NP-MRD: Showing NP-Card for (1r,2r,3s,5s,6r,9s,11s,13r,14s)-5-hydroxy-3-isopropyl-6,9,13-trimethyltetracyclo[7.5.0.0²,⁶.0¹¹,¹³]tetradecan-14-yl acetate (NP0262399)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-08 05:11:01 UTC

Updated at

2022-09-08 05:11:01 UTC

NP-MRD ID

NP0262399

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,3s,5s,6r,9s,11s,13r,14s)-5-hydroxy-3-isopropyl-6,9,13-trimethyltetracyclo[7.5.0.0²,⁶.0¹¹,¹³]tetradecan-14-yl acetate

Description

(?)-2Beta-Acetoxy-11alpha-hydroxyverrucosane belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. (1r,2r,3s,5s,6r,9s,11s,13r,14s)-5-hydroxy-3-isopropyl-6,9,13-trimethyltetracyclo[7.5.0.0²,⁶.0¹¹,¹³]tetradecan-14-yl acetate is found in Scapania bolanderi. Based on a literature review very few articles have been published on (?)-2Beta-Acetoxy-11alpha-hydroxyverrucosane.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082207112D          

 25 28  0  0  1  0            999 V2000
    3.1245    0.9783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8400    0.2039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0271    0.0630    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3684   -0.4297    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0839   -1.2041    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6123   -1.8377    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4252   -1.6969    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8645   -0.9985    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5578   -0.2327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7411   -0.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0676    0.4159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6644   -1.2005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7195   -2.0237    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4178   -2.4630    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9536   -2.3304    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5454   -2.9053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6691   -3.1048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8563   -3.2456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3279   -2.6121    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0434   -3.3865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5150   -2.7529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9866   -2.1193    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4582   -1.4857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2710   -1.3449    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1302   -0.5320    0.0000 C   0  0  0  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
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  1  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
  7 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  6 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 22 24  1  0  0  0  0
  5 24  1  0  0  0  0
 24 25  1  6  0  0  0
M  END

     RDKit          3D

 61 64  0  0  0  0  0  0  0  0999 V2000
    1.7268    3.1176    2.5286 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9611    1.8628    1.7780 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7246    0.9571    2.2412 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3810    1.5752    0.5336 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5982    0.4072   -0.1706 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4240   -0.4176   -0.5637 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7548   -0.4110    0.3312 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8235    0.5623    0.0390 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7300    1.9662    0.4561 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5272    2.2192    1.9176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1175    2.5731    0.1350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0330   -0.0075    0.8068 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6800   -1.4760    1.0804 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2301   -1.6686    2.3716 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6056   -1.6671    0.0600 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2837   -1.5743   -1.3059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8505   -2.9234    0.1118 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0691   -2.8693   -1.1220 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0444   -1.7879   -0.8270 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8546   -2.2651    0.3876 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0020   -1.6834   -1.9684 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8040   -0.4712   -2.0913 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0650    0.7124   -2.7437 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4633    0.7275   -1.3629 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6083    1.6789   -0.9762 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7001    3.4664    2.9810 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0659    2.9248    3.4174 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2794    3.8618    1.8716 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3002   -0.2043    0.4813 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0238   -0.1150   -1.5801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5375   -0.4238    1.4010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1391    0.5562   -1.0344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0606    2.6009   -0.1877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5009    2.2810    2.4773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8374    1.5383    2.4239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1086    3.2517    2.0130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0396    3.6694    0.0655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8683    2.2451    0.8576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3848    2.2159   -0.8937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1052    0.4551    1.8202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9623    0.1052    0.2508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5579   -2.1006    0.8380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7420   -2.4211    2.7701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2926   -1.1142   -1.2353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6647   -1.1283   -2.0790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4860   -2.6334   -1.6437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2075   -3.0355    0.9997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5288   -3.7693    0.0555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4826   -2.7872   -2.0500 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6198   -3.8219   -1.1308 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7757   -3.3895    0.4969 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4809   -1.8603    1.3278 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9527   -2.1087    0.2179 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6478   -2.6094   -1.9364 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3970   -1.8202   -2.9125 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8751   -0.6216   -2.3526 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7239    1.2721   -3.4639 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0819    0.5335   -3.1777 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0747    2.0866   -1.9150 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3240    1.2015   -0.3082 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0926    2.5616   -0.5126 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0
  9 11  1  0
  9  8  1  0
  8 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  6
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  1
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  1
 24  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7 15  1  0
  6 19  1  0
 24 22  1  0
 10 34  1  0
 10 35  1  0
 10 36  1  0
  9 33  1  0
 11 37  1  0
 11 38  1  0
 11 39  1  0
  8 32  1  6
 12 40  1  0
 12 41  1  0
 13 42  1  6
 14 43  1  0
 16 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 18 49  1  0
 18 50  1  0
 20 51  1  0
 20 52  1  0
 20 53  1  0
 21 54  1  0
 21 55  1  0
 22 56  1  6
 23 57  1  0
 23 58  1  0
 25 59  1  0
 25 60  1  0
 25 61  1  0
  5 29  1  1
  1 26  1  0
  1 27  1  0
  1 28  1  0
  6 30  1  6
  7 31  1  1
M  END


  Mrv1652309082207112D          

 25 28  0  0  1  0            999 V2000
    3.1245    0.9783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8400    0.2039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0271    0.0630    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3684   -0.4297    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0839   -1.2041    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6123   -1.8377    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4252   -1.6969    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8645   -0.9985    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5578   -0.2327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7411   -0.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0676    0.4159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6644   -1.2005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7195   -2.0237    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4178   -2.4630    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9536   -2.3304    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5454   -2.9053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6691   -3.1048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8563   -3.2456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3279   -2.6121    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0434   -3.3865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5150   -2.7529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9866   -2.1193    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4582   -1.4857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2710   -1.3449    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1302   -0.5320    0.0000 C   0  0  0  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
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  1  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
  7 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  6 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 22 24  1  0  0  0  0
  5 24  1  0  0  0  0
 24 25  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0262399

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@@H]1C[C@H](O)[C@]2(C)CC[C@@]3(C)C[C@H]4C[C@@]4(C)[C@@H](OC(C)=O)[C@@H]3[C@@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C22H36O3/c1-12(2)15-9-16(24)21(5)8-7-20(4)10-14-11-22(14,6)19(25-13(3)23)18(20)17(15)21/h12,14-19,24H,7-11H2,1-6H3/t14-,15-,16-,17+,18-,19-,20-,21-,22+/m0/s1

> <INCHI_KEY>
PLRAZEQRSYIUSJ-GFAORHGDSA-N

> <FORMULA>
C22H36O3

> <MOLECULAR_WEIGHT>
348.527

> <EXACT_MASS>
348.266445019

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
40.519566737452664

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R,3S,5S,6R,9S,11S,13R,14S)-5-hydroxy-6,9,13-trimethyl-3-(propan-2-yl)tetracyclo[7.5.0.0^{2,6}.0^{11,13}]tetradecan-14-yl acetate

> <JCHEM_LOGP>
3.8636914140000016

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.717729221510748

> <JCHEM_PKA_STRONGEST_BASIC>
-0.7352650048555324

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
97.92199999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,3S,5S,6R,9S,11S,13R,14S)-5-hydroxy-3-isopropyl-6,9,13-trimethyltetracyclo[7.5.0.0^{2,6}.0^{11,13}]tetradecan-14-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       5.832   1.826   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.301   0.381   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       3.784   0.118   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       6.288  -0.802   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       5.757  -2.248   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.743  -3.430   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.260  -3.167   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.080  -1.864   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.508  -0.434   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.983  -0.215   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.460   0.776   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.574  -2.241   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.676  -3.778   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      11.980  -4.598   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       9.247  -4.350   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.351  -5.423   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.716  -5.796   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.198  -6.059   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.212  -4.876   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.681  -6.321   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.695  -5.139   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.708  -3.956   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.722  -2.773   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.239  -2.511   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.976  -0.993   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   24                                                  
CONECT    6    5    7   19                                                  
CONECT    7    6    8   15                                                  
CONECT    8    7    9   12                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    8   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    7   16   17                                             
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18    6   20   21                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22   24                                                       
CONECT   24   23   22    5   25                                             
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Value	Source
(?)-2b-acetoxy-11a-hydroxyverrucosane	Generator
(?)-2β-acetoxy-11α-hydroxyverrucosane	Generator

Chemical Formula

C₂₂H₃₆O₃

Average Mass

348.5270 Da

Monoisotopic Mass

348.26645 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)[C@@H]1C[C@H](O)[C@]2(C)CC[C@@]3(C)C[C@H]4C[C@@]4(C)[C@@H](OC(C)=O)[C@@H]3[C@@H]12

InChI Identifier

InChI=1S/C22H36O3/c1-12(2)15-9-16(24)21(5)8-7-20(4)10-14-11-22(14,6)19(25-13(3)23)18(20)17(15)21/h12,14-19,24H,7-11H2,1-6H3/t14-,15-,16-,17+,18-,19-,20-,21-,22+/m0/s1

InChI Key

PLRAZEQRSYIUSJ-GFAORHGDSA-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
Scapania bolanderi	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Verrucosane, neoverrucosane, homoverrucosane, or homoneoverrucosane diterpenoid
Diterpenoid
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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

Bracket

METLIN ID

Not Available

PubChem Compound

101596694

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,3s,5s,6r,9s,11s,13r,14s)-5-hydroxy-3-isopropyl-6,9,13-trimethyltetracyclo[7.5.0.0²,⁶.0¹¹,¹³]tetradecan-14-yl acetate (NP0262399)

MOL for NP0262399 ((1r,2r,3s,5s,6r,9s,11s,13r,14s)-5-hydroxy-3-isopropyl-6,9,13-trimethyltetracyclo[7.5.0.0²,⁶.0¹¹,¹³]tetradecan-14-yl acetate)

3D MOL for NP0262399 ((1r,2r,3s,5s,6r,9s,11s,13r,14s)-5-hydroxy-3-isopropyl-6,9,13-trimethyltetracyclo[7.5.0.0²,⁶.0¹¹,¹³]tetradecan-14-yl acetate)

3D SDF for NP0262399 ((1r,2r,3s,5s,6r,9s,11s,13r,14s)-5-hydroxy-3-isopropyl-6,9,13-trimethyltetracyclo[7.5.0.0²,⁶.0¹¹,¹³]tetradecan-14-yl acetate)

3D-SDF for NP0262399 ((1r,2r,3s,5s,6r,9s,11s,13r,14s)-5-hydroxy-3-isopropyl-6,9,13-trimethyltetracyclo[7.5.0.0²,⁶.0¹¹,¹³]tetradecan-14-yl acetate)

PDB for NP0262399 ((1r,2r,3s,5s,6r,9s,11s,13r,14s)-5-hydroxy-3-isopropyl-6,9,13-trimethyltetracyclo[7.5.0.0²,⁶.0¹¹,¹³]tetradecan-14-yl acetate)

3D PDB for NP0262399 ((1r,2r,3s,5s,6r,9s,11s,13r,14s)-5-hydroxy-3-isopropyl-6,9,13-trimethyltetracyclo[7.5.0.0²,⁶.0¹¹,¹³]tetradecan-14-yl acetate)

SMILES for NP0262399 ((1r,2r,3s,5s,6r,9s,11s,13r,14s)-5-hydroxy-3-isopropyl-6,9,13-trimethyltetracyclo[7.5.0.0²,⁶.0¹¹,¹³]tetradecan-14-yl acetate)

INCHI for NP0262399 ((1r,2r,3s,5s,6r,9s,11s,13r,14s)-5-hydroxy-3-isopropyl-6,9,13-trimethyltetracyclo[7.5.0.0²,⁶.0¹¹,¹³]tetradecan-14-yl acetate)

Structure for NP0262399 ((1r,2r,3s,5s,6r,9s,11s,13r,14s)-5-hydroxy-3-isopropyl-6,9,13-trimethyltetracyclo[7.5.0.0²,⁶.0¹¹,¹³]tetradecan-14-yl acetate)

3D Structure for NP0262399 ((1r,2r,3s,5s,6r,9s,11s,13r,14s)-5-hydroxy-3-isopropyl-6,9,13-trimethyltetracyclo[7.5.0.0²,⁶.0¹¹,¹³]tetradecan-14-yl acetate)