NP-MRD: Showing NP-Card for (18e)-2,20,24,27-tetrahydroxy-10-methyl-21,26-diazatetracyclo[23.2.1.0⁷,¹⁴.0⁹,¹³]octacosa-1,5,11,16,18,20,26-heptaen-28-one (NP0193180)

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Record Information

Version

2.0

Created at

2022-09-04 10:33:37 UTC

Updated at

2022-09-04 10:33:37 UTC

NP-MRD ID

NP0193180

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(18e)-2,20,24,27-tetrahydroxy-10-methyl-21,26-diazatetracyclo[23.2.1.0⁷,¹⁴.0⁹,¹³]octacosa-1,5,11,16,18,20,26-heptaen-28-one

Description

(18E)-2,20,24,27-tetrahydroxy-10-methyl-21,26-diazatetracyclo[23.2.1.0⁷,¹⁴.0⁹,¹³]Octacosa-1,5,11,16,18,20,26-heptaen-28-one belongs to the class of organic compounds known as pyrrolines. Pyrrolines are compounds containing a pyrroline ring, which is a five-member unsaturated aliphatic ring with one nitrogen atom and four carbon atoms (18E)-2,20,24,27-tetrahydroxy-10-methyl-21,26-diazatetracyclo[23.2.1.0⁷,¹⁴.0⁹,¹³]Octacosa-1,5,11,16,18,20,26-heptaen-28-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004241503372D          

 34 37  0  0  0  0            999 V2000
   13.0874    0.2635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4637   -0.2766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5341   -1.0986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7741   -1.4195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3092   -0.7066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4305   -0.6087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1775   -0.9588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2479   -1.7808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5712   -2.2527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8242   -1.9026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1475   -2.3746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4004   -2.0245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3301   -1.2025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7237   -2.4964    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9767   -2.1464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3000   -2.6183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5529   -2.2682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8763   -2.7401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4826   -1.4462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8803   -0.8824    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2304   -0.1354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7946    0.5651    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0889   -0.1523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7656    0.3196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6953    1.1416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5127   -0.0304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1894    0.4415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9364    0.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6131    0.5633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3601    0.2133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1202    0.5342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6602   -0.0895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1593   -0.9743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9063   -1.3244    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
  3  4  2  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
  8  7  1  4  0  0  0
  8  9  2  0  0  0  0
  9 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
 12 14  1  0  0  0  0
 14 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
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  4  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 28 27  1  4  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
  6 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
  2 32  1  0  0  0  0
  5 32  1  0  0  0  0
 23 33  1  0  0  0  0
 19 33  1  0  0  0  0
 33 34  2  0  0  0  0
M  END


  Mrv1533004241503372D          

 34 37  0  0  0  0            999 V2000
   13.0874    0.2635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4637   -0.2766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5341   -1.0986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7741   -1.4195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3092   -0.7066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4305   -0.6087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1775   -0.9588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2479   -1.7808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5712   -2.2527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8242   -1.9026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1475   -2.3746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4004   -2.0245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3301   -1.2025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7237   -2.4964    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9767   -2.1464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3000   -2.6183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5529   -2.2682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8763   -2.7401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4826   -1.4462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8803   -0.8824    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2304   -0.1354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7946    0.5651    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0889   -0.1523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7656    0.3196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6953    1.1416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5127   -0.0304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1894    0.4415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9364    0.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6131    0.5633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3601    0.2133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1202    0.5342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6602   -0.0895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1593   -0.9743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9063   -1.3244    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
  3  4  2  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
  8  7  1  4  0  0  0
  8  9  2  0  0  0  0
  9 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
 12 14  1  0  0  0  0
 14 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
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  4  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 28 27  1  4  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
  6 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
  2 32  1  0  0  0  0
  5 32  1  0  0  0  0
 23 33  1  0  0  0  0
 19 33  1  0  0  0  0
 33 34  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0193180

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C=CC2C1CC1C=CCCC(O)=C3C(=O)NC(C(O)CCNC(=O)\C=C\C=CCC21)C3=O

> <INCHI_IDENTIFIER>
InChI=1S/C27H34N2O5/c1-16-11-12-19-18-8-3-2-4-10-23(32)28-14-13-22(31)25-26(33)24(27(34)29-25)21(30)9-6-5-7-17(18)15-20(16)19/h2-5,7,10-12,16-20,22,25,30-31H,6,8-9,13-15H2,1H3,(H,28,32)(H,29,34)/b3-2?,7-5?,10-4+,24-21?

> <INCHI_KEY>
YVLAFZPZBWKPAA-BAIKISOQSA-N

> <FORMULA>
C27H34N2O5

> <MOLECULAR_WEIGHT>
466.578

> <EXACT_MASS>
466.246772203

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
49.59780543876805

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(18E)-2,24-dihydroxy-10-methyl-21,26-diazatetracyclo[23.2.1.0⁷,¹⁴.0⁹,¹³]octacosa-1,5,11,16,18-pentaene-20,27,28-trione

> <ALOGPS_LOGP>
2.37

> <JCHEM_LOGP>
1.8934016833333336

> <ALOGPS_LOGS>
-4.78

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
10.096117582249367

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.938714245074207

> <JCHEM_PKA_STRONGEST_BASIC>
-0.17208927045668687

> <JCHEM_POLAR_SURFACE_AREA>
115.73000000000002

> <JCHEM_REFRACTIVITY>
135.17959999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.76e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(18E)-2,24-dihydroxy-10-methyl-21,26-diazatetracyclo[23.2.1.0⁷,¹⁴.0⁹,¹³]octacosa-1,5,11,16,18-pentaene-20,27,28-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      24.430   0.492   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      23.266  -0.516   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      23.397  -2.051   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      21.978  -2.650   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      21.110  -1.319   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      19.470  -1.136   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      20.865  -1.790   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      20.996  -3.324   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      19.733  -4.205   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      18.338  -3.552   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      17.075  -4.433   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      15.681  -3.779   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      15.549  -2.245   0.000  0.00  0.00           O+0
HETATM   14  N   UNK     0      14.418  -4.660   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      13.023  -4.007   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.760  -4.887   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.366  -4.234   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       9.102  -5.115   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      10.234  -2.700   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       9.110  -1.647   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       9.763  -0.253   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       8.950   1.055   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      11.366  -0.284   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.629   0.597   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      12.498   2.131   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      14.024  -0.057   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      15.287   0.824   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      16.681   0.171   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      17.944   1.052   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      19.339   0.398   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      20.758   0.997   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      21.766  -0.167   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      11.497  -1.819   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      12.892  -2.472   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   32                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   32                                                  
CONECT    6    5    7   30                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   33                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   33                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29    6   31                                                  
CONECT   31   30   32                                                       
CONECT   32   31    2    5                                                  
CONECT   33   23   19   34                                                  
CONECT   34   33                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₄N₂O₅

Average Mass

466.5780 Da

Monoisotopic Mass

466.24677 Da

IUPAC Name

(18E)-2,24-dihydroxy-10-methyl-21,26-diazatetracyclo[23.2.1.0⁷,¹⁴.0⁹,¹³]octacosa-1,5,11,16,18-pentaene-20,27,28-trione

Traditional Name

(18E)-2,24-dihydroxy-10-methyl-21,26-diazatetracyclo[23.2.1.0⁷,¹⁴.0⁹,¹³]octacosa-1,5,11,16,18-pentaene-20,27,28-trione

CAS Registry Number

Not Available

SMILES

CC1C=CC2C1CC1C=CCCC(O)=C3C(=O)NC(C(O)CCNC(=O)\C=C\C=CCC21)C3=O

InChI Identifier

InChI=1S/C27H34N2O5/c1-16-11-12-19-18-8-3-2-4-10-23(32)28-14-13-22(31)25-26(33)24(27(34)29-25)21(30)9-6-5-7-17(18)15-20(16)19/h2-5,7,10-12,16-20,22,25,30-31H,6,8-9,13-15H2,1H3,(H,28,32)(H,29,34)/b3-2?,7-5?,10-4+,24-21?

InChI Key

YVLAFZPZBWKPAA-BAIKISOQSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrrolines. Pyrrolines are compounds containing a pyrroline ring, which is a five-member unsaturated aliphatic ring with one nitrogen atom and four carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrrolines

Sub Class

Not Available

Direct Parent

Pyrrolines

Alternative Parents

Substituents

Vinylogous acid
Cyclic carboximidic acid
Pyrroline
Secondary alcohol
Ketone
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Polyol
Enol
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
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	2.37	ALOGPS
logP	1.89	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	4.94	ChemAxon
pKa (Strongest Basic)	-0.17	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	115.73 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	135.18 m³·mol⁻¹	ChemAxon
Polarizability	49.6 Å³	ChemAxon
Number of Rings	4	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (18e)-2,20,24,27-tetrahydroxy-10-methyl-21,26-diazatetracyclo[23.2.1.0⁷,¹⁴.0⁹,¹³]octacosa-1,5,11,16,18,20,26-heptaen-28-one (NP0193180)

MOL for NP0193180 ((18e)-2,20,24,27-tetrahydroxy-10-methyl-21,26-diazatetracyclo[23.2.1.0⁷,¹⁴.0⁹,¹³]octacosa-1,5,11,16,18,20,26-heptaen-28-one)

3D MOL for NP0193180 ((18e)-2,20,24,27-tetrahydroxy-10-methyl-21,26-diazatetracyclo[23.2.1.0⁷,¹⁴.0⁹,¹³]octacosa-1,5,11,16,18,20,26-heptaen-28-one)

3D SDF for NP0193180 ((18e)-2,20,24,27-tetrahydroxy-10-methyl-21,26-diazatetracyclo[23.2.1.0⁷,¹⁴.0⁹,¹³]octacosa-1,5,11,16,18,20,26-heptaen-28-one)

3D-SDF for NP0193180 ((18e)-2,20,24,27-tetrahydroxy-10-methyl-21,26-diazatetracyclo[23.2.1.0⁷,¹⁴.0⁹,¹³]octacosa-1,5,11,16,18,20,26-heptaen-28-one)

PDB for NP0193180 ((18e)-2,20,24,27-tetrahydroxy-10-methyl-21,26-diazatetracyclo[23.2.1.0⁷,¹⁴.0⁹,¹³]octacosa-1,5,11,16,18,20,26-heptaen-28-one)

3D PDB for NP0193180 ((18e)-2,20,24,27-tetrahydroxy-10-methyl-21,26-diazatetracyclo[23.2.1.0⁷,¹⁴.0⁹,¹³]octacosa-1,5,11,16,18,20,26-heptaen-28-one)

SMILES for NP0193180 ((18e)-2,20,24,27-tetrahydroxy-10-methyl-21,26-diazatetracyclo[23.2.1.0⁷,¹⁴.0⁹,¹³]octacosa-1,5,11,16,18,20,26-heptaen-28-one)

INCHI for NP0193180 ((18e)-2,20,24,27-tetrahydroxy-10-methyl-21,26-diazatetracyclo[23.2.1.0⁷,¹⁴.0⁹,¹³]octacosa-1,5,11,16,18,20,26-heptaen-28-one)

Structure for NP0193180 ((18e)-2,20,24,27-tetrahydroxy-10-methyl-21,26-diazatetracyclo[23.2.1.0⁷,¹⁴.0⁹,¹³]octacosa-1,5,11,16,18,20,26-heptaen-28-one)

3D Structure for NP0193180 ((18e)-2,20,24,27-tetrahydroxy-10-methyl-21,26-diazatetracyclo[23.2.1.0⁷,¹⁴.0⁹,¹³]octacosa-1,5,11,16,18,20,26-heptaen-28-one)