NP-MRD: Showing NP-Card for Preechinulin (NP0057996)

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Record Information

Version

2.0

Created at

2022-04-28 03:20:11 UTC

Updated at

2022-04-28 03:20:11 UTC

NP-MRD ID

NP0057996

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Preechinulin

Description

(3S)-3alpha-Methyl-6beta-[[2-(1,1-dimethyl-2-propenyl)-1H-indole-3-yl]methyl]hexahydropyrazine-2,5-dione belongs to the class of organic compounds known as 3-alkylindoles. 3-Alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position. Preechinulin is found in Eurotium amstelodami, Eurotium chevalieri, Aspergillus variecolor and Eurotium echinulatum. Based on a literature review very few articles have been published on (3S)-3alpha-Methyl-6beta-[[2-(1,1-dimethyl-2-propenyl)-1H-indole-3-yl]methyl]hexahydropyrazine-2,5-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 49  0  0  0  0  0  0  0  0999 V2000
   -2.1323   -3.2596    0.6840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4664   -2.0476    0.3603 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1251   -0.8003    1.1269 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1594   -0.9768    2.2161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4741   -0.4693    1.8258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8518    0.2698    0.1275 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5834    1.4195   -0.0170 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1220    2.1443   -1.0505 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5295    3.3539   -1.5663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8529    3.8901   -2.6622 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7718    3.1930   -3.2244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3684    1.9835   -2.7058 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0575    1.4881   -1.6272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9054    0.3216   -0.8749 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1877   -0.6181   -1.1126 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5570   -0.2023   -0.7089 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7645    0.3777    0.5609 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0558    0.2927    1.2120 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5173    1.2577    1.8764 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8037   -0.9670    1.0602 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2745   -0.7513    1.4249 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7457   -1.4107   -0.3103 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5055   -1.3293   -0.9994 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1601   -2.1708   -1.8556 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5639   -3.5631    1.5452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4436   -4.0859    0.0326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0555   -1.8650   -0.5486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1021   -0.9266    2.0041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4393   -1.9242    2.7555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3616   -0.1855    3.0052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7014   -1.2464    2.5724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3054   -0.4612    1.0784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4630    0.4974    2.3086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3892    1.6556    0.6181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3626    3.8680   -1.1141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1891    4.8409   -3.0471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2825    3.6518   -4.0719 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4629    1.4886   -3.1698 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1928   -0.9763   -2.1685 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0029   -1.5961   -0.5386 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9439    0.6021   -1.4422 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0294    0.8923    1.0645 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3481   -1.7309    1.7481 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4560   -0.9471    2.4875 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8830   -1.4549    0.7829 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6068    0.2675    1.1701 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5617   -1.7894   -0.8322 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 20  1  0
 20 22  1  0
 22 23  1  0
 23 24  2  0
 23 16  1  0
 16 15  1  0
 15 14  1  0
 14  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
  6  3  1  0
  3  4  1  1
  3  5  1  0
  3  2  1  0
  2  1  2  3
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 13 14  1  0
 13  8  1  0
 21 44  1  0
 21 45  1  0
 21 46  1  0
 20 43  1  1
 22 47  1  0
 16 41  1  6
 15 39  1  0
 15 40  1  0
  7 34  1  0
  9 35  1  0
 10 36  1  0
 11 37  1  0
 12 38  1  0
  4 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  5 33  1  0
  2 27  1  0
  1 25  1  0
  1 26  1  0
 17 42  1  0
M  END


  Mrv1652304282205202D          

 24 26  0  0  1  0            999 V2000
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7846    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2695    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7846   -0.2549    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0945    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0945   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0945    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9195    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3320    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0396    1.8646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4875    2.4777    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3194    2.3061    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8715    2.9192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6784    2.7477    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6165    3.7038    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1904    3.8754    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7425    3.2623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5494    3.4338    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1686    4.3169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  3  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  2  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  2  0  0  0  0
  7 15  1  0  0  0  0
 16 15  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 16 22  1  0  0  0  0
 22 23  2  0  0  0  0
 20 24  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0057996

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1NC(=O)[C@@H](CC2=C(NC3=CC=CC=C23)C(C)(C)C=C)NC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H23N3O2/c1-5-19(3,4)16-13(12-8-6-7-9-14(12)21-16)10-15-18(24)20-11(2)17(23)22-15/h5-9,11,15,21H,1,10H2,2-4H3,(H,20,24)(H,22,23)/t11-,15+/m0/s1

> <INCHI_KEY>
LVPZJIGICMPWFH-XHDPSFHLSA-N

> <FORMULA>
C19H23N3O2

> <MOLECULAR_WEIGHT>
325.412

> <EXACT_MASS>
325.179026993

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
34.60067937562937

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,6R)-3-methyl-6-{[2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methyl}piperazine-2,5-dione

> <ALOGPS_LOGP>
2.58

> <JCHEM_LOGP>
2.287688439000001

> <ALOGPS_LOGS>
-4.53

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.458892643791707

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.29020253773774

> <JCHEM_PKA_STRONGEST_BASIC>
-4.38363524687558

> <JCHEM_POLAR_SURFACE_AREA>
73.99000000000001

> <JCHEM_REFRACTIVITY>
93.48879999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.53e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,6R)-3-methyl-6-{[2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methyl}piperazine-2,5-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.000   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.465   2.016   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.370   0.770   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      -1.465  -0.476   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      -3.910   0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.910  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.910   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.450   0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -6.220   2.104   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.941   3.481   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.910   4.625   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       0.596   4.305   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       1.627   5.449   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       3.133   5.129   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.151   6.914   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0      -0.355   7.234   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0      -1.386   6.090   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -2.892   6.410   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.181   8.058   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3    9                                                  
CONECT    3    2    4    7                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    1                                                       
CONECT    7    3    8   15                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8    2                                                       
CONECT   10    8   11   12   13                                             
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13   10   14                                                       
CONECT   14   13                                                            
CONECT   15    7   16                                                       
CONECT   16   15   17   22                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   24                                                  
CONECT   21   20   22                                                       
CONECT   22   21   16   23                                                  
CONECT   23   22                                                            
CONECT   24   20                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Value	Source
(3S)-3a-Methyl-6b-[[2-(1,1-dimethyl-2-propenyl)-1H-indole-3-yl]methyl]hexahydropyrazine-2,5-dione	Generator
(3S)-3Α-methyl-6β-[[2-(1,1-dimethyl-2-propenyl)-1H-indole-3-yl]methyl]hexahydropyrazine-2,5-dione	Generator

Chemical Formula

C₁₉H₂₃N₃O₂

Average Mass

325.4120 Da

Monoisotopic Mass

325.17903 Da

IUPAC Name

(3S,6R)-3-methyl-6-{[2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methyl}piperazine-2,5-dione

Traditional Name

(3S,6R)-3-methyl-6-{[2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methyl}piperazine-2,5-dione

CAS Registry Number

Not Available

SMILES

C[C@@H]1NC(=O)[C@@H](CC2=C(NC3=CC=CC=C23)C(C)(C)C=C)NC1=O

InChI Identifier

InChI=1S/C19H23N3O2/c1-5-19(3,4)16-13(12-8-6-7-9-14(12)21-16)10-15-18(24)20-11(2)17(23)22-15/h5-9,11,15,21H,1,10H2,2-4H3,(H,20,24)(H,22,23)/t11-,15+/m0/s1

InChI Key

LVPZJIGICMPWFH-XHDPSFHLSA-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
Aspergillus amstelodami	Fungi	KNApSAcK
Aspergillus chevalieri	Fungi	KNApSAcK
Aspergillus stellatus	Fungi	KNApSAcK
Eurotium echinulatum	Fungi	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 3-alkylindoles. 3-Alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indoles

Direct Parent

3-alkylindoles

Alternative Parents

Substituents

3-alkylindole
Benzenoid
Substituted pyrrole
Heteroaromatic compound
Cyclic carboximidic acid
Pyrrole
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	2.58	ALOGPS
logP	2.29	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	11.29	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	73.99 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	93.49 m³·mol⁻¹	ChemAxon
Polarizability	34.6 Å³	ChemAxon
Number of Rings	3	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

102413446

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Preechinulin (NP0057996)

MOL for NP0057996 (Preechinulin)

3D MOL for NP0057996 (Preechinulin)

3D SDF for NP0057996 (Preechinulin)

3D-SDF for NP0057996 (Preechinulin)

PDB for NP0057996 (Preechinulin)

3D PDB for NP0057996 (Preechinulin)

SMILES for NP0057996 (Preechinulin)

INCHI for NP0057996 (Preechinulin)

Structure for NP0057996 (Preechinulin)

3D Structure for NP0057996 (Preechinulin)