NP-MRD: Showing NP-Card for Murrayamine I (NP0070137)

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Record Information

Version

2.0

Created at

2022-04-28 15:24:16 UTC

Updated at

2022-04-28 15:24:16 UTC

NP-MRD ID

NP0070137

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Murrayamine I

Description

[(5R)-14-hydroxy-5,8-dimethyl-6-oxa-17-azatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]Heptadeca-1,3,7,9,11(16),12,14-heptaen-5-yl]methyl acetate belongs to the class of organic compounds known as carbazoles. Carbazoles are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring. Murrayamine I is found in Murraya euchrestifolia. Based on a literature review very few articles have been published on [(5R)-14-hydroxy-5,8-dimethyl-6-oxa-17-azatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]Heptadeca-1,3,7,9,11(16),12,14-heptaen-5-yl]methyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 44 47  0  0  0  0  0  0  0  0999 V2000
    6.3630   -0.2549    2.2425 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4882   -0.1740    1.0357 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8258   -0.8026    0.0313 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3760    0.5665    1.0706 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4132    0.7995    0.1454 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5381   -0.3683   -0.2000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2114   -1.5458   -0.8257 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8971   -0.8315    1.0431 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6046   -0.7669    1.2847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2826   -0.2054    0.2779 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2342    0.2493   -0.9083 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5931    0.7956   -1.8987 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0207    1.2830   -3.1761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9487    0.8693   -1.6587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4550    0.4092   -0.4631 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6341   -0.1269    0.5060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4099   -0.4913    1.5654 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6899   -0.2054    1.3014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8830   -0.3540    1.9968 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1002    0.0341    1.4825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2909   -0.1245    2.1998 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1083    0.5916    0.2206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9502    0.7605   -0.5102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7451    0.3561    0.0448 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5711    0.1737   -1.1386 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7641   -0.5783    3.1145 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2097   -0.9528    2.0861 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7750    0.7415    2.4743 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7481    1.6796    0.4260 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8856    1.2080   -0.8258 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8880   -1.3256   -1.6524 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6237   -2.2381   -0.0707 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3773   -2.1934   -1.3016 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5543   -1.2483    1.7909 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1607   -1.1201    2.2191 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0843    1.3910   -3.0840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2161    0.5810   -4.0103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4465    2.2899   -3.4291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6272    1.2842   -2.3957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0809   -0.9236    2.4469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8660   -0.7943    2.9903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2363   -0.5348    3.1139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0647    0.9008   -0.1932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9443    1.1963   -1.5003 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  6  5  1  1
  6  7  1  0
  6 25  1  0
 25 11  1  0
 11 10  2  0
 10  9  1  0
  9  8  2  0
 10 16  1  0
 16 15  2  0
 15 14  1  0
 14 12  2  0
 12 13  1  0
 15 24  1  0
 24 18  2  0
 18 17  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 20 22  1  0
 22 23  2  0
  8  6  1  0
 17 16  1  0
 12 11  1  0
 23 24  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  5 29  1  0
  5 30  1  0
  7 31  1  0
  7 32  1  0
  7 33  1  0
  9 35  1  0
  8 34  1  0
 14 39  1  0
 13 36  1  0
 13 37  1  0
 13 38  1  0
 17 40  1  0
 19 41  1  0
 21 42  1  0
 22 43  1  0
 23 44  1  0
M  END


  Mrv1652304282217242D          

 25 28  0  0  1  0            999 V2000
    5.0376   -0.0335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0768    0.7906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3828    1.2366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6495    0.8585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6103    0.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3043   -0.4116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8144   -0.1829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3618    0.5068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8779    1.1504    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5381    0.4596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1671   -0.2772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6198   -0.9670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4434   -0.9198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2488   -1.7038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3435   -0.3244    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1092    0.3654    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2618    1.1022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0855    1.1494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8143   -0.0630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8586    0.7104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5321    0.2340    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2814    0.5790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9550    0.1026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3573    1.4005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8101    1.1687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  1  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  7 13  1  0  0  0  0
 12 14  1  0  0  0  0
 11 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 10 18  1  0  0  0  0
 16 19  1  6  0  0  0
 16 20  1  1  0  0  0
 20 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
  2 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0070137

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC[C@]1(C)OC2=C(C=C1)C1=C(C=C2C)C2=C(N1)C=C(O)C=C2

> <INCHI_IDENTIFIER>
InChI=1S/C20H19NO4/c1-11-8-16-14-5-4-13(23)9-17(14)21-18(16)15-6-7-20(3,25-19(11)15)10-24-12(2)22/h4-9,21,23H,10H2,1-3H3/t20-/m1/s1

> <INCHI_KEY>
HGIQTDGMLIBTAD-HXUWFJFHSA-N

> <FORMULA>
C20H19NO4

> <MOLECULAR_WEIGHT>
337.375

> <EXACT_MASS>
337.131408096

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
36.55901988094472

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(5R)-14-hydroxy-5,8-dimethyl-6-oxa-17-azatetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-1(10),2(7),3,8,11(16),12,14-heptaen-5-yl]methyl acetate

> <ALOGPS_LOGP>
4.14

> <JCHEM_LOGP>
3.5955806026666672

> <ALOGPS_LOGS>
-4.79

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.497881449712889

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.76961764198103

> <JCHEM_PKA_STRONGEST_BASIC>
-4.928207556935371

> <JCHEM_POLAR_SURFACE_AREA>
71.55

> <JCHEM_REFRACTIVITY>
95.5829

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.42e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(5R)-14-hydroxy-5,8-dimethyl-6-oxa-17-azatetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-1(10),2(7),3,8,11(16),12,14-heptaen-5-yl]methyl acetate

> <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       9.404  -0.063   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.477   1.476   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.181   2.308   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.812   1.603   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.739   0.064   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.035  -0.768   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.254  -0.341   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.409   0.946   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       5.372   2.147   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       2.871   0.858   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.179  -0.517   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.024  -1.805   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.561  -1.717   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.331  -3.180   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.641  -0.606   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -0.204   0.682   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.489   2.057   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.026   2.146   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.520  -0.118   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.603   1.326   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -2.860   0.437   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -4.259   1.081   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -5.516   0.191   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -4.400   2.614   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      10.845   2.181   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   25                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8   13                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8    4                                                       
CONECT   10    8   11   18                                                  
CONECT   11   10   12   15                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12    7                                                       
CONECT   14   12                                                            
CONECT   15   11   16                                                       
CONECT   16   15   17   19   20                                             
CONECT   17   16   18                                                       
CONECT   18   17   10                                                       
CONECT   19   16                                                            
CONECT   20   16   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25    2                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Value	Source
[(5R)-14-Hydroxy-5,8-dimethyl-6-oxa-17-azatetracyclo[8.7.0.0,.0,]heptadeca-1,3,7,9,11(16),12,14-heptaen-5-yl]methyl acetic acid	Generator

Chemical Formula

C₂₀H₁₉NO₄

Average Mass

337.3750 Da

Monoisotopic Mass

337.13141 Da

IUPAC Name

[(5R)-14-hydroxy-5,8-dimethyl-6-oxa-17-azatetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-1(10),2(7),3,8,11(16),12,14-heptaen-5-yl]methyl acetate

Traditional Name

[(5R)-14-hydroxy-5,8-dimethyl-6-oxa-17-azatetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-1(10),2(7),3,8,11(16),12,14-heptaen-5-yl]methyl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC[C@]1(C)OC2=C(C=C1)C1=C(C=C2C)C2=C(N1)C=C(O)C=C2

InChI Identifier

InChI=1S/C20H19NO4/c1-11-8-16-14-5-4-13(23)9-17(14)21-18(16)15-6-7-20(3,25-19(11)15)10-24-12(2)22/h4-9,21,23H,10H2,1-3H3/t20-/m1/s1

InChI Key

HGIQTDGMLIBTAD-HXUWFJFHSA-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
Murraya euchrestifolia	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as carbazoles. Carbazoles are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Carbazoles

Direct Parent

Carbazoles

Alternative Parents

Substituents

Carbazole
Benzopyran
Hydroxyindole
1-benzopyran
Indole
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Pyrrole
Heteroaromatic compound
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Azacycle
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic oxide
Organic nitrogen compound
Carbonyl group
Organopnictogen compound
Organic oxygen 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	4.14	ALOGPS
logP	3.6	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	9.77	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	71.55 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	95.58 m³·mol⁻¹	ChemAxon
Polarizability	36.56 Å³	ChemAxon
Number of Rings	4	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

137348811

PDB ID

9ET

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Murrayamine I (NP0070137)

MOL for NP0070137 (Murrayamine I)

3D MOL for NP0070137 (Murrayamine I)

3D SDF for NP0070137 (Murrayamine I)

3D-SDF for NP0070137 (Murrayamine I)

PDB for NP0070137 (Murrayamine I)

3D PDB for NP0070137 (Murrayamine I)

SMILES for NP0070137 (Murrayamine I)

INCHI for NP0070137 (Murrayamine I)

Structure for NP0070137 (Murrayamine I)

3D Structure for NP0070137 (Murrayamine I)