NP-MRD: Showing NP-Card for (1r,3s,4s,6s,8r,10s,13r,14r,16r)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.0¹,¹⁰.0³,⁸]hexadecane-3,4,6,14,16-pentol (NP0173596)

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Record Information

Version

2.0

Created at

2022-09-03 10:45:31 UTC

Updated at

2022-09-03 10:45:31 UTC

NP-MRD ID

NP0173596

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3s,4s,6s,8r,10s,13r,14r,16r)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.0¹,¹⁰.0³,⁸]hexadecane-3,4,6,14,16-pentol

Description

Leucothol B belongs to the class of organic compounds known as leucothol and grayanotoxane diterpenoids. These are diterpenoids with a structure based either on the leucothol or the grayanotoxane skeleton. Based on a literature review very few articles have been published on Leucothol B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032212452D          

 25 28  0  0  1  0            999 V2000
    3.6704   -1.1396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4720   -0.3387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6713   -0.1051    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1143   -0.7723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2839   -0.5673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0345    0.2636    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7471    0.4672    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0160   -0.3127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4183    0.7398    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0794    1.2787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8792    1.0419    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6883    1.8445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4801    1.6073    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2909    2.4103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2701    1.3696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3670    2.1889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0938    1.4165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4593    0.5666    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2493    0.3289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8585    0.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0684    0.2389    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8326    1.4220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0092    1.1288    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6446    1.8688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1873    1.2000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  3  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 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  1  0  0  0
 18 20  1  0  0  0  0
 21 20  1  6  0  0  0
  2 21  1  0  0  0  0
 11 21  1  0  0  0  0
  9 22  1  1  0  0  0
 22 23  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  6  0  0  0
M  END

     RDKit          3D

 57 60  0  0  0  0  0  0  0  0999 V2000
   -0.1413   -3.0337   -1.1314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0570   -1.7374   -0.8571 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3069   -1.2126   -0.6574 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1165   -2.0438    0.3252 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4120   -1.3489    0.6746 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2346    0.0450    1.1666 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7170    0.3103    1.2051 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5922    1.5842    1.7335 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4061    0.2103   -0.2472 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1880    0.9606   -0.6971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0160    0.3536   -0.0653 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8817    0.0342    1.2757 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2252    1.2303   -0.3198 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3873    1.3415   -1.6847 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4794    0.6188    0.2681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6511    1.3388   -0.4154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6210    0.9477    1.7519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6418   -0.8348   -0.0118 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2625   -0.9762   -1.2538 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3663   -1.6405    0.0538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3112   -0.9580   -0.7902 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6155    0.8171   -0.9639 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6330    1.0661    0.1256 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0455    0.8585   -0.3620 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4233    2.3532    0.5981 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1118   -3.4751   -1.2959 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7315   -3.6866   -1.2004 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8178   -1.3409   -1.6606 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4081   -2.9805   -0.2307 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5508   -2.3768    1.1974 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0973   -1.3981   -0.2059 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8950   -1.9512    1.4724 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6918    0.2409    2.1516 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3099   -0.4646    1.8512 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8947    2.1310    1.3524 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2673    2.0570   -0.5860 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1058    0.7830   -1.8048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0296    0.7747    1.8894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0474    2.1984    0.1478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7078    1.9734   -2.0797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6108    0.8686   -0.1817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6111    2.3978   -0.0320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4366    1.4198   -1.4992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7103    1.1179    1.9932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2846    0.1356    2.4008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1344    1.9249    1.9438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3393   -1.2666    0.7394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6475   -1.2923   -1.9376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0012   -1.6254    1.0962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6199   -2.6540   -0.2684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6800   -0.7585   -1.8192 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3407    1.7231   -1.5195 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0606    0.1113   -1.6864 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6111    0.1787    0.3103 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0994    0.5589   -1.4201 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5601    1.8515   -0.2808 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8817    2.5394    1.4421 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  1  0
 23 25  1  1
 23 22  1  0
  9 22  1  6
  9 10  1  0
 10 11  1  0
 11 12  1  1
 11 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 15 17  1  0
 15 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  6 23  1  0
  3  9  1  0
  7  9  1  0
 21 11  1  0
 24 54  1  0
 24 55  1  0
 24 56  1  0
 25 57  1  0
 22 52  1  0
 22 53  1  0
 10 36  1  0
 10 37  1  0
 12 38  1  0
 13 39  1  1
 14 40  1  0
 16 41  1  0
 16 42  1  0
 16 43  1  0
 17 44  1  0
 17 45  1  0
 17 46  1  0
 18 47  1  1
 19 48  1  0
 20 49  1  0
 20 50  1  0
 21 51  1  6
  1 26  1  0
  1 27  1  0
  3 28  1  6
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  1
  7 34  1  1
  8 35  1  0
M  END


  Mrv1652309032212452D          

 25 28  0  0  1  0            999 V2000
    3.6704   -1.1396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4720   -0.3387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6713   -0.1051    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1143   -0.7723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2839   -0.5673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0345    0.2636    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7471    0.4672    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0160   -0.3127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4183    0.7398    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0794    1.2787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8792    1.0419    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6883    1.8445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4801    1.6073    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2909    2.4103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2701    1.3696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3670    2.1889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0938    1.4165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4593    0.5666    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2493    0.3289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8585    0.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0684    0.2389    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8326    1.4220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0092    1.1288    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6446    1.8688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1873    1.2000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  3  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 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  1  0  0  0
 18 20  1  0  0  0  0
 21 20  1  6  0  0  0
  2 21  1  0  0  0  0
 11 21  1  0  0  0  0
  9 22  1  1  0  0  0
 22 23  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0173596

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@]1(O)C[C@@]23C[C@@]4(O)[C@@H](O)C(C)(C)[C@@H](O)C[C@@H]4C(=C)[C@@H]2CC[C@@H]1[C@H]3O

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O5/c1-10-11-5-6-12-15(22)19(11,8-18(12,4)24)9-20(25)13(10)7-14(21)17(2,3)16(20)23/h11-16,21-25H,1,5-9H2,2-4H3/t11-,12+,13+,14-,15+,16-,18+,19+,20-/m0/s1

> <INCHI_KEY>
LBZHIHYQQXRTHW-ZNXXBGFSSA-N

> <FORMULA>
C20H32O5

> <MOLECULAR_WEIGHT>
352.471

> <EXACT_MASS>
352.22497413

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
38.700305380436475

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,3S,4S,6S,8R,10S,13R,14R,16R)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.0^{1,10}.0^{3,8}]hexadecane-3,4,6,14,16-pentol

> <ALOGPS_LOGP>
0.55

> <JCHEM_LOGP>
-0.28841213233333374

> <ALOGPS_LOGS>
-1.67

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.00313442255062

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.168796631112112

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9367859023199214

> <JCHEM_POLAR_SURFACE_AREA>
101.15

> <JCHEM_REFRACTIVITY>
93.14679999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.48e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3S,4S,6S,8R,10S,13R,14R,16R)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.0^{1,10}.0^{3,8}]hexadecane-3,4,6,14,16-pentol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       6.851  -2.127   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.481  -0.632   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.986  -0.196   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.947  -1.442   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.397  -1.059   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.931   0.492   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.261   0.872   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       3.763  -0.584   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.514   1.381   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.748   2.387   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.241   1.945   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.885   3.443   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       8.363   3.000   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       8.010   4.499   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       9.838   2.557   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.018   4.086   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.375   2.644   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.191   1.058   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      11.665   0.614   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.069   0.002   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.594   0.446   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.421   2.654   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.884   2.107   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.203   3.488   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       0.350   2.240   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   21                                                  
CONECT    3    2    4    9                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   23                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7    3   10   22                                             
CONECT   10    9   11                                                       
CONECT   11   10   12   13   21                                             
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17   18                                             
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   15   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20    2   11                                                  
CONECT   22    9   23                                                       
CONECT   23   22    6   24   25                                             
CONECT   24   23                                                            
CONECT   25   23                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₂O₅

Average Mass

352.4710 Da

Monoisotopic Mass

352.22497 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@]1(O)C[C@@]23C[C@@]4(O)[C@@H](O)C(C)(C)[C@@H](O)C[C@@H]4C(=C)[C@@H]2CC[C@@H]1[C@H]3O

InChI Identifier

InChI=1S/C20H32O5/c1-10-11-5-6-12-15(22)19(11,8-18(12,4)24)9-20(25)13(10)7-14(21)17(2,3)16(20)23/h11-16,21-25H,1,5-9H2,2-4H3/t11-,12+,13+,14-,15+,16-,18+,19+,20-/m0/s1

InChI Key

LBZHIHYQQXRTHW-ZNXXBGFSSA-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 leucothol and grayanotoxane diterpenoids. These are diterpenoids with a structure based either on the leucothol or the grayanotoxane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Leucothol and grayanotoxane diterpenoids

Alternative Parents

Substituents

Leucothol diterpenoid
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Polyol
Organic oxygen compound
Hydrocarbon derivative
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	0.55	ALOGPS
logS	-1.7	ALOGPS

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

88297976

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101324717

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3s,4s,6s,8r,10s,13r,14r,16r)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.0¹,¹⁰.0³,⁸]hexadecane-3,4,6,14,16-pentol (NP0173596)

MOL for NP0173596 ((1r,3s,4s,6s,8r,10s,13r,14r,16r)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.0¹,¹⁰.0³,⁸]hexadecane-3,4,6,14,16-pentol)

3D MOL for NP0173596 ((1r,3s,4s,6s,8r,10s,13r,14r,16r)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.0¹,¹⁰.0³,⁸]hexadecane-3,4,6,14,16-pentol)

3D SDF for NP0173596 ((1r,3s,4s,6s,8r,10s,13r,14r,16r)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.0¹,¹⁰.0³,⁸]hexadecane-3,4,6,14,16-pentol)

3D-SDF for NP0173596 ((1r,3s,4s,6s,8r,10s,13r,14r,16r)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.0¹,¹⁰.0³,⁸]hexadecane-3,4,6,14,16-pentol)

PDB for NP0173596 ((1r,3s,4s,6s,8r,10s,13r,14r,16r)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.0¹,¹⁰.0³,⁸]hexadecane-3,4,6,14,16-pentol)

3D PDB for NP0173596 ((1r,3s,4s,6s,8r,10s,13r,14r,16r)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.0¹,¹⁰.0³,⁸]hexadecane-3,4,6,14,16-pentol)

SMILES for NP0173596 ((1r,3s,4s,6s,8r,10s,13r,14r,16r)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.0¹,¹⁰.0³,⁸]hexadecane-3,4,6,14,16-pentol)

INCHI for NP0173596 ((1r,3s,4s,6s,8r,10s,13r,14r,16r)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.0¹,¹⁰.0³,⁸]hexadecane-3,4,6,14,16-pentol)

Structure for NP0173596 ((1r,3s,4s,6s,8r,10s,13r,14r,16r)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.0¹,¹⁰.0³,⁸]hexadecane-3,4,6,14,16-pentol)

3D Structure for NP0173596 ((1r,3s,4s,6s,8r,10s,13r,14r,16r)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.0¹,¹⁰.0³,⁸]hexadecane-3,4,6,14,16-pentol)