NP-MRD: Showing NP-Card for (1s,12s,16r)-16-ethyl-15-methyl-11-methylidene-9,15-diazatetracyclo[10.3.1.0²,¹⁰.0³,⁸]hexadeca-2(10),3,5,7-tetraene (NP0184892)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

1.0

Created at

2022-09-04 00:08:12 UTC

Updated at

2022-09-04 00:08:12 UTC

NP-MRD ID

NP0184892

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,12s,16r)-16-ethyl-15-methyl-11-methylidene-9,15-diazatetracyclo[10.3.1.0²,¹⁰.0³,⁸]hexadeca-2(10),3,5,7-tetraene

Description

ZINC100002737 belongs to the class of organic compounds known as carbazoles. Carbazoles are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring. It was first documented in 2022 (PMID: 36057450). Based on a literature review a significant number of articles have been published on ZINC100002737 (PMID: 36057449) (PMID: 36057448) (PMID: 36057447) (PMID: 36057446).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          2D

 42 45  0  0  0  0  0  0  0  0999 V2000
    2.1328    3.1443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7062    2.6807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3943    1.2135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2760    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3943   -1.2135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7062   -2.6807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -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
   -2.1470   -1.7537    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
   -2.1470    1.7537    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
   -3.3342    3.2733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8333    3.3256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4086    3.6844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5233    4.6881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9499    4.2246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2617    2.7574    0.0000 N   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
    2.4446    4.6115    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2475    2.1406    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7760    0.0000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1328   -3.1443    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0967   -5.1517    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9499   -4.2246    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5736   -1.2902    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4190    0.9587    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3971    4.6117    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6462    4.7405    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5689    1.7917    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3324    3.3780    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9641    4.8199    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2468    1.8837    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0798    5.1027    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4626    5.7488    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2275    6.0126    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1586    5.7100    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3917    4.6381    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1149    1.8303    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6324    3.4595    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4021    0.8214    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 13  1  0
 13 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 12  1  0
 12 11  1  0
 11  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
  3  2  1  0
  2  1  2  3
 12 13  1  0
 10 11  1  0
  2 16  1  0
 10  5  1  0
 15 32  1  0
 15 33  1  0
 15 34  1  0
 14 30  1  0
 14 31  1  0
 13 29  1  1
 16 35  1  1
 17 36  1  0
 17 37  1  0
 18 38  1  0
 18 39  1  0
 20 40  1  0
 20 41  1  0
 20 42  1  0
 12 28  1  6
  4 23  1  0
  6 24  1  0
  7 25  1  0
  8 26  1  0
  9 27  1  0
  1 21  1  0
  1 22  1  0
M  END


  Mrv1652309042202082D          

 20 23  0  0  1  0            999 V2000
    1.3509   -1.3340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6716   -0.5043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1670    0.2425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0776   -0.4564    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6863    0.1005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5075    0.0207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9871    0.6919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6457    1.4429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8245    1.5227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3449    0.8515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5251    0.7588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0703    1.4471    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6901    0.4031    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2508   -0.4384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4457   -1.3236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8633   -0.3391    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4085    0.3492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5737    1.1575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2620    1.6123    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1329    2.4666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
  3 11  2  0  0  0  0
 12 11  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16  2  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 12 19  1  0  0  0  0
 19 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0184892

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@H]1[C@@H]2CCN(C)[C@@H]1C1=C(NC3=CC=CC=C13)C2=C

> <INCHI_IDENTIFIER>
InChI=1S/C18H22N2/c1-4-12-13-9-10-20(3)18(12)16-14-7-5-6-8-15(14)19-17(16)11(13)2/h5-8,12-13,18-19H,2,4,9-10H2,1,3H3/t12-,13-,18+/m1/s1

> <INCHI_KEY>
MFFIRXGJJPPAMA-VFVRVIDISA-N

> <FORMULA>
C18H22N2

> <MOLECULAR_WEIGHT>
266.388

> <EXACT_MASS>
266.178298716

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
21.640212549851604

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,12S,16R)-16-ethyl-15-methyl-11-methylidene-9,15-diazatetracyclo[10.3.1.0^{2,10}.0^{3,8}]hexadeca-2(10),3,5,7-tetraene

> <JCHEM_LOGP>
3.6233329293333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.859332710804072

> <JCHEM_PKA_STRONGEST_BASIC>
8.592000403815542

> <JCHEM_POLAR_SURFACE_AREA>
19.03

> <JCHEM_REFRACTIVITY>
83.9622

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,12S,16R)-16-ethyl-15-methyl-11-methylidene-9,15-diazatetracyclo[10.3.1.0^{2,10}.0^{3,8}]hexadeca-2(10),3,5,7-tetraene

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       2.522  -2.490   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.120  -0.941   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.045   0.453   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0       5.745  -0.852   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       6.881   0.188   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.414   0.039   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.309   1.292   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.672   2.693   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.139   2.842   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.244   1.589   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.713   1.416   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.865   2.701   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.155   0.753   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.201  -0.818   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.565  -2.471   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.611  -0.633   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.763   0.652   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.071   2.161   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       2.356   3.010   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       2.115   4.604   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   16                                                  
CONECT    3    2    4   11                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    5   11                                                  
CONECT   11   10    3   12                                                  
CONECT   12   11   13   19                                                  
CONECT   13   12   14   16                                                  
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16   13    2   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   12   20                                                  
CONECT   20   19                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₂N₂

Average Mass

266.3880 Da

Monoisotopic Mass

266.17830 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC[C@@H]1[C@@H]2CCN(C)[C@@H]1C1=C(NC3=CC=CC=C13)C2=C

InChI Identifier

InChI=1S/C18H22N2/c1-4-12-13-9-10-20(3)18(12)16-14-7-5-6-8-15(14)19-17(16)11(13)2/h5-8,12-13,18-19H,2,4,9-10H2,1,3H3/t12-,13-,18+/m1/s1

InChI Key

MFFIRXGJJPPAMA-VFVRVIDISA-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 carbazoles. Carbazoles are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Carbazoles

Direct Parent

Carbazoles

Alternative Parents

Substituents

Carbazole
3-alkylindole
Indole
Aralkylamine
Piperidine
Benzenoid
Heteroaromatic compound
Pyrrole
Tertiary aliphatic amine
Tertiary amine
Azacycle
Organonitrogen compound
Hydrocarbon derivative
Organic nitrogen 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

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

98042957

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Micalizzi E, Vaudano AE, Ballerini A, Talami F, Giovannini G, Turchi G, Cioclu MC, Giunta L, Meletti S: Ictal Apnea: a prospective monocentric study in patients with epilepsy. Eur J Neurol. 2022 Sep 3. doi: 10.1111/ene.15547. [PubMed:36057450 ]
Jiang S, Guo P, Heo HY, Zhang Y, Wu J, Jin Y, Laterra J, Eberhart CG, Lim M, Blakeley JO: Radiomics analysis of amide proton transfer-weighted and structural MR images for treatment response assessment in malignant gliomas. NMR Biomed. 2022 Sep 3:e4824. doi: 10.1002/nbm.4824. [PubMed:36057449 ]
Agarwal K, Saikia P, Podder I: Metabolic syndrome and Dyslipidemia in xanthelasma palpebrarum and associated risk-factors- a case-control study. J Cosmet Dermatol. 2022 Sep 3. doi: 10.1111/jocd.15353. [PubMed:36057448 ]
Lebel V, Argiropoulos N, Robins S, Charbonneau L, Feeley N: Family-centred care and breastfeeding self-efficacy determined how ready mothers were for their infants to be discharged from a neonatal intensive care unit. Acta Paediatr. 2022 Sep 3. doi: 10.1111/apa.16538. [PubMed:36057447 ]
Park JI, Kim SJ, Kim YJ, Lee SJ: Protective role of Caesalpinia sappan extract and its main component brazilin against blue light-induced damage in human fibroblasts. J Cosmet Dermatol. 2022 Sep 3. doi: 10.1111/jocd.15354. [PubMed:36057446 ]
LOTUS database [Link]

Showing NP-Card for (1s,12s,16r)-16-ethyl-15-methyl-11-methylidene-9,15-diazatetracyclo[10.3.1.0²,¹⁰.0³,⁸]hexadeca-2(10),3,5,7-tetraene (NP0184892)

MOL for NP0184892 ((1s,12s,16r)-16-ethyl-15-methyl-11-methylidene-9,15-diazatetracyclo[10.3.1.0²,¹⁰.0³,⁸]hexadeca-2(10),3,5,7-tetraene)

3D MOL for NP0184892 ((1s,12s,16r)-16-ethyl-15-methyl-11-methylidene-9,15-diazatetracyclo[10.3.1.0²,¹⁰.0³,⁸]hexadeca-2(10),3,5,7-tetraene)

3D SDF for NP0184892 ((1s,12s,16r)-16-ethyl-15-methyl-11-methylidene-9,15-diazatetracyclo[10.3.1.0²,¹⁰.0³,⁸]hexadeca-2(10),3,5,7-tetraene)

3D-SDF for NP0184892 ((1s,12s,16r)-16-ethyl-15-methyl-11-methylidene-9,15-diazatetracyclo[10.3.1.0²,¹⁰.0³,⁸]hexadeca-2(10),3,5,7-tetraene)

PDB for NP0184892 ((1s,12s,16r)-16-ethyl-15-methyl-11-methylidene-9,15-diazatetracyclo[10.3.1.0²,¹⁰.0³,⁸]hexadeca-2(10),3,5,7-tetraene)

3D PDB for NP0184892 ((1s,12s,16r)-16-ethyl-15-methyl-11-methylidene-9,15-diazatetracyclo[10.3.1.0²,¹⁰.0³,⁸]hexadeca-2(10),3,5,7-tetraene)

SMILES for NP0184892 ((1s,12s,16r)-16-ethyl-15-methyl-11-methylidene-9,15-diazatetracyclo[10.3.1.0²,¹⁰.0³,⁸]hexadeca-2(10),3,5,7-tetraene)

INCHI for NP0184892 ((1s,12s,16r)-16-ethyl-15-methyl-11-methylidene-9,15-diazatetracyclo[10.3.1.0²,¹⁰.0³,⁸]hexadeca-2(10),3,5,7-tetraene)

Structure for NP0184892 ((1s,12s,16r)-16-ethyl-15-methyl-11-methylidene-9,15-diazatetracyclo[10.3.1.0²,¹⁰.0³,⁸]hexadeca-2(10),3,5,7-tetraene)

3D Structure for NP0184892 ((1s,12s,16r)-16-ethyl-15-methyl-11-methylidene-9,15-diazatetracyclo[10.3.1.0²,¹⁰.0³,⁸]hexadeca-2(10),3,5,7-tetraene)