NP-MRD: Showing NP-Card for Lasiodin (NP0139715)

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Record Information

Version

2.0

Created at

2022-06-29 20:07:14 UTC

Updated at

2022-06-29 20:07:14 UTC

NP-MRD ID

NP0139715

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Lasiodin

Description

Lasiokaurin belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D. Lasiodin is found in Isodon excisoides, Isodon japonicus, Isodon rubescens, Isodon rugosus, Isodon serra and Isodon trichocarpus. Lasiokaurin is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171519432D          

 29 33  0  0  0  0            999 V2000
    6.8246    2.7025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9159    1.8826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6716    1.5517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2515    1.3936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3428    0.5736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1069    0.2229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2497   -0.6083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6918   -1.2384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3527   -1.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2546   -1.9380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9307   -0.8465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4623   -1.6486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7931   -2.4043    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5598   -1.4498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0237   -2.0769    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2047   -1.0972    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0212   -0.3594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6583    0.0511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7332    0.2200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3657    0.9964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5156    1.0369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9163    0.4210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6307    0.0160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1345    0.6693    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2249   -0.5938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4316   -0.9557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3297   -1.7744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7705   -0.4256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9990   -0.7179    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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
  5 18  1  0  0  0  0
 11 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
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 14 25  1  0  0  0  0
 19 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 22 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END

     RDKit          3D

 59 63  0  0  0  0  0  0  0  0999 V2000
    4.5504    1.0249   -1.2410 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6564    0.2973   -0.5926 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6041   -0.5247   -1.1806 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5977   -0.8652   -2.3807 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6834   -0.7825   -0.0490 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6913   -1.0588    1.0316 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4778   -2.1239    0.5910 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5708    0.1913    0.8764 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7895    1.2696    1.5331 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3834    1.4538    1.0559 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8235    0.4270    0.1534 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5851   -0.0386    0.4526 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4325   -1.1102    1.5394 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2349   -2.2084    1.0708 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8481   -2.0196   -0.1818 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6919   -3.0900   -0.4291 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1723   -1.8313   -1.2540 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8194   -3.0250   -1.5217 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0812   -0.7128   -0.8329 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5181   -1.0643   -0.8492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9878   -2.1879   -0.0315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8452   -1.3735   -2.3225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3249    0.1609   -0.5200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9598    0.6627    0.8477 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4747    1.0424    0.9058 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4114    2.2510    0.1854 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2520    3.4403    0.8710 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1867    4.6981    0.0671 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1577    3.5517    2.1109 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2921    1.6015   -0.7304 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5432    1.0472   -2.3221 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3125   -1.1943    2.0321 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8739   -1.8801   -0.2641 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5257    0.0792    1.3799 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4105    2.1944    1.5215 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7418    0.9959    2.6295 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4092    2.4750    0.5655 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6915    1.5675    1.9152 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7181    0.9063   -0.8707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4272   -1.4348    1.9252 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0372   -0.5872    2.3965 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7397   -3.7289    0.3194 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3966   -1.5961   -2.2025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1267   -3.7193   -1.6043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9497    0.0981   -1.6094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2840   -2.9509    0.2824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7926   -2.7462   -0.6007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5439   -1.8790    0.9013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8471   -0.9700   -2.5943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0918   -0.9841   -3.0093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8892   -2.4740   -2.4547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1648    0.9852   -1.2303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3829   -0.1009   -0.5306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1994   -0.0290    1.6760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5584    1.5787    1.0271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3158    1.2618    1.9764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6085    4.5181   -0.8719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2297    5.0286   -0.1818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6747    5.4833    0.6231 H   0  0  0  0  0  0  0  0  0  0  0  0
 28 27  1  0
 27 29  2  0
 27 26  1  0
 26 25  1  0
 25 24  1  0
 24 23  1  0
 23 20  1  0
 20 21  1  0
 20 22  1  0
 20 19  1  0
 19 17  1  0
 17 18  1  0
 17 15  1  0
 15 16  1  6
 15 14  1  0
 14 13  1  0
 12 13  1  1
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  6  1  0
  6  7  1  0
  6  5  1  0
  5  3  1  6
  3  4  2  0
  3  2  1  0
  2  1  2  3
 12 25  1  0
  5 11  1  0
 12 19  1  0
  2  8  1  0
  5 15  1  0
 28 57  1  0
 28 58  1  0
 28 59  1  0
 25 56  1  1
 24 54  1  0
 24 55  1  0
 23 52  1  0
 23 53  1  0
 21 46  1  0
 21 47  1  0
 21 48  1  0
 22 49  1  0
 22 50  1  0
 22 51  1  0
 19 45  1  6
 17 43  1  6
 18 44  1  0
 16 42  1  0
 13 40  1  0
 13 41  1  0
 11 39  1  6
 10 37  1  0
 10 38  1  0
  9 35  1  0
  9 36  1  0
  8 34  1  1
  6 32  1  1
  7 33  1  0
  1 30  1  0
  1 31  1  0
M  END


  Mrv1533004171519432D          

 29 33  0  0  0  0            999 V2000
    6.8246    2.7025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9159    1.8826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6716    1.5517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2515    1.3936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3428    0.5736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1069    0.2229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2497   -0.6083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6918   -1.2384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3527   -1.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2546   -1.9380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9307   -0.8465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4623   -1.6486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7931   -2.4043    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5598   -1.4498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0237   -2.0769    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2047   -1.0972    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0212   -0.3594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6583    0.0511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7332    0.2200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3657    0.9964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5156    1.0369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9163    0.4210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6307    0.0160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1345    0.6693    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2249   -0.5938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4316   -0.9557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3297   -1.7744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7705   -0.4256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9990   -0.7179    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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
  5 18  1  0  0  0  0
 11 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
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 14 25  1  0  0  0  0
 19 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 22 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0139715

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1CCC(C)(C)C2C(O)C3(O)OCC12C1CCC2C(O)C31C(=O)C2=C

> <INCHI_IDENTIFIER>
InChI=1S/C22H30O7/c1-10-12-5-6-13-20-9-28-22(27,21(13,16(10)24)17(12)25)18(26)15(20)19(3,4)8-7-14(20)29-11(2)23/h12-15,17-18,25-27H,1,5-9H2,2-4H3

> <INCHI_KEY>
DJQLJZNVICMJRV-UHFFFAOYSA-N

> <FORMULA>
C22H30O7

> <MOLECULAR_WEIGHT>
406.475

> <EXACT_MASS>
406.199153306

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
42.03104538610863

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-15-yl acetate

> <ALOGPS_LOGP>
1.01

> <JCHEM_LOGP>
0.9817336043333331

> <ALOGPS_LOGS>
-2.22

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.630431464149545

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.513344480126326

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2196213200803125

> <JCHEM_POLAR_SURFACE_AREA>
113.29000000000002

> <JCHEM_REFRACTIVITY>
101.0288

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.43e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-15-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      12.739   5.045   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.910   3.514   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      14.320   2.896   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      11.669   2.601   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      11.840   1.071   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.266   0.416   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.533  -1.135   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.491  -2.312   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.725  -3.233   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.675  -3.618   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.071  -1.580   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.196  -3.077   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      10.814  -4.488   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       8.512  -2.706   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       7.511  -3.877   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       9.715  -2.048   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       9.373  -0.671   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.562   0.095   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.835   0.411   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.149   1.860   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.562   1.936   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.444   0.786   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.777   0.030   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       7.718   1.249   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       7.886  -1.108   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.406  -1.784   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       6.215  -3.312   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       5.172  -0.794   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.731  -1.340   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   18                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10   11                                             
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    8   12   18                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16   25                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17    5   11   19                                             
CONECT   19   18   20   25                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   28                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   14   19   26                                             
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   22   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₀O₇

Average Mass

406.4750 Da

Monoisotopic Mass

406.19915 Da

IUPAC Name

9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-15-yl acetate

Traditional Name

9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-15-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1CCC(C)(C)C2C(O)C3(O)OCC12C1CCC2C(O)C31C(=O)C2=C

InChI Identifier

InChI=1S/C22H30O7/c1-10-12-5-6-13-20-9-28-22(27,21(13,16(10)24)17(12)25)18(26)15(20)19(3,4)8-7-14(20)29-11(2)23/h12-15,17-18,25-27H,1,5-9H2,2-4H3

InChI Key

DJQLJZNVICMJRV-UHFFFAOYSA-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
Isodon excisoides	LOTUS Database	35616633
Isodon japonicus	LOTUS Database	35616633
Isodon rubescens	LOTUS Database	35616633
Isodon rugosus	LOTUS Database	35616633
Isodon serra	LOTUS Database	35616633
Isodon trichocarpus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Kaurane diterpenoids

Alternative Parents

Substituents

Kaurane diterpenoid
Oxane
Cyclic alcohol
Carboxylic acid ester
Hemiacetal
Ketone
Secondary alcohol
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Organic oxide
Organooxygen compound
Carbonyl group
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	1.01	ALOGPS
logP	0.98	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	10.51	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	113.29 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	101.03 m³·mol⁻¹	ChemAxon
Polarizability	42.03 Å³	ChemAxon
Number of Rings	5	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

429192

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Lasiodin (NP0139715)

MOL for NP0139715 (Lasiodin)

3D MOL for NP0139715 (Lasiodin)

3D SDF for NP0139715 (Lasiodin)

3D-SDF for NP0139715 (Lasiodin)

PDB for NP0139715 (Lasiodin)

3D PDB for NP0139715 (Lasiodin)

SMILES for NP0139715 (Lasiodin)

INCHI for NP0139715 (Lasiodin)

Structure for NP0139715 (Lasiodin)

3D Structure for NP0139715 (Lasiodin)