NP-MRD: Showing NP-Card for Aspartyl-L-proline (NP0086951)

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Record Information

Version

2.0

Created at

2022-05-11 16:35:32 UTC

Updated at

2022-05-11 16:35:32 UTC

NP-MRD ID

NP0086951

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Aspartyl-L-proline

Description

Aspartyl-L-proline, also known as asp-pro, belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond. Aspartyl-L-proline is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 30 30  0  0  0  0  0  0  0  0999 V2000
    2.5917   -0.1737   -1.7541 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6395   -0.2679   -0.6360 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0843    0.7210    0.4436 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4357    0.3325    0.8705 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6402   -0.6799    1.5986 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5287    1.0828    0.4752 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2678   -0.0507   -1.0789 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1244    0.5548   -2.1971 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9051   -0.4489   -0.3876 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9472   -1.1738    0.8568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2712   -0.6581    1.4475 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1373   -0.8881    0.1976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2871   -0.1788   -0.8356 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5748    1.2903   -0.6496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6890    1.7799   -0.9570 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6098    2.1386   -0.1322 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1842   -0.7913   -2.5129 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4645   -0.6611   -1.4169 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7452   -1.2759   -0.2126 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1180    1.7256   -0.0403 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3743    0.7031    1.2787 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4658    0.8872    0.8367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1725   -2.2541    0.6217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1193   -1.0501    1.5327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5962   -1.2347    2.3099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1579    0.4112    1.6122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1413   -0.4936    0.3032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0611   -1.9632   -0.0316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4608   -0.5095   -1.8570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5339    3.1263   -0.3347 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  6  1  0
  4  5  2  0
  2  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 16  1  0
 14 15  2  0
 13  9  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  1
  3 20  1  0
  3 21  1  0
  6 22  1  0
 10 23  1  0
 10 24  1  0
 11 25  1  0
 11 26  1  0
 12 27  1  0
 12 28  1  0
 13 29  1  6
 16 30  1  0
M  END


  Mrv0541 02231219292D          

 16 16  0  0  1  0            999 V2000
   27.6563  -15.3419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.0070  -13.3223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.5655  -14.6814    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.5128  -17.4044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.7983  -16.1669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.9418  -14.1043    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   25.5128  -14.9294    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   27.6093  -13.6194    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   27.3544  -12.8348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.5293  -12.8348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.2744  -13.6194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.9418  -14.9294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.2274  -15.3419    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   28.3939  -13.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.2274  -16.1669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.5128  -16.5794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1 12  2  0  0  0  0
  2 14  1  0  0  0  0
  3 14  2  0  0  0  0
  4 16  1  0  0  0  0
  5 16  2  0  0  0  0
  6  8  1  0  0  0  0
  6 11  1  0  0  0  0
  6 12  1  0  0  0  0
 13  7  1  6  0  0  0
  8  9  1  0  0  0  0
  8 14  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 13  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0086951

> <DATABASE_NAME>
NP-MRD

> <SMILES>
N[C@@H](CC(O)=O)C(=O)N1CCC[C@H]1C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C9H14N2O5/c10-5(4-7(12)13)8(14)11-3-1-2-6(11)9(15)16/h5-6H,1-4,10H2,(H,12,13)(H,15,16)/t5-,6-/m0/s1

> <INCHI_KEY>
UKGGPJNBONZZCM-WDSKDSINSA-N

> <FORMULA>
C9H14N2O5

> <MOLECULAR_WEIGHT>
230.2179

> <EXACT_MASS>
230.090271568

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_AVERAGE_POLARIZABILITY>
21.34772753198195

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-1-[(2S)-2-amino-3-carboxypropanoyl]pyrrolidine-2-carboxylic acid

> <ALOGPS_LOGP>
-3.30

> <JCHEM_LOGP>
-4.044969406461262

> <ALOGPS_LOGS>
-0.86

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
3.820681277258631

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.1016266674010042

> <JCHEM_PKA_STRONGEST_BASIC>
8.519373304334216

> <JCHEM_POLAR_SURFACE_AREA>
120.92999999999998

> <JCHEM_REFRACTIVITY>
51.51920000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.21e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
asp-pro

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  O   UNK     0      51.625 -28.638   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0      54.146 -24.868   0.000  0.00  0.00           O+0
HETATM    3  O   UNK     0      53.322 -27.405   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      47.624 -32.488   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      46.290 -30.178   0.000  0.00  0.00           O+0
HETATM    6  N   UNK     0      50.291 -26.328   0.000  0.00  0.00           N+0
HETATM    7  N   UNK     0      47.624 -27.868   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      51.537 -25.423   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      51.062 -23.958   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      49.521 -23.958   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      49.046 -25.423   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      50.291 -27.868   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      48.958 -28.638   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      53.002 -25.899   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      48.958 -30.178   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      47.624 -30.948   0.000  0.00  0.00           C+0
CONECT    1   12                                                            
CONECT    2   14                                                            
CONECT    3   14                                                            
CONECT    4   16                                                            
CONECT    5   16                                                            
CONECT    6    8   11   12                                                  
CONECT    7   13                                                            
CONECT    8    6    9   14                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11    6   10                                                       
CONECT   12    1    6   13                                                  
CONECT   13    7   12   15                                                  
CONECT   14    2    3    8                                                  
CONECT   15   13   16                                                       
CONECT   16    4    5   15                                                  
MASTER        0    0    0    0    0    0    0    0   16    0   32    0
END

View in JSmol

Synonyms

Value	Source
1-L-alpha-Aspartyl-L-proline	HMDB
Asp-pro	HMDB
Aspartylproline	HMDB
Aspartyl-proline	HMDB
(2S)-1-[(2S)-2-Amino-3-carboxypropanoyl]pyrrolidine-2-carboxylate	HMDB

Chemical Formula

C₉H₁₄N₂O₅

Average Mass

230.2179 Da

Monoisotopic Mass

230.09027 Da

IUPAC Name

(2S)-1-[(2S)-2-amino-3-carboxypropanoyl]pyrrolidine-2-carboxylic acid

Traditional Name

asp-pro

CAS Registry Number

Not Available

SMILES

N[C@@H](CC(O)=O)C(=O)N1CCC[C@H]1C(O)=O

InChI Identifier

InChI=1S/C9H14N2O5/c10-5(4-7(12)13)8(14)11-3-1-2-6(11)9(15)16/h5-6H,1-4,10H2,(H,12,13)(H,15,16)/t5-,6-/m0/s1

InChI Key

UKGGPJNBONZZCM-WDSKDSINSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Anas platyrhynchos	FooDB	FooDB
Anatidae	FooDB	FooDB
Anser anser	FooDB	FooDB
Bison bison	FooDB	FooDB
Bos taurus	FooDB	FooDB
Bos taurus X Bison bison	FooDB	FooDB
Bubalus bubalis	FooDB	FooDB
Capra aegagrus hircus	FooDB	FooDB
Cervidae	FooDB	FooDB
Cervus canadensis	FooDB	FooDB
Columba	FooDB	FooDB
Columbidae	FooDB	FooDB
Dromaius novaehollandiae	FooDB	FooDB
Equus caballus	FooDB	FooDB
Gallus gallus	FooDB	FooDB
Lagopus muta	FooDB	FooDB
Leporidae	FooDB	FooDB
Lepus timidus	FooDB	FooDB
Melanitta fusca	FooDB	FooDB
Meleagris gallopavo	FooDB	FooDB
Numida meleagris	FooDB	FooDB
Odocoileus	FooDB	FooDB
Oryctolagus	FooDB	FooDB
Ovis aries	FooDB	FooDB
Phasianidae	FooDB	FooDB
Phasianus colchicus	FooDB	FooDB
Struthio camelus	FooDB	FooDB
Sus scrofa	FooDB	FooDB
Sus scrofa domestica	FooDB	FooDB

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Dipeptides

Alternative Parents

Substituents

Alpha-dipeptide
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
Proline or derivatives
N-acyl-l-alpha-amino acid
Alpha-amino acid amide
Alpha-amino acid or derivatives
N-acylpyrrolidine
Pyrrolidine carboxylic acid
Pyrrolidine carboxylic acid or derivatives
Heterocyclic fatty acid
Fatty acyl
Fatty acid
Dicarboxylic acid or derivatives
Tertiary carboxylic acid amide
Pyrrolidine
Amino acid
Amino acid or derivatives
Carboxamide group
Organoheterocyclic compound
Azacycle
Carboxylic acid
Hydrocarbon derivative
Organopnictogen compound
Primary aliphatic amine
Organic oxide
Organonitrogen compound
Organooxygen compound
Carbonyl group
Primary amine
Amine
Organic nitrogen compound
Organic oxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	-3.3	ALOGPS
logP	-4	ChemAxon
logS	-0.86	ALOGPS
pKa (Strongest Acidic)	3.1	ChemAxon
pKa (Strongest Basic)	8.52	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	120.93 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	51.52 m³·mol⁻¹	ChemAxon
Polarizability	21.35 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

External Links

HMDB ID

HMDB0002335

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB022967

KNApSAcK ID

Not Available

Chemspider ID

149163

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

6629

PubChem Compound

170612

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Aspartyl-L-proline (NP0086951)

MOL for NP0086951 (Aspartyl-L-proline)

3D MOL for NP0086951 (Aspartyl-L-proline)

3D SDF for NP0086951 (Aspartyl-L-proline)

3D-SDF for NP0086951 (Aspartyl-L-proline)

PDB for NP0086951 (Aspartyl-L-proline)

3D PDB for NP0086951 (Aspartyl-L-proline)

SMILES for NP0086951 (Aspartyl-L-proline)

INCHI for NP0086951 (Aspartyl-L-proline)

Structure for NP0086951 (Aspartyl-L-proline)

3D Structure for NP0086951 (Aspartyl-L-proline)