NP-MRD: Showing NP-Card for (3s)-5-[(1s,2r,4ar,8ar)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentyl acetate (NP0253349)

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Record Information

Version

2.0

Created at

2022-09-07 17:11:46 UTC

Updated at

2022-09-07 17:11:46 UTC

NP-MRD ID

NP0253349

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s)-5-[(1s,2r,4ar,8ar)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentyl acetate

Description

(3S)-5-[(1S,2R,4aR,8aR)-5-(hydroxymethyl)-1,2,4a-trimethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl]-3-methylpentyl acetate belongs to the class of organic compounds known as colensane and clerodane diterpenoids. These are diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations. (3s)-5-[(1s,2r,4ar,8ar)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentyl acetate is found in Baccharis trinervis. Based on a literature review very few articles have been published on (3S)-5-[(1S,2R,4aR,8aR)-5-(hydroxymethyl)-1,2,4a-trimethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl]-3-methylpentyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072219112D          

 25 26  0  0  1  0            999 V2000
    6.2697    0.4979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9842    0.9104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9842    1.7354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6986    0.4979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4131    0.9104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1276    0.4979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8421    0.9104    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.8421    1.7354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5565    0.4979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2710    0.9104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9855    0.4979    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.4552   -0.1341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2676    1.2732    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.7373    1.9052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0801    1.4164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6104    0.7844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3282    0.0092    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.1407    0.1525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8585   -0.6228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6710   -0.4795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9532    0.2957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5764   -1.3980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7639   -1.5413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2336   -0.9093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5158   -0.1341    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 25 24  1  6  0  0  0
 11 25  1  0  0  0  0
 17 25  1  0  0  0  0
M  END

     RDKit          3D

 63 64  0  0  0  0  0  0  0  0999 V2000
    7.0883    2.5042    0.2559 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7531    1.8367    0.4009 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4583    1.3062    1.5008 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8546    1.7954   -0.6379 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5866    1.1778   -0.5572 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7693   -0.2674   -0.2817 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4508   -1.0598   -0.1982 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9247   -2.4864    0.0787 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5455   -0.5485    0.8560 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2874   -1.2034    1.1399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8357   -1.2564    0.1370 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4855   -1.9367   -1.1376 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8821   -2.1106    0.8744 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4925   -3.1914    0.0423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8692   -1.2639    1.6188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6094   -0.2666    0.8027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8008    0.3144   -0.3361 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3446   -0.1633   -1.6548 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0659    1.7818   -0.3534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4719    2.2412   -0.2044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5604    3.6371   -0.2961 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1343    2.6945   -0.5391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6953    2.3782   -0.7584 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6225    0.8914   -1.1909 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3368    0.1395   -0.1308 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1757    3.2319    1.1011 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1370    3.0907   -0.6799 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9190    1.7889    0.3781 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0801    1.2771   -1.5476 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9896    1.7138    0.2389 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2759   -0.4734    0.6813 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4028   -0.7140   -1.1025 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0660   -1.0458   -1.2297 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8712   -2.4773    0.6934 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2307   -2.8993   -0.9010 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1615   -3.1336    0.5000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4789    0.5619    0.7079 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1586   -0.5950    1.8172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2018   -0.7541    2.0678 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5226   -2.2542    1.5199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3731   -2.4520   -1.5952 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3290   -2.6595   -0.9538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1440   -1.2633   -1.9590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3731   -2.7067    1.7125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1477   -2.8954   -0.7632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1588   -3.7675    0.7619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7741   -3.9465   -0.3054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5888   -1.9710    2.0955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3523   -0.7579    2.4624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5336   -0.7224    0.4031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9493    0.5225    1.5381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6388   -0.6083   -2.3375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8492    0.6565   -2.2540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1702   -0.8781   -1.4600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9135    1.9834    0.7701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1491    1.7717   -0.9727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2618    4.0093    0.5762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4326    3.7339   -0.5314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2488    3.0402   -1.4995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1340    2.4549    0.1927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1802    0.9004   -2.1754 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3936    0.6102   -1.4278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1292    0.6838    0.8500 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  7  9  1  0
  9 10  1  0
 11 10  1  1
 11 12  1  0
 11 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  6
 17 25  1  0
 25 24  1  0
 24 23  1  0
 23 22  1  0
 22 19  2  0
 19 20  1  0
 20 21  1  0
 25 11  1  0
 19 17  1  0
  8 34  1  0
  8 35  1  0
  8 36  1  0
  7 33  1  6
  6 31  1  0
  6 32  1  0
  5 29  1  0
  5 30  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  9 37  1  0
  9 38  1  0
 10 39  1  0
 10 40  1  0
 12 41  1  0
 12 42  1  0
 12 43  1  0
 13 44  1  1
 14 45  1  0
 14 46  1  0
 14 47  1  0
 15 48  1  0
 15 49  1  0
 16 50  1  0
 16 51  1  0
 18 52  1  0
 18 53  1  0
 18 54  1  0
 25 63  1  1
 24 61  1  0
 24 62  1  0
 23 59  1  0
 23 60  1  0
 22 58  1  0
 20 55  1  0
 20 56  1  0
 21 57  1  0
M  END


  Mrv1652309072219112D          

 25 26  0  0  1  0            999 V2000
    6.2697    0.4979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9842    0.9104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9842    1.7354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6986    0.4979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4131    0.9104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1276    0.4979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8421    0.9104    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.8421    1.7354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5565    0.4979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2710    0.9104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9855    0.4979    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.4552   -0.1341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2676    1.2732    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.7373    1.9052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0801    1.4164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6104    0.7844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3282    0.0092    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.1407    0.1525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8585   -0.6228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6710   -0.4795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9532    0.2957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5764   -1.3980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7639   -1.5413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2336   -0.9093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5158   -0.1341    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 25 24  1  6  0  0  0
 11 25  1  0  0  0  0
 17 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0253349

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](CCOC(C)=O)CC[C@@]1(C)[C@H](C)CC[C@]2(C)[C@@H]1CCC=C2CO

> <INCHI_IDENTIFIER>
InChI=1S/C22H38O3/c1-16(11-14-25-18(3)24)9-12-21(4)17(2)10-13-22(5)19(15-23)7-6-8-20(21)22/h7,16-17,20,23H,6,8-15H2,1-5H3/t16-,17+,20+,21-,22-/m0/s1

> <INCHI_KEY>
JXJUDJCWRDJMCG-HFQQBTNDSA-N

> <FORMULA>
C22H38O3

> <MOLECULAR_WEIGHT>
350.543

> <EXACT_MASS>
350.282095084

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
42.33121888272069

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S)-5-[(1S,2R,4aR,8aR)-5-(hydroxymethyl)-1,2,4a-trimethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl]-3-methylpentyl acetate

> <JCHEM_LOGP>
4.511403051

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.500113043060097

> <JCHEM_PKA_STRONGEST_BASIC>
-1.7052483203563744

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
103.3565

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3S)-5-[(1S,2R,4aR,8aR)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentyl acetate

> <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      11.703   0.929   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.037   1.699   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      13.037   3.239   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      14.371   0.929   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      15.704   1.699   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      17.038   0.929   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      18.372   1.699   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      18.372   3.239   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      19.706   0.929   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      21.039   1.699   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      22.373   0.929   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      21.383  -0.250   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      22.900   2.377   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      21.910   3.556   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      24.416   2.644   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      25.406   1.464   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      24.879   0.017   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      26.396   0.285   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      25.869  -1.163   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      27.386  -0.895   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      27.913   0.552   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      25.343  -2.610   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      23.826  -2.877   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      22.836  -1.697   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      23.363  -0.250   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   25                                             
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19   25                                             
CONECT   18   17                                                            
CONECT   19   17   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   11   17                                                  
MASTER        0    0    0    0    0    0    0    0   25    0   52    0
END

View in JSmol

Synonyms

Value	Source
(3S)-5-[(1S,2R,4AR,8ar)-5-(hydroxymethyl)-1,2,4a-trimethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl]-3-methylpentyl acetic acid	Generator

Chemical Formula

C₂₂H₃₈O₃

Average Mass

350.5430 Da

Monoisotopic Mass

350.28210 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H](CCOC(C)=O)CC[C@@]1(C)[C@H](C)CC[C@]2(C)[C@@H]1CCC=C2CO

InChI Identifier

InChI=1S/C22H38O3/c1-16(11-14-25-18(3)24)9-12-21(4)17(2)10-13-22(5)19(15-23)7-6-8-20(21)22/h7,16-17,20,23H,6,8-15H2,1-5H3/t16-,17+,20+,21-,22-/m0/s1

InChI Key

JXJUDJCWRDJMCG-HFQQBTNDSA-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
Baccharis trinervis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as colensane and clerodane diterpenoids. These are diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Colensane and clerodane diterpenoids

Alternative Parents

Substituents

Clerodane diterpenoid
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
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

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

162899053

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s)-5-[(1s,2r,4ar,8ar)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentyl acetate (NP0253349)

MOL for NP0253349 ((3s)-5-[(1s,2r,4ar,8ar)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentyl acetate)

3D MOL for NP0253349 ((3s)-5-[(1s,2r,4ar,8ar)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentyl acetate)

3D SDF for NP0253349 ((3s)-5-[(1s,2r,4ar,8ar)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentyl acetate)

3D-SDF for NP0253349 ((3s)-5-[(1s,2r,4ar,8ar)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentyl acetate)

PDB for NP0253349 ((3s)-5-[(1s,2r,4ar,8ar)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentyl acetate)

3D PDB for NP0253349 ((3s)-5-[(1s,2r,4ar,8ar)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentyl acetate)

SMILES for NP0253349 ((3s)-5-[(1s,2r,4ar,8ar)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentyl acetate)

INCHI for NP0253349 ((3s)-5-[(1s,2r,4ar,8ar)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentyl acetate)

Structure for NP0253349 ((3s)-5-[(1s,2r,4ar,8ar)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentyl acetate)

3D Structure for NP0253349 ((3s)-5-[(1s,2r,4ar,8ar)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentyl acetate)