NP-MRD: Showing NP-Card for bauhispirorin A (NP0032933)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2021-06-19 23:37:03 UTC

Updated at

2021-06-30 00:02:25 UTC

NP-MRD ID

NP0032933

Secondary Accession Numbers

None

Natural Product Identification

Common Name

bauhispirorin A

Provided By

JEOL Database JEOL Logo

Description

bauhispirorin A is found in Bauhinia purpurea. bauhispirorin A was first documented in 2007 (Boonphong, S., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202101373D          

 33 35  0  0  0  0            999 V2000
   -0.4718    2.6106   -1.9048 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2871    3.6142   -1.2342 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1097    3.6594    0.1382 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1036    4.1072    0.9122 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9633    4.2566    2.3769 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8842    4.7661    3.0121 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3303    3.8512    3.0461 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0670    2.7693    2.2502 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4303    2.5069    2.9072 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1613    1.3477    2.2390 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2170    0.2360    1.8933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7238   -1.0097    1.4976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8589   -2.0572    1.1778 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4808   -1.8688    1.2504 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0306   -0.6299    1.6337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8343    0.4216    1.9383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2397    1.5970    2.3006 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1812    3.2920    0.8076 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2533    3.4420    0.2256 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4510    1.6571   -1.3659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4991    2.9476   -2.0684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0167    2.4510   -2.8871 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0534    4.4145    0.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0748    3.4726    4.0434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9411    4.7554    3.1535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2705    2.2419    3.9617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0662    3.4001    2.8924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6615    1.6839    1.3242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9408    0.9811    2.9178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7984   -1.1711    1.4418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2612   -3.0214    0.8772 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1948   -2.6854    1.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1060   -0.4836    1.6911 H   0  0  0  0  0  0  0  0  0  0  0  0
 18  3  1  0  0  0  0
 16 15  2  0  0  0  0
 15 14  1  0  0  0  0
 16 11  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  7  1  0  0  0  0
  8 18  1  0  0  0  0
 16 17  1  0  0  0  0
 11 10  1  0  0  0  0
 10  9  1  0  0  0  0
  9  8  1  0  0  0  0
  8 17  1  0  0  0  0
 14 13  2  0  0  0  0
  5  6  2  0  0  0  0
  8  7  1  0  0  0  0
 18 19  2  0  0  0  0
 13 12  1  0  0  0  0
  3  2  1  0  0  0  0
 12 11  2  0  0  0  0
  2  1  1  0  0  0  0
  4 23  1  0  0  0  0
  7 24  1  0  0  0  0
  7 25  1  0  0  0  0
 14 32  1  0  0  0  0
 13 31  1  0  0  0  0
 12 30  1  0  0  0  0
 15 33  1  0  0  0  0
 10 28  1  0  0  0  0
 10 29  1  0  0  0  0
  9 26  1  0  0  0  0
  9 27  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
M  END

     RDKit          3D

 33 35  0  0  0  0  0  0  0  0999 V2000
   -0.4718    2.6106   -1.9048 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2871    3.6142   -1.2342 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1097    3.6594    0.1382 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1036    4.1072    0.9122 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9633    4.2566    2.3769 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8842    4.7661    3.0121 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3303    3.8512    3.0461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0670    2.7693    2.2502 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4303    2.5069    2.9072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1613    1.3477    2.2390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2170    0.2360    1.8933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7238   -1.0097    1.4976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8589   -2.0572    1.1778 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4808   -1.8688    1.2504 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0306   -0.6299    1.6337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8343    0.4216    1.9383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2397    1.5970    2.3006 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1812    3.2920    0.8076 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2533    3.4420    0.2256 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4510    1.6571   -1.3659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4991    2.9476   -2.0684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0167    2.4510   -2.8871 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0534    4.4145    0.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0748    3.4726    4.0434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9411    4.7554    3.1535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2705    2.2419    3.9617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0662    3.4001    2.8924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6615    1.6839    1.3242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9408    0.9811    2.9178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7984   -1.1711    1.4418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2612   -3.0214    0.8772 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1948   -2.6854    1.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1060   -0.4836    1.6911 H   0  0  0  0  0  0  0  0  0  0  0  0
 18  3  1  0
 16 15  2  0
 15 14  1  0
 16 11  1  0
  3  4  2  0
  4  5  1  0
  5  7  1  0
  8 18  1  0
 16 17  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8 17  1  0
 14 13  2  0
  5  6  2  0
  8  7  1  0
 18 19  2  0
 13 12  1  0
  3  2  1  0
 12 11  2  0
  2  1  1  0
  4 23  1  0
  7 24  1  0
  7 25  1  0
 14 32  1  0
 13 31  1  0
 12 30  1  0
 15 33  1  0
 10 28  1  0
 10 29  1  0
  9 26  1  0
  9 27  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
M  END


  Mrv1652306202101373D          

 33 35  0  0  0  0            999 V2000
   -0.4718    2.6106   -1.9048 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2871    3.6142   -1.2342 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1097    3.6594    0.1382 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1036    4.1072    0.9122 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9633    4.2566    2.3769 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8842    4.7661    3.0121 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3303    3.8512    3.0461 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0670    2.7693    2.2502 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4303    2.5069    2.9072 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1613    1.3477    2.2390 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2170    0.2360    1.8933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7238   -1.0097    1.4976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8589   -2.0572    1.1778 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4808   -1.8688    1.2504 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0306   -0.6299    1.6337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8343    0.4216    1.9383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2397    1.5970    2.3006 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1812    3.2920    0.8076 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2533    3.4420    0.2256 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4510    1.6571   -1.3659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4991    2.9476   -2.0684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0167    2.4510   -2.8871 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0534    4.4145    0.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0748    3.4726    4.0434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9411    4.7554    3.1535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2705    2.2419    3.9617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0662    3.4001    2.8924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6615    1.6839    1.3242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9408    0.9811    2.9178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7984   -1.1711    1.4418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2612   -3.0214    0.8772 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1948   -2.6854    1.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1060   -0.4836    1.6911 H   0  0  0  0  0  0  0  0  0  0  0  0
 18  3  1  0  0  0  0
 16 15  2  0  0  0  0
 15 14  1  0  0  0  0
 16 11  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  7  1  0  0  0  0
  8 18  1  0  0  0  0
 16 17  1  0  0  0  0
 11 10  1  0  0  0  0
 10  9  1  0  0  0  0
  9  8  1  0  0  0  0
  8 17  1  0  0  0  0
 14 13  2  0  0  0  0
  5  6  2  0  0  0  0
  8  7  1  0  0  0  0
 18 19  2  0  0  0  0
 13 12  1  0  0  0  0
  3  2  1  0  0  0  0
 12 11  2  0  0  0  0
  2  1  1  0  0  0  0
  4 23  1  0  0  0  0
  7 24  1  0  0  0  0
  7 25  1  0  0  0  0
 14 32  1  0  0  0  0
 13 31  1  0  0  0  0
 12 30  1  0  0  0  0
 15 33  1  0  0  0  0
 10 28  1  0  0  0  0
 10 29  1  0  0  0  0
  9 26  1  0  0  0  0
  9 27  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0032933

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C1=C([H])C([H])=C2C(O[C@@]3(C(=O)C(OC([H])([H])[H])=C([H])C(=O)C3([H])[H])C([H])([H])C2([H])[H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H14O4/c1-18-13-8-11(16)9-15(14(13)17)7-6-10-4-2-3-5-12(10)19-15/h2-5,8H,6-7,9H2,1H3/t15-/m0/s1

> <INCHI_KEY>
ZYXVNXXRKJOSNN-HNNXBMFYSA-N

> <FORMULA>
C15H14O4

> <MOLECULAR_WEIGHT>
258.273

> <EXACT_MASS>
258.089208931

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
26.085469844231245

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-3'-methoxy-3,4-dihydrospiro[1-benzopyran-2,1'-cyclohexan]-3'-ene-2',5'-dione

> <ALOGPS_LOGP>
1.88

> <JCHEM_LOGP>
2.4401231443333335

> <ALOGPS_LOGS>
-3.74

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.38430403118144

> <JCHEM_PKA_STRONGEST_BASIC>
-4.630736148097069

> <JCHEM_POLAR_SURFACE_AREA>
52.6

> <JCHEM_REFRACTIVITY>
70.1508

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.73e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-3'-methoxy-3,4-dihydrospiro[1-benzopyran-2,1'-cyclohexan]-3'-ene-2',5'-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 33 35  0  0  0  0  0  0  0  0999 V2000
   -0.4718    2.6106   -1.9048 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2871    3.6142   -1.2342 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1097    3.6594    0.1382 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1036    4.1072    0.9122 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9633    4.2566    2.3769 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8842    4.7661    3.0121 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3303    3.8512    3.0461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0670    2.7693    2.2502 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4303    2.5069    2.9072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1613    1.3477    2.2390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2170    0.2360    1.8933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7238   -1.0097    1.4976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8589   -2.0572    1.1778 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4808   -1.8688    1.2504 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0306   -0.6299    1.6337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8343    0.4216    1.9383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2397    1.5970    2.3006 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1812    3.2920    0.8076 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2533    3.4420    0.2256 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4510    1.6571   -1.3659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4991    2.9476   -2.0684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0167    2.4510   -2.8871 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0534    4.4145    0.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0748    3.4726    4.0434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9411    4.7554    3.1535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2705    2.2419    3.9617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0662    3.4001    2.8924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6615    1.6839    1.3242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9408    0.9811    2.9178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7984   -1.1711    1.4418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2612   -3.0214    0.8772 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1948   -2.6854    1.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1060   -0.4836    1.6911 H   0  0  0  0  0  0  0  0  0  0  0  0
 18  3  1  0
 16 15  2  0
 15 14  1  0
 16 11  1  0
  3  4  2  0
  4  5  1  0
  5  7  1  0
  8 18  1  0
 16 17  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8 17  1  0
 14 13  2  0
  5  6  2  0
  8  7  1  0
 18 19  2  0
 13 12  1  0
  3  2  1  0
 12 11  2  0
  2  1  1  0
  4 23  1  0
  7 24  1  0
  7 25  1  0
 14 32  1  0
 13 31  1  0
 12 30  1  0
 15 33  1  0
 10 28  1  0
 10 29  1  0
  9 26  1  0
  9 27  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0      -0.472   2.611  -1.905  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.287   3.614  -1.234  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.110   3.659   0.138  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.104   4.107   0.912  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.963   4.257   2.377  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.884   4.766   3.012  0.00  0.00           O+0
HETATM    7  C   UNK     0      -0.330   3.851   3.046  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.067   2.769   2.250  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.430   2.507   2.907  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.161   1.348   2.239  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.217   0.236   1.893  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.724  -1.010   1.498  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.859  -2.057   1.178  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.481  -1.869   1.250  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.031  -0.630   1.634  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.834   0.422   1.938  0.00  0.00           C+0
HETATM   17  O   UNK     0      -0.240   1.597   2.301  0.00  0.00           O+0
HETATM   18  C   UNK     0      -1.181   3.292   0.808  0.00  0.00           C+0
HETATM   19  O   UNK     0      -2.253   3.442   0.226  0.00  0.00           O+0
HETATM   20  H   UNK     0      -0.451   1.657  -1.366  0.00  0.00           H+0
HETATM   21  H   UNK     0      -1.499   2.948  -2.068  0.00  0.00           H+0
HETATM   22  H   UNK     0      -0.017   2.451  -2.887  0.00  0.00           H+0
HETATM   23  H   UNK     0       2.053   4.415   0.490  0.00  0.00           H+0
HETATM   24  H   UNK     0      -0.075   3.473   4.043  0.00  0.00           H+0
HETATM   25  H   UNK     0      -0.941   4.755   3.154  0.00  0.00           H+0
HETATM   26  H   UNK     0      -2.271   2.242   3.962  0.00  0.00           H+0
HETATM   27  H   UNK     0      -3.066   3.400   2.892  0.00  0.00           H+0
HETATM   28  H   UNK     0      -3.662   1.684   1.324  0.00  0.00           H+0
HETATM   29  H   UNK     0      -3.941   0.981   2.918  0.00  0.00           H+0
HETATM   30  H   UNK     0      -3.798  -1.171   1.442  0.00  0.00           H+0
HETATM   31  H   UNK     0      -2.261  -3.021   0.877  0.00  0.00           H+0
HETATM   32  H   UNK     0       0.195  -2.685   1.010  0.00  0.00           H+0
HETATM   33  H   UNK     0       1.106  -0.484   1.691  0.00  0.00           H+0
CONECT    1    2   20   21   22                                             
CONECT    2    3    1                                                       
CONECT    3   18    4    2                                                  
CONECT    4    3    5   23                                                  
CONECT    5    4    7    6                                                  
CONECT    6    5                                                            
CONECT    7    5    8   24   25                                             
CONECT    8   18    9   17    7                                             
CONECT    9   10    8   26   27                                             
CONECT   10   11    9   28   29                                             
CONECT   11   16   10   12                                                  
CONECT   12   13   11   30                                                  
CONECT   13   14   12   31                                                  
CONECT   14   15   13   32                                                  
CONECT   15   16   14   33                                                  
CONECT   16   15   11   17                                                  
CONECT   17   16    8                                                       
CONECT   18    3    8   19                                                  
CONECT   19   18                                                            
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    4                                                            
CONECT   24    7                                                            
CONECT   25    7                                                            
CONECT   26    9                                                            
CONECT   27    9                                                            
CONECT   28   10                                                            
CONECT   29   10                                                            
CONECT   30   12                                                            
CONECT   31   13                                                            
CONECT   32   14                                                            
CONECT   33   15                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   70    0
END

RDKit          3D

33 35  0  0  0  0  0  0  0  0999 V2000
   -0.4718    2.6106   -1.9048 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2871    3.6142   -1.2342 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1097    3.6594    0.1382 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1036    4.1072    0.9122 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9633    4.2566    2.3769 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8842    4.7661    3.0121 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3303    3.8512    3.0461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0670    2.7693    2.2502 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4303    2.5069    2.9072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1613    1.3477    2.2390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2170    0.2360    1.8933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7238   -1.0097    1.4976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8589   -2.0572    1.1778 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4808   -1.8688    1.2504 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0306   -0.6299    1.6337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8343    0.4216    1.9383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2397    1.5970    2.3006 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1812    3.2920    0.8076 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2533    3.4420    0.2256 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4510    1.6571   -1.3659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4991    2.9476   -2.0684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0167    2.4510   -2.8871 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0534    4.4145    0.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0748    3.4726    4.0434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9411    4.7554    3.1535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2705    2.2419    3.9617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0662    3.4001    2.8924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6615    1.6839    1.3242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9408    0.9811    2.9178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7984   -1.1711    1.4418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2612   -3.0214    0.8772 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1948   -2.6854    1.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1060   -0.4836    1.6911 H   0  0  0  0  0  0  0  0  0  0  0  0
 18  3  1  0
 16 15  2  0
 15 14  1  0
 16 11  1  0
  3  4  2  0
  4  5  1  0
  5  7  1  0
  8 18  1  0
 16 17  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8 17  1  0
 14 13  2  0
  5  6  2  0
  8  7  1  0
 18 19  2  0
 13 12  1  0
  3  2  1  0
 12 11  2  0
  2  1  1  0
  4 23  1  0
  7 24  1  0
  7 25  1  0
 14 32  1  0
 13 31  1  0
 12 30  1  0
 15 33  1  0
 10 28  1  0
 10 29  1  0
  9 26  1  0
  9 27  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₁₄O₄

Average Mass

258.2730 Da

Monoisotopic Mass

258.08921 Da

IUPAC Name

(2S)-3'-methoxy-3,4-dihydrospiro[1-benzopyran-2,1'-cyclohexan]-3'-ene-2',5'-dione

Traditional Name

(2S)-3'-methoxy-3,4-dihydrospiro[1-benzopyran-2,1'-cyclohexan]-3'-ene-2',5'-dione

CAS Registry Number

Not Available

SMILES

[H]C1=C([H])C([H])=C2C(O[C@@]3(C(=O)C(OC([H])([H])[H])=C([H])C(=O)C3([H])[H])C([H])([H])C2([H])[H])=C1[H]

InChI Identifier

InChI=1S/C15H14O4/c1-18-13-8-11(16)9-15(14(13)17)7-6-10-4-2-3-5-12(10)19-15/h2-5,8H,6-7,9H2,1H3/t15-/m0/s1

InChI Key

ZYXVNXXRKJOSNN-HNNXBMFYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Bauhinia purpurea	JEOL database	Boonphong, S., et al, J. Nat. Prod. 70, 795 (2007)

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	1.88	ALOGPS
logP	2.44	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	15.38	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	52.6 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	70.15 m³·mol⁻¹	ChemAxon
Polarizability	26.09 Å³	ChemAxon
Number of Rings	3	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

Not Available

References

General References

Boonphong, S., et al. (2007). Boonphong, S., et al, J. Nat. Prod. 70, 795 (2007). J. Nat. Prod..

Showing NP-Card for bauhispirorin A (NP0032933)

MOL for NP0032933 (bauhispirorin A)

3D MOL for NP0032933 (bauhispirorin A)

3D SDF for NP0032933 (bauhispirorin A)

3D-SDF for NP0032933 (bauhispirorin A)

PDB for NP0032933 (bauhispirorin A)

3D PDB for NP0032933 (bauhispirorin A)

SMILES for NP0032933 (bauhispirorin A)

INCHI for NP0032933 (bauhispirorin A)

Structure for NP0032933 (bauhispirorin A)

3D Structure for NP0032933 (bauhispirorin A)