NP-MRD: Showing NP-Card for (1r,4r,9r,10s,12r,13s)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadec-15-en-13-ol (NP0255701)

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Record Information

Version

2.0

Created at

2022-09-07 20:16:45 UTC

Updated at

2022-09-07 20:16:45 UTC

NP-MRD ID

NP0255701

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,4r,9r,10s,12r,13s)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadec-15-en-13-ol

Description

(+)-Serradiol belongs to the class of organic compounds known as atisane diterpenoids. These are diterpenoids with a structure based on the atisane skeleton, which is a tetracyclic compound containing the [2,2,2]bicyc1ic ring system with the C15-C16 bridge attached at C12. Thus, (+)-serradiol is considered to be an isoprenoid. Based on a literature review very few articles have been published on (+)-serradiol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
    3.6390   -1.5205   -0.4747 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9904   -0.1261   -0.4923 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3950    0.4569   -1.8568 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6563    0.6814    0.5535 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8188    1.6610    1.2818 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4122    1.7981    0.7950 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8418    0.4012    0.7173 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9957   -0.2919    2.0356 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6067    0.4974    0.3020 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4398    1.3325    1.2153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8623    0.7959    1.1731 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7927   -0.5620    1.8334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9115   -1.3821    1.2719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2420   -0.8435    0.0447 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3817   -1.8432   -0.6105 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0847   -1.7592   -0.3010 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5413   -0.3000   -0.4144 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4108   -0.5385   -0.9138 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2897    0.5089   -0.2663 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3382    1.6857   -1.0115 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6906   -0.0670   -0.1835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5774    0.8076    0.4248 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5826   -2.0084   -1.4543 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7352   -1.3063   -0.3073 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3162   -2.1169    0.3757 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5563    0.3341   -2.5683 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5982    1.5472   -1.7555 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2748   -0.0283   -2.2701 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5293    1.2556    0.1161 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1655    0.0160    1.3139 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2581    2.7019    1.2862 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7523    1.4060    2.3807 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8219    2.3581    1.5389 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3700    2.2354   -0.2140 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0330   -0.5822    2.2276 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3668   -1.1707    2.1773 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6848    0.4429    2.8342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5880    1.0335   -0.6945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0989    1.2428    2.2520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4103    2.4123    0.9577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5942    1.4508    1.6347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4205   -0.7678    2.6639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6757   -2.3660    1.6484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4994   -1.8414   -1.7201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7137   -2.8726   -0.2887 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3011   -2.1896    0.6781 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6150   -2.3729   -1.0615 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0666    0.0523   -1.3792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9299   -0.0571   -1.7975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9604   -1.4612   -1.1705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9954    1.5642   -1.7414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0632   -0.3903   -1.1710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6481   -0.9888    0.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2614    1.0747   -0.2558 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  1
  7 17  1  0
 17 16  1  0
 16 15  1  0
 14 15  1  6
 14 18  1  0
 18 19  1  0
 19 20  1  6
 19 21  1  0
 21 22  1  0
 19 11  1  0
 11 10  1  0
 10  9  1  0
 11 12  1  0
 12 13  2  0
 17  2  1  0
  9 14  1  0
  9  7  1  0
 13 14  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  6 34  1  0
  8 35  1  0
  8 36  1  0
  8 37  1  0
 17 48  1  6
 16 46  1  0
 16 47  1  0
 15 44  1  0
 15 45  1  0
 18 49  1  0
 18 50  1  0
 20 51  1  0
 21 52  1  0
 21 53  1  0
 22 54  1  0
 11 41  1  1
 10 39  1  0
 10 40  1  0
  9 38  1  6
 12 42  1  0
 13 43  1  0
M  END


  Mrv1652309072222162D          

 22 25  0  0  1  0            999 V2000
    5.9541    2.0919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1618    1.8618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0728    2.6820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5259    1.1215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0669    0.4360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2437    0.4908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8796    1.2311    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4620    0.5196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0278    1.1866    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6987    0.3221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7747    0.1529    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1947    0.7255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0028    1.4239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5311    1.9681    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0940    2.6209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9219    2.6686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3386    1.9166    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5848    1.8330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3018    0.9545    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5280    1.2408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6098    0.5054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6528   -0.3185    0.0000 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
  2  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  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 14 13  1  6  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 17 16  1  6  0  0  0
  2 17  1  0  0  0  0
  7 17  1  0  0  0  0
 14 18  1  0  0  0  0
 18 19  1  0  0  0  0
 11 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0255701

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)CCC[C@]2(C)[C@@H]1CC[C@]13C[C@@](O)(CO)[C@H](C[C@@H]21)C=C3

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O2/c1-17(2)7-4-8-18(3)15(17)6-10-19-9-5-14(11-16(18)19)20(22,12-19)13-21/h5,9,14-16,21-22H,4,6-8,10-13H2,1-3H3/t14-,15+,16-,18+,19+,20+/m0/s1

> <INCHI_KEY>
YLPLMBSVCFKOSP-ICHMTLFLSA-N

> <FORMULA>
C20H32O2

> <MOLECULAR_WEIGHT>
304.474

> <EXACT_MASS>
304.24023027

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
36.130616821546795

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,4R,9R,10S,12R,13S)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[10.2.2.0^{1,10}.0^{4,9}]hexadec-15-en-13-ol

> <JCHEM_LOGP>
3.239745128

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.2864536063258

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.62390415268882

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0803575594627803

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
90.21129999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4R,9R,10S,12R,13S)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[10.2.2.0^{1,10}.0^{4,9}]hexadec-15-en-13-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      11.114   3.905   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.635   3.475   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.469   5.006   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.315   2.094   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.458   0.814   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.922   0.916   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.242   2.298   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.462   0.970   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.652   2.215   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.038   0.601   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.313   0.285   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.097   1.354   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.739   2.658   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.725   3.674   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.775   4.892   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.321   4.981   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.099   3.578   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.958   3.422   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.430   1.782   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.986   2.316   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.138   0.943   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.218  -0.595   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   17                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   17                                             
CONECT    8    7                                                            
CONECT    9    7   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   19                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9   15   18                                             
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16    2    7                                                  
CONECT   18   14   19                                                       
CONECT   19   18   11   20   21                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₂O₂

Average Mass

304.4740 Da

Monoisotopic Mass

304.24023 Da

IUPAC Name

(1R,4R,9R,10S,12R,13S)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[10.2.2.0^{1,10}.0^{4,9}]hexadec-15-en-13-ol

Traditional Name

(1R,4R,9R,10S,12R,13S)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[10.2.2.0^{1,10}.0^{4,9}]hexadec-15-en-13-ol

CAS Registry Number

Not Available

SMILES

CC1(C)CCC[C@]2(C)[C@@H]1CC[C@]13C[C@@](O)(CO)[C@H](C[C@@H]21)C=C3

InChI Identifier

InChI=1S/C20H32O2/c1-17(2)7-4-8-18(3)15(17)6-10-19-9-5-14(11-16(18)19)20(22,12-19)13-21/h5,9,14-16,21-22H,4,6-8,10-13H2,1-3H3/t14-,15+,16-,18+,19+,20+/m0/s1

InChI Key

YLPLMBSVCFKOSP-ICHMTLFLSA-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 atisane diterpenoids. These are diterpenoids with a structure based on the atisane skeleton, which is a tetracyclic compound containing the [2,2,2]bicyc1ic ring system with the C15-C16 bridge attached at C12.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Atisane diterpenoids

Alternative Parents

Substituents

Atisane diterpenoid
Alkaloid or derivatives
Tertiary alcohol
Cyclic alcohol
1,2-diol
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	3.24	ChemAxon
pKa (Strongest Acidic)	13.62	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	40.46 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	90.21 m³·mol⁻¹	ChemAxon
Polarizability	36.13 Å³	ChemAxon
Number of Rings	4	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

113385727

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101277423

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,4r,9r,10s,12r,13s)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadec-15-en-13-ol (NP0255701)

MOL for NP0255701 ((1r,4r,9r,10s,12r,13s)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadec-15-en-13-ol)

3D MOL for NP0255701 ((1r,4r,9r,10s,12r,13s)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadec-15-en-13-ol)

3D SDF for NP0255701 ((1r,4r,9r,10s,12r,13s)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadec-15-en-13-ol)

3D-SDF for NP0255701 ((1r,4r,9r,10s,12r,13s)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadec-15-en-13-ol)

PDB for NP0255701 ((1r,4r,9r,10s,12r,13s)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadec-15-en-13-ol)

3D PDB for NP0255701 ((1r,4r,9r,10s,12r,13s)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadec-15-en-13-ol)

SMILES for NP0255701 ((1r,4r,9r,10s,12r,13s)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadec-15-en-13-ol)

INCHI for NP0255701 ((1r,4r,9r,10s,12r,13s)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadec-15-en-13-ol)

Structure for NP0255701 ((1r,4r,9r,10s,12r,13s)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadec-15-en-13-ol)

3D Structure for NP0255701 ((1r,4r,9r,10s,12r,13s)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadec-15-en-13-ol)