NP-MRD: Showing NP-Card for (1r,4s,7s,9s)-6,9-dihydroxy-7-methyl-14-(3-methylbut-2-en-1-yl)-4-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-2,5,16-triazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-5,10(15),11,13-tetraen-3-one (NP0238160)

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Record Information

Version

2.0

Created at

2022-09-06 21:30:17 UTC

Updated at

2022-09-06 21:30:17 UTC

NP-MRD ID

NP0238160

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,4s,7s,9s)-6,9-dihydroxy-7-methyl-14-(3-methylbut-2-en-1-yl)-4-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-2,5,16-triazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-5,10(15),11,13-tetraen-3-one

Description

(1R,4S,7S,9S)-6,9-dihydroxy-7-methyl-14-(3-methylbut-2-en-1-yl)-4-{[7-(3-methylbut-2-en-1-yl)-1H-indol-3-yl]methyl}-2,5,16-triazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]Hexadeca-5,10,12,14-tetraen-3-one belongs to the class of organic compounds known as pyrroloindoles. Pyrroloindoles are compounds containing a pyrroloindole moiety, which is a tricyclic heterocycle which consists of a pyrrole ring fused to an indole. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Indole is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. (1r,4s,7s,9s)-6,9-dihydroxy-7-methyl-14-(3-methylbut-2-en-1-yl)-4-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-2,5,16-triazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-5,10(15),11,13-tetraen-3-one is found in Aspergillus taichungensis. Based on a literature review very few articles have been published on (1R,4S,7S,9S)-6,9-dihydroxy-7-methyl-14-(3-methylbut-2-en-1-yl)-4-{[7-(3-methylbut-2-en-1-yl)-1H-indol-3-yl]methyl}-2,5,16-triazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]Hexadeca-5,10,12,14-tetraen-3-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062223302D          

 40 45  0  0  1  0            999 V2000
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 39 40  1  1  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309062223302D          

 40 45  0  0  1  0            999 V2000
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    6.6726   -1.8585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5174   -1.0482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7706   -0.6976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8733    0.1210    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.6836    0.2763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1104    0.9823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7123    1.7049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8875    1.7215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4894    2.4441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6646    2.4607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9162    3.1501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9352    0.9657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3332    0.2431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9065   -0.4630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0816   -0.4464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2038   -3.2083    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5797   -3.7479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7350   -4.5582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8004   -3.4773    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8701   -4.2993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0778   -3.8753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4759   -3.3111    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1253   -4.0578    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
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 23 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 19 32  1  0  0  0  0
 22 32  1  0  0  0  0
 17 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 14 36  1  0  0  0  0
 36 37  1  1  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 10 39  1  0  0  0  0
 13 39  1  0  0  0  0
 39 40  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0238160

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC1=CC=CC2=C1N[C@@H]1N3C(=O)[C@H](CC4=CNC5=C(CC=C(C)C)C=CC=C45)N=C(O)[C@]3(C)C[C@]21O

> <INCHI_IDENTIFIER>
InChI=1S/C33H38N4O3/c1-19(2)12-14-21-8-6-10-24-23(17-34-27(21)24)16-26-29(38)37-30-33(40,18-32(37,5)31(39)35-26)25-11-7-9-22(28(25)36-30)15-13-20(3)4/h6-13,17,26,30,34,36,40H,14-16,18H2,1-5H3,(H,35,39)/t26-,30+,32-,33-/m0/s1

> <INCHI_KEY>
HBASCSQGGWRHEV-PLURVQFNSA-N

> <FORMULA>
C33H38N4O3

> <MOLECULAR_WEIGHT>
538.692

> <EXACT_MASS>
538.2943911

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
60.78143717882123

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,4S,7S,9S)-6,9-dihydroxy-7-methyl-14-(3-methylbut-2-en-1-yl)-4-{[7-(3-methylbut-2-en-1-yl)-1H-indol-3-yl]methyl}-2,5,16-triazatetracyclo[7.7.0.0^{2,7}.0^{10,15}]hexadeca-5,10,12,14-tetraen-3-one

> <JCHEM_LOGP>
5.791895427666667

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.879891796555189

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.371793875691214

> <JCHEM_PKA_STRONGEST_BASIC>
1.094079062705535

> <JCHEM_POLAR_SURFACE_AREA>
100.95

> <JCHEM_REFRACTIVITY>
160.49250000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4S,7S,9S)-6,9-dihydroxy-7-methyl-14-(3-methylbut-2-en-1-yl)-4-{[7-(3-methylbut-2-en-1-yl)-1H-indol-3-yl]methyl}-2,5,16-triazatetracyclo[7.7.0.0^{2,7}.0^{10,15}]hexadeca-5,10,12,14-tetraen-3-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.273   0.064   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.181  -0.441   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.346   0.566   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.471  -1.953   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.926  -2.459   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.216  -3.971   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.051  -4.978   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.341  -6.491   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.795  -6.996   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.960  -5.989   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.671  -4.476   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       6.019  -3.733   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       7.143  -4.787   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       8.671  -4.978   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       9.836  -3.971   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       9.546  -2.459   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      11.291  -4.476   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.456  -3.469   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.166  -1.957   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.772  -1.302   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0      10.964   0.226   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0      12.476   0.516   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.273   1.834   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.530   3.182   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.990   3.213   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.247   4.562   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.707   4.593   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.044   5.880   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      14.812   1.803   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      15.555   0.454   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      14.759  -0.864   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      13.219  -0.833   0.000  0.00  0.00           C+0
HETATM   33  N   UNK     0      11.580  -5.989   0.000  0.00  0.00           N+0
HETATM   34  C   UNK     0      10.416  -6.996   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      10.705  -8.509   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       8.961  -6.491   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       9.091  -8.025   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       7.612  -7.234   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       6.488  -6.181   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       5.834  -7.575   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   39                                                  
CONECT   11   10    6   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   39                                                  
CONECT   14   13   15   36                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   33                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   32                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   32                                                  
CONECT   23   22   24   29                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   23   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   19   22                                                  
CONECT   33   17   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   14   37   38                                             
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   10   13   40                                             
CONECT   40   39                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   90    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₃H₃₈N₄O₃

Average Mass

538.6920 Da

Monoisotopic Mass

538.29439 Da

IUPAC Name

(1R,4S,7S,9S)-6,9-dihydroxy-7-methyl-14-(3-methylbut-2-en-1-yl)-4-{[7-(3-methylbut-2-en-1-yl)-1H-indol-3-yl]methyl}-2,5,16-triazatetracyclo[7.7.0.0^{2,7}.0^{10,15}]hexadeca-5,10,12,14-tetraen-3-one

Traditional Name

(1R,4S,7S,9S)-6,9-dihydroxy-7-methyl-14-(3-methylbut-2-en-1-yl)-4-{[7-(3-methylbut-2-en-1-yl)-1H-indol-3-yl]methyl}-2,5,16-triazatetracyclo[7.7.0.0^{2,7}.0^{10,15}]hexadeca-5,10,12,14-tetraen-3-one

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1=CC=CC2=C1N[C@@H]1N3C(=O)[C@H](CC4=CNC5=C(CC=C(C)C)C=CC=C45)N=C(O)[C@]3(C)C[C@]21O

InChI Identifier

InChI=1S/C33H38N4O3/c1-19(2)12-14-21-8-6-10-24-23(17-34-27(21)24)16-26-29(38)37-30-33(40,18-32(37,5)31(39)35-26)25-11-7-9-22(28(25)36-30)15-13-20(3)4/h6-13,17,26,30,34,36,40H,14-16,18H2,1-5H3,(H,35,39)/t26-,30+,32-,33-/m0/s1

InChI Key

HBASCSQGGWRHEV-PLURVQFNSA-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
Aspergillus taichungensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrroloindoles. Pyrroloindoles are compounds containing a pyrroloindole moiety, which is a tricyclic heterocycle which consists of a pyrrole ring fused to an indole. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Indole is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Pyrroloindoles

Direct Parent

Pyrroloindoles

Alternative Parents

Substituents

Pyrroloindole
3-alkylindole
Alpha-amino acid or derivatives
Dihydroindole
Indole
Secondary aliphatic/aromatic amine
Benzenoid
Substituted pyrrole
Heteroaromatic compound
Cyclic carboximidic acid
Tertiary carboxylic acid amide
Tertiary alcohol
Pyrrolidine
Pyrrole
Lactam
Carboxamide group
Amino acid or derivatives
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Secondary amine
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
Alcohol
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	5.79	ChemAxon
pKa (Strongest Acidic)	4.37	ChemAxon
pKa (Strongest Basic)	1.09	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	100.95 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	160.49 m³·mol⁻¹	ChemAxon
Polarizability	60.78 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

78438693

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139588746

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,4s,7s,9s)-6,9-dihydroxy-7-methyl-14-(3-methylbut-2-en-1-yl)-4-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-2,5,16-triazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-5,10(15),11,13-tetraen-3-one (NP0238160)

MOL for NP0238160 ((1r,4s,7s,9s)-6,9-dihydroxy-7-methyl-14-(3-methylbut-2-en-1-yl)-4-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-2,5,16-triazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-5,10(15),11,13-tetraen-3-one)

3D MOL for NP0238160 ((1r,4s,7s,9s)-6,9-dihydroxy-7-methyl-14-(3-methylbut-2-en-1-yl)-4-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-2,5,16-triazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-5,10(15),11,13-tetraen-3-one)

3D SDF for NP0238160 ((1r,4s,7s,9s)-6,9-dihydroxy-7-methyl-14-(3-methylbut-2-en-1-yl)-4-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-2,5,16-triazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-5,10(15),11,13-tetraen-3-one)

3D-SDF for NP0238160 ((1r,4s,7s,9s)-6,9-dihydroxy-7-methyl-14-(3-methylbut-2-en-1-yl)-4-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-2,5,16-triazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-5,10(15),11,13-tetraen-3-one)

PDB for NP0238160 ((1r,4s,7s,9s)-6,9-dihydroxy-7-methyl-14-(3-methylbut-2-en-1-yl)-4-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-2,5,16-triazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-5,10(15),11,13-tetraen-3-one)

3D PDB for NP0238160 ((1r,4s,7s,9s)-6,9-dihydroxy-7-methyl-14-(3-methylbut-2-en-1-yl)-4-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-2,5,16-triazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-5,10(15),11,13-tetraen-3-one)

SMILES for NP0238160 ((1r,4s,7s,9s)-6,9-dihydroxy-7-methyl-14-(3-methylbut-2-en-1-yl)-4-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-2,5,16-triazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-5,10(15),11,13-tetraen-3-one)

INCHI for NP0238160 ((1r,4s,7s,9s)-6,9-dihydroxy-7-methyl-14-(3-methylbut-2-en-1-yl)-4-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-2,5,16-triazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-5,10(15),11,13-tetraen-3-one)

Structure for NP0238160 ((1r,4s,7s,9s)-6,9-dihydroxy-7-methyl-14-(3-methylbut-2-en-1-yl)-4-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-2,5,16-triazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-5,10(15),11,13-tetraen-3-one)

3D Structure for NP0238160 ((1r,4s,7s,9s)-6,9-dihydroxy-7-methyl-14-(3-methylbut-2-en-1-yl)-4-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-2,5,16-triazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-5,10(15),11,13-tetraen-3-one)