NP-MRD: Showing NP-Card for Lupinacidin B (NP0007048)

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Record Information

Version

2.0

Created at

2020-12-09 03:56:55 UTC

Updated at

2021-07-15 16:56:30 UTC

NP-MRD ID

NP0007048

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Lupinacidin B

Provided By

NPAtlas

Description

4-Butyl-1,3,5-trihydroxy-2-methyl-9,10-dihydroanthracene-9,10-dione belongs to the class of organic compounds known as hydroxyanthraquinones. Hydroxyanthraquinones are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group. Lupinacidin B is found in Micromonospora lupini. Based on a literature review very few articles have been published on 4-butyl-1,3,5-trihydroxy-2-methyl-9,10-dihydroanthracene-9,10-dione.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118373D          

 42 44  0  0  0  0            999 V2000
    3.8312    1.2699   -1.8528 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6384    1.0926   -0.9029 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0621    0.5328    0.4033 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9696    0.3008    1.4168 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9295   -0.6148    0.9647 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1688   -1.9998    0.9074 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4566   -2.4063    1.3107 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2610   -2.8937    0.5035 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5657   -4.3390    0.4613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0203   -2.4737    0.1034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9048   -3.4142   -0.2973 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3068   -1.1136    0.1419 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3225   -0.2013    0.5741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6973    1.2013    0.5861 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2066    1.9977    0.9791 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9964    1.6720    0.1847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3120    3.0160    0.2092 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4439    3.9659    0.6046 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6103    3.3985   -0.2029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5541    2.4960   -0.6199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2097    1.1632   -0.6332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9387    0.7516   -0.2338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6147   -0.6592   -0.2641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4992   -1.4445   -0.6488 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6966    0.7455   -1.3661 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6273    0.8987   -2.8581 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1243    2.3370   -1.8836 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9148    0.4617   -1.4551 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1862    2.1002   -0.8419 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8588    1.2176    0.8204 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6248   -0.4208    0.1929 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7316    1.1181    2.0779 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5485   -0.3738    2.1934 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7244   -3.3830    1.3039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3449   -4.9656    0.3712 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0508   -4.6672    1.4252 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3128   -4.5776   -0.3490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8079   -3.4452   -0.6125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5401    3.9412    0.9152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8635    4.4552   -0.1857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5536    2.8036   -0.9359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9495    0.4562   -0.9592 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 13  5  1  0  0  0  0
 22 16  1  0  0  0  0
 23 12  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  2 28  1  0  0  0  0
  2 29  1  0  0  0  0
  3 30  1  0  0  0  0
  3 31  1  0  0  0  0
  4 32  1  0  0  0  0
  4 33  1  0  0  0  0
  7 34  1  0  0  0  0
  9 35  1  0  0  0  0
  9 36  1  0  0  0  0
  9 37  1  0  0  0  0
 11 38  1  0  0  0  0
 18 39  1  0  0  0  0
 19 40  1  0  0  0  0
 20 41  1  0  0  0  0
 21 42  1  0  0  0  0
M  END

     RDKit          3D

 42 44  0  0  0  0  0  0  0  0999 V2000
    3.8312    1.2699   -1.8528 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6384    1.0926   -0.9029 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0621    0.5328    0.4033 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9696    0.3008    1.4168 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9295   -0.6148    0.9647 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1688   -1.9998    0.9074 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4566   -2.4063    1.3107 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2610   -2.8937    0.5035 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5657   -4.3390    0.4613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0203   -2.4737    0.1034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9048   -3.4142   -0.2973 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3068   -1.1136    0.1419 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3225   -0.2013    0.5741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6973    1.2013    0.5861 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2066    1.9977    0.9791 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9964    1.6720    0.1847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3120    3.0160    0.2092 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4439    3.9659    0.6046 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6103    3.3985   -0.2029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5541    2.4960   -0.6199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2097    1.1632   -0.6332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9387    0.7516   -0.2338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6147   -0.6592   -0.2641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4992   -1.4445   -0.6488 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6966    0.7455   -1.3661 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6273    0.8987   -2.8581 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1243    2.3370   -1.8836 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9148    0.4617   -1.4551 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1862    2.1002   -0.8419 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8588    1.2176    0.8204 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6248   -0.4208    0.1929 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7316    1.1181    2.0779 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5485   -0.3738    2.1934 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7244   -3.3830    1.3039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3449   -4.9656    0.3712 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0508   -4.6672    1.4252 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3128   -4.5776   -0.3490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8079   -3.4452   -0.6125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5401    3.9412    0.9152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8635    4.4552   -0.1857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5536    2.8036   -0.9359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9495    0.4562   -0.9592 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 13  5  1  0
 22 16  1  0
 23 12  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  7 34  1  0
  9 35  1  0
  9 36  1  0
  9 37  1  0
 11 38  1  0
 18 39  1  0
 19 40  1  0
 20 41  1  0
 21 42  1  0
M  END


  Mrv1652306242118373D          

 42 44  0  0  0  0            999 V2000
    3.8312    1.2699   -1.8528 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6384    1.0926   -0.9029 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0621    0.5328    0.4033 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9696    0.3008    1.4168 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9295   -0.6148    0.9647 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1688   -1.9998    0.9074 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4566   -2.4063    1.3107 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2610   -2.8937    0.5035 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5657   -4.3390    0.4613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0203   -2.4737    0.1034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9048   -3.4142   -0.2973 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3068   -1.1136    0.1419 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3225   -0.2013    0.5741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6973    1.2013    0.5861 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2066    1.9977    0.9791 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9964    1.6720    0.1847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3120    3.0160    0.2092 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4439    3.9659    0.6046 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6103    3.3985   -0.2029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5541    2.4960   -0.6199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2097    1.1632   -0.6332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9387    0.7516   -0.2338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6147   -0.6592   -0.2641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4992   -1.4445   -0.6488 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6966    0.7455   -1.3661 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6273    0.8987   -2.8581 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1243    2.3370   -1.8836 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9148    0.4617   -1.4551 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1862    2.1002   -0.8419 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8588    1.2176    0.8204 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6248   -0.4208    0.1929 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7316    1.1181    2.0779 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5485   -0.3738    2.1934 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7244   -3.3830    1.3039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3449   -4.9656    0.3712 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0508   -4.6672    1.4252 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3128   -4.5776   -0.3490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8079   -3.4452   -0.6125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5401    3.9412    0.9152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8635    4.4552   -0.1857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5536    2.8036   -0.9359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9495    0.4562   -0.9592 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 13  5  1  0  0  0  0
 22 16  1  0  0  0  0
 23 12  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  2 28  1  0  0  0  0
  2 29  1  0  0  0  0
  3 30  1  0  0  0  0
  3 31  1  0  0  0  0
  4 32  1  0  0  0  0
  4 33  1  0  0  0  0
  7 34  1  0  0  0  0
  9 35  1  0  0  0  0
  9 36  1  0  0  0  0
  9 37  1  0  0  0  0
 11 38  1  0  0  0  0
 18 39  1  0  0  0  0
 19 40  1  0  0  0  0
 20 41  1  0  0  0  0
 21 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0007048

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C(=O)C3=C(C(=O)C2=C([H])C([H])=C1[H])C(O[H])=C(C(O[H])=C3C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C19H18O5/c1-3-4-6-11-14-15(17(22)9(2)16(11)21)18(23)10-7-5-8-12(20)13(10)19(14)24/h5,7-8,20-22H,3-4,6H2,1-2H3

> <INCHI_KEY>
IVQKRDHUECCAJE-UHFFFAOYSA-N

> <FORMULA>
C19H18O5

> <MOLECULAR_WEIGHT>
326.348

> <EXACT_MASS>
326.11542368

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
34.29538101525726

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-butyl-1,3,5-trihydroxy-2-methyl-9,10-dihydroanthracene-9,10-dione

> <ALOGPS_LOGP>
3.48

> <JCHEM_LOGP>
5.668558883333334

> <ALOGPS_LOGS>
-3.75

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.479006478946003

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.87413443187422

> <JCHEM_PKA_STRONGEST_BASIC>
-5.2864268349832395

> <JCHEM_POLAR_SURFACE_AREA>
94.83000000000001

> <JCHEM_REFRACTIVITY>
90.9791

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.78e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-butyl-1,3,5-trihydroxy-2-methylanthracene-9,10-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 42 44  0  0  0  0  0  0  0  0999 V2000
    3.8312    1.2699   -1.8528 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6384    1.0926   -0.9029 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0621    0.5328    0.4033 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9696    0.3008    1.4168 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9295   -0.6148    0.9647 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1688   -1.9998    0.9074 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4566   -2.4063    1.3107 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2610   -2.8937    0.5035 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5657   -4.3390    0.4613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0203   -2.4737    0.1034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9048   -3.4142   -0.2973 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3068   -1.1136    0.1419 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3225   -0.2013    0.5741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6973    1.2013    0.5861 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2066    1.9977    0.9791 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9964    1.6720    0.1847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3120    3.0160    0.2092 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4439    3.9659    0.6046 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6103    3.3985   -0.2029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5541    2.4960   -0.6199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2097    1.1632   -0.6332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9387    0.7516   -0.2338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6147   -0.6592   -0.2641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4992   -1.4445   -0.6488 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6966    0.7455   -1.3661 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6273    0.8987   -2.8581 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1243    2.3370   -1.8836 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9148    0.4617   -1.4551 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1862    2.1002   -0.8419 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8588    1.2176    0.8204 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6248   -0.4208    0.1929 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7316    1.1181    2.0779 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5485   -0.3738    2.1934 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7244   -3.3830    1.3039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3449   -4.9656    0.3712 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0508   -4.6672    1.4252 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3128   -4.5776   -0.3490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8079   -3.4452   -0.6125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5401    3.9412    0.9152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8635    4.4552   -0.1857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5536    2.8036   -0.9359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9495    0.4562   -0.9592 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 13  5  1  0
 22 16  1  0
 23 12  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  7 34  1  0
  9 35  1  0
  9 36  1  0
  9 37  1  0
 11 38  1  0
 18 39  1  0
 19 40  1  0
 20 41  1  0
 21 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       3.831   1.270  -1.853  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.638   1.093  -0.903  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.062   0.533   0.403  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.970   0.301   1.417  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.930  -0.615   0.965  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.169  -2.000   0.907  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.457  -2.406   1.311  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.261  -2.894   0.503  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.566  -4.339   0.461  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.020  -2.474   0.103  0.00  0.00           C+0
HETATM   11  O   UNK     0      -1.905  -3.414  -0.297  0.00  0.00           O+0
HETATM   12  C   UNK     0      -1.307  -1.114   0.142  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.323  -0.201   0.574  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.697   1.201   0.586  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.207   1.998   0.979  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.996   1.672   0.185  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.312   3.016   0.209  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.444   3.966   0.605  0.00  0.00           O+0
HETATM   19  C   UNK     0      -3.610   3.398  -0.203  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.554   2.496  -0.620  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.210   1.163  -0.633  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.939   0.752  -0.234  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.615  -0.659  -0.264  0.00  0.00           C+0
HETATM   24  O   UNK     0      -3.499  -1.444  -0.649  0.00  0.00           O+0
HETATM   25  H   UNK     0       4.697   0.746  -1.366  0.00  0.00           H+0
HETATM   26  H   UNK     0       3.627   0.899  -2.858  0.00  0.00           H+0
HETATM   27  H   UNK     0       4.124   2.337  -1.884  0.00  0.00           H+0
HETATM   28  H   UNK     0       1.915   0.462  -1.455  0.00  0.00           H+0
HETATM   29  H   UNK     0       2.186   2.100  -0.842  0.00  0.00           H+0
HETATM   30  H   UNK     0       3.859   1.218   0.820  0.00  0.00           H+0
HETATM   31  H   UNK     0       3.625  -0.421   0.193  0.00  0.00           H+0
HETATM   32  H   UNK     0       1.732   1.118   2.078  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.549  -0.374   2.193  0.00  0.00           H+0
HETATM   34  H   UNK     0       2.724  -3.383   1.304  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.345  -4.966   0.371  0.00  0.00           H+0
HETATM   36  H   UNK     0       1.051  -4.667   1.425  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.313  -4.578  -0.349  0.00  0.00           H+0
HETATM   38  H   UNK     0      -2.808  -3.445  -0.613  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.540   3.941   0.915  0.00  0.00           H+0
HETATM   40  H   UNK     0      -3.864   4.455  -0.186  0.00  0.00           H+0
HETATM   41  H   UNK     0      -5.554   2.804  -0.936  0.00  0.00           H+0
HETATM   42  H   UNK     0      -4.949   0.456  -0.959  0.00  0.00           H+0
CONECT    1    2   25   26   27                                             
CONECT    2    1    3   28   29                                             
CONECT    3    2    4   30   31                                             
CONECT    4    3    5   32   33                                             
CONECT    5    4    6   13                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6   34                                                       
CONECT    8    6    9   10                                                  
CONECT    9    8   35   36   37                                             
CONECT   10    8   11   12                                                  
CONECT   11   10   38                                                       
CONECT   12   10   13   23                                                  
CONECT   13   12   14    5                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   22                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17   39                                                       
CONECT   19   17   20   40                                                  
CONECT   20   19   21   41                                                  
CONECT   21   20   22   42                                                  
CONECT   22   21   23   16                                                  
CONECT   23   22   24   12                                                  
CONECT   24   23                                                            
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    2                                                            
CONECT   29    2                                                            
CONECT   30    3                                                            
CONECT   31    3                                                            
CONECT   32    4                                                            
CONECT   33    4                                                            
CONECT   34    7                                                            
CONECT   35    9                                                            
CONECT   36    9                                                            
CONECT   37    9                                                            
CONECT   38   11                                                            
CONECT   39   18                                                            
CONECT   40   19                                                            
CONECT   41   20                                                            
CONECT   42   21                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   88    0
END

RDKit          3D

42 44  0  0  0  0  0  0  0  0999 V2000
    3.8312    1.2699   -1.8528 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6384    1.0926   -0.9029 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0621    0.5328    0.4033 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9696    0.3008    1.4168 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9295   -0.6148    0.9647 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1688   -1.9998    0.9074 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4566   -2.4063    1.3107 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2610   -2.8937    0.5035 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5657   -4.3390    0.4613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0203   -2.4737    0.1034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9048   -3.4142   -0.2973 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3068   -1.1136    0.1419 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3225   -0.2013    0.5741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6973    1.2013    0.5861 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2066    1.9977    0.9791 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9964    1.6720    0.1847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3120    3.0160    0.2092 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4439    3.9659    0.6046 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6103    3.3985   -0.2029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5541    2.4960   -0.6199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2097    1.1632   -0.6332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9387    0.7516   -0.2338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6147   -0.6592   -0.2641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4992   -1.4445   -0.6488 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6966    0.7455   -1.3661 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6273    0.8987   -2.8581 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1243    2.3370   -1.8836 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9148    0.4617   -1.4551 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1862    2.1002   -0.8419 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8588    1.2176    0.8204 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6248   -0.4208    0.1929 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7316    1.1181    2.0779 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5485   -0.3738    2.1934 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7244   -3.3830    1.3039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3449   -4.9656    0.3712 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0508   -4.6672    1.4252 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3128   -4.5776   -0.3490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8079   -3.4452   -0.6125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5401    3.9412    0.9152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8635    4.4552   -0.1857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5536    2.8036   -0.9359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9495    0.4562   -0.9592 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 13  5  1  0
 22 16  1  0
 23 12  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  7 34  1  0
  9 35  1  0
  9 36  1  0
  9 37  1  0
 11 38  1  0
 18 39  1  0
 19 40  1  0
 20 41  1  0
 21 42  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
Lupinacidins b	ChEMBL

Chemical Formula

C₁₉H₁₈O₅

Average Mass

326.3480 Da

Monoisotopic Mass

326.11542 Da

IUPAC Name

4-butyl-1,3,5-trihydroxy-2-methyl-9,10-dihydroanthracene-9,10-dione

Traditional Name

4-butyl-1,3,5-trihydroxy-2-methylanthracene-9,10-dione

CAS Registry Number

Not Available

SMILES

CCCCC1=C(O)C(C)=C(O)C2=C1C(=O)C1=C(C=CC=C1O)C2=O

InChI Identifier

InChI=1S/C19H18O5/c1-3-4-6-11-14-15(17(22)9(2)16(11)21)18(23)10-7-5-8-12(20)13(10)19(14)24/h5,7-8,20-22H,3-4,6H2,1-2H3

InChI Key

IVQKRDHUECCAJE-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, 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
Micromonospora lupini	NPAtlas	17475486

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxyanthraquinones. Hydroxyanthraquinones are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Hydroxyanthraquinones

Alternative Parents

Substituents

Hydroxyanthraquinone
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Vinylogous acid
Ketone
Polyol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic 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	3.48	ALOGPS
logP	5.67	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	7.87	ChemAxon
pKa (Strongest Basic)	-5.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	94.83 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	90.98 m³·mol⁻¹	ChemAxon
Polarizability	34.3 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA004414

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

23285973

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23628281

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Lupinacidin B (NP0007048)

MOL for NP0007048 (Lupinacidin B)

3D MOL for NP0007048 (Lupinacidin B)

3D SDF for NP0007048 (Lupinacidin B)

3D-SDF for NP0007048 (Lupinacidin B)

PDB for NP0007048 (Lupinacidin B)

3D PDB for NP0007048 (Lupinacidin B)

SMILES for NP0007048 (Lupinacidin B)

INCHI for NP0007048 (Lupinacidin B)

Structure for NP0007048 (Lupinacidin B)

3D Structure for NP0007048 (Lupinacidin B)