NP-MRD: Showing NP-Card for 14-methyl-1,4-diazapentacyclo[7.7.1.0²,¹².0³,⁸.0¹¹,¹⁶]heptadec-4-ene-3,5-diol (NP0281275)

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Record Information

Version

2.0

Created at

2022-09-09 07:31:00 UTC

Updated at

2022-09-09 07:31:00 UTC

NP-MRD ID

NP0281275

Secondary Accession Numbers

None

Natural Product Identification

Common Name

14-methyl-1,4-diazapentacyclo[7.7.1.0²,¹².0³,⁸.0¹¹,¹⁶]heptadec-4-ene-3,5-diol

Description

14-Methyl-1,4-diazapentacyclo[7.7.1.0²,¹².0³,⁸.0¹¹,¹⁶]Heptadec-4-ene-3,5-diol belongs to the class of organic compounds known as naphthyridines. Naphthyridines are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings. The naphthyridine skeleton can also be described as an assembly two fused pyridine rings, which do not share their nitrogen atom. 14-Methyl-1,4-diazapentacyclo[7.7.1.0²,¹².0³,⁸.0¹¹,¹⁶]Heptadec-4-ene-3,5-diol is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 44 48  0  0  0  0  0  0  0  0999 V2000
    4.5618    0.6352   -0.0792 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2740    0.0128    0.4524 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7038   -0.8139   -0.6840 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3528   -1.3755   -0.3809 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9731   -0.9921    1.0569 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3426   -1.6278    1.3876 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4410   -1.2619    0.4108 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8987   -1.4553   -0.9750 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2979   -0.6414   -1.1015 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1821    0.6320   -0.4418 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8798    0.5120    0.8968 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2713    1.0858    0.8195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2445    1.0793   -0.2511 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1819    2.3296    0.3995 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9107    1.2192   -1.5093 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3114    1.0307   -1.6102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9541    1.6054   -2.5191 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0517    0.1652   -0.6642 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4268    0.2537    0.6850 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9290    0.1218    0.6852 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3674   -0.1409    0.0329 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8903    1.4925    0.5335 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5048    0.8549   -1.1582 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5723   -0.6041    1.3208 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6996   -0.1277   -1.5797 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4585   -1.6065   -0.9009 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2580   -2.4547   -0.5059 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7122   -1.3156    1.7842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6178   -1.3739    2.4349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2159   -2.7191    1.3320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2571   -2.0152    0.5483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6178   -1.3157   -1.7772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5604   -2.5262   -1.0350 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6773    1.4277   -1.0653 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3564    1.0094    1.7136 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3130    1.8619    0.0286 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5490    1.5907    1.7685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1726    3.0604   -0.2823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3694    1.4662   -2.3884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0993    0.5751   -0.5685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1755   -0.8663   -1.0375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6573    1.2768    1.0954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8247   -0.4796    1.4041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5950    0.4153    1.7245 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2 12  1  0
 12 11  1  0
 11  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9  4  1  0
  4  3  1  0
  9 10  1  0
 10 13  1  0
 13 14  1  1
 13 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
  3  2  1  0
 20 13  1  0
 10 11  1  0
  4  5  1  0
 20  7  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  2 24  1  1
 12 36  1  0
 12 37  1  0
 11 35  1  1
  5 28  1  1
  6 29  1  0
  6 30  1  0
  7 31  1  1
  8 32  1  0
  8 33  1  0
  4 27  1  1
  3 25  1  0
  3 26  1  0
 10 34  1  6
 14 38  1  0
 15 39  1  0
 18 40  1  0
 18 41  1  0
 19 42  1  0
 19 43  1  0
 20 44  1  1
M  END


  Mrv1533004231520082D          

 20 24  0  0  0  0            999 V2000
   -1.4116   -1.9206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7469   -1.4319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0083   -1.7496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5526   -1.1256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4627   -0.1053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9599    0.8146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9293    0.4908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3879    0.4294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0268   -0.3937    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0035   -0.2031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8272   -0.5942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3509   -1.0729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1963   -0.9914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8745   -1.7510    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7108   -1.6363    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5265   -1.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0410   -2.1581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8278   -0.7452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3133   -0.1002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4976   -0.2233    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  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
  9 10  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
  2 11  1  0  0  0  0
  9 12  1  0  0  0  0
  4 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
  7 20  1  0  0  0  0
 13 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0281275

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC2C3CC4CN(C3C1)C2C1(O)NC(=O)CCC41

> <INCHI_IDENTIFIER>
InChI=1S/C16H24N2O2/c1-8-4-11-10-6-9-7-18(13(10)5-8)15(11)16(20)12(9)2-3-14(19)17-16/h8-13,15,20H,2-7H2,1H3,(H,17,19)

> <INCHI_KEY>
NVAVRHCNQUQCGY-UHFFFAOYSA-N

> <FORMULA>
C16H24N2O2

> <MOLECULAR_WEIGHT>
276.38

> <EXACT_MASS>
276.183778021

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
30.391945015744703

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-hydroxy-14-methyl-1,4-diazapentacyclo[7.7.1.0²,¹².0³,⁸.0¹¹,¹⁶]heptadecan-5-one

> <ALOGPS_LOGP>
1.04

> <JCHEM_LOGP>
0.34582481442990565

> <ALOGPS_LOGS>
-1.75

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
12.314215452107423

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.020390834564138

> <JCHEM_PKA_STRONGEST_BASIC>
10.881973796404381

> <JCHEM_POLAR_SURFACE_AREA>
52.57

> <JCHEM_REFRACTIVITY>
74.72270000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.94e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-hydroxy-14-methyl-1,4-diazapentacyclo[7.7.1.0²,¹².0³,⁸.0¹¹,¹⁶]heptadecan-5-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0      -2.635  -3.585   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.394  -2.673   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.015  -3.266   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.032  -2.101   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.864  -0.196   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.792   1.521   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.601   0.916   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.591   0.802   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       1.917  -0.735   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      -0.006  -0.379   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.544  -1.109   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.522  -2.003   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.100  -1.851   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.499  -3.269   0.000  0.00  0.00           O+0
HETATM   15  N   UNK     0       5.060  -3.054   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       6.583  -2.825   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       7.543  -4.028   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       7.145  -1.391   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.185  -0.187   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.662  -0.417   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   11                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   12                                                  
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   20                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   12                                                  
CONECT   10    9    5   11                                                  
CONECT   11   10    2                                                       
CONECT   12    9    4   13                                                  
CONECT   13   12   14   15   20                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19    7   13                                                  
MASTER        0    0    0    0    0    0    0    0   20    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₂₄N₂O₂

Average Mass

276.3800 Da

Monoisotopic Mass

276.18378 Da

IUPAC Name

3-hydroxy-14-methyl-1,4-diazapentacyclo[7.7.1.0²,¹².0³,⁸.0¹¹,¹⁶]heptadecan-5-one

Traditional Name

3-hydroxy-14-methyl-1,4-diazapentacyclo[7.7.1.0²,¹².0³,⁸.0¹¹,¹⁶]heptadecan-5-one

CAS Registry Number

Not Available

SMILES

CC1CC2C3CC4CN(C3C1)C2C1(O)NC(=O)CCC41

InChI Identifier

InChI=1S/C16H24N2O2/c1-8-4-11-10-6-9-7-18(13(10)5-8)15(11)16(20)12(9)2-3-14(19)17-16/h8-13,15,20H,2-7H2,1H3,(H,17,19)

InChI Key

NVAVRHCNQUQCGY-UHFFFAOYSA-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 naphthyridines. Naphthyridines are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings. The naphthyridine skeleton can also be described as an assembly two fused pyridine rings, which do not share their nitrogen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Diazanaphthalenes

Sub Class

Naphthyridines

Direct Parent

Naphthyridines

Alternative Parents

Substituents

Naphthyridine
Quinolidine
Indolizidine
Azepane
Tetrahydropyridine
Piperidine
N-alkylpyrrolidine
Cyclic alcohol
Cyclic carboximidic acid
Pyrrolidine
Tertiary aliphatic amine
Tertiary amine
Alkanolamine
Azacycle
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Amine
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Organopnictogen compound
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	1.04	ALOGPS
logP	0.35	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	10.02	ChemAxon
pKa (Strongest Basic)	10.88	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	52.57 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	74.72 m³·mol⁻¹	ChemAxon
Polarizability	30.39 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

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HMDB ID

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References

General References

LOTUS database [Link]

Showing NP-Card for 14-methyl-1,4-diazapentacyclo[7.7.1.0²,¹².0³,⁸.0¹¹,¹⁶]heptadec-4-ene-3,5-diol (NP0281275)

MOL for NP0281275 (14-methyl-1,4-diazapentacyclo[7.7.1.0²,¹².0³,⁸.0¹¹,¹⁶]heptadec-4-ene-3,5-diol)

3D MOL for NP0281275 (14-methyl-1,4-diazapentacyclo[7.7.1.0²,¹².0³,⁸.0¹¹,¹⁶]heptadec-4-ene-3,5-diol)

3D SDF for NP0281275 (14-methyl-1,4-diazapentacyclo[7.7.1.0²,¹².0³,⁸.0¹¹,¹⁶]heptadec-4-ene-3,5-diol)

3D-SDF for NP0281275 (14-methyl-1,4-diazapentacyclo[7.7.1.0²,¹².0³,⁸.0¹¹,¹⁶]heptadec-4-ene-3,5-diol)

PDB for NP0281275 (14-methyl-1,4-diazapentacyclo[7.7.1.0²,¹².0³,⁸.0¹¹,¹⁶]heptadec-4-ene-3,5-diol)

3D PDB for NP0281275 (14-methyl-1,4-diazapentacyclo[7.7.1.0²,¹².0³,⁸.0¹¹,¹⁶]heptadec-4-ene-3,5-diol)

SMILES for NP0281275 (14-methyl-1,4-diazapentacyclo[7.7.1.0²,¹².0³,⁸.0¹¹,¹⁶]heptadec-4-ene-3,5-diol)

INCHI for NP0281275 (14-methyl-1,4-diazapentacyclo[7.7.1.0²,¹².0³,⁸.0¹¹,¹⁶]heptadec-4-ene-3,5-diol)

Structure for NP0281275 (14-methyl-1,4-diazapentacyclo[7.7.1.0²,¹².0³,⁸.0¹¹,¹⁶]heptadec-4-ene-3,5-diol)

3D Structure for NP0281275 (14-methyl-1,4-diazapentacyclo[7.7.1.0²,¹².0³,⁸.0¹¹,¹⁶]heptadec-4-ene-3,5-diol)