NP-MRD: Showing NP-Card for Arecoic acid D (NP0011183)

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Record Information

Version

2.0

Created at

2021-01-05 20:57:49 UTC

Updated at

2021-07-15 17:08:11 UTC

NP-MRD ID

NP0011183

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Arecoic acid D

Provided By

NPAtlas

Description

Arecoic acid D, also known as arecoate D, belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups. Arecoic acid D is found in Arecophila. Based on a literature review very few articles have been published on Arecoic acid D.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242107443D          

 42 43  0  0  0  0            999 V2000
    3.7015    0.7466    0.0799 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2149    0.5624    0.0596 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6515   -0.5151   -0.3969 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4832   -1.5950   -0.9118 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9441   -2.6605   -1.3628 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8779   -1.5523   -0.9513 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1790   -0.7424   -0.4409 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2299   -0.8358   -1.8908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1277   -2.0650    0.2374 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3766   -1.9701    1.0873 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4495   -1.1448    0.4114 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0104    0.2989    0.2249 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5416    1.0765    1.4384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5757    0.8743   -0.9984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3152    0.1727   -1.7249 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3415    2.1685   -1.4125 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5258    0.3306    0.3084 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0738    1.6757   -0.0648 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4283    1.7000    0.6049 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1989    1.3966    1.9651 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9818    1.7438    0.4886 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1569   -0.0094    0.7318 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1323    0.7325   -0.9417 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3617   -1.4865   -1.8439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9710   -1.6292   -2.0733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6001    0.1523   -2.2736 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6587   -1.0890   -2.5052 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7073   -2.3401    0.9151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2224   -2.8746   -0.5161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1812   -1.5214    2.0716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7843   -2.9933    1.1940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3378   -1.1821    1.1035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8103   -1.6001   -0.5341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1623    0.4350    2.0952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1633    1.9303    1.0900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7277    1.4876    2.0559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5087    2.9947   -0.8798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2670    0.1885    1.3982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5110    2.5087    0.3653 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1845    1.7851   -1.1599 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9479    2.6700    0.4964 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8569    2.1754    2.4599 H   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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  3  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  6  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19  2  1  0  0  0  0
 17  7  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  6 24  1  0  0  0  0
  8 25  1  0  0  0  0
  8 26  1  0  0  0  0
  8 27  1  0  0  0  0
  9 28  1  0  0  0  0
  9 29  1  0  0  0  0
 10 30  1  0  0  0  0
 10 31  1  0  0  0  0
 11 32  1  0  0  0  0
 11 33  1  0  0  0  0
 13 34  1  0  0  0  0
 13 35  1  0  0  0  0
 13 36  1  0  0  0  0
 16 37  1  0  0  0  0
 17 38  1  1  0  0  0
 18 39  1  0  0  0  0
 18 40  1  0  0  0  0
 19 41  1  1  0  0  0
 20 42  1  0  0  0  0
M  END

     RDKit          3D

 42 43  0  0  0  0  0  0  0  0999 V2000
    3.7015    0.7466    0.0799 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2149    0.5624    0.0596 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6515   -0.5151   -0.3969 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4832   -1.5950   -0.9118 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9441   -2.6605   -1.3628 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8779   -1.5523   -0.9513 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1790   -0.7424   -0.4409 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2299   -0.8358   -1.8908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1277   -2.0650    0.2374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3766   -1.9701    1.0873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4495   -1.1448    0.4114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0104    0.2989    0.2249 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5416    1.0765    1.4384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5757    0.8743   -0.9984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3152    0.1727   -1.7249 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3415    2.1685   -1.4125 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5258    0.3306    0.3084 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0738    1.6757   -0.0648 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4283    1.7000    0.6049 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1989    1.3966    1.9651 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9818    1.7438    0.4886 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1569   -0.0094    0.7318 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1323    0.7325   -0.9417 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3617   -1.4865   -1.8439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9710   -1.6292   -2.0733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6001    0.1523   -2.2736 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6587   -1.0890   -2.5052 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7073   -2.3401    0.9151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2224   -2.8746   -0.5161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1812   -1.5214    2.0716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7843   -2.9933    1.1940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3378   -1.1821    1.1035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8103   -1.6001   -0.5341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1623    0.4350    2.0952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1633    1.9303    1.0900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7277    1.4876    2.0559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5087    2.9947   -0.8798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2670    0.1885    1.3982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5110    2.5087    0.3653 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1845    1.7851   -1.1599 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9479    2.6700    0.4964 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8569    2.1754    2.4599 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  3  7  1  0
  7  8  1  6
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  6
 14 15  2  0
 14 16  1  0
 12 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19  2  1  0
 17  7  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  6 24  1  0
  8 25  1  0
  8 26  1  0
  8 27  1  0
  9 28  1  0
  9 29  1  0
 10 30  1  0
 10 31  1  0
 11 32  1  0
 11 33  1  0
 13 34  1  0
 13 35  1  0
 13 36  1  0
 16 37  1  0
 17 38  1  1
 18 39  1  0
 18 40  1  0
 19 41  1  1
 20 42  1  0
M  END


  Mrv1652306242107443D          

 42 43  0  0  0  0            999 V2000
    3.7015    0.7466    0.0799 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2149    0.5624    0.0596 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6515   -0.5151   -0.3969 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4832   -1.5950   -0.9118 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9441   -2.6605   -1.3628 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8779   -1.5523   -0.9513 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1790   -0.7424   -0.4409 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2299   -0.8358   -1.8908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1277   -2.0650    0.2374 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3766   -1.9701    1.0873 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4495   -1.1448    0.4114 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0104    0.2989    0.2249 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5416    1.0765    1.4384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5757    0.8743   -0.9984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3152    0.1727   -1.7249 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3415    2.1685   -1.4125 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5258    0.3306    0.3084 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0738    1.6757   -0.0648 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4283    1.7000    0.6049 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1989    1.3966    1.9651 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9818    1.7438    0.4886 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1569   -0.0094    0.7318 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1323    0.7325   -0.9417 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3617   -1.4865   -1.8439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9710   -1.6292   -2.0733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6001    0.1523   -2.2736 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6587   -1.0890   -2.5052 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7073   -2.3401    0.9151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2224   -2.8746   -0.5161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1812   -1.5214    2.0716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7843   -2.9933    1.1940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3378   -1.1821    1.1035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8103   -1.6001   -0.5341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1623    0.4350    2.0952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1633    1.9303    1.0900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7277    1.4876    2.0559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5087    2.9947   -0.8798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2670    0.1885    1.3982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5110    2.5087    0.3653 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1845    1.7851   -1.1599 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9479    2.6700    0.4964 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8569    2.1754    2.4599 H   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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  3  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  6  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19  2  1  0  0  0  0
 17  7  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  6 24  1  0  0  0  0
  8 25  1  0  0  0  0
  8 26  1  0  0  0  0
  8 27  1  0  0  0  0
  9 28  1  0  0  0  0
  9 29  1  0  0  0  0
 10 30  1  0  0  0  0
 10 31  1  0  0  0  0
 11 32  1  0  0  0  0
 11 33  1  0  0  0  0
 13 34  1  0  0  0  0
 13 35  1  0  0  0  0
 13 36  1  0  0  0  0
 16 37  1  0  0  0  0
 17 38  1  1  0  0  0
 18 39  1  0  0  0  0
 18 40  1  0  0  0  0
 19 41  1  1  0  0  0
 20 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0011183

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)C1=C(C([H])([H])[H])[C@]([H])(O[H])C([H])([H])[C@@]2([H])[C@](C(=O)O[H])(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])[C@]12C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H22O5/c1-8-9(16)7-10-14(2,11(8)12(17)18)5-4-6-15(10,3)13(19)20/h9-10,16H,4-7H2,1-3H3,(H,17,18)(H,19,20)/t9-,10-,14+,15+/m1/s1

> <INCHI_KEY>
CEIDCYCXCMFPMO-RPVFDAQASA-N

> <FORMULA>
C15H22O5

> <MOLECULAR_WEIGHT>
282.336

> <EXACT_MASS>
282.146723808

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
29.289490903206293

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,4aS,7R,8aR)-7-hydroxy-1,4a,6-trimethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalene-1,5-dicarboxylic acid

> <ALOGPS_LOGP>
1.13

> <JCHEM_LOGP>
1.8313499640000008

> <ALOGPS_LOGS>
-1.98

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
4.81060534837352

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.111163711102738

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0036492294978974

> <JCHEM_POLAR_SURFACE_AREA>
94.83

> <JCHEM_REFRACTIVITY>
72.2323

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.96e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4aS,7R,8aR)-7-hydroxy-1,4a,6-trimethyl-2,3,4,7,8,8a-hexahydronaphthalene-1,5-dicarboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 42 43  0  0  0  0  0  0  0  0999 V2000
    3.7015    0.7466    0.0799 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2149    0.5624    0.0596 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6515   -0.5151   -0.3969 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4832   -1.5950   -0.9118 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9441   -2.6605   -1.3628 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8779   -1.5523   -0.9513 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1790   -0.7424   -0.4409 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2299   -0.8358   -1.8908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1277   -2.0650    0.2374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3766   -1.9701    1.0873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4495   -1.1448    0.4114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0104    0.2989    0.2249 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5416    1.0765    1.4384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5757    0.8743   -0.9984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3152    0.1727   -1.7249 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3415    2.1685   -1.4125 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5258    0.3306    0.3084 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0738    1.6757   -0.0648 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4283    1.7000    0.6049 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1989    1.3966    1.9651 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9818    1.7438    0.4886 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1569   -0.0094    0.7318 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1323    0.7325   -0.9417 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3617   -1.4865   -1.8439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9710   -1.6292   -2.0733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6001    0.1523   -2.2736 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6587   -1.0890   -2.5052 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7073   -2.3401    0.9151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2224   -2.8746   -0.5161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1812   -1.5214    2.0716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7843   -2.9933    1.1940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3378   -1.1821    1.1035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8103   -1.6001   -0.5341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1623    0.4350    2.0952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1633    1.9303    1.0900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7277    1.4876    2.0559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5087    2.9947   -0.8798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2670    0.1885    1.3982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5110    2.5087    0.3653 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1845    1.7851   -1.1599 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9479    2.6700    0.4964 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8569    2.1754    2.4599 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  3  7  1  0
  7  8  1  6
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  6
 14 15  2  0
 14 16  1  0
 12 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19  2  1  0
 17  7  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  6 24  1  0
  8 25  1  0
  8 26  1  0
  8 27  1  0
  9 28  1  0
  9 29  1  0
 10 30  1  0
 10 31  1  0
 11 32  1  0
 11 33  1  0
 13 34  1  0
 13 35  1  0
 13 36  1  0
 16 37  1  0
 17 38  1  1
 18 39  1  0
 18 40  1  0
 19 41  1  1
 20 42  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       3.701   0.747   0.080  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.215   0.562   0.060  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.652  -0.515  -0.397  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.483  -1.595  -0.912  0.00  0.00           C+0
HETATM    5  O   UNK     0       1.944  -2.660  -1.363  0.00  0.00           O+0
HETATM    6  O   UNK     0       3.878  -1.552  -0.951  0.00  0.00           O+0
HETATM    7  C   UNK     0       0.179  -0.742  -0.441  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.230  -0.836  -1.891  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.128  -2.065   0.237  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.377  -1.970   1.087  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.450  -1.145   0.411  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.010   0.299   0.225  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.542   1.077   1.438  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.576   0.874  -0.998  0.00  0.00           C+0
HETATM   15  O   UNK     0      -3.315   0.173  -1.725  0.00  0.00           O+0
HETATM   16  O   UNK     0      -2.341   2.168  -1.413  0.00  0.00           O+0
HETATM   17  C   UNK     0      -0.526   0.331   0.308  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.074   1.676  -0.065  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.428   1.700   0.605  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.199   1.397   1.965  0.00  0.00           O+0
HETATM   21  H   UNK     0       3.982   1.744   0.489  0.00  0.00           H+0
HETATM   22  H   UNK     0       4.157  -0.009   0.732  0.00  0.00           H+0
HETATM   23  H   UNK     0       4.132   0.733  -0.942  0.00  0.00           H+0
HETATM   24  H   UNK     0       4.362  -1.486  -1.844  0.00  0.00           H+0
HETATM   25  H   UNK     0      -0.971  -1.629  -2.073  0.00  0.00           H+0
HETATM   26  H   UNK     0      -0.600   0.152  -2.274  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.659  -1.089  -2.505  0.00  0.00           H+0
HETATM   28  H   UNK     0       0.707  -2.340   0.915  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.222  -2.875  -0.516  0.00  0.00           H+0
HETATM   30  H   UNK     0      -1.181  -1.521   2.072  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.784  -2.993   1.194  0.00  0.00           H+0
HETATM   32  H   UNK     0      -3.338  -1.182   1.103  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.810  -1.600  -0.534  0.00  0.00           H+0
HETATM   34  H   UNK     0      -3.162   0.435   2.095  0.00  0.00           H+0
HETATM   35  H   UNK     0      -3.163   1.930   1.090  0.00  0.00           H+0
HETATM   36  H   UNK     0      -1.728   1.488   2.056  0.00  0.00           H+0
HETATM   37  H   UNK     0      -2.509   2.995  -0.880  0.00  0.00           H+0
HETATM   38  H   UNK     0      -0.267   0.189   1.398  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.511   2.509   0.365  0.00  0.00           H+0
HETATM   40  H   UNK     0       0.185   1.785  -1.160  0.00  0.00           H+0
HETATM   41  H   UNK     0       1.948   2.670   0.496  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.857   2.175   2.460  0.00  0.00           H+0
CONECT    1    2   21   22   23                                             
CONECT    2    1    3   19                                                  
CONECT    3    2    4    7                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4   24                                                       
CONECT    7    3    8    9   17                                             
CONECT    8    7   25   26   27                                             
CONECT    9    7   10   28   29                                             
CONECT   10    9   11   30   31                                             
CONECT   11   10   12   32   33                                             
CONECT   12   11   13   14   17                                             
CONECT   13   12   34   35   36                                             
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   37                                                       
CONECT   17   12   18    7   38                                             
CONECT   18   17   19   39   40                                             
CONECT   19   18   20    2   41                                             
CONECT   20   19   42                                                       
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    6                                                            
CONECT   25    8                                                            
CONECT   26    8                                                            
CONECT   27    8                                                            
CONECT   28    9                                                            
CONECT   29    9                                                            
CONECT   30   10                                                            
CONECT   31   10                                                            
CONECT   32   11                                                            
CONECT   33   11                                                            
CONECT   34   13                                                            
CONECT   35   13                                                            
CONECT   36   13                                                            
CONECT   37   16                                                            
CONECT   38   17                                                            
CONECT   39   18                                                            
CONECT   40   18                                                            
CONECT   41   19                                                            
CONECT   42   20                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   86    0
END

RDKit          3D

42 43  0  0  0  0  0  0  0  0999 V2000
    3.7015    0.7466    0.0799 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2149    0.5624    0.0596 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6515   -0.5151   -0.3969 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4832   -1.5950   -0.9118 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9441   -2.6605   -1.3628 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8779   -1.5523   -0.9513 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1790   -0.7424   -0.4409 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2299   -0.8358   -1.8908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1277   -2.0650    0.2374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3766   -1.9701    1.0873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4495   -1.1448    0.4114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0104    0.2989    0.2249 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5416    1.0765    1.4384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5757    0.8743   -0.9984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3152    0.1727   -1.7249 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3415    2.1685   -1.4125 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5258    0.3306    0.3084 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0738    1.6757   -0.0648 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4283    1.7000    0.6049 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1989    1.3966    1.9651 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9818    1.7438    0.4886 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1569   -0.0094    0.7318 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1323    0.7325   -0.9417 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3617   -1.4865   -1.8439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9710   -1.6292   -2.0733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6001    0.1523   -2.2736 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6587   -1.0890   -2.5052 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7073   -2.3401    0.9151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2224   -2.8746   -0.5161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1812   -1.5214    2.0716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7843   -2.9933    1.1940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3378   -1.1821    1.1035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8103   -1.6001   -0.5341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1623    0.4350    2.0952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1633    1.9303    1.0900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7277    1.4876    2.0559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5087    2.9947   -0.8798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2670    0.1885    1.3982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5110    2.5087    0.3653 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1845    1.7851   -1.1599 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9479    2.6700    0.4964 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8569    2.1754    2.4599 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  3  7  1  0
  7  8  1  6
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  6
 14 15  2  0
 14 16  1  0
 12 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19  2  1  0
 17  7  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  6 24  1  0
  8 25  1  0
  8 26  1  0
  8 27  1  0
  9 28  1  0
  9 29  1  0
 10 30  1  0
 10 31  1  0
 11 32  1  0
 11 33  1  0
 13 34  1  0
 13 35  1  0
 13 36  1  0
 16 37  1  0
 17 38  1  1
 18 39  1  0
 18 40  1  0
 19 41  1  1
 20 42  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
Arecoate D	Generator
(1S,4AS,7R,8ar)-7-hydroxy-1,4a,6-trimethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalene-1,5-dicarboxylate	Generator

Chemical Formula

C₁₅H₂₂O₅

Average Mass

282.3360 Da

Monoisotopic Mass

282.14672 Da

IUPAC Name

(1S,4aS,7R,8aR)-7-hydroxy-1,4a,6-trimethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalene-1,5-dicarboxylic acid

Traditional Name

(1S,4aS,7R,8aR)-7-hydroxy-1,4a,6-trimethyl-2,3,4,7,8,8a-hexahydronaphthalene-1,5-dicarboxylic acid

CAS Registry Number

Not Available

SMILES

CC1=C(C(O)=O)[C@@]2(C)CCC[C@@](C)([C@@H]2C[C@H]1O)C(O)=O

InChI Identifier

InChI=1S/C15H22O5/c1-8-9(16)7-10-14(2,11(8)12(17)18)5-4-6-15(10,3)13(19)20/h9-10,16H,4-7H2,1-3H3,(H,17,18)(H,19,20)/t9-,10-,14+,15+/m1/s1

InChI Key

CEIDCYCXCMFPMO-RPVFDAQASA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Arecophila	NPAtlas	23079766

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Dicarboxylic acids and derivatives

Direct Parent

Dicarboxylic acids and derivatives

Alternative Parents

Substituents

Dicarboxylic acid or derivatives
Secondary alcohol
Carboxylic acid
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.13	ALOGPS
logP	1.83	ChemAxon
logS	-2	ALOGPS
pKa (Strongest Acidic)	4.11	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	94.83 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	72.23 m³·mol⁻¹	ChemAxon
Polarizability	29.29 Å³	ChemAxon
Number of Rings	2	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

NPAtlas ID

NPA003363

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78442281

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71545927

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Arecoic acid D (NP0011183)

MOL for NP0011183 (Arecoic acid D)

3D MOL for NP0011183 (Arecoic acid D)

3D SDF for NP0011183 (Arecoic acid D)

3D-SDF for NP0011183 (Arecoic acid D)

PDB for NP0011183 (Arecoic acid D)

3D PDB for NP0011183 (Arecoic acid D)

SMILES for NP0011183 (Arecoic acid D)

INCHI for NP0011183 (Arecoic acid D)

Structure for NP0011183 (Arecoic acid D)

3D Structure for NP0011183 (Arecoic acid D)