NP-MRD: Showing NP-Card for 1-(3-hydroxy-2,4-dimethyldodec-4-enoyl)pyrrolidine-2-carboxylic acid (NP0193732)

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Record Information

Version

2.0

Created at

2022-09-04 11:16:10 UTC

Updated at

2022-09-04 11:16:10 UTC

NP-MRD ID

NP0193732

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-(3-hydroxy-2,4-dimethyldodec-4-enoyl)pyrrolidine-2-carboxylic acid

Description

1-(3-Hydroxy-2,4-dimethyldodec-4-enoyl)pyrrolidine-2-carboxylic acid belongs to the class of organic compounds known as n-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 1-(3-Hydroxy-2,4-dimethyldodec-4-enoyl)pyrrolidine-2-carboxylic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 57 57  0  0  0  0  0  0  0  0999 V2000
    7.7947    1.0712   -0.2883 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4947   -0.3257    0.2235 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0930   -0.7506   -0.1433 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0577    0.1833    0.4454 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6632   -0.2213    0.0930 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3134   -1.6009    0.5851 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9077   -1.9791    0.2164 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9030   -1.0494    0.7913 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1107   -0.3855   -0.0351 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2388   -0.5795   -1.5034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9178    0.5647    0.5249 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5827    1.8289    0.1027 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3088    0.1391    0.1125 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5233   -1.2542    0.6658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3023    1.1151    0.6214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8987    2.0957    1.3085 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6832    1.0064    0.3779 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7345    1.8978    0.8269 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9505    1.5469    0.0238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8036    0.0552   -0.1400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2955   -0.0652   -0.3989 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1108    0.1500   -1.8476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5813   -0.6907   -2.6484 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4294    1.2613   -2.3218 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6347    1.7964    0.5528 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1314    1.3534   -1.1283 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8731    1.0710   -0.6099 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5956   -0.3379    1.3165 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1852   -1.0611   -0.2569 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9708   -1.7923    0.2550 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9805   -0.8396   -1.2488 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2763    1.1944    0.0461 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2165    0.1965    1.5437 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9698    0.4985    0.5725 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5651   -0.2283   -1.0086 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9862   -2.3501    0.1004 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -1.6675    1.6667 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8122   -2.0236   -0.8667 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7069   -2.9767    0.7028 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8041   -0.9027    1.8695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4292    0.0749   -2.0766 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0306   -1.6448   -1.8040 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2844   -0.3065   -1.8329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8872    0.5142    1.6322 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0439    2.2707    0.7105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3003    0.1187   -1.0111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7892   -1.9227   -0.1895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2219   -1.2948    1.5027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5600   -1.6965    1.0573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9877    1.7472    1.9032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4622    2.9651    0.6813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0167    2.0664   -0.9438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8945    1.7143    0.6046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0579   -0.4461    0.8192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3324   -0.3567   -0.9996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0210   -1.0640   -0.0621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0607    1.3166   -3.2624 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  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 24  1  0
 22 23  2  0
 21 17  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  0
  6 37  1  0
  7 38  1  0
  7 39  1  0
  8 40  1  0
 10 41  1  0
 10 42  1  0
 10 43  1  0
 11 44  1  1
 12 45  1  0
 13 46  1  6
 14 47  1  0
 14 48  1  0
 14 49  1  0
 18 50  1  0
 18 51  1  0
 19 52  1  0
 19 53  1  0
 20 54  1  0
 20 55  1  0
 21 56  1  1
 24 57  1  0
M  END


  Mrv1533004201503022D          

 24 24  0  0  0  0            999 V2000
   -5.3155   -4.3751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6011   -3.9626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8866   -4.3751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1721   -3.9626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4576   -4.3751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7432   -3.9626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0287   -4.3751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3142   -3.9626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4002   -4.3751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4002   -5.2001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1147   -3.9626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8292   -4.3751    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1147   -3.1376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4002   -2.7251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8292   -2.7251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5437   -3.1376    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8292   -1.9001    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1617   -1.4152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4167   -0.6305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2417   -0.6305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4966   -1.4152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2812   -1.6701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8943   -1.1181    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4528   -2.4771    0.0000 O   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 17 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0193732

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCC=C(C)C(O)C(C)C(=O)N1CCCC1C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H33NO4/c1-4-5-6-7-8-9-11-14(2)17(21)15(3)18(22)20-13-10-12-16(20)19(23)24/h11,15-17,21H,4-10,12-13H2,1-3H3,(H,23,24)

> <INCHI_KEY>
JFFANXXIOVCBBG-UHFFFAOYSA-N

> <FORMULA>
C19H33NO4

> <MOLECULAR_WEIGHT>
339.476

> <EXACT_MASS>
339.240958547

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
38.749475879081565

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-(3-hydroxy-2,4-dimethyldodec-4-enoyl)pyrrolidine-2-carboxylic acid

> <ALOGPS_LOGP>
3.36

> <JCHEM_LOGP>
3.563976984333334

> <ALOGPS_LOGS>
-3.18

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
14.154932870773322

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.9906566638927923

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2451081910946122

> <JCHEM_POLAR_SURFACE_AREA>
77.84

> <JCHEM_REFRACTIVITY>
95.00069999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.23e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-(3-hydroxy-2,4-dimethyldodec-4-enoyl)pyrrolidine-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  C   UNK     0      -9.922  -8.167   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.589  -7.397   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -7.255  -8.167   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.921  -7.397   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.588  -8.167   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.254  -7.397   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.920  -8.167   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.587  -7.397   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.747  -8.167   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.747  -9.707   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.081  -7.397   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.414  -8.167   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.081  -5.857   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.747  -5.087   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.414  -5.087   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.748  -5.857   0.000  0.00  0.00           O+0
HETATM   17  N   UNK     0       3.414  -3.547   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       2.169  -2.642   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.644  -1.177   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.184  -1.177   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.660  -2.642   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.125  -3.118   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       7.269  -2.087   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       6.445  -4.624   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   21                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   17   22                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   48    0
END

View in JSmol

Synonyms

Value	Source
1-(3-Hydroxy-2,4-dimethyldodec-4-enoyl)pyrrolidine-2-carboxylate	Generator

Chemical Formula

C₁₉H₃₃NO₄

Average Mass

339.4760 Da

Monoisotopic Mass

339.24096 Da

IUPAC Name

1-(3-hydroxy-2,4-dimethyldodec-4-enoyl)pyrrolidine-2-carboxylic acid

Traditional Name

1-(3-hydroxy-2,4-dimethyldodec-4-enoyl)pyrrolidine-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

CCCCCCCC=C(C)C(O)C(C)C(=O)N1CCCC1C(O)=O

InChI Identifier

InChI=1S/C19H33NO4/c1-4-5-6-7-8-9-11-14(2)17(21)15(3)18(22)20-13-10-12-16(20)19(23)24/h11,15-17,21H,4-10,12-13H2,1-3H3,(H,23,24)

InChI Key

JFFANXXIOVCBBG-UHFFFAOYSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

N-acyl-alpha amino acids

Alternative Parents

Substituents

N-acyl-alpha-amino acid
Proline or derivatives
N-acylpyrrolidine
Pyrrolidine carboxylic acid
Pyrrolidine carboxylic acid or derivatives
Pyrrolidine
Tertiary carboxylic acid amide
Carboxamide group
Secondary alcohol
Carboxylic acid
Monocarboxylic acid or derivatives
Azacycle
Organoheterocyclic compound
Organonitrogen compound
Organic oxide
Organic oxygen compound
Alcohol
Organooxygen compound
Hydrocarbon derivative
Carbonyl group
Organic nitrogen 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	3.36	ALOGPS
logP	3.56	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	3.99	ChemAxon
pKa (Strongest Basic)	-1.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	77.84 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	95 m³·mol⁻¹	ChemAxon
Polarizability	38.75 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73836736

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-(3-hydroxy-2,4-dimethyldodec-4-enoyl)pyrrolidine-2-carboxylic acid (NP0193732)

MOL for NP0193732 (1-(3-hydroxy-2,4-dimethyldodec-4-enoyl)pyrrolidine-2-carboxylic acid)

3D MOL for NP0193732 (1-(3-hydroxy-2,4-dimethyldodec-4-enoyl)pyrrolidine-2-carboxylic acid)

3D SDF for NP0193732 (1-(3-hydroxy-2,4-dimethyldodec-4-enoyl)pyrrolidine-2-carboxylic acid)

3D-SDF for NP0193732 (1-(3-hydroxy-2,4-dimethyldodec-4-enoyl)pyrrolidine-2-carboxylic acid)

PDB for NP0193732 (1-(3-hydroxy-2,4-dimethyldodec-4-enoyl)pyrrolidine-2-carboxylic acid)

3D PDB for NP0193732 (1-(3-hydroxy-2,4-dimethyldodec-4-enoyl)pyrrolidine-2-carboxylic acid)

SMILES for NP0193732 (1-(3-hydroxy-2,4-dimethyldodec-4-enoyl)pyrrolidine-2-carboxylic acid)

INCHI for NP0193732 (1-(3-hydroxy-2,4-dimethyldodec-4-enoyl)pyrrolidine-2-carboxylic acid)

Structure for NP0193732 (1-(3-hydroxy-2,4-dimethyldodec-4-enoyl)pyrrolidine-2-carboxylic acid)

3D Structure for NP0193732 (1-(3-hydroxy-2,4-dimethyldodec-4-enoyl)pyrrolidine-2-carboxylic acid)