NP-MRD: Showing NP-Card for (3'-hydroxybutan-20-yl)5-oxopyrrolidine-2-carboxylate (NP0010803)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2021-01-05 20:38:29 UTC

Updated at

2021-07-15 17:07:07 UTC

NP-MRD ID

NP0010803

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3'-hydroxybutan-20-yl)5-oxopyrrolidine-2-carboxylate

Provided By

NPAtlas

Description

(3'-Hydroxybutan-20-yl)5-oxopyrrolidine-2-carboxylate belongs to the class of organic compounds known as alpha amino acid esters. These are ester derivatives of alpha amino acids. (3'-hydroxybutan-20-yl)5-oxopyrrolidine-2-carboxylate is found in Trichoderma and Trichoderma atroviride. Based on a literature review very few articles have been published on (3'-hydroxybutan-20-yl)5-oxopyrrolidine-2-carboxylate.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242107413D          

 29 29  0  0  0  0            999 V2000
   -2.5093   -0.4899    1.1160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7430    0.0520   -0.2811 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9111    0.8176   -0.2160 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6409    0.9790   -0.7250 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0811    1.6753   -1.9754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3908    0.3480   -0.8385 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7172    0.6496   -0.1009 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6065    1.5691    0.7497 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0315   -0.0172   -0.2236 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9887   -1.4878    0.0083 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3825   -1.7953    0.5103 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8258   -0.5408    1.1427 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7665   -0.4350    1.9565 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0127    0.5001    0.6731 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8188    0.3241    1.8271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4685   -0.8147    1.2716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2387   -1.3095    1.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9429   -0.7587   -1.0032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7135    0.2526   -0.3085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5384    1.7547    0.0711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1510    1.9558   -2.5366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6081    2.6366   -1.7727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6563    1.0165   -2.6581 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3901    0.1604   -1.2712 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8892   -2.0344   -0.9689 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2237   -1.8165    0.7189 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3958   -2.6609    1.2032 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0715   -2.0337   -0.3226 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1108    1.5029    0.9398 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14  9  1  0  0  0  0
  1 15  1  0  0  0  0
  1 16  1  0  0  0  0
  1 17  1  0  0  0  0
  2 18  1  6  0  0  0
  3 19  1  0  0  0  0
  4 20  1  1  0  0  0
  5 21  1  0  0  0  0
  5 22  1  0  0  0  0
  5 23  1  0  0  0  0
  9 24  1  6  0  0  0
 10 25  1  0  0  0  0
 10 26  1  0  0  0  0
 11 27  1  0  0  0  0
 11 28  1  0  0  0  0
 14 29  1  0  0  0  0
M  END

     RDKit          3D

 29 29  0  0  0  0  0  0  0  0999 V2000
   -2.5093   -0.4899    1.1160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7430    0.0520   -0.2811 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9111    0.8176   -0.2160 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6409    0.9790   -0.7250 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0811    1.6753   -1.9754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3908    0.3480   -0.8385 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7172    0.6496   -0.1009 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6065    1.5691    0.7497 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0315   -0.0172   -0.2236 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9887   -1.4878    0.0083 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3825   -1.7953    0.5103 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8258   -0.5408    1.1427 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7665   -0.4350    1.9565 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0127    0.5001    0.6731 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8188    0.3241    1.8271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4685   -0.8147    1.2716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2387   -1.3095    1.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9429   -0.7587   -1.0032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7135    0.2526   -0.3085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5384    1.7547    0.0711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1510    1.9558   -2.5366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6081    2.6366   -1.7727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6563    1.0165   -2.6581 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3901    0.1604   -1.2712 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8892   -2.0344   -0.9689 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2237   -1.8165    0.7189 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3958   -2.6609    1.2032 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0715   -2.0337   -0.3226 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1108    1.5029    0.9398 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  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  2  0
 12 14  1  0
 14  9  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  6
  3 19  1  0
  4 20  1  1
  5 21  1  0
  5 22  1  0
  5 23  1  0
  9 24  1  6
 10 25  1  0
 10 26  1  0
 11 27  1  0
 11 28  1  0
 14 29  1  0
M  END


  Mrv1652306242107413D          

 29 29  0  0  0  0            999 V2000
   -2.5093   -0.4899    1.1160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7430    0.0520   -0.2811 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9111    0.8176   -0.2160 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6409    0.9790   -0.7250 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0811    1.6753   -1.9754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3908    0.3480   -0.8385 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7172    0.6496   -0.1009 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6065    1.5691    0.7497 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0315   -0.0172   -0.2236 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9887   -1.4878    0.0083 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3825   -1.7953    0.5103 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8258   -0.5408    1.1427 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7665   -0.4350    1.9565 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0127    0.5001    0.6731 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8188    0.3241    1.8271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4685   -0.8147    1.2716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2387   -1.3095    1.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9429   -0.7587   -1.0032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7135    0.2526   -0.3085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5384    1.7547    0.0711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1510    1.9558   -2.5366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6081    2.6366   -1.7727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6563    1.0165   -2.6581 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3901    0.1604   -1.2712 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8892   -2.0344   -0.9689 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2237   -1.8165    0.7189 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3958   -2.6609    1.2032 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0715   -2.0337   -0.3226 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1108    1.5029    0.9398 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14  9  1  0  0  0  0
  1 15  1  0  0  0  0
  1 16  1  0  0  0  0
  1 17  1  0  0  0  0
  2 18  1  6  0  0  0
  3 19  1  0  0  0  0
  4 20  1  1  0  0  0
  5 21  1  0  0  0  0
  5 22  1  0  0  0  0
  5 23  1  0  0  0  0
  9 24  1  6  0  0  0
 10 25  1  0  0  0  0
 10 26  1  0  0  0  0
 11 27  1  0  0  0  0
 11 28  1  0  0  0  0
 14 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0010803

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@]([H])(C([H])([H])[H])[C@@]([H])(OC(=O)[C@@]1([H])N([H])C(=O)C([H])([H])C1([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C9H15NO4/c1-5(11)6(2)14-9(13)7-3-4-8(12)10-7/h5-7,11H,3-4H2,1-2H3,(H,10,12)/t5-,6+,7+/m1/s1

> <INCHI_KEY>
KGVMXZGSVPGTNQ-AHXFUIDQSA-N

> <FORMULA>
C9H15NO4

> <MOLECULAR_WEIGHT>
201.222

> <EXACT_MASS>
201.100107967

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
29

> <JCHEM_AVERAGE_POLARIZABILITY>
20.520765660920638

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R)-3-hydroxybutan-2-yl (2S)-5-oxopyrrolidine-2-carboxylate

> <ALOGPS_LOGP>
-0.50

> <JCHEM_LOGP>
-0.6007276090000001

> <ALOGPS_LOGS>
-0.07

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.49200088539898

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.140490747009533

> <JCHEM_PKA_STRONGEST_BASIC>
-2.224654023480619

> <JCHEM_POLAR_SURFACE_AREA>
75.63

> <JCHEM_REFRACTIVITY>
47.9868

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.73e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R)-3-hydroxybutan-2-yl (2S)-5-oxopyrrolidine-2-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 29 29  0  0  0  0  0  0  0  0999 V2000
   -2.5093   -0.4899    1.1160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7430    0.0520   -0.2811 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9111    0.8176   -0.2160 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6409    0.9790   -0.7250 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0811    1.6753   -1.9754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3908    0.3480   -0.8385 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7172    0.6496   -0.1009 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6065    1.5691    0.7497 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0315   -0.0172   -0.2236 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9887   -1.4878    0.0083 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3825   -1.7953    0.5103 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8258   -0.5408    1.1427 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7665   -0.4350    1.9565 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0127    0.5001    0.6731 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8188    0.3241    1.8271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4685   -0.8147    1.2716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2387   -1.3095    1.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9429   -0.7587   -1.0032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7135    0.2526   -0.3085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5384    1.7547    0.0711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1510    1.9558   -2.5366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6081    2.6366   -1.7727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6563    1.0165   -2.6581 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3901    0.1604   -1.2712 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8892   -2.0344   -0.9689 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2237   -1.8165    0.7189 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3958   -2.6609    1.2032 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0715   -2.0337   -0.3226 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1108    1.5029    0.9398 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  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  2  0
 12 14  1  0
 14  9  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  6
  3 19  1  0
  4 20  1  1
  5 21  1  0
  5 22  1  0
  5 23  1  0
  9 24  1  6
 10 25  1  0
 10 26  1  0
 11 27  1  0
 11 28  1  0
 14 29  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -2.509  -0.490   1.116  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.743   0.052  -0.281  0.00  0.00           C+0
HETATM    3  O   UNK     0      -3.911   0.818  -0.216  0.00  0.00           O+0
HETATM    4  C   UNK     0      -1.641   0.979  -0.725  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.081   1.675  -1.975  0.00  0.00           C+0
HETATM    6  O   UNK     0      -0.391   0.348  -0.839  0.00  0.00           O+0
HETATM    7  C   UNK     0       0.717   0.650  -0.101  0.00  0.00           C+0
HETATM    8  O   UNK     0       0.607   1.569   0.750  0.00  0.00           O+0
HETATM    9  C   UNK     0       2.031  -0.017  -0.224  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.989  -1.488   0.008  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.382  -1.795   0.510  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.826  -0.541   1.143  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.766  -0.435   1.956  0.00  0.00           O+0
HETATM   14  N   UNK     0       3.013   0.500   0.673  0.00  0.00           N+0
HETATM   15  H   UNK     0      -2.819   0.324   1.827  0.00  0.00           H+0
HETATM   16  H   UNK     0      -1.468  -0.815   1.272  0.00  0.00           H+0
HETATM   17  H   UNK     0      -3.239  -1.310   1.272  0.00  0.00           H+0
HETATM   18  H   UNK     0      -2.943  -0.759  -1.003  0.00  0.00           H+0
HETATM   19  H   UNK     0      -4.713   0.253  -0.309  0.00  0.00           H+0
HETATM   20  H   UNK     0      -1.538   1.755   0.071  0.00  0.00           H+0
HETATM   21  H   UNK     0      -1.151   1.956  -2.537  0.00  0.00           H+0
HETATM   22  H   UNK     0      -2.608   2.637  -1.773  0.00  0.00           H+0
HETATM   23  H   UNK     0      -2.656   1.016  -2.658  0.00  0.00           H+0
HETATM   24  H   UNK     0       2.390   0.160  -1.271  0.00  0.00           H+0
HETATM   25  H   UNK     0       1.889  -2.034  -0.969  0.00  0.00           H+0
HETATM   26  H   UNK     0       1.224  -1.817   0.719  0.00  0.00           H+0
HETATM   27  H   UNK     0       3.396  -2.661   1.203  0.00  0.00           H+0
HETATM   28  H   UNK     0       4.072  -2.034  -0.323  0.00  0.00           H+0
HETATM   29  H   UNK     0       3.111   1.503   0.940  0.00  0.00           H+0
CONECT    1    2   15   16   17                                             
CONECT    2    1    3    4   18                                             
CONECT    3    2   19                                                       
CONECT    4    2    5    6   20                                             
CONECT    5    4   21   22   23                                             
CONECT    6    4    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   14   24                                             
CONECT   10    9   11   25   26                                             
CONECT   11   10   12   27   28                                             
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12    9   29                                                  
CONECT   15    1                                                            
CONECT   16    1                                                            
CONECT   17    1                                                            
CONECT   18    2                                                            
CONECT   19    3                                                            
CONECT   20    4                                                            
CONECT   21    5                                                            
CONECT   22    5                                                            
CONECT   23    5                                                            
CONECT   24    9                                                            
CONECT   25   10                                                            
CONECT   26   10                                                            
CONECT   27   11                                                            
CONECT   28   11                                                            
CONECT   29   14                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   58    0
END

RDKit          3D

29 29  0  0  0  0  0  0  0  0999 V2000
   -2.5093   -0.4899    1.1160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7430    0.0520   -0.2811 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9111    0.8176   -0.2160 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6409    0.9790   -0.7250 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0811    1.6753   -1.9754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3908    0.3480   -0.8385 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7172    0.6496   -0.1009 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6065    1.5691    0.7497 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0315   -0.0172   -0.2236 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9887   -1.4878    0.0083 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3825   -1.7953    0.5103 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8258   -0.5408    1.1427 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7665   -0.4350    1.9565 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0127    0.5001    0.6731 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8188    0.3241    1.8271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4685   -0.8147    1.2716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2387   -1.3095    1.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9429   -0.7587   -1.0032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7135    0.2526   -0.3085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5384    1.7547    0.0711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1510    1.9558   -2.5366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6081    2.6366   -1.7727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6563    1.0165   -2.6581 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3901    0.1604   -1.2712 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8892   -2.0344   -0.9689 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2237   -1.8165    0.7189 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3958   -2.6609    1.2032 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0715   -2.0337   -0.3226 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1108    1.5029    0.9398 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  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  2  0
 12 14  1  0
 14  9  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  6
  3 19  1  0
  4 20  1  1
  5 21  1  0
  5 22  1  0
  5 23  1  0
  9 24  1  6
 10 25  1  0
 10 26  1  0
 11 27  1  0
 11 28  1  0
 14 29  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
(3'-Hydroxybutan-20-yl)5-oxopyrrolidine-2-carboxylic acid	Generator
3-Hydroxybutan-2-yl (2S)-5-hydroxy-3,4-dihydro-2H-pyrrole-2-carboxylic acid	Generator

Chemical Formula

C₉H₁₅NO₄

Average Mass

201.2220 Da

Monoisotopic Mass

201.10011 Da

IUPAC Name

(2S,3R)-3-hydroxybutan-2-yl (2S)-5-oxopyrrolidine-2-carboxylate

Traditional Name

(2S,3R)-3-hydroxybutan-2-yl (2S)-5-oxopyrrolidine-2-carboxylate

CAS Registry Number

Not Available

SMILES

CC(O)C(C)OC(=O)[C@@H]1CCC(=O)N1

InChI Identifier

InChI=1S/C9H15NO4/c1-5(11)6(2)14-9(13)7-3-4-8(12)10-7/h5-7,11H,3-4H2,1-2H3,(H,10,12)/t5?,6?,7-/m0/s1

InChI Key

KGVMXZGSVPGTNQ-AHXFUIDQSA-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
Trichoderma	NPAtlas	22582864
Trichoderma atroviride	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha amino acid esters. These are ester derivatives of alpha amino acids.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Alpha amino acid esters

Alternative Parents

Substituents

Alpha-amino acid ester
Pyrroline carboxylic acid or derivatives
Pyrroline carboxylic acid
Cyclic carboximidic acid
Pyrroline
Lactim
Secondary alcohol
Carboxylic acid ester
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Monocarboxylic acid or derivatives
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
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	-0.5	ALOGPS
logP	-0.6	ChemAxon
logS	-0.07	ALOGPS
pKa (Strongest Acidic)	11.14	ChemAxon
pKa (Strongest Basic)	-2.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.63 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	47.99 m³·mol⁻¹	ChemAxon
Polarizability	20.52 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

NPAtlas ID

NPA002137

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

29214931

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139583695

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for (3'-hydroxybutan-20-yl)5-oxopyrrolidine-2-carboxylate (NP0010803)

MOL for NP0010803 ((3'-hydroxybutan-20-yl)5-oxopyrrolidine-2-carboxylate)

3D MOL for NP0010803 ((3'-hydroxybutan-20-yl)5-oxopyrrolidine-2-carboxylate)

3D SDF for NP0010803 ((3'-hydroxybutan-20-yl)5-oxopyrrolidine-2-carboxylate)

3D-SDF for NP0010803 ((3'-hydroxybutan-20-yl)5-oxopyrrolidine-2-carboxylate)

PDB for NP0010803 ((3'-hydroxybutan-20-yl)5-oxopyrrolidine-2-carboxylate)

3D PDB for NP0010803 ((3'-hydroxybutan-20-yl)5-oxopyrrolidine-2-carboxylate)

SMILES for NP0010803 ((3'-hydroxybutan-20-yl)5-oxopyrrolidine-2-carboxylate)

INCHI for NP0010803 ((3'-hydroxybutan-20-yl)5-oxopyrrolidine-2-carboxylate)

Structure for NP0010803 ((3'-hydroxybutan-20-yl)5-oxopyrrolidine-2-carboxylate)

3D Structure for NP0010803 ((3'-hydroxybutan-20-yl)5-oxopyrrolidine-2-carboxylate)