NP-MRD: Showing NP-Card for aracarpene-1 (NP0039828)

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Record Information

Version

2.0

Created at

2021-06-20 22:08:52 UTC

Updated at

2021-06-30 00:13:22 UTC

NP-MRD ID

NP0039828

Secondary Accession Numbers

None

Natural Product Identification

Common Name

aracarpene-1

Provided By

JEOL Database JEOL Logo

Description

Aracarpene 1 belongs to the class of organic compounds known as pterocarpans. These are benzo-pyrano-furano-benzene compounds, containing the 6H-[1]benzofuro[3,2-c]chromene skeleton. They are derivatives of isoflavonoids. aracarpene-1 is found in Arachis hypogaea and Aspergillus caelatus. aracarpene-1 was first documented in 2010 (PMID: 21030054). Based on a literature review very few articles have been published on Aracarpene 1.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212100083D          

 34 37  0  0  0  0            999 V2000
    4.8853   -1.3444   -3.1413 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8306   -0.2069   -2.2881 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7553   -0.1204   -1.4362 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7166   -1.0512   -1.3383 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6578   -0.8679   -0.4294 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6482    0.2731    0.3933 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7980    0.8010    1.3953 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3802    1.9680    1.8018 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5281    2.2316    1.1467 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6996    1.1881    0.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7554    1.0220   -0.6197 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7747    1.9390   -0.7131 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8426    2.8284    2.8117 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4405    4.0232    3.2265 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8336    4.7931    4.2228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3591    4.3599    4.7894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9481    5.1157    5.7624 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9553    3.1709    4.3775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1316    2.7926    4.9713 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3649    2.3910    3.3863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0265    1.2281    3.0411 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4697    0.3560    2.0087 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9562   -2.2699   -2.5605 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0287   -1.3676   -3.8229 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7918   -1.2624   -3.7488 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6929   -1.9425   -1.9580 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8605   -1.6034   -0.3693 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3701    1.5875   -1.4018 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3741    4.3561    2.7785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2880    5.7226    4.5534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7570    4.6210    6.0031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3700    1.9473    4.5422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3342   -0.6273    2.4721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2412    0.2551    1.2376 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 20  2  0  0  0  0
  7  6  1  0  0  0  0
 10  9  1  0  0  0  0
  9  8  1  0  0  0  0
 16 18  2  0  0  0  0
 10  6  1  0  0  0  0
 18 20  1  0  0  0  0
  6  5  2  0  0  0  0
 15 16  1  0  0  0  0
  5  4  1  0  0  0  0
 13  8  1  0  0  0  0
  4  3  2  0  0  0  0
 20 21  1  0  0  0  0
  3 11  1  0  0  0  0
 11 10  2  0  0  0  0
 21 22  1  0  0  0  0
 11 12  1  0  0  0  0
 22  7  1  0  0  0  0
  3  2  1  0  0  0  0
  8  7  2  0  0  0  0
  2  1  1  0  0  0  0
 13 14  1  0  0  0  0
 18 19  1  0  0  0  0
 14 15  2  0  0  0  0
 16 17  1  0  0  0  0
 15 30  1  0  0  0  0
 14 29  1  0  0  0  0
 22 33  1  0  0  0  0
 22 34  1  0  0  0  0
  5 27  1  0  0  0  0
  4 26  1  0  0  0  0
 12 28  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
 19 32  1  0  0  0  0
 17 31  1  0  0  0  0
M  END

     RDKit          3D

 34 37  0  0  0  0  0  0  0  0999 V2000
    4.8853   -1.3444   -3.1413 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8306   -0.2069   -2.2881 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7553   -0.1204   -1.4362 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7166   -1.0512   -1.3383 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6578   -0.8679   -0.4294 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6482    0.2731    0.3933 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7980    0.8010    1.3953 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3802    1.9680    1.8018 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5281    2.2316    1.1467 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6996    1.1881    0.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7554    1.0220   -0.6197 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7747    1.9390   -0.7131 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8426    2.8284    2.8117 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4405    4.0232    3.2265 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8336    4.7931    4.2228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3591    4.3599    4.7894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9481    5.1157    5.7624 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9553    3.1709    4.3775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1316    2.7926    4.9713 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3649    2.3910    3.3863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0265    1.2281    3.0411 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4697    0.3560    2.0087 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9562   -2.2699   -2.5605 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0287   -1.3676   -3.8229 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7918   -1.2624   -3.7488 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6929   -1.9425   -1.9580 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8605   -1.6034   -0.3693 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3701    1.5875   -1.4018 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3741    4.3561    2.7785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2880    5.7226    4.5534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7570    4.6210    6.0031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3700    1.9473    4.5422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3342   -0.6273    2.4721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2412    0.2551    1.2376 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 20  2  0
  7  6  1  0
 10  9  1  0
  9  8  1  0
 16 18  2  0
 10  6  1  0
 18 20  1  0
  6  5  2  0
 15 16  1  0
  5  4  1  0
 13  8  1  0
  4  3  2  0
 20 21  1  0
  3 11  1  0
 11 10  2  0
 21 22  1  0
 11 12  1  0
 22  7  1  0
  3  2  1  0
  8  7  2  0
  2  1  1  0
 13 14  1  0
 18 19  1  0
 14 15  2  0
 16 17  1  0
 15 30  1  0
 14 29  1  0
 22 33  1  0
 22 34  1  0
  5 27  1  0
  4 26  1  0
 12 28  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
 19 32  1  0
 17 31  1  0
M  END


  Mrv1652306212100083D          

 34 37  0  0  0  0            999 V2000
    4.8853   -1.3444   -3.1413 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8306   -0.2069   -2.2881 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7553   -0.1204   -1.4362 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7166   -1.0512   -1.3383 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6578   -0.8679   -0.4294 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6482    0.2731    0.3933 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7980    0.8010    1.3953 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3802    1.9680    1.8018 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5281    2.2316    1.1467 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6996    1.1881    0.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7554    1.0220   -0.6197 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7747    1.9390   -0.7131 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8426    2.8284    2.8117 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4405    4.0232    3.2265 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8336    4.7931    4.2228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3591    4.3599    4.7894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9481    5.1157    5.7624 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9553    3.1709    4.3775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1316    2.7926    4.9713 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3649    2.3910    3.3863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0265    1.2281    3.0411 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4697    0.3560    2.0087 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9562   -2.2699   -2.5605 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0287   -1.3676   -3.8229 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7918   -1.2624   -3.7488 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6929   -1.9425   -1.9580 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8605   -1.6034   -0.3693 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3701    1.5875   -1.4018 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3741    4.3561    2.7785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2880    5.7226    4.5534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7570    4.6210    6.0031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3700    1.9473    4.5422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3342   -0.6273    2.4721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2412    0.2551    1.2376 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 20  2  0  0  0  0
  7  6  1  0  0  0  0
 10  9  1  0  0  0  0
  9  8  1  0  0  0  0
 16 18  2  0  0  0  0
 10  6  1  0  0  0  0
 18 20  1  0  0  0  0
  6  5  2  0  0  0  0
 15 16  1  0  0  0  0
  5  4  1  0  0  0  0
 13  8  1  0  0  0  0
  4  3  2  0  0  0  0
 20 21  1  0  0  0  0
  3 11  1  0  0  0  0
 11 10  2  0  0  0  0
 21 22  1  0  0  0  0
 11 12  1  0  0  0  0
 22  7  1  0  0  0  0
  3  2  1  0  0  0  0
  8  7  2  0  0  0  0
  2  1  1  0  0  0  0
 13 14  1  0  0  0  0
 18 19  1  0  0  0  0
 14 15  2  0  0  0  0
 16 17  1  0  0  0  0
 15 30  1  0  0  0  0
 14 29  1  0  0  0  0
 22 33  1  0  0  0  0
 22 34  1  0  0  0  0
  5 27  1  0  0  0  0
  4 26  1  0  0  0  0
 12 28  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
 19 32  1  0  0  0  0
 17 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0039828

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C(O[H])C2=C(C([H])=C1[H])C1=C(C3=C([H])C([H])=C(OC([H])([H])[H])C(O[H])=C3O1)C([H])([H])O2

> <INCHI_IDENTIFIER>
InChI=1S/C16H12O6/c1-20-11-5-3-7-9-6-21-15-8(2-4-10(17)12(15)18)14(9)22-16(7)13(11)19/h2-5,17-19H,6H2,1H3

> <INCHI_KEY>
LVXFNHZELZMOCC-UHFFFAOYSA-N

> <FORMULA>
C16H12O6

> <MOLECULAR_WEIGHT>
300.266

> <EXACT_MASS>
300.063388106

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
30.705414501643773

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
14-methoxy-8,17-dioxatetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-1(10),2(7),3,5,11,13,15-heptaene-5,6,15-triol

> <ALOGPS_LOGP>
2.52

> <JCHEM_LOGP>
2.2247845073333328

> <ALOGPS_LOGS>
-2.62

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.188008988377351

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.87740946441714

> <JCHEM_PKA_STRONGEST_BASIC>
-2.932712787665742

> <JCHEM_POLAR_SURFACE_AREA>
92.29

> <JCHEM_REFRACTIVITY>
77.3365

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.25e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
14-methoxy-8,17-dioxatetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-1(10),2(7),3,5,11,13,15-heptaene-5,6,15-triol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 34 37  0  0  0  0  0  0  0  0999 V2000
    4.8853   -1.3444   -3.1413 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8306   -0.2069   -2.2881 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7553   -0.1204   -1.4362 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7166   -1.0512   -1.3383 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6578   -0.8679   -0.4294 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6482    0.2731    0.3933 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7980    0.8010    1.3953 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3802    1.9680    1.8018 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5281    2.2316    1.1467 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6996    1.1881    0.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7554    1.0220   -0.6197 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7747    1.9390   -0.7131 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8426    2.8284    2.8117 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4405    4.0232    3.2265 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8336    4.7931    4.2228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3591    4.3599    4.7894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9481    5.1157    5.7624 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9553    3.1709    4.3775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1316    2.7926    4.9713 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3649    2.3910    3.3863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0265    1.2281    3.0411 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4697    0.3560    2.0087 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9562   -2.2699   -2.5605 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0287   -1.3676   -3.8229 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7918   -1.2624   -3.7488 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6929   -1.9425   -1.9580 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8605   -1.6034   -0.3693 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3701    1.5875   -1.4018 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3741    4.3561    2.7785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2880    5.7226    4.5534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7570    4.6210    6.0031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3700    1.9473    4.5422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3342   -0.6273    2.4721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2412    0.2551    1.2376 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 20  2  0
  7  6  1  0
 10  9  1  0
  9  8  1  0
 16 18  2  0
 10  6  1  0
 18 20  1  0
  6  5  2  0
 15 16  1  0
  5  4  1  0
 13  8  1  0
  4  3  2  0
 20 21  1  0
  3 11  1  0
 11 10  2  0
 21 22  1  0
 11 12  1  0
 22  7  1  0
  3  2  1  0
  8  7  2  0
  2  1  1  0
 13 14  1  0
 18 19  1  0
 14 15  2  0
 16 17  1  0
 15 30  1  0
 14 29  1  0
 22 33  1  0
 22 34  1  0
  5 27  1  0
  4 26  1  0
 12 28  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
 19 32  1  0
 17 31  1  0
M  END

HEADER    PROTEIN                                 21-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   21-JUN-21         0                                  
HETATM    1  C   UNK     0       4.885  -1.344  -3.141  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.831  -0.207  -2.288  0.00  0.00           O+0
HETATM    3  C   UNK     0       3.755  -0.120  -1.436  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.717  -1.051  -1.338  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.658  -0.868  -0.429  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.648   0.273   0.393  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.798   0.801   1.395  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.380   1.968   1.802  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.528   2.232   1.147  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.700   1.188   0.275  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.755   1.022  -0.620  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.775   1.939  -0.713  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.843   2.828   2.812  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.440   4.023   3.227  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.834   4.793   4.223  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.359   4.360   4.789  0.00  0.00           C+0
HETATM   17  O   UNK     0      -0.948   5.116   5.762  0.00  0.00           O+0
HETATM   18  C   UNK     0      -0.955   3.171   4.378  0.00  0.00           C+0
HETATM   19  O   UNK     0      -2.132   2.793   4.971  0.00  0.00           O+0
HETATM   20  C   UNK     0      -0.365   2.391   3.386  0.00  0.00           C+0
HETATM   21  O   UNK     0      -1.026   1.228   3.041  0.00  0.00           O+0
HETATM   22  C   UNK     0      -0.470   0.356   2.009  0.00  0.00           C+0
HETATM   23  H   UNK     0       4.956  -2.270  -2.561  0.00  0.00           H+0
HETATM   24  H   UNK     0       4.029  -1.368  -3.823  0.00  0.00           H+0
HETATM   25  H   UNK     0       5.792  -1.262  -3.749  0.00  0.00           H+0
HETATM   26  H   UNK     0       2.693  -1.942  -1.958  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.861  -1.603  -0.369  0.00  0.00           H+0
HETATM   28  H   UNK     0       5.370   1.587  -1.402  0.00  0.00           H+0
HETATM   29  H   UNK     0       2.374   4.356   2.779  0.00  0.00           H+0
HETATM   30  H   UNK     0       1.288   5.723   4.553  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.757   4.621   6.003  0.00  0.00           H+0
HETATM   32  H   UNK     0      -2.370   1.947   4.542  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.334  -0.627   2.472  0.00  0.00           H+0
HETATM   34  H   UNK     0      -1.241   0.255   1.238  0.00  0.00           H+0
CONECT    1    2   23   24   25                                             
CONECT    2    3    1                                                       
CONECT    3    4   11    2                                                  
CONECT    4    5    3   26                                                  
CONECT    5    6    4   27                                                  
CONECT    6    7   10    5                                                  
CONECT    7    6   22    8                                                  
CONECT    8    9   13    7                                                  
CONECT    9   10    8                                                       
CONECT   10    9    6   11                                                  
CONECT   11    3   10   12                                                  
CONECT   12   11   28                                                       
CONECT   13   20    8   14                                                  
CONECT   14   13   15   29                                                  
CONECT   15   16   14   30                                                  
CONECT   16   18   15   17                                                  
CONECT   17   16   31                                                       
CONECT   18   16   20   19                                                  
CONECT   19   18   32                                                       
CONECT   20   13   18   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21    7   33   34                                             
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    4                                                            
CONECT   27    5                                                            
CONECT   28   12                                                            
CONECT   29   14                                                            
CONECT   30   15                                                            
CONECT   31   17                                                            
CONECT   32   19                                                            
CONECT   33   22                                                            
CONECT   34   22                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

RDKit          3D

34 37  0  0  0  0  0  0  0  0999 V2000
    4.8853   -1.3444   -3.1413 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8306   -0.2069   -2.2881 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7553   -0.1204   -1.4362 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7166   -1.0512   -1.3383 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6578   -0.8679   -0.4294 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6482    0.2731    0.3933 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7980    0.8010    1.3953 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3802    1.9680    1.8018 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5281    2.2316    1.1467 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6996    1.1881    0.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7554    1.0220   -0.6197 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7747    1.9390   -0.7131 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8426    2.8284    2.8117 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4405    4.0232    3.2265 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8336    4.7931    4.2228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3591    4.3599    4.7894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9481    5.1157    5.7624 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9553    3.1709    4.3775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1316    2.7926    4.9713 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3649    2.3910    3.3863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0265    1.2281    3.0411 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4697    0.3560    2.0087 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9562   -2.2699   -2.5605 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0287   -1.3676   -3.8229 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7918   -1.2624   -3.7488 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6929   -1.9425   -1.9580 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8605   -1.6034   -0.3693 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3701    1.5875   -1.4018 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3741    4.3561    2.7785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2880    5.7226    4.5534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7570    4.6210    6.0031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3700    1.9473    4.5422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3342   -0.6273    2.4721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2412    0.2551    1.2376 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 20  2  0
  7  6  1  0
 10  9  1  0
  9  8  1  0
 16 18  2  0
 10  6  1  0
 18 20  1  0
  6  5  2  0
 15 16  1  0
  5  4  1  0
 13  8  1  0
  4  3  2  0
 20 21  1  0
  3 11  1  0
 11 10  2  0
 21 22  1  0
 11 12  1  0
 22  7  1  0
  3  2  1  0
  8  7  2  0
  2  1  1  0
 13 14  1  0
 18 19  1  0
 14 15  2  0
 16 17  1  0
 15 30  1  0
 14 29  1  0
 22 33  1  0
 22 34  1  0
  5 27  1  0
  4 26  1  0
 12 28  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
 19 32  1  0
 17 31  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₁₆H₁₂O₆

Average Mass

300.2660 Da

Monoisotopic Mass

300.06339 Da

IUPAC Name

14-methoxy-8,17-dioxatetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-1(10),2(7),3,5,11,13,15-heptaene-5,6,15-triol

Traditional Name

14-methoxy-8,17-dioxatetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-1(10),2(7),3,5,11,13,15-heptaene-5,6,15-triol

CAS Registry Number

Not Available

SMILES

[H]OC1=C(O[H])C2=C(C([H])=C1[H])C1=C(C3=C([H])C([H])=C(OC([H])([H])[H])C(O[H])=C3O1)C([H])([H])O2

InChI Identifier

InChI=1S/C16H12O6/c1-20-11-5-3-7-9-6-21-15-8(2-4-10(17)12(15)18)14(9)22-16(7)13(11)19/h2-5,17-19H,6H2,1H3

InChI Key

LVXFNHZELZMOCC-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, 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, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Arachis hypogaea	Plant	KNApSAcK
Aspergillus caelatus	JEOL database	Sobolev, V.S., et al, Phytochem. 71, 2099 (2010)

Chemical Taxonomy

Classification

Not classified

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	2.52	ALOGPS
logP	2.22	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	7.88	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	92.29 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	77.34 m³·mol⁻¹	ChemAxon
Polarizability	30.71 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

28288191

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

50908262

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Sobolev VS, Neff SA, Gloer JB, Khan SI, Tabanca N, De Lucca AJ, Wedge DE: Pterocarpenes elicited by Aspergillus caelatus in peanut (Arachis hypogaea) seeds. Phytochemistry. 2010 Dec;71(17-18):2099-107. doi: 10.1016/j.phytochem.2010.09.018. Epub 2010 Oct 26. [PubMed:21030054 ]
Sobolev, V.S., et al. (2010). Sobolev, V.S., et al, Phytochem. 71, 2099 (2010). Phytochem..

Showing NP-Card for aracarpene-1 (NP0039828)

MOL for NP0039828 (aracarpene-1)

3D MOL for NP0039828 (aracarpene-1)

3D SDF for NP0039828 (aracarpene-1)

3D-SDF for NP0039828 (aracarpene-1)

PDB for NP0039828 (aracarpene-1)

3D PDB for NP0039828 (aracarpene-1)

SMILES for NP0039828 (aracarpene-1)

INCHI for NP0039828 (aracarpene-1)

Structure for NP0039828 (aracarpene-1)

3D Structure for NP0039828 (aracarpene-1)