NP-MRD: Showing NP-Card for (1s,2s,3r,4r,7r,8s,10z,12s,13r,14s,16r,17s)-2,14,16,17-tetrakis(acetyloxy)-8-chloro-3-hydroxy-4,13,17-trimethyl-9-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-10-en-12-yl acetate (NP0186904)

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Record Information

Version

2.0

Created at

2022-09-04 02:54:03 UTC

Updated at

2022-09-04 02:54:03 UTC

NP-MRD ID

NP0186904

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,3r,4r,7r,8s,10z,12s,13r,14s,16r,17s)-2,14,16,17-tetrakis(acetyloxy)-8-chloro-3-hydroxy-4,13,17-trimethyl-9-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-10-en-12-yl acetate

Description

Briarein A belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. (1s,2s,3r,4r,7r,8s,10z,12s,13r,14s,16r,17s)-2,14,16,17-tetrakis(acetyloxy)-8-chloro-3-hydroxy-4,13,17-trimethyl-9-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-10-en-12-yl acetate is found in Briareum asbestinum. Based on a literature review very few articles have been published on Briarein A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042204542D          

 44 46  0  0  1  0            999 V2000
    2.8939    2.1648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3972    1.5112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1744    1.7879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9659    1.5549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4692    0.9013    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2464    1.1780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3954    1.9894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7671    2.5241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1726    2.2661    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4922    0.0766    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0897    0.6455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3148    0.0133    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.7809    0.6940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6035    0.6306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0696    1.3113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9599   -0.1134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6712   -0.7308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2051   -1.4115    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5616   -2.1555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3841   -2.2188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.7406   -2.9628    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1999   -1.0956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5463   -1.5990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1769   -0.2709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.9311    0.8305    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1397    1.0634    0.0000 Cl  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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  6  7  1  0  0  0  0
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 29 23  1  6  0  0  0
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 31 32  1  0  0  0  0
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 37 38  1  1  0  0  0
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 42 41  1  1  0  0  0
 35 42  1  0  0  0  0
 42 43  1  0  0  0  0
  2 43  1  0  0  0  0
 43 44  1  1  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309042204542D          

 44 46  0  0  1  0            999 V2000
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    6.6712   -0.7308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2051   -1.4115    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5616   -2.1555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3841   -2.2188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8502   -1.5381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7406   -2.9628    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3825   -1.3481    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5879   -1.5700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4630   -2.1692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7922   -2.6494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8727   -3.4705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0409   -2.3086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0261   -0.6041    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2489   -0.8808    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2719   -1.7055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9976   -2.0979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7003   -1.6657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0206   -2.9226    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4575   -0.6479    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7342   -1.4251    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9913   -1.3286    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2681   -2.1058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1999   -1.0956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5463   -1.5990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1769   -0.2709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9541    0.0058    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9311    0.8305    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1397    1.0634    0.0000 Cl  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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 12 17  1  0  0  0  0
 17 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
 20 22  2  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 29 23  1  6  0  0  0
 10 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
 30 35  1  0  0  0  0
 35 36  1  1  0  0  0
 35 37  1  0  0  0  0
 37 38  1  1  0  0  0
 37 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 42 41  1  1  0  0  0
 35 42  1  0  0  0  0
 42 43  1  0  0  0  0
  2 43  1  0  0  0  0
 43 44  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0186904

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1C(=O)O[C@H]2[C@@H](Cl)C(=C)\C=C/[C@H](OC(C)=O)[C@@]3(C)[C@H](C[C@@H](OC(C)=O)[C@@](C)(OC(C)=O)[C@@H]3[C@H](OC(C)=O)[C@]12O)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H39ClO13/c1-13-10-11-20(39-15(3)32)28(8)21(40-16(4)33)12-22(41-17(5)34)29(9,44-19(7)36)24(28)26(42-18(6)35)30(38)14(2)27(37)43-25(30)23(13)31/h10-11,14,20-26,38H,1,12H2,2-9H3/b11-10-/t14-,20-,21-,22+,23-,24+,25-,26-,28-,29+,30-/m0/s1

> <INCHI_KEY>
RLUYXGRXKZCZRM-YAHQTALESA-N

> <FORMULA>
C30H39ClO13

> <MOLECULAR_WEIGHT>
643.08

> <EXACT_MASS>
642.207919

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
62.18950497322555

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,3R,4R,7R,8S,10Z,12S,13R,14S,16R,17S)-2,14,16,17-tetrakis(acetyloxy)-8-chloro-3-hydroxy-4,13,17-trimethyl-9-methylidene-5-oxo-6-oxatricyclo[11.4.0.0^{3,7}]heptadec-10-en-12-yl acetate

> <JCHEM_LOGP>
0.8335105110000001

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.367639258661224

> <JCHEM_PKA_STRONGEST_BASIC>
-3.9501945882615788

> <JCHEM_POLAR_SURFACE_AREA>
178.03

> <JCHEM_REFRACTIVITY>
148.916

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3R,4R,7R,8S,10Z,12S,13R,14S,16R,17S)-2,14,16,17-tetrakis(acetyloxy)-8-chloro-3-hydroxy-4,13,17-trimethyl-9-methylidene-5-oxo-6-oxatricyclo[11.4.0.0^{3,7}]heptadec-10-en-12-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       5.402   4.041   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.342   2.821   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.792   3.337   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.270   2.903   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.209   1.682   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      11.660   2.199   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      11.938   3.714   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.765   4.712   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      13.389   4.230   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      10.252   0.143   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.367   1.205   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.788   0.025   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      12.658   1.295   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      14.193   1.177   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      15.063   2.448   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      14.859  -0.212   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      12.453  -1.364   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.583  -2.635   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      12.248  -4.024   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      13.784  -4.142   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      14.654  -2.871   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      14.449  -5.531   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      10.047  -2.517   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.564  -2.931   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      10.198  -4.049   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.945  -4.946   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.096  -6.478   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       7.543  -4.309   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       9.382  -1.128   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.931  -1.644   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       7.974  -3.184   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       9.329  -3.916   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      10.641  -3.109   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       9.372  -5.456   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       6.454  -1.209   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       6.970  -2.660   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       5.584  -2.480   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       6.100  -3.931   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       4.107  -2.045   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       2.886  -2.985   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0       4.064  -0.506   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       5.514   0.011   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       5.471   1.550   0.000  0.00  0.00           C+0
HETATM   44 Cl   UNK     0       3.994   1.985   0.000  0.00  0.00          Cl+0
CONECT    1    2                                                            
CONECT    2    1    3   43                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    5   11   12   29                                             
CONECT   11   10                                                            
CONECT   12   10   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   12   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   18   24   25   29                                             
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   23   10   30                                                  
CONECT   30   29   31   35                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35   30   36   37   42                                             
CONECT   36   35                                                            
CONECT   37   35   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   35   43                                                  
CONECT   43   42    2   44                                                  
CONECT   44   43                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₃₉ClO₁₃

Average Mass

643.0800 Da

Monoisotopic Mass

642.20792 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H]1C(=O)O[C@H]2[C@@H](Cl)C(=C)\C=C/[C@H](OC(C)=O)[C@@]3(C)[C@H](C[C@@H](OC(C)=O)[C@@](C)(OC(C)=O)[C@@H]3[C@H](OC(C)=O)[C@]12O)OC(C)=O

InChI Identifier

InChI=1S/C30H39ClO13/c1-13-10-11-20(39-15(3)32)28(8)21(40-16(4)33)12-22(41-17(5)34)29(9,44-19(7)36)24(28)26(42-18(6)35)30(38)14(2)27(37)43-25(30)23(13)31/h10-11,14,20-26,38H,1,12H2,2-9H3/b11-10-/t14-,20-,21-,22+,23-,24+,25-,26-,28-,29+,30-/m0/s1

InChI Key

RLUYXGRXKZCZRM-YAHQTALESA-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
Briareum asbestinum	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
Hexacarboxylic acid or derivatives
Briarane diterpenoid
Cyclitol or derivatives
Gamma butyrolactone
Tetrahydrofuran
Tertiary alcohol
Carboxylic acid ester
Lactone
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Organohalogen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Organic oxygen compound
Alkyl halide
Alkyl chloride
Organochloride
Organooxygen compound
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

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

10200281

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21585458

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,3r,4r,7r,8s,10z,12s,13r,14s,16r,17s)-2,14,16,17-tetrakis(acetyloxy)-8-chloro-3-hydroxy-4,13,17-trimethyl-9-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-10-en-12-yl acetate (NP0186904)

MOL for NP0186904 ((1s,2s,3r,4r,7r,8s,10z,12s,13r,14s,16r,17s)-2,14,16,17-tetrakis(acetyloxy)-8-chloro-3-hydroxy-4,13,17-trimethyl-9-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-10-en-12-yl acetate)

3D MOL for NP0186904 ((1s,2s,3r,4r,7r,8s,10z,12s,13r,14s,16r,17s)-2,14,16,17-tetrakis(acetyloxy)-8-chloro-3-hydroxy-4,13,17-trimethyl-9-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-10-en-12-yl acetate)

3D SDF for NP0186904 ((1s,2s,3r,4r,7r,8s,10z,12s,13r,14s,16r,17s)-2,14,16,17-tetrakis(acetyloxy)-8-chloro-3-hydroxy-4,13,17-trimethyl-9-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-10-en-12-yl acetate)

3D-SDF for NP0186904 ((1s,2s,3r,4r,7r,8s,10z,12s,13r,14s,16r,17s)-2,14,16,17-tetrakis(acetyloxy)-8-chloro-3-hydroxy-4,13,17-trimethyl-9-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-10-en-12-yl acetate)

PDB for NP0186904 ((1s,2s,3r,4r,7r,8s,10z,12s,13r,14s,16r,17s)-2,14,16,17-tetrakis(acetyloxy)-8-chloro-3-hydroxy-4,13,17-trimethyl-9-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-10-en-12-yl acetate)

3D PDB for NP0186904 ((1s,2s,3r,4r,7r,8s,10z,12s,13r,14s,16r,17s)-2,14,16,17-tetrakis(acetyloxy)-8-chloro-3-hydroxy-4,13,17-trimethyl-9-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-10-en-12-yl acetate)

SMILES for NP0186904 ((1s,2s,3r,4r,7r,8s,10z,12s,13r,14s,16r,17s)-2,14,16,17-tetrakis(acetyloxy)-8-chloro-3-hydroxy-4,13,17-trimethyl-9-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-10-en-12-yl acetate)

INCHI for NP0186904 ((1s,2s,3r,4r,7r,8s,10z,12s,13r,14s,16r,17s)-2,14,16,17-tetrakis(acetyloxy)-8-chloro-3-hydroxy-4,13,17-trimethyl-9-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-10-en-12-yl acetate)

Structure for NP0186904 ((1s,2s,3r,4r,7r,8s,10z,12s,13r,14s,16r,17s)-2,14,16,17-tetrakis(acetyloxy)-8-chloro-3-hydroxy-4,13,17-trimethyl-9-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-10-en-12-yl acetate)

3D Structure for NP0186904 ((1s,2s,3r,4r,7r,8s,10z,12s,13r,14s,16r,17s)-2,14,16,17-tetrakis(acetyloxy)-8-chloro-3-hydroxy-4,13,17-trimethyl-9-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-10-en-12-yl acetate)