000000-112f0c10008b73308350	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - L-cis-3-Amino-2-pyrrolidinecarboxylic acid 10V, Negative-QTOF	splash10-004i-0900000000-02ef78896b309f4af9f0	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - L-cis-3-Amino-2-pyrrolidinecarboxylic acid 20V, Negative-QTOF	splash10-0096-9500000000-56e0f99e3cbf9915eae9	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - L-cis-3-Amino-2-pyrrolidinecarboxylic acid 40V, Negative-QTOF	splash10-0a4l-9000000000-94451bd5935c37630fd5	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - L-cis-3-Amino-2-pyrrolidinecarboxylic acid 10V, Positive-QTOF	splash10-000i-9400000000-60554e6045afe585dddd	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - L-cis-3-Amino-2-pyrrolidinecarboxylic acid 20V, Positive-QTOF	splash10-00kr-9000000000-0142ce47b13403efce84	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - L-cis-3-Amino-2-pyrrolidinecarboxylic acid 40V, Positive-QTOF	splash10-0596-9000000000-5407f402ee66c25513d1	2021-09-25	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
Extracellular

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB000485

KNApSAcK ID

Not Available

Chemspider ID

13605823

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21998160

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

Showing metabocard for L-cis-3-Amino-2-pyrrolidinecarboxylic acid (HMDB0029396)

MOL for HMDB0029396 (L-cis-3-Amino-2-pyrrolidinecarboxylic acid)

3D MOL for HMDB0029396 (L-cis-3-Amino-2-pyrrolidinecarboxylic acid)

3D SDF for HMDB0029396 (L-cis-3-Amino-2-pyrrolidinecarboxylic acid)

3D-SDF for HMDB0029396 (L-cis-3-Amino-2-pyrrolidinecarboxylic acid)

PDB for HMDB0029396 (L-cis-3-Amino-2-pyrrolidinecarboxylic acid)

3D PDB for HMDB0029396 (L-cis-3-Amino-2-pyrrolidinecarboxylic acid)

SMILES for HMDB0029396 (L-cis-3-Amino-2-pyrrolidinecarboxylic acid)

INCHI for HMDB0029396 (L-cis-3-Amino-2-pyrrolidinecarboxylic acid)

Structure for HMDB0029396 (L-cis-3-Amino-2-pyrrolidinecarboxylic acid)

3D Structure for HMDB0029396 (L-cis-3-Amino-2-pyrrolidinecarboxylic acid)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra