NP-MRD: Showing NP-Card for Cannabinol (NP0044855)

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Record Information

Version

2.0

Created at

2022-03-10 18:36:40 UTC

Updated at

2022-03-10 22:19:14 UTC

NP-MRD ID

NP0044855

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Cannabinol

Description

Cannabinol (CBN), belongs to the class of organic compounds known as dibenzopyrans. These are organic heterocyclic compounds with a structure containing a dibenzopyran moiety, made up of two benzene rings fused to a central pyran ring. Cannabinol is the best known and most abundant member of the cannabinoid subclass of cannabis compounds known as cannabinols or CBNs. Cannabinol is psychoactive, although in a lesser degree as THC and related compounds. CBN is most likely a degradation product of tetrahydrocannabinoic acid (THCA) or of tetrahydrocannabinol (THC). CBN can also be obtained through the decarboxilation of cannabinolic acid (CBNA), another product of the degradation of THCA (PMID: 1140243 ). Independently of the routes by which CBN is produced, it is found in higher quantities in Cannabis products that have been stored over an extended period of time or that have been exposed to sunlight or heat (PMID: 26870049 ). CBN is mildly psychoactive (PMID: 1221432 ) And acts as a partial agonist of the CB1 and CB2 receptors, with a higher affinity for the CB2 receptors (PMID: 11020293 ). In both cases the affinity of CBN to these receptors is lower than that of THC (PMID: 9667767 ). The legal status of CBN is uncertain, as it is not included in the United Nations‚Äö√Ñ√¥ Convention on Psychotropic Substances. However, it could still be considered as an analogue of THC in some states of the United States of America, leaving open the possibility of penal prosecution. The main pharmacological characteristics of Cannabinol are sedative, antibiotic, anticonvulsant and anti-inflammatory (PMID: 6991645 ). Cannabinol (CBN) is also found in cannabis smoke and is volatilized during the combustion of cannabis (https://Doi.Org/10.1007/978-1-59259-947-9_2).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 49 51  0  0  0  0  0  0  0  0999 V2000
    5.4619    1.5653   -0.9964 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9951    1.9697    0.3821 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1074    0.8553    0.8988 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5817    1.1605    2.2832 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7218    0.0070    2.7163 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5561   -0.2276    1.8067 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6262   -1.0717    0.7395 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5312   -1.3007   -0.1245 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7014   -2.1651   -1.1665 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6602   -0.6640    0.0934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7406    0.2056    1.1885 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3578    0.4080    2.0193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9323    0.8452    1.4099 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0929    0.7295    0.6592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1880    0.1911    1.5657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5546    2.1072    0.1878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9721   -0.1919   -0.4817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0790   -0.3657   -1.2784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0483   -1.2044   -2.3578 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8644   -1.8899   -2.6432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8302   -2.8033   -3.8183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7422   -1.7364   -1.8649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7936   -0.8885   -0.7843 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1228    2.3528   -1.6951 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5842    1.5645   -1.0276 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1119    0.5494   -1.2855 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4068    2.8993    0.3838 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8373    2.0659    1.0980 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2177    0.7177    0.2442 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6508   -0.1080    0.9512 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4660    1.2587    2.9434 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0390    2.1294    2.3156 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2817   -0.9254    2.7903 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3544    0.2228    3.7620 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5474   -1.5964    0.5288 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5494   -2.6533   -1.3671 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2753    1.0886    2.8664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1962    0.3603    1.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0740   -0.8992    1.6950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1871    0.7008    2.5540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4633    2.8584    0.9847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6198    2.0164   -0.0784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9440    2.4574   -0.6785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0232    0.1573   -1.0818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9083   -1.3591   -3.0026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4198   -2.2142   -4.6656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0764   -3.6250   -3.6427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7943   -3.2705   -4.0290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8806   -2.2834   -2.1349 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
  8 10  2  0
 10 11  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 14 17  1  0
 17 23  2  0
 23 22  1  0
 22 20  2  0
 20 21  1  0
 20 19  1  0
 19 18  2  0
 11 12  2  0
 12  6  1  0
 23 10  1  0
 18 17  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  7 35  1  0
  9 36  1  0
 15 38  1  0
 15 39  1  0
 15 40  1  0
 16 41  1  0
 16 42  1  0
 16 43  1  0
 22 49  1  0
 21 46  1  0
 21 47  1  0
 21 48  1  0
 19 45  1  0
 18 44  1  0
 12 37  1  0
M  END


  Mrv1652309272007282D          

 23 25  0  0  0  0            999 V2000
 9996.990010000.5485    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9999.851910000.5485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.566410000.1377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.280810000.5485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.999310000.1377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.713810000.5485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.2238 9997.0174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.1744 9997.0256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9994.8421 9999.3117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.2733 9999.3093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9995.5590 9998.8968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9995.5590 9998.0718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.2733 9997.6594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.134110000.1365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.419810000.5489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.705410000.1364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.1342 9999.3116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.7041 9999.3098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.9896 9998.8973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.9896 9998.0723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.7041 9997.6600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.4185 9998.0723    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9998.4185 9998.8973    0.0000 C   0  0  0  0  0  0  0  0  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
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 11  9  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 17 14  1  0  0  0  0
 14  2  1  0  0  0  0
  1 16  1  0  0  0  0
 18 19  1  0  0  0  0
 18 23  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 21  8  1  0  0  0  0
 21  7  1  0  0  0  0
 13 20  1  0  0  0  0
 19 10  1  0  0  0  0
 16 18  2  0  0  0  0
 23 17  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0044855

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCC1=CC(O)=C2C(OC(C)(C)C3=C2C=C(C)C=C3)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H26O2/c1-5-6-7-8-15-12-18(22)20-16-11-14(2)9-10-17(16)21(3,4)23-19(20)13-15/h9-13,22H,5-8H2,1-4H3

> <INCHI_KEY>
VBGLYOIFKLUMQG-UHFFFAOYSA-N

> <FORMULA>
C21H26O2

> <MOLECULAR_WEIGHT>
310.437

> <EXACT_MASS>
310.193280077

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
37.75262448976888

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6,6,9-trimethyl-3-pentyl-6H-benzo[c]chromen-1-ol

> <ALOGPS_LOGP>
6.58

> <JCHEM_LOGP>
6.412731023666666

> <ALOGPS_LOGS>
-5.96

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.318134306693421

> <JCHEM_PKA_STRONGEST_BASIC>
-4.922121880517445

> <JCHEM_POLAR_SURFACE_AREA>
29.46

> <JCHEM_REFRACTIVITY>
95.73629999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.39e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
cannabinol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 27-SEP-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-SEP-20         0                                  
HETATM    1  O   UNK     0    8661.0488667.691   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0    8666.3908667.691   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0    8667.7248666.924   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0    8669.0588667.691   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0    8670.3998666.924   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0    8671.7338667.691   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0    8663.3518661.099   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0    8661.3928661.115   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0    8657.0398665.382   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0    8659.7108665.377   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0    8658.3778664.607   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0    8658.3778663.067   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0    8659.7108662.297   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8665.0508666.921   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0    8663.7178667.691   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0    8662.3838666.921   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0    8665.0508665.382   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0    8662.3818665.378   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0    8661.0478664.608   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0    8661.0478663.068   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0    8662.3818662.299   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0    8663.7148663.068   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0    8663.7148664.608   0.000  0.00  0.00           C+0
CONECT    1   16                                                            
CONECT    2    3   14                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5                                                            
CONECT    7   21                                                            
CONECT    8   21                                                            
CONECT    9   11                                                            
CONECT   10   11   19                                                       
CONECT   11   10   12    9                                                  
CONECT   12   11   13                                                       
CONECT   13   12   20                                                       
CONECT   14   15   17    2                                                  
CONECT   15   14   16                                                       
CONECT   16   15    1   18                                                  
CONECT   17   14   23                                                       
CONECT   18   19   23   16                                                  
CONECT   19   18   20   10                                                  
CONECT   20   19   21   13                                                  
CONECT   21   20   22    8    7                                             
CONECT   22   21   23                                                       
CONECT   23   18   22   17                                                  
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Value	Source
6,6,9-Trimethyl-3-pentyl-6H-dibenzo[b,d]pyran-1-ol	PhytoBank
3-Amyl-1-hydroxy-6,6,9-trimethyl-6H-dibenzo[b,d]pyran	PhytoBank
CBN	PhytoBank

Chemical Formula

C₂₁H₂₆O₂

Average Mass

310.4370 Da

Monoisotopic Mass

310.19328 Da

IUPAC Name

6,6,9-trimethyl-3-pentyl-6H-benzo[c]chromen-1-ol

Traditional Name

cannabinol

CAS Registry Number

521-35-7

SMILES

CCCCCC1=CC(O)=C2C(OC(C)(C)C3=C2C=C(C)C=C3)=C1

InChI Identifier

InChI=1S/C21H26O2/c1-5-6-7-8-15-12-18(22)20-16-11-14(2)9-10-17(16)21(3,4)23-19(20)13-15/h9-13,22H,5-8H2,1-4H3

InChI Key

VBGLYOIFKLUMQG-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Cannabis sativa	NULL	Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dibenzopyrans. These are organic heterocyclic compounds with a structure containing a dibenzopyran moiety, made up of two benzene rings fused to a central pyran ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Dibenzopyrans

Alternative Parents

Substituents

Dibenzopyran
2-benzopyran
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Oxacycle
Ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

dibenzopyran (CHEBI:3360 )
Other aromatic polyketides (C07580 )
Cannabinoids (C07580 )
Other aromatic polyketides (LMPK13120002 )

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	6.58	ALOGPS
logP	6.41	ChemAxon
logS	-6	ALOGPS
pKa (Strongest Acidic)	9.32	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	29.46 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	95.74 m³·mol⁻¹	ChemAxon
Polarizability	37.75 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

Not Available

Chemspider ID

Not Available

KEGG Compound ID

C07580

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Cannabinol

METLIN ID

Not Available

PubChem Compound

2543

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

McCallum ND, Yagen B, Levy S, Mechoulam R: Cannabinol: a rapidly formed metabolite of delta-1- and delta-6-tetrahydrocannabinol. Experientia. 1975 May 15;31(5):520-1. doi: 10.1007/BF01932433. [PubMed:1140243 ]
Karniol IG, Shirakawa I, Takahashi RN, Knobel E, Musty RE: Effects of delta9-tetrahydrocannabinol and cannabinol in man. Pharmacology. 1975;13(6):502-12. doi: 10.1159/000136944. [PubMed:1221432 ]
Mahadevan A, Siegel C, Martin BR, Abood ME, Beletskaya I, Razdan RK: Novel cannabinol probes for CB1 and CB2 cannabinoid receptors. J Med Chem. 2000 Oct 5;43(20):3778-85. doi: 10.1021/jm0001572. [PubMed:11020293 ]
Petitet F, Jeantaud B, Reibaud M, Imperato A, Dubroeucq MC: Complex pharmacology of natural cannabinoids: evidence for partial agonist activity of delta9-tetrahydrocannabinol and antagonist activity of cannabidiol on rat brain cannabinoid receptors. Life Sci. 1998;63(1):PL1-6. doi: 10.1016/s0024-3205(98)00238-0. [PubMed:9667767 ]

Showing NP-Card for Cannabinol (NP0044855)

MOL for NP0044855 (Cannabinol)

3D MOL for NP0044855 (Cannabinol)

3D SDF for NP0044855 (Cannabinol)

3D-SDF for NP0044855 (Cannabinol)

PDB for NP0044855 (Cannabinol)

3D PDB for NP0044855 (Cannabinol)

SMILES for NP0044855 (Cannabinol)

INCHI for NP0044855 (Cannabinol)

Structure for NP0044855 (Cannabinol)

3D Structure for NP0044855 (Cannabinol)