NP-MRD: Showing NP-Card for 9-hydroxy-4,4,4',4',14'-pentamethyl-12'-methylidene-9',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-one (NP0185319)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 00:41:30 UTC

Updated at

2022-09-04 00:41:30 UTC

NP-MRD ID

NP0185319

Secondary Accession Numbers

None

Natural Product Identification

Common Name

9-hydroxy-4,4,4',4',14'-pentamethyl-12'-methylidene-9',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-one

Description

9-Hydroxy-4,4,4',4',14'-pentamethyl-12'-methylidene-4H-9',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]Tetradecane]-13'-one belongs to the class of organic compounds known as azaspirodecane derivatives. These are organic compounds containing a spirodecane moiety with at least one nitrogen atom. 9-hydroxy-4,4,4',4',14'-pentamethyl-12'-methylidene-9',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-one is found in Penicillium dierckxii. 9-Hydroxy-4,4,4',4',14'-pentamethyl-12'-methylidene-4H-9',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]Tetradecane]-13'-one is a very strong basic compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004171502522D          

 35 41  0  0  0  0            999 V2000
    2.3782   -0.2010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1044    0.5772    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2256    0.7291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7605    0.0478    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7646    1.4912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4998    2.2268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3766    2.0854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0123    2.6535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3929    3.1984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4792    3.3337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7546    2.2657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5380    1.4491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6961    1.2478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8924    1.3113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2275    1.7968    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2489    1.7365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3924    2.2630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4351    2.3621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8628    3.0676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9248    3.0730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3717    3.6852    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7451    3.1606    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0819    2.4074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8669    2.1538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3899    2.7919    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2148    2.7809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7205    2.1291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5263    1.3273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3512    1.3163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6991    0.5206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7783    0.9793    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0398    1.3471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4276    0.7941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6426    1.0477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4697    1.8544    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  2 13  1  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  5 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
  5 18  1  0  0  0  0
 18 19  2  0  0  0  0
 11 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  1  0  0  0  0
 24 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 11 35  1  0  0  0  0
 23 35  1  0  0  0  0
M  END


  Mrv1533004171502522D          

 35 41  0  0  0  0            999 V2000
    2.3782   -0.2010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1044    0.5772    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2256    0.7291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7605    0.0478    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7646    1.4912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4998    2.2268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3766    2.0854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0123    2.6535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3929    3.1984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4792    3.3337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7546    2.2657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5380    1.4491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6961    1.2478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8924    1.3113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2275    1.7968    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2489    1.7365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3924    2.2630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4351    2.3621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8628    3.0676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9248    3.0730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3717    3.6852    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7451    3.1606    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0819    2.4074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8669    2.1538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3899    2.7919    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2148    2.7809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7205    2.1291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5263    1.3273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3512    1.3163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6991    0.5206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7783    0.9793    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0398    1.3471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4276    0.7941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6426    1.0477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4697    1.8544    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  2 13  1  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  5 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
  5 18  1  0  0  0  0
 18 19  2  0  0  0  0
 11 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  1  0  0  0  0
 24 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 11 35  1  0  0  0  0
 23 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0185319

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1C(=O)C23CC4C(C)(C)C5(CC14CN2CCC3=C)C(=O)NC1=C2OC=CC(C)(C)OC2=CC=C51

> <INCHI_IDENTIFIER>
InChI=1S/C28H33N3O4/c1-16-9-11-31-15-26-14-27(25(4,5)19(26)13-28(16,31)23(33)30(26)6)17-7-8-18-21(20(17)29-22(27)32)34-12-10-24(2,3)35-18/h7-8,10,12,19H,1,9,11,13-15H2,2-6H3,(H,29,32)

> <INCHI_KEY>
XSESDTUYLDKCBE-UHFFFAOYSA-N

> <FORMULA>
C28H33N3O4

> <MOLECULAR_WEIGHT>
475.589

> <EXACT_MASS>
475.247106555

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
52.185872288781596

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,4,4',4',14'-pentamethyl-12'-methylidene-9,10-dihydro-4H-9',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-9,13'-dione

> <ALOGPS_LOGP>
4.16

> <JCHEM_LOGP>
2.567549857333332

> <ALOGPS_LOGS>
-3.84

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.591660340142196

> <JCHEM_PKA_STRONGEST_BASIC>
7.5992890340019725

> <JCHEM_POLAR_SURFACE_AREA>
71.11000000000001

> <JCHEM_REFRACTIVITY>
133.1266

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.85e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,4,4',4',14'-pentamethyl-12'-methylidene-10H-9',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-9,13'-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       4.435  -0.339   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       3.990   1.135   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       2.347   1.605   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       1.394   0.395   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.507   3.092   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.772   4.480   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.432   4.013   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.726   4.951   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.642   6.045   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.641   6.190   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.114   4.224   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.676   2.715   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.106   2.443   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.671   2.327   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       2.774   3.447   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       1.241   4.098   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.149   2.745   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.074   4.164   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.651   5.522   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.455   5.726   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.441   6.885   0.000  0.00  0.00           O+0
HETATM   22  N   UNK     0       8.989   5.866   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0       9.596   4.450   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      11.054   3.954   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      12.048   5.130   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      13.588   5.085   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      14.513   3.854   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      14.127   2.363   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      15.666   2.319   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      14.426   0.853   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      12.721   1.735   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      11.353   2.443   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      10.194   1.429   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       8.736   1.925   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       8.437   3.436   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   13                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   15   18                                             
CONECT    6    5    7                                                       
CONECT    7    6    8   13                                                  
CONECT    8    7    9   10   11                                             
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    8   12   20   35                                             
CONECT   12   11   13                                                       
CONECT   13   12    2    7   14                                             
CONECT   14   13   15                                                       
CONECT   15   14    5   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17    5   19                                                  
CONECT   19   18                                                            
CONECT   20   11   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24   35                                                  
CONECT   24   23   25   32                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30   31                                             
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   28   32                                                       
CONECT   32   31   24   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   11   23                                                  
MASTER        0    0    0    0    0    0    0    0   35    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₃₃N₃O₄

Average Mass

475.5890 Da

Monoisotopic Mass

475.24711 Da

IUPAC Name

4,4,4',4',14'-pentamethyl-12'-methylidene-9,10-dihydro-4H-9',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-9,13'-dione

Traditional Name

4,4,4',4',14'-pentamethyl-12'-methylidene-10H-9',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-9,13'-dione

CAS Registry Number

Not Available

SMILES

CN1C(=O)C23CC4C(C)(C)C5(CC14CN2CCC3=C)C(=O)NC1=C2OC=CC(C)(C)OC2=CC=C51

InChI Identifier

InChI=1S/C28H33N3O4/c1-16-9-11-31-15-26-14-27(25(4,5)19(26)13-28(16,31)23(33)30(26)6)17-7-8-18-21(20(17)29-22(27)32)34-12-10-24(2,3)35-18/h7-8,10,12,19H,1,9,11,13-15H2,2-6H3,(H,29,32)

InChI Key

XSESDTUYLDKCBE-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Penicillium dierckxii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as azaspirodecane derivatives. These are organic compounds containing a spirodecane moiety with at least one nitrogen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Azaspirodecane derivatives

Sub Class

Not Available

Direct Parent

Azaspirodecane derivatives

Alternative Parents

Substituents

Alpha-amino acid or derivatives
Azaspirodecane
3-alkylindole
Indole or derivatives
Indolizidine
1,4-dioxepine
Alkyl aryl ether
Delta-lactam
Dioxepine
Aralkylamine
Piperidinone
N-methylpiperazine
N-alkylpiperazine
1,4-diazinane
Piperazine
Piperidine
Benzenoid
N-alkylpyrrolidine
Pyrrolidine
Tertiary carboxylic acid amide
Cyclic carboximidic acid
Amino acid or derivatives
Tertiary aliphatic amine
Tertiary amine
Lactam
Carboxamide group
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Ether
Azacycle
Oxacycle
Carboxylic acid derivative
Organic oxide
Organic nitrogen compound
Carbonyl group
Hydrocarbon derivative
Organonitrogen compound
Organooxygen 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
logP	4.16	ALOGPS
logP	2.57	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	11.59	ChemAxon
pKa (Strongest Basic)	7.6	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	71.11 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	133.13 m³·mol⁻¹	ChemAxon
Polarizability	52.19 Å³	ChemAxon
Number of Rings	7	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

14734718

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 9-hydroxy-4,4,4',4',14'-pentamethyl-12'-methylidene-9',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-one (NP0185319)

MOL for NP0185319 (9-hydroxy-4,4,4',4',14'-pentamethyl-12'-methylidene-9',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-one)

3D MOL for NP0185319 (9-hydroxy-4,4,4',4',14'-pentamethyl-12'-methylidene-9',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-one)

3D SDF for NP0185319 (9-hydroxy-4,4,4',4',14'-pentamethyl-12'-methylidene-9',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-one)

3D-SDF for NP0185319 (9-hydroxy-4,4,4',4',14'-pentamethyl-12'-methylidene-9',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-one)

PDB for NP0185319 (9-hydroxy-4,4,4',4',14'-pentamethyl-12'-methylidene-9',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-one)

3D PDB for NP0185319 (9-hydroxy-4,4,4',4',14'-pentamethyl-12'-methylidene-9',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-one)

SMILES for NP0185319 (9-hydroxy-4,4,4',4',14'-pentamethyl-12'-methylidene-9',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-one)

INCHI for NP0185319 (9-hydroxy-4,4,4',4',14'-pentamethyl-12'-methylidene-9',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-one)

Structure for NP0185319 (9-hydroxy-4,4,4',4',14'-pentamethyl-12'-methylidene-9',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-one)

3D Structure for NP0185319 (9-hydroxy-4,4,4',4',14'-pentamethyl-12'-methylidene-9',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-one)