NP-MRD: Showing NP-Card for (1r,2r,3r,5r,7s,8r,11r,12r,13s,14s,15s,16r,18s)-2,15,16,18-tetrakis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9-dioxatetracyclo[12.4.0.0³,⁵.0⁸,¹²]octadecan-13-yl acetate (NP0326058)

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Record Information

Version

2.0

Created at

2022-09-12 07:17:16 UTC

Updated at

2022-09-12 07:17:16 UTC

NP-MRD ID

NP0326058

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,3r,5r,7s,8r,11r,12r,13s,14s,15s,16r,18s)-2,15,16,18-tetrakis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9-dioxatetracyclo[12.4.0.0³,⁵.0⁸,¹²]octadecan-13-yl acetate

Description

Briarein D belongs to the class of organic compounds known as hexacarboxylic acids and derivatives. These are carboxylic acids containing exactly six carboxyl groups. (1r,2r,3r,5r,7s,8r,11r,12r,13s,14s,15s,16r,18s)-2,15,16,18-tetrakis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9-dioxatetracyclo[12.4.0.0³,⁵.0⁸,¹²]octadecan-13-yl acetate is found in Briareum asbestinum. Based on a literature review very few articles have been published on Briarein D.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122209172D          

 45 48  0  0  1  0            999 V2000
    2.5524    0.5415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7821   -0.2509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6066   -0.2773    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8865    0.4988    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    4.2582   -0.7833    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9408   -0.3200    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5924   -0.8260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3848   -0.5963    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3125   -1.6021    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7758   -2.2847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4879   -1.5757    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9512   -2.2583    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2080   -2.3517    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8596   -2.8578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7471   -3.6751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9831   -3.9863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3987   -4.1811    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5254   -2.8151    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9148   -3.5424    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5634   -3.0326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5295   -4.0926    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3134   -3.8354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4826   -3.0279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9281   -4.3856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4797   -4.2433    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8691   -4.9706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4339   -5.6715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8234   -6.3988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6094   -5.6451    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6551   -4.2169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2657   -3.4896    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4411   -3.4632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0059   -4.1641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3953   -4.8914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1813   -4.1377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7008   -2.7887    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8888   -2.9343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0492   -2.2826    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3666   -2.7459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6241   -2.3864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0586   -2.8498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5641   -1.5636    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8195   -1.4902    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2874   -0.8598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0994   -0.7142    0.0000 C   0  0  2  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  1  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
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 27 28  1  0  0  0  0
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 25 30  1  0  0  0  0
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 31 32  1  6  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  2  0  0  0  0
 31 36  1  0  0  0  0
 18 36  1  0  0  0  0
 36 37  1  1  0  0  0
 36 38  1  0  0  0  0
 38 39  1  1  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  2  0  0  0  0
 38 43  1  0  0  0  0
 43 44  1  6  0  0  0
 45 44  1  6  0  0  0
  2 45  1  0  0  0  0
 43 45  1  0  0  0  0
M  END

     RDKit          3D

 84 87  0  0  0  0  0  0  0  0999 V2000
   -3.7604    3.2106   -1.4730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5030    2.1862   -0.6824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6436    0.8269   -1.2955 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8598    0.0300   -0.2502 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -2.4190    0.0822   -1.5764 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5227   -0.5260   -2.8888 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8104   -1.8657   -2.7378 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6523   -2.5574   -3.3597 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8606   -2.2688   -1.6466 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2988   -3.5486   -0.9914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9806   -1.0441   -0.7335 C   0  0  2  0  0  0  0  0  0  0  0  0
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    3.5569   -1.3971    0.4082 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8913   -1.6420    0.1332 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.4764   -0.8538   -0.6466 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6526    0.5865    1.0868 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6422    1.6284    1.1094 C   0  0  2  0  0  0  0  0  0  0  0  0
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    1.7498    3.8026    2.9025 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9711    2.0743   -1.0691 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.1793    5.3912   -1.7431 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.1475   -1.4372   -2.7439 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.5771    2.3631    4.4937 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.1724    2.3515   -1.7739 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.2455    3.1135   -0.6588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1572    3.0647    1.1676 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.3064    6.0308   -1.9861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4346    4.7458   -2.6030 H   0  0  0  0  0  0  0  0  0  0  0  0
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  9  7  1  0
  7  8  2  0
  7  6  1  0
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 12 54  1  0
 34 73  1  0
 34 74  1  0
 34 75  1  0
M  END


  Mrv1652309122209172D          

 45 48  0  0  1  0            999 V2000
    2.5524    0.5415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7821   -0.2509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6066   -0.2773    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8865    0.4988    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    4.2582   -0.7833    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9408   -0.3200    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5924   -0.8260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3848   -0.5963    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3125   -1.6021    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    4.9512   -2.2583    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2080   -2.3517    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8596   -2.8578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7471   -3.6751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9831   -3.9863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3987   -4.1811    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5254   -2.8151    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9148   -3.5424    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5634   -3.0326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5295   -4.0926    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3134   -3.8354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4826   -3.0279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9281   -4.3856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4797   -4.2433    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8691   -4.9706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4339   -5.6715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8234   -6.3988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6094   -5.6451    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6551   -4.2169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2657   -3.4896    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4411   -3.4632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0059   -4.1641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3953   -4.8914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1813   -4.1377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7008   -2.7887    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8888   -2.9343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0492   -2.2826    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3666   -2.7459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6241   -2.3864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0586   -2.8498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5641   -1.5636    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8195   -1.4902    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2874   -0.8598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0994   -0.7142    0.0000 C   0  0  2  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  1  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  1  0  0  0
 19 21  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 19 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 25 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  6  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  2  0  0  0  0
 31 36  1  0  0  0  0
 18 36  1  0  0  0  0
 36 37  1  1  0  0  0
 36 38  1  0  0  0  0
 38 39  1  1  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  2  0  0  0  0
 38 43  1  0  0  0  0
 43 44  1  6  0  0  0
 45 44  1  6  0  0  0
  2 45  1  0  0  0  0
 43 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0326058

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1C(=O)O[C@H]2[C@@H](Cl)C(=C)[C@H]3O[C@H]3[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/C30H39ClO14/c1-11-20(31)24-30(38,12(2)27(37)44-24)26(42-16(6)35)23-28(8,25(41-15(5)34)22-21(11)43-22)18(39-13(3)32)10-19(40-14(4)33)29(23,9)45-17(7)36/h12,18-26,38H,1,10H2,2-9H3/t12-,18-,19+,20-,21+,22+,23+,24-,25-,26-,28-,29+,30-/m0/s1

> <INCHI_KEY>
SDYQCNCTAOUPSK-SIZDLAHDSA-N

> <FORMULA>
C30H39ClO14

> <MOLECULAR_WEIGHT>
659.08

> <EXACT_MASS>
658.2028336

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
62.38113403720905

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,3R,5R,7S,8R,11R,12R,13S,14S,15S,16R,18S)-2,15,16,18-tetrakis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9-dioxatetracyclo[12.4.0.0^{3,5}.0^{8,12}]octadecan-13-yl acetate

> <JCHEM_LOGP>
0.2073285260000004

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.368094308310742

> <JCHEM_PKA_STRONGEST_BASIC>
-3.949995549544881

> <JCHEM_POLAR_SURFACE_AREA>
190.56

> <JCHEM_REFRACTIVITY>
147.0123

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,3R,5R,7S,8R,11R,12R,13S,14S,15S,16R,18S)-2,15,16,18-tetrakis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9-dioxatetracyclo[12.4.0.0^{3,5}.0^{8,12}]octadecan-13-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       4.764   1.011   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.193  -0.468   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.732  -0.518   0.000  0.00  0.00           C+0
HETATM    4 Cl   UNK     0       7.255   0.931   0.000  0.00  0.00          Cl+0
HETATM    5  C   UNK     0       7.949  -1.462   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       9.223  -0.597   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      10.439  -1.542   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      11.918  -1.113   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       9.917  -2.991   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.782  -4.265   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.377  -2.941   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       9.242  -4.215   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       7.855  -4.390   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       9.071  -5.335   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       8.861  -6.860   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.435  -7.441   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      10.078  -7.805   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       6.581  -5.255   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.308  -6.612   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.518  -5.661   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.455  -7.640   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.918  -7.159   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.234  -5.652   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      11.066  -8.187   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       6.495  -7.921   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       7.222  -9.278   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       6.410 -10.587   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.137 -11.944   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.871 -10.537   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       4.956  -7.871   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.229  -6.514   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       2.690  -6.465   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       1.878  -7.773   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.605  -9.131   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       0.339  -7.724   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       5.041  -5.205   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       3.526  -5.477   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       3.825  -4.261   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       2.551  -5.126   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       1.165  -4.455   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -0.109  -5.320   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       1.053  -2.919   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       3.396  -2.782   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       2.403  -1.605   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       3.919  -1.333   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   45                                                  
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   36                                                  
CONECT   19   18   20   21   25                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   19   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   25   31                                                       
CONECT   31   30   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36   31   18   37   38                                             
CONECT   37   36                                                            
CONECT   38   36   39   43                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40                                                            
CONECT   43   38   44   45                                                  
CONECT   44   43   45                                                       
CONECT   45   44    2   43                                                  
MASTER        0    0    0    0    0    0    0    0   45    0   96    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₃₉ClO₁₄

Average Mass

659.0800 Da

Monoisotopic Mass

658.20283 Da

IUPAC Name

(1R,2R,3R,5R,7S,8R,11R,12R,13S,14S,15S,16R,18S)-2,15,16,18-tetrakis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9-dioxatetracyclo[12.4.0.0^{3,5}.0^{8,12}]octadecan-13-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]3O[C@H]3[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/C30H39ClO14/c1-11-20(31)24-30(38,12(2)27(37)44-24)26(42-16(6)35)23-28(8,25(41-15(5)34)22-21(11)43-22)18(39-13(3)32)10-19(40-14(4)33)29(23,9)45-17(7)36/h12,18-26,38H,1,10H2,2-9H3/t12-,18-,19+,20-,21+,22+,23+,24-,25-,26-,28-,29+,30-/m0/s1

InChI Key

SDYQCNCTAOUPSK-SIZDLAHDSA-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 hexacarboxylic acids and derivatives. These are carboxylic acids containing exactly six carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Hexacarboxylic acids and derivatives

Direct Parent

Hexacarboxylic acids and derivatives

Alternative Parents

Substituents

Hexacarboxylic acid or derivatives
Gamma butyrolactone
Cyclitol or derivatives
Tetrahydrofuran
Tertiary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organochloride
Organohalogen compound
Carbonyl group
Alkyl halide
Alkyl chloride
Alcohol
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	0.21	ChemAxon
pKa (Strongest Acidic)	12.37	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	190.56 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	147.01 m³·mol⁻¹	ChemAxon
Polarizability	62.38 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

10200284

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21585461

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,3r,5r,7s,8r,11r,12r,13s,14s,15s,16r,18s)-2,15,16,18-tetrakis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9-dioxatetracyclo[12.4.0.0³,⁵.0⁸,¹²]octadecan-13-yl acetate (NP0326058)

MOL for NP0326058 ((1r,2r,3r,5r,7s,8r,11r,12r,13s,14s,15s,16r,18s)-2,15,16,18-tetrakis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9-dioxatetracyclo[12.4.0.0³,⁵.0⁸,¹²]octadecan-13-yl acetate)

3D MOL for NP0326058 ((1r,2r,3r,5r,7s,8r,11r,12r,13s,14s,15s,16r,18s)-2,15,16,18-tetrakis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9-dioxatetracyclo[12.4.0.0³,⁵.0⁸,¹²]octadecan-13-yl acetate)

3D SDF for NP0326058 ((1r,2r,3r,5r,7s,8r,11r,12r,13s,14s,15s,16r,18s)-2,15,16,18-tetrakis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9-dioxatetracyclo[12.4.0.0³,⁵.0⁸,¹²]octadecan-13-yl acetate)

3D-SDF for NP0326058 ((1r,2r,3r,5r,7s,8r,11r,12r,13s,14s,15s,16r,18s)-2,15,16,18-tetrakis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9-dioxatetracyclo[12.4.0.0³,⁵.0⁸,¹²]octadecan-13-yl acetate)

PDB for NP0326058 ((1r,2r,3r,5r,7s,8r,11r,12r,13s,14s,15s,16r,18s)-2,15,16,18-tetrakis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9-dioxatetracyclo[12.4.0.0³,⁵.0⁸,¹²]octadecan-13-yl acetate)

3D PDB for NP0326058 ((1r,2r,3r,5r,7s,8r,11r,12r,13s,14s,15s,16r,18s)-2,15,16,18-tetrakis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9-dioxatetracyclo[12.4.0.0³,⁵.0⁸,¹²]octadecan-13-yl acetate)

SMILES for NP0326058 ((1r,2r,3r,5r,7s,8r,11r,12r,13s,14s,15s,16r,18s)-2,15,16,18-tetrakis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9-dioxatetracyclo[12.4.0.0³,⁵.0⁸,¹²]octadecan-13-yl acetate)

INCHI for NP0326058 ((1r,2r,3r,5r,7s,8r,11r,12r,13s,14s,15s,16r,18s)-2,15,16,18-tetrakis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9-dioxatetracyclo[12.4.0.0³,⁵.0⁸,¹²]octadecan-13-yl acetate)

Structure for NP0326058 ((1r,2r,3r,5r,7s,8r,11r,12r,13s,14s,15s,16r,18s)-2,15,16,18-tetrakis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9-dioxatetracyclo[12.4.0.0³,⁵.0⁸,¹²]octadecan-13-yl acetate)

3D Structure for NP0326058 ((1r,2r,3r,5r,7s,8r,11r,12r,13s,14s,15s,16r,18s)-2,15,16,18-tetrakis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9-dioxatetracyclo[12.4.0.0³,⁵.0⁸,¹²]octadecan-13-yl acetate)