NP-MRD: Showing NP-Card for 15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadec-10-ene (NP0303374)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-10 17:40:47 UTC

Updated at

2022-09-10 17:40:47 UTC

NP-MRD ID

NP0303374

Secondary Accession Numbers

None

Natural Product Identification

Common Name

15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadec-10-ene

Description

Anhydrodihydrolycopodine belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. 15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadec-10-ene is found in Diphasiastrum tristachyum. Based on a literature review very few articles have been published on Anhydrodihydrolycopodine.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 45  0  0  0  0  0  0  0  0999 V2000
    2.9869   -1.2442    1.7384 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1433   -0.1738    1.0326 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3455   -0.3814   -0.4362 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5700    0.5663   -1.2995 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8768   -0.2448   -2.3707 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0493   -1.2648   -1.6910 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4587   -1.0362   -0.5078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3515   -2.0855    0.0788 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6422   -1.3776    0.4430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2559   -0.3224    1.4811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4242    0.6851    0.9196 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2392    1.4451   -0.0239 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4195    2.7106   -0.3064 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2804    2.2216   -1.1777 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5272    1.2484   -0.4077 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2225    0.1836    0.3057 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6988   -0.2683    1.4520 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6263   -1.3313    2.7640 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9457   -2.1978    1.1706 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0404   -0.8945    1.7799 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5798    0.7959    1.3502 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4204   -0.2421   -0.6502 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1214   -1.4477   -0.6765 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2038    1.3052   -1.8068 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6820   -0.7223   -2.9767 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2688    0.3438   -3.0531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1260   -2.2091   -2.1991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9497   -2.5142    1.0058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5257   -2.9254   -0.6223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3998   -2.0576    0.8473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0348   -0.9312   -0.4778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8190   -0.8531    2.3417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2207    0.1583    1.7764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2151    1.6588    0.3902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3260    0.9178   -1.0074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0130    3.0367    0.6724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0177    3.4951   -0.7610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7095    1.8669   -2.1117 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3588    3.1160   -1.3872 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1467    1.8356    0.3340 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4964   -1.2915    1.7638 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5627    0.4264    2.3032 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  1
 17  2  1  0
 15  4  1  0
 16  7  1  0
 16 11  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  1
  3 22  1  0
  3 23  1  0
  4 24  1  6
  5 25  1  0
  5 26  1  0
  6 27  1  0
  8 28  1  0
  8 29  1  0
  9 30  1  0
  9 31  1  0
 10 32  1  0
 10 33  1  0
 12 34  1  0
 12 35  1  0
 13 36  1  0
 13 37  1  0
 14 38  1  0
 14 39  1  0
 15 40  1  1
 17 41  1  0
 17 42  1  0
M  END


  Mrv1652309102219402D          

 17 20  0  0  0  0            999 V2000
    1.9625    2.5168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9403    1.6921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3005    1.0524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8691    0.3739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8931    1.1986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6193    1.5901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3214    1.1570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0476    1.5485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7498    1.1153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7257    0.2907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9996   -0.1008    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9755   -0.9255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2494   -1.3170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5472   -0.8839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5712   -0.0592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2974    0.3323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6054    0.9515    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  2  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
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  4 15  1  0  0  0  0
 15 16  1  0  0  0  0
  7 16  1  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
  2 17  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0303374

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC2CC=C3CCCN4CCCC2C34C1

> <INCHI_IDENTIFIER>
InChI=1S/C16H25N/c1-12-10-13-6-7-14-4-2-8-17-9-3-5-15(13)16(14,17)11-12/h7,12-13,15H,2-6,8-11H2,1H3

> <INCHI_KEY>
YJVNTACRBUGVBH-UHFFFAOYSA-N

> <FORMULA>
C16H25N

> <MOLECULAR_WEIGHT>
231.383

> <EXACT_MASS>
231.198699809

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
28.07273754178124

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
15-methyl-6-azatetracyclo[8.6.0.0^{1,6}.0^{2,13}]hexadec-10-ene

> <JCHEM_LOGP>
3.2472428159999986

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
8.540966456503675

> <JCHEM_POLAR_SURFACE_AREA>
3.24

> <JCHEM_REFRACTIVITY>
72.9145

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
15-methyl-6-azatetracyclo[8.6.0.0^{1,6}.0^{2,13}]hexadec-10-ene

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       3.663   4.698   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.622   3.159   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.428   1.964   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.489   0.698   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.534   2.237   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.889   2.968   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.200   2.160   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.556   2.890   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.866   2.082   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.821   0.543   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       7.466  -0.188   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       7.421  -1.728   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.065  -2.458   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.755  -1.650   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.800  -0.111   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.155   0.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.863   1.776   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   17                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   15                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   16                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14    4   16                                                  
CONECT   16   15    7   11   17                                             
CONECT   17   16    2                                                       
MASTER        0    0    0    0    0    0    0    0   17    0   40    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₂₅N

Average Mass

231.3830 Da

Monoisotopic Mass

231.19870 Da

IUPAC Name

15-methyl-6-azatetracyclo[8.6.0.0^{1,6}.0^{2,13}]hexadec-10-ene

Traditional Name

15-methyl-6-azatetracyclo[8.6.0.0^{1,6}.0^{2,13}]hexadec-10-ene

CAS Registry Number

Not Available

SMILES

CC1CC2CC=C3CCCN4CCCC2C34C1

InChI Identifier

InChI=1S/C16H25N/c1-12-10-13-6-7-14-4-2-8-17-9-3-5-15(13)16(14,17)11-12/h7,12-13,15H,2-6,8-11H2,1H3

InChI Key

YJVNTACRBUGVBH-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

Species Name	Source	Reference
Diphasiastrum tristachyum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Quinolidine
Quinolizidine
Azaspirodecane
Piperidine
Tertiary aliphatic amine
Tertiary amine
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Organopnictogen compound
Hydrocarbon derivative
Organonitrogen compound
Amine
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	3.25	ChemAxon
pKa (Strongest Basic)	8.54	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	3.24 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	72.91 m³·mol⁻¹	ChemAxon
Polarizability	28.07 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

C00027862

Chemspider ID

521597

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

599965

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadec-10-ene (NP0303374)

MOL for NP0303374 (15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadec-10-ene)

3D MOL for NP0303374 (15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadec-10-ene)

3D SDF for NP0303374 (15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadec-10-ene)

3D-SDF for NP0303374 (15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadec-10-ene)

PDB for NP0303374 (15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadec-10-ene)

3D PDB for NP0303374 (15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadec-10-ene)

SMILES for NP0303374 (15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadec-10-ene)

INCHI for NP0303374 (15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadec-10-ene)

Structure for NP0303374 (15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadec-10-ene)

3D Structure for NP0303374 (15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadec-10-ene)