NP-MRD: Showing NP-Card for Peimisine (NP0137310)

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Record Information

Version

2.0

Created at

2022-05-30 16:48:32 UTC

Updated at

2022-05-30 16:48:32 UTC

NP-MRD ID

NP0137310

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Peimisine

Description

Ebeiensine, also known as peimisine, belongs to the class of organic compounds known as jerveratrum-type alkaloids. These are steroidal alkaloids with a structure that is based on the jervane ring system. Jerveratrum alkaloids have alkamines with 1-3 oxygen atoms, and occur as such or as monoglycosides. Peimisine is found in Fritillaria cirrhosa, Fritillaria thunbergii and Fritillaria unibracteata. Ebeiensine is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533005011512432D          

 31 36  0  0  0  0            999 V2000
    8.5708   -0.0032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7724    0.2047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5532    1.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7548    1.2078    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1756    0.6203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3948   -0.1750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1932   -0.3828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7062   -0.6292    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0613   -0.1146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8535   -0.9130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0581   -1.1322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4706   -0.5530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6471   -0.6021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1325   -1.2469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3167   -1.1237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8021   -1.7685    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0156   -0.3556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1999   -0.2323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1013    0.5358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9170    0.6590    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4133    1.1806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2291    1.0573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5302    0.2892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0448    0.9341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3460    0.1660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9834    0.6897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6785    0.2454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4738    0.4646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6817    1.2629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3515    0.6577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1323    1.4530    0.0000 C   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
  2  7  1  0  0  0  0
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 15 17  1  0  0  0  0
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 17 23  1  0  0  0  0
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  9 28  1  0  0  0  0
 28 29  1  0  0  0  0
  9 30  1  0  0  0  0
  5 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END

     RDKit          3D

 72 77  0  0  0  0  0  0  0  0999 V2000
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    0.3871    0.7546    0.5669 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3228   -0.3467    1.5945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9850   -1.0717    1.5522 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8700   -0.7101    0.3791 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5103    0.4927    0.6016 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7849    0.4506    0.1245 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6955    1.0060    1.2286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0927    1.0333    0.6487 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.1100    2.1272   -0.4078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3562   -0.3292    0.0605 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3475   -1.3071    0.4995 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1317   -0.9493   -0.2401 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9370   -1.7388    0.2162 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2268   -2.4875    1.4921 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8078   -0.7283   -2.9451 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.3240   -0.4220    1.4990 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6119   -0.5153    1.4387 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.7228   -1.1362   -1.4656 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4599   -1.3741   -1.7330 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0470   -1.2887   -0.0238 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1905    1.1233   -2.4630 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5538    1.6292   -2.9130 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9879   -0.0850   -3.0352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4199    1.4694    0.8185 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5007    0.1143    2.5872 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1131   -1.1269    1.3808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8564   -2.1925    1.4906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4972   -0.9065    2.5225 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.6526    0.2741    2.0608 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1533005011512432D          

 31 36  0  0  0  0            999 V2000
    8.5708   -0.0032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.4706   -0.5530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.8021   -1.7685    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.2291    1.0573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5302    0.2892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0448    0.9341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.6817    1.2629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.1323    1.4530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0137310

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C2NCC(C)CC2OC11CCC2C3CC(=O)C4CC(O)CCC4(C)C3CC2=C1C

> <INCHI_IDENTIFIER>
InChI=1S/C27H41NO3/c1-14-9-24-25(28-13-14)16(3)27(31-24)8-6-18-19(15(27)2)11-21-20(18)12-23(30)22-10-17(29)5-7-26(21,22)4/h14,16-18,20-22,24-25,28-29H,5-13H2,1-4H3

> <INCHI_KEY>
KYELXPJVGNZIGC-UHFFFAOYSA-N

> <FORMULA>
C27H41NO3

> <MOLECULAR_WEIGHT>
427.629

> <EXACT_MASS>
427.308644184

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
72

> <JCHEM_AVERAGE_POLARIZABILITY>
50.726270066322016

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5'-hydroxy-2',3,6,15'-tetramethyl-3a,4,5,6,7,7a-hexahydro-3H-spiro[furo[3,2-b]pyridine-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadecan]-15'-en-8'-one

> <ALOGPS_LOGP>
3.28

> <JCHEM_LOGP>
3.2787955483333335

> <ALOGPS_LOGS>
-4.83

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
19.418424241734304

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.234279099870616

> <JCHEM_PKA_STRONGEST_BASIC>
9.934024597163146

> <JCHEM_POLAR_SURFACE_AREA>
58.56

> <JCHEM_REFRACTIVITY>
121.98639999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.33e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5'-hydroxy-2',3,6,15'-tetramethyl-3a,4,5,6,7,7a-hexahydro-3H-spiro[furo[3,2-b]pyridine-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadecan]-15'-en-8'-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 01-MAY-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   01-MAY-15         0                                  
HETATM    1  C   UNK     0      15.999  -0.006   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.509   0.382   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      14.099   1.867   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0      12.609   2.255   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0      11.528   1.158   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.937  -0.327   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.427  -0.715   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      10.651  -1.175   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       9.448  -0.214   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.060  -1.704   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.575  -2.113   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.479  -1.032   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.941  -1.124   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.981  -2.328   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.458  -2.097   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.497  -3.301   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.896  -0.664   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.373  -0.434   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.189   1.000   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -1.712   1.230   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.772   2.204   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.294   1.974   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.856   0.540   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.817   1.744   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.379   0.310   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.569   1.288   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.866   0.458   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.351   0.867   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.739   2.357   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.989   1.228   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.580   2.712   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   30                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6    2                                                       
CONECT    8    6    9                                                       
CONECT    9    8   10   28   30                                             
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   27                                                  
CONECT   13   12   14   25                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   23                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   17   24   25                                             
CONECT   24   23                                                            
CONECT   25   23   13   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   12   28                                                  
CONECT   28   27    9   29                                                  
CONECT   29   28                                                            
CONECT   30    9    5   31                                                  
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   72    0
END

View in JSmol

Synonyms

Value	Source
Peimisine	MeSH
Peimissine	MeSH

Chemical Formula

C₂₇H₄₁NO₃

Average Mass

427.6290 Da

Monoisotopic Mass

427.30864 Da

IUPAC Name

5'-hydroxy-2',3,6,15'-tetramethyl-3a,4,5,6,7,7a-hexahydro-3H-spiro[furo[3,2-b]pyridine-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadecan]-15'-en-8'-one

Traditional Name

5'-hydroxy-2',3,6,15'-tetramethyl-3a,4,5,6,7,7a-hexahydro-3H-spiro[furo[3,2-b]pyridine-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadecan]-15'-en-8'-one

CAS Registry Number

Not Available

SMILES

CC1C2NCC(C)CC2OC11CCC2C3CC(=O)C4CC(O)CCC4(C)C3CC2=C1C

InChI Identifier

InChI=1S/C27H41NO3/c1-14-9-24-25(28-13-14)16(3)27(31-24)8-6-18-19(15(27)2)11-21-20(18)12-23(30)22-10-17(29)5-7-26(21,22)4/h14,16-18,20-22,24-25,28-29H,5-13H2,1-4H3

InChI Key

KYELXPJVGNZIGC-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

Species Name	Source	Reference
Fritillaria cirrhosa	LOTUS Database	35616633
Fritillaria thunbergii	LOTUS Database	35616633
Fritillaria unibracteata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as jerveratrum-type alkaloids. These are steroidal alkaloids with a structure that is based on the jervane ring system. Jerveratrum alkaloids have alkamines with 1-3 oxygen atoms, and occur as such or as monoglycosides.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal alkaloids

Direct Parent

Jerveratrum-type alkaloids

Alternative Parents

Substituents

Jerveratrum-type alkaloid
Azasteroid
Alkaloid or derivatives
Piperidine
Cyclic alcohol
Tetrahydrofuran
Ketone
Secondary alcohol
Dialkyl ether
Secondary aliphatic amine
Ether
Oxacycle
Secondary amine
Azacycle
Organoheterocyclic compound
Organic oxide
Organopnictogen compound
Amine
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Organic nitrogen compound
Carbonyl group
Organic oxygen compound
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	3.28	ALOGPS
logP	3.28	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	15.23	ChemAxon
pKa (Strongest Basic)	9.93	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	58.56 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	121.99 m³·mol⁻¹	ChemAxon
Polarizability	50.73 Å³	ChemAxon
Number of Rings	6	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

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

5320448

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Peimisine (NP0137310)

MOL for NP0137310 (Peimisine)

3D MOL for NP0137310 (Peimisine)

3D SDF for NP0137310 (Peimisine)

3D-SDF for NP0137310 (Peimisine)

PDB for NP0137310 (Peimisine)

3D PDB for NP0137310 (Peimisine)

SMILES for NP0137310 (Peimisine)

INCHI for NP0137310 (Peimisine)

Structure for NP0137310 (Peimisine)

3D Structure for NP0137310 (Peimisine)