NP-MRD: Showing NP-Card for Gardneramine (NP0138760)

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Record Information

Version

2.0

Created at

2022-06-29 18:34:59 UTC

Updated at

2022-06-29 18:34:59 UTC

NP-MRD ID

NP0138760

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Gardneramine

Description

Gardneramine 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. It was first documented in 1993 (PMID: 35862567). Based on a literature review a significant number of articles have been published on Gardneramine (PMID: 35863886) (PMID: 35863885) (PMID: 35863884) (PMID: 31683708).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652306292220352D          

 30 35  0  0  1  0            999 V2000
   -1.3183   -2.5124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5414   -2.2350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3932   -1.4234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3838   -1.1459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5319   -0.3344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1019    0.3827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8603    0.7858    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8662    1.6336    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8030    1.5602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5036    1.0749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8084    0.5233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8237   -0.3410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1902    0.1866    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3868    1.1117    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4644    2.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1695    2.5227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7623    1.9052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5495    2.1711    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9064    1.4151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3475    0.8083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5936    0.0208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3986   -0.1598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9575    0.4471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7114    1.2345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2703    1.8413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0242    2.6288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6447   -0.9472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4497   -1.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0347   -0.5860    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2808   -1.3735    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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  7 11  1  0  0  0  0
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 13 12  1  6  0  0  0
  5 13  1  0  0  0  0
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  8 14  1  0  0  0  0
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 22 27  1  0  0  0  0
 27 28  1  0  0  0  0
 21 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END

     RDKit          2D

 58 63  0  0  0  0  0  0  0  0999 V2000
   -6.7207    9.7405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3651    8.2833    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9253    7.8627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4855    7.4420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1298    5.9848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2140    4.9482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8584    3.4909    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5172    0.9620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.6900    5.5641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3344    4.1069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4086   -3.6844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8351   -3.2209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9499   -4.2246    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.5736   -1.2902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6883   -2.2939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0323   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0323    0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6832    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4186    3.0703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.6361    0.1182    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.6847    2.2660    0.0000 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  2  0
  5  6  1  0
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 30 29  1  0
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 25 26  1  0
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 22 23  1  0
 21 20  1  0
 20 17  2  0
 17 18  1  0
 18 19  1  0
 10  5  1  0
 17 16  1  0
  8  7  1  0
 11 30  1  0
 14 28  1  0
 27 28  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  0
  6 37  1  0
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 30 58  1  1
 29 56  1  0
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  8 39  1  0
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 26 53  1  0
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 23 50  1  0
 23 51  1  0
 23 52  1  0
 20 49  1  0
 19 46  1  0
 19 47  1  0
 19 48  1  0
M  END


  Mrv1652306292220352D          

 30 35  0  0  1  0            999 V2000
   -1.3183   -2.5124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5414   -2.2350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3932   -1.4234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3838   -1.1459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5319   -0.3344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1019    0.3827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8603    0.7858    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8662    1.6336    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8030    1.5602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5036    1.0749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8084    0.5233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8237   -0.3410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1902    0.1866    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3868    1.1117    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4644    2.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1695    2.5227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7623    1.9052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5495    2.1711    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9064    1.4151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3475    0.8083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5936    0.0208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3986   -0.1598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9575    0.4471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7114    1.2345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2703    1.8413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0242    2.6288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6447   -0.9472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4497   -1.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0347   -0.5860    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2808   -1.3735    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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  6  0  0  0
  5 13  1  0  0  0  0
 13 14  1  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 10 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 10 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 22 27  1  0  0  0  0
 27 28  1  0  0  0  0
 21 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0138760

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC\C=C1/CN2[C@H]3CC45C2C[C@H]1[C@@H]3COC4=NC1=C5C(OC)=C(OC)C=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C23H28N2O5/c1-26-6-5-12-10-25-15-9-23-18(25)7-13(12)14(15)11-30-22(23)24-20-16(27-2)8-17(28-3)21(29-4)19(20)23/h5,8,13-15,18H,6-7,9-11H2,1-4H3/b12-5+/t13-,14+,15+,18?,23?/m1/s1

> <INCHI_KEY>
RIMDDIPKIZTBHU-KPDHXFAYSA-N

> <FORMULA>
C23H28N2O5

> <MOLECULAR_WEIGHT>
412.486

> <EXACT_MASS>
412.19982201

> <ALOGPS_LOGP>
1.91

> <ALOGPS_LOGS>
-3.67

> <ALOGPS_SOLUBILITY>
8.90e-02 g/l

$$$$

HEADER    PROTEIN                                 29-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-JUN-22         0                                  
HETATM    1  C   UNK     0      -2.461  -4.690   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.011  -4.172   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.734  -2.657   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.716  -2.139   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.993  -0.624   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.190   0.714   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       1.606   1.467   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       1.617   3.049   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.366   2.912   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.673   2.006   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.376   0.977   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.404  -0.637   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.222   0.348   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.589   2.075   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.733   3.832   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.050   4.709   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.156   3.556   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0       6.626   4.053   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       7.292   2.642   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.249   1.509   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.708   0.039   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.211  -0.298   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.254   0.834   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.795   2.304   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       9.838   3.437   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       9.379   4.907   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.670  -1.768   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      10.173  -2.105   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       5.665  -1.094   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       6.124  -2.564   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   13                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   11                                                  
CONECT    8    7    9   14                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   17   20                                             
CONECT   11   10    7   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12    5   14                                                  
CONECT   14   13    8   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   10   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   24                                                  
CONECT   20   19   10   21                                                  
CONECT   21   20   22   29                                                  
CONECT   22   21   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   19   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   22   28                                                       
CONECT   28   27                                                            
CONECT   29   21   30                                                       
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₈N₂O₅

Average Mass

412.4860 Da

Monoisotopic Mass

412.19982 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

34274-91-4

SMILES

COC\C=C1/CN2[C@H]3CC45C2C[C@H]1[C@@H]3COC4=NC1=C5C(OC)=C(OC)C=C1OC

InChI Identifier

InChI=1S/C23H28N2O5/c1-26-6-5-12-10-25-15-9-23-18(25)7-13(12)14(15)11-30-22(23)24-20-16(27-2)8-17(28-3)21(29-4)19(20)23/h5,8,13-15,18H,6-7,9-11H2,1-4H3/b12-5+/t13-,14+,15+,18?,23?/m1/s1

InChI Key

RIMDDIPKIZTBHU-KPDHXFAYSA-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 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
Indolizidine
Anisole
Quinuclidine
Alkyl aryl ether
Oxepane
Aralkylamine
Piperidine
N-alkylpyrrolidine
Benzenoid
Pyrrolidine
Tertiary amine
Tertiary aliphatic amine
Organic 1,3-dipolar compound
Azacycle
Oxacycle
Ether
Dialkyl ether
Propargyl-type 1,3-dipolar organic compound
Organic nitrogen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Amine
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

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

4945708

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6441560

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Morales Corado JA, Lee CU, Enns GM: Carnitine-Acylcarnitine Translocase Deficiency. 1993. [PubMed:35862567 ]
Kaorop W, Maneechote C, Kumfu S, Chattipakorn SC, Chattipakorn N: Mitochondrial-derived peptides as a novel intervention for obesity and cardiac diseases: bench evidence for potential bedside application. J Clin Pathol. 2022 Jul 21. pii: jcp-2022-208321. doi: 10.1136/jcp-2022-208321. [PubMed:35863886 ]
Zheng T, Zheng S, Wang K, Quan H, Bai Q, Li S, Qi R, Zhao Y, Cui X, Gao X: Automatic CD30 scoring method for whole slide images of primary cutaneous CD30(+) lymphoproliferative diseases. J Clin Pathol. 2022 Jul 21. pii: jcp-2022-208344. doi: 10.1136/jcp-2022-208344. [PubMed:35863885 ]
Humphreys H, Burke L, O'Connell K, Keogan M: Answering Ireland's call: pathology during the COVID-19 pandemic. J Clin Pathol. 2022 Nov;75(11):721-723. doi: 10.1136/jclinpath-2022-208323. Epub 2022 Jul 21. [PubMed:35863884 ]
Zhao N, Tan HR, Chen QL, Sun Q, Wang L, Song Y, Olounfeh KM, Meng FH: Development and Validation of a Sensitive UHPLC-MS/MS Method for the Measurement of Gardneramine in Rat Plasma and Tissues and its Application to Pharmacokinetics and Tissue Distribution Study. Molecules. 2019 Oct 31;24(21):3953. doi: 10.3390/molecules24213953. [PubMed:31683708 ]

Showing NP-Card for Gardneramine (NP0138760)

MOL for NP0138760 (Gardneramine)

3D MOL for NP0138760 (Gardneramine)

3D SDF for NP0138760 (Gardneramine)

3D-SDF for NP0138760 (Gardneramine)

PDB for NP0138760 (Gardneramine)

3D PDB for NP0138760 (Gardneramine)

SMILES for NP0138760 (Gardneramine)

INCHI for NP0138760 (Gardneramine)

Structure for NP0138760 (Gardneramine)

3D Structure for NP0138760 (Gardneramine)