NP-MRD: Showing NP-Card for (1's,2r,2's,3'r,4'r,7'r,8's,10'r,12's,13'r,14's)-12',14'-bis(acetyloxy)-8'-chloro-3',10'-dihydroxy-4',13'-dimethyl-9'-methylidene-5'-oxo-6'-oxaspiro[oxirane-2,17'-tricyclo[11.4.0.0³,⁷]heptadecan]-2'-yl acetate (NP0220344)

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Record Information

Version

2.0

Created at

2022-09-05 21:37:56 UTC

Updated at

2022-09-05 21:37:57 UTC

NP-MRD ID

NP0220344

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1's,2r,2's,3'r,4'r,7'r,8's,10'r,12's,13'r,14's)-12',14'-bis(acetyloxy)-8'-chloro-3',10'-dihydroxy-4',13'-dimethyl-9'-methylidene-5'-oxo-6'-oxaspiro[oxirane-2,17'-tricyclo[11.4.0.0³,⁷]heptadecan]-2'-yl acetate

Description

(1'S,2R,2'S,3'R,4'R,7'R,8'S,10'R,12'S,13'R,14'S)-2',14'-bis(acetyloxy)-8'-chloro-3',10'-dihydroxy-4',13'-dimethyl-9'-methylidene-5'-oxo-6'-oxaspiro[oxirane-2,17'-tricyclo[11.4.0.0³,⁷]Heptadecane]-12'-yl acetate belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. (1's,2r,2's,3'r,4'r,7'r,8's,10'r,12's,13'r,14's)-12',14'-bis(acetyloxy)-8'-chloro-3',10'-dihydroxy-4',13'-dimethyl-9'-methylidene-5'-oxo-6'-oxaspiro[oxirane-2,17'-tricyclo[11.4.0.0³,⁷]heptadecan]-2'-yl acetate is found in Junceella fragilis. Based on a literature review very few articles have been published on (1'S,2R,2'S,3'R,4'R,7'R,8'S,10'R,12'S,13'R,14'S)-2',14'-bis(acetyloxy)-8'-chloro-3',10'-dihydroxy-4',13'-dimethyl-9'-methylidene-5'-oxo-6'-oxaspiro[oxirane-2,17'-tricyclo[11.4.0.0³,⁷]Heptadecane]-12'-yl acetate.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309052223372D          

 38 41  0  0  1  0            999 V2000
    5.1616    4.4113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1148    3.5876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8047    3.1353    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5415    3.5066    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    5.7580    2.3116    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3388    1.7257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9610    0.9922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3323    0.2555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3208    1.2802    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5608    0.5441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0212    1.9403    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5698    1.3976    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0702    2.1596    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2845    1.5690    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9745    1.1166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7112    1.4879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9277    0.2929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5946    2.0213    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5478    1.1976    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8111    0.8263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1212    1.2787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1680    2.1024    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4780    2.5547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7413    2.1834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6945    1.3597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0514    2.6358    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9047    2.4737    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2147    2.9260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9515    3.2973    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2615    3.7497    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3083    4.5734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6184    5.0257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0450    4.9447    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6882    3.6687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3781    3.2163    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3313    2.3926    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3715    1.1509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9191    0.4609    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  1  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  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 22 27  1  0  0  0  0
 18 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  1  1  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 29 34  1  0  0  0  0
 34 35  1  0  0  0  0
  2 35  1  0  0  0  0
 35 36  1  6  0  0  0
 19 37  1  0  0  0  0
 37 38  1  0  0  0  0
 19 38  1  6  0  0  0
M  END


  Mrv1652309052223372D          

 38 41  0  0  1  0            999 V2000
    5.1616    4.4113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1148    3.5876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8047    3.1353    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5415    3.5066    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    5.7580    2.3116    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3388    1.7257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9610    0.9922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3323    0.2555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3208    1.2802    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5608    0.5441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0212    1.9403    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5698    1.3976    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0702    2.1596    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2845    1.5690    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9745    1.1166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7112    1.4879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9277    0.2929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5946    2.0213    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5478    1.1976    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8111    0.8263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1212    1.2787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1680    2.1024    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4780    2.5547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7413    2.1834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6945    1.3597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0514    2.6358    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9047    2.4737    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2147    2.9260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9515    3.2973    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2615    3.7497    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3083    4.5734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6184    5.0257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0450    4.9447    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6882    3.6687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3781    3.2163    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3313    2.3926    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3715    1.1509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9191    0.4609    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  1  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  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 22 27  1  0  0  0  0
 18 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  1  1  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 29 34  1  0  0  0  0
 34 35  1  0  0  0  0
  2 35  1  0  0  0  0
 35 36  1  6  0  0  0
 19 37  1  0  0  0  0
 37 38  1  0  0  0  0
 19 38  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0220344

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1C(=O)O[C@H]2[C@@H](Cl)C(=C)[C@H](O)C[C@H](OC(C)=O)[C@@]3(C)[C@H](CC[C@]4(CO4)[C@@H]3[C@H](OC(C)=O)[C@]12O)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C26H35ClO11/c1-11-16(31)9-18(36-14(4)29)24(6)17(35-13(3)28)7-8-25(10-34-25)20(24)22(37-15(5)30)26(33)12(2)23(32)38-21(26)19(11)27/h12,16-22,31,33H,1,7-10H2,2-6H3/t12-,16+,17-,18-,19-,20+,21-,22-,24+,25-,26-/m0/s1

> <INCHI_KEY>
SELXBNJIEIRRMW-PPGLDISYSA-N

> <FORMULA>
C26H35ClO11

> <MOLECULAR_WEIGHT>
559.01

> <EXACT_MASS>
558.1867896

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
54.07570088346924

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1'S,2R,2'S,3'R,4'R,7'R,8'S,10'R,12'S,13'R,14'S)-12',14'-bis(acetyloxy)-8'-chloro-3',10'-dihydroxy-4',13'-dimethyl-9'-methylidene-5'-oxo-6'-oxaspiro[oxirane-2,17'-tricyclo[11.4.0.0^{3,7}]heptadecane]-2'-yl acetate

> <JCHEM_LOGP>
0.11616003266666677

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.504108887561724

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.364941018219472

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0171604064414685

> <JCHEM_POLAR_SURFACE_AREA>
158.19000000000003

> <JCHEM_REFRACTIVITY>
127.83800000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,2R,2'S,3'R,4'R,7'R,8'S,10'R,12'S,13'R,14'S)-12',14'-bis(acetyloxy)-8'-chloro-3',10'-dihydroxy-4',13'-dimethyl-9'-methylidene-5'-oxo-6'-oxaspiro[oxirane-2,17'-tricyclo[11.4.0.0^{3,7}]heptadecane]-2'-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       9.635   8.234   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.548   6.697   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.836   5.852   0.000  0.00  0.00           C+0
HETATM    4 Cl   UNK     0      12.211   6.546   0.000  0.00  0.00          Cl+0
HETATM    5  C   UNK     0      10.748   4.315   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      11.832   3.221   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      11.127   1.852   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      11.820   0.477   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       9.932   2.390   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.514   1.016   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.373   3.622   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.530   2.609   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       7.598   4.031   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       7.998   2.929   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       9.286   2.084   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.661   2.777   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       9.198   0.547   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       6.710   3.773   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.623   2.236   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.247   1.542   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.960   2.387   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.047   3.924   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.759   4.769   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.384   4.076   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.296   2.538   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.096   4.920   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       5.422   4.618   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.134   5.462   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.509   6.155   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       4.222   6.999   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       4.309   8.537   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.021   9.381   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       5.684   9.230   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       6.885   6.848   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       8.172   6.004   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       8.085   4.466   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       8.160   2.148   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       7.316   0.860   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   35                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   11                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9    5   12   13                                             
CONECT   12   11                                                            
CONECT   13   11   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   13   19   27                                                  
CONECT   19   18   20   37   38                                             
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   22   18   28   29                                             
CONECT   28   27                                                            
CONECT   29   27   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   29   35                                                       
CONECT   35   34    2   36                                                  
CONECT   36   35                                                            
CONECT   37   19   38                                                       
CONECT   38   37   19                                                       
MASTER        0    0    0    0    0    0    0    0   38    0   82    0
END

View in JSmol

Synonyms

Value	Source
(1's,2R,2's,3'r,4'r,7'r,8's,10'r,12's,13'r,14's)-2',14'-Bis(acetyloxy)-8'-chloro-3',10'-dihydroxy-4',13'-dimethyl-9'-methylidene-5'-oxo-6'-oxaspiro[oxirane-2,17'-tricyclo[11.4.0.0,]heptadecane]-12'-yl acetic acid	Generator

Chemical Formula

C₂₆H₃₅ClO₁₁

Average Mass

559.0100 Da

Monoisotopic Mass

558.18679 Da

IUPAC Name

(1'S,2R,2'S,3'R,4'R,7'R,8'S,10'R,12'S,13'R,14'S)-12',14'-bis(acetyloxy)-8'-chloro-3',10'-dihydroxy-4',13'-dimethyl-9'-methylidene-5'-oxo-6'-oxaspiro[oxirane-2,17'-tricyclo[11.4.0.0^{3,7}]heptadecane]-2'-yl acetate

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@H]1C(=O)O[C@H]2[C@@H](Cl)C(=C)[C@H](O)C[C@H](OC(C)=O)[C@@]3(C)[C@H](CC[C@]4(CO4)[C@@H]3[C@H](OC(C)=O)[C@]12O)OC(C)=O

InChI Identifier

InChI=1S/C26H35ClO11/c1-11-16(31)9-18(36-14(4)29)24(6)17(35-13(3)28)7-8-25(10-34-25)20(24)22(37-15(5)30)26(33)12(2)23(32)38-21(26)19(11)27/h12,16-22,31,33H,1,7-10H2,2-6H3/t12-,16+,17-,18-,19-,20+,21-,22-,24+,25-,26-/m0/s1

InChI Key

SELXBNJIEIRRMW-PPGLDISYSA-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
Junceella fragilis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpene lactone
Diterpenoid
Briarane diterpenoid
Tetracarboxylic acid or derivatives
Gamma butyrolactone
Tertiary alcohol
Tetrahydrofuran
Carboxylic acid ester
Lactone
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Organohalogen compound
Carbonyl group
Alkyl halide
Alkyl chloride
Organochloride
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	0.12	ChemAxon
pKa (Strongest Acidic)	12.36	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	158.19 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	127.84 m³·mol⁻¹	ChemAxon
Polarizability	54.08 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

163032987

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1's,2r,2's,3'r,4'r,7'r,8's,10'r,12's,13'r,14's)-12',14'-bis(acetyloxy)-8'-chloro-3',10'-dihydroxy-4',13'-dimethyl-9'-methylidene-5'-oxo-6'-oxaspiro[oxirane-2,17'-tricyclo[11.4.0.0³,⁷]heptadecan]-2'-yl acetate (NP0220344)

MOL for NP0220344 ((1's,2r,2's,3'r,4'r,7'r,8's,10'r,12's,13'r,14's)-12',14'-bis(acetyloxy)-8'-chloro-3',10'-dihydroxy-4',13'-dimethyl-9'-methylidene-5'-oxo-6'-oxaspiro[oxirane-2,17'-tricyclo[11.4.0.0³,⁷]heptadecan]-2'-yl acetate)

3D MOL for NP0220344 ((1's,2r,2's,3'r,4'r,7'r,8's,10'r,12's,13'r,14's)-12',14'-bis(acetyloxy)-8'-chloro-3',10'-dihydroxy-4',13'-dimethyl-9'-methylidene-5'-oxo-6'-oxaspiro[oxirane-2,17'-tricyclo[11.4.0.0³,⁷]heptadecan]-2'-yl acetate)

3D SDF for NP0220344 ((1's,2r,2's,3'r,4'r,7'r,8's,10'r,12's,13'r,14's)-12',14'-bis(acetyloxy)-8'-chloro-3',10'-dihydroxy-4',13'-dimethyl-9'-methylidene-5'-oxo-6'-oxaspiro[oxirane-2,17'-tricyclo[11.4.0.0³,⁷]heptadecan]-2'-yl acetate)

3D-SDF for NP0220344 ((1's,2r,2's,3'r,4'r,7'r,8's,10'r,12's,13'r,14's)-12',14'-bis(acetyloxy)-8'-chloro-3',10'-dihydroxy-4',13'-dimethyl-9'-methylidene-5'-oxo-6'-oxaspiro[oxirane-2,17'-tricyclo[11.4.0.0³,⁷]heptadecan]-2'-yl acetate)

PDB for NP0220344 ((1's,2r,2's,3'r,4'r,7'r,8's,10'r,12's,13'r,14's)-12',14'-bis(acetyloxy)-8'-chloro-3',10'-dihydroxy-4',13'-dimethyl-9'-methylidene-5'-oxo-6'-oxaspiro[oxirane-2,17'-tricyclo[11.4.0.0³,⁷]heptadecan]-2'-yl acetate)

3D PDB for NP0220344 ((1's,2r,2's,3'r,4'r,7'r,8's,10'r,12's,13'r,14's)-12',14'-bis(acetyloxy)-8'-chloro-3',10'-dihydroxy-4',13'-dimethyl-9'-methylidene-5'-oxo-6'-oxaspiro[oxirane-2,17'-tricyclo[11.4.0.0³,⁷]heptadecan]-2'-yl acetate)

SMILES for NP0220344 ((1's,2r,2's,3'r,4'r,7'r,8's,10'r,12's,13'r,14's)-12',14'-bis(acetyloxy)-8'-chloro-3',10'-dihydroxy-4',13'-dimethyl-9'-methylidene-5'-oxo-6'-oxaspiro[oxirane-2,17'-tricyclo[11.4.0.0³,⁷]heptadecan]-2'-yl acetate)

INCHI for NP0220344 ((1's,2r,2's,3'r,4'r,7'r,8's,10'r,12's,13'r,14's)-12',14'-bis(acetyloxy)-8'-chloro-3',10'-dihydroxy-4',13'-dimethyl-9'-methylidene-5'-oxo-6'-oxaspiro[oxirane-2,17'-tricyclo[11.4.0.0³,⁷]heptadecan]-2'-yl acetate)

Structure for NP0220344 ((1's,2r,2's,3'r,4'r,7'r,8's,10'r,12's,13'r,14's)-12',14'-bis(acetyloxy)-8'-chloro-3',10'-dihydroxy-4',13'-dimethyl-9'-methylidene-5'-oxo-6'-oxaspiro[oxirane-2,17'-tricyclo[11.4.0.0³,⁷]heptadecan]-2'-yl acetate)

3D Structure for NP0220344 ((1's,2r,2's,3'r,4'r,7'r,8's,10'r,12's,13'r,14's)-12',14'-bis(acetyloxy)-8'-chloro-3',10'-dihydroxy-4',13'-dimethyl-9'-methylidene-5'-oxo-6'-oxaspiro[oxirane-2,17'-tricyclo[11.4.0.0³,⁷]heptadecan]-2'-yl acetate)