NP-MRD: Showing NP-Card for Ethoxy-cannabitriolvarin (NP0045230)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-03-10 19:10:06 UTC

Updated at

2022-03-10 22:20:39 UTC

NP-MRD ID

NP0045230

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Ethoxy-cannabitriolvarin

Description

Ethoxy-cannabitriolvarin (CBTVE) is an ethoxylated derivative of cannabivarin (CBV). Unlike the methylated derivatives, which are naturally produced by the action of the SAM enzyme (PMID: 16766004 ), Ethoxylated metabolites are very rarely found as plant natural products and are instead often found as artifacts produced during extraction procedures employing ethanol as the extraction solvent. CBTVE was isolated from a 140-year-old Cannabis sativa extract and reported in 1985 (PMID: 6991645 ). Regardless, ethoxy-cannabitriolvarin is one of more than 120 cannabinoid compounds reported to have been isolated from in Cannabis sativa (PMID: 6991645 ).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 55 57  0  0  0  0  0  0  0  0999 V2000
    5.3030    0.2284   -0.9932 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3875    1.4638   -0.1565 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6997    1.2171    1.1724 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2901    0.8797    0.8969 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3260    1.8494    0.8268 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0009    1.5250    0.5670 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0430    2.5212    0.4969 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6562    0.2247    0.3804 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5989   -0.8016    0.4410 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9090   -0.4294    0.7024 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2853   -2.1377    0.2560 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0133   -2.5170   -0.0662 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1110   -3.2254   -1.4025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4418   -3.5399    0.9779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0127   -1.4068   -0.1236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7300   -0.1395    0.0792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8046    0.9281    0.0298 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0567    1.2288   -1.2373 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3300    2.4285   -1.7213 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5222    3.1617   -1.2007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0593    0.1166    0.4989 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7307   -0.5083    1.8388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1484    0.9290    0.6635 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3752   -0.9148   -0.5466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3658   -1.9738   -0.4450 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2456    0.0901   -1.3022 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6687   -0.6250   -0.3953 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9562    0.4031   -1.8955 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4369    1.7411    0.0802 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9420    2.3075   -0.7001 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1851    0.4085    1.7284 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7221    2.1305    1.8123 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5636    2.8947    0.9706 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3424    3.4737    0.6417 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6481   -1.2269    0.7506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8377   -4.0632   -1.3679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4489   -2.5442   -2.2115 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8591   -3.6477   -1.7334 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4576   -4.1328    1.2431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8342   -3.0094    1.8449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1618   -4.2608    0.5350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7880    1.6486    0.8227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5235    2.3135   -2.8356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4535    3.1038   -1.6916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4581    2.6297   -1.4716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4607    3.4618   -0.1481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5772    4.1322   -1.7806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1122   -1.5345    1.9359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2203    0.0726    2.6750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6373   -0.4447    2.0582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7053    0.5656    1.3843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3767   -1.3233   -0.3083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3605   -0.4210   -1.5357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3183   -2.5407   -1.3947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5773   -2.7104    0.3537 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 10  2  0
 10  9  1  0
  9  8  2  0
  8  6  1  0
  6  7  1  0
  6  5  2  0
  8 16  1  0
 16 15  2  0
 15 25  1  0
 25 24  1  0
 24 21  1  0
 21 22  1  0
 21 23  1  1
 21 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 15 12  1  0
 12 13  1  6
 12 14  1  0
 12 11  1  0
  5  4  1  0
 17 16  1  0
 11  9  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  0
  2 30  1  0
  3 31  1  0
  3 32  1  0
 10 35  1  0
  7 34  1  0
  5 33  1  0
 25 54  1  0
 25 55  1  0
 24 52  1  0
 24 53  1  0
 22 48  1  0
 22 49  1  0
 22 50  1  0
 23 51  1  0
 17 42  1  1
 19 43  1  0
 19 44  1  0
 20 45  1  0
 20 46  1  0
 20 47  1  0
 13 36  1  0
 13 37  1  0
 13 38  1  0
 14 39  1  0
 14 40  1  0
 14 41  1  0
M  END


  Mrv1652303192001373D          

 25 27  0  0  0  0            999 V2000
    5.1414    1.2775    1.5275 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6303    0.4975    0.3174 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8594    0.9271   -0.8919 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3985    0.6805   -0.7312 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8547   -0.5204   -1.1271 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4996   -0.7571   -0.9824 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6749    0.2413   -0.4252 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2057    1.4353   -0.0275 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4234    2.4125    0.5241 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5816    1.6450   -0.1883 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7285   -0.0200   -0.2070 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1592   -1.2601   -0.5553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5935   -1.5348   -0.3304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9760   -1.1525    1.0751 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4539    0.2049    1.5152 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5346   -0.0352    2.6690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4962    0.9500    2.0098 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7706    0.8745    0.3102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9819    2.1367    0.0643 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8154    2.6779   -0.8359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2561    2.3224   -0.6306 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3270   -2.3302   -1.1133 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9469   -2.8711   -2.3932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2971   -3.4854   -0.1148 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9740   -1.9753   -1.3898 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  1  0  0  0  0
  4  5  2  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
  8 10  2  0  0  0  0
  7 11  1  0  0  0  0
 11 12  2  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
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 12 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
 10  4  1  0  0  0  0
 18 11  1  0  0  0  0
 25  6  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0045230

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC1=CC2=C(C(O)=C1)C1=C(CC[C@](C)(O)C1OCC)C(C)(C)O2

> <INCHI_IDENTIFIER>
InChI=1S/C21H30O4/c1-6-8-13-11-15(22)18-16(12-13)25-20(3,4)14-9-10-21(5,23)19(17(14)18)24-7-2/h11-12,19,22-23H,6-10H2,1-5H3/t19-,21-/m0/s1

> <INCHI_KEY>
RFAYJRLIEJZHOI-FPOVZHCZSA-N

> <FORMULA>
C21H30O4

> <MOLECULAR_WEIGHT>
346.467

> <EXACT_MASS>
346.214409446

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
39.85507314353155

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(9S)-10-ethoxy-6,6,9-trimethyl-3-propyl-6H,7H,8H,9H,10H-cyclohexa[c]chromene-1,9-diol

> <ALOGPS_LOGP>
3.86

> <JCHEM_LOGP>
3.915826372333332

> <ALOGPS_LOGS>
-4.07

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.959419391427726

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.240901736664402

> <JCHEM_PKA_STRONGEST_BASIC>
-3.254033136952607

> <JCHEM_POLAR_SURFACE_AREA>
58.92

> <JCHEM_REFRACTIVITY>
99.6543

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.97e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(9S)-10-ethoxy-6,6,9-trimethyl-3-propyl-7H,8H,10H-cyclohexa[c]chromene-1,9-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-MAR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-MAR-20         0                                  
HETATM    1  C   UNK     0       5.141   1.278   1.528  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.630   0.498   0.317  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.859   0.927  -0.892  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.398   0.681  -0.731  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.855  -0.520  -1.127  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.500  -0.757  -0.982  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.675   0.241  -0.425  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.206   1.435  -0.028  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.423   2.413   0.524  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.582   1.645  -0.188  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.729  -0.020  -0.207  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.159  -1.260  -0.555  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.594  -1.535  -0.330  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.976  -1.153   1.075  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.454   0.205   1.515  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.535  -0.035   2.669  0.00  0.00           C+0
HETATM   17  O   UNK     0      -3.496   0.950   2.010  0.00  0.00           O+0
HETATM   18  C   UNK     0      -1.771   0.875   0.310  0.00  0.00           C+0
HETATM   19  O   UNK     0      -1.982   2.137   0.064  0.00  0.00           O+0
HETATM   20  C   UNK     0      -2.815   2.678  -0.836  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.256   2.322  -0.631  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.327  -2.330  -1.113  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.947  -2.871  -2.393  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.297  -3.485  -0.115  0.00  0.00           C+0
HETATM   25  O   UNK     0       0.974  -1.975  -1.390  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   25                                                  
CONECT    7    6    8   11                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8    4                                                       
CONECT   11    7   12   18                                                  
CONECT   12   11   13   22                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17   18                                             
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   15   19   11                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   12   23   24   25                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   22    6                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₃₀O₄

Average Mass

346.4670 Da

Monoisotopic Mass

346.21441 Da

IUPAC Name

(9S)-10-ethoxy-6,6,9-trimethyl-3-propyl-6H,7H,8H,9H,10H-cyclohexa[c]chromene-1,9-diol

Traditional Name

(9S)-10-ethoxy-6,6,9-trimethyl-3-propyl-7H,8H,10H-cyclohexa[c]chromene-1,9-diol

CAS Registry Number

Not Available

SMILES

CCCC1=CC2=C(C(O)=C1)C1=C(CC[C@](C)(O)C1OCC)C(C)(C)O2

InChI Identifier

InChI=1S/C21H30O4/c1-6-8-13-11-15(22)18-16(12-13)25-20(3,4)14-9-10-21(5,23)19(17(14)18)24-7-2/h11-12,19,22-23H,6-10H2,1-5H3/t19-,21-/m0/s1

InChI Key

RFAYJRLIEJZHOI-FPOVZHCZSA-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

Classification

Not classified

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	3.86	ALOGPS
logP	3.92	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	9.24	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	58.92 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	99.65 m³·mol⁻¹	ChemAxon
Polarizability	39.86 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

Showing NP-Card for Ethoxy-cannabitriolvarin (NP0045230)

MOL for NP0045230 (Ethoxy-cannabitriolvarin)

3D MOL for NP0045230 (Ethoxy-cannabitriolvarin)

3D SDF for NP0045230 (Ethoxy-cannabitriolvarin)

3D-SDF for NP0045230 (Ethoxy-cannabitriolvarin)

PDB for NP0045230 (Ethoxy-cannabitriolvarin)

3D PDB for NP0045230 (Ethoxy-cannabitriolvarin)

SMILES for NP0045230 (Ethoxy-cannabitriolvarin)

INCHI for NP0045230 (Ethoxy-cannabitriolvarin)

Structure for NP0045230 (Ethoxy-cannabitriolvarin)

3D Structure for NP0045230 (Ethoxy-cannabitriolvarin)