NP-MRD: Showing NP-Card for (-)-Furaquinocin H (NP0061612)

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Record Information

Version

2.0

Created at

2022-04-28 06:22:16 UTC

Updated at

2022-04-28 06:22:16 UTC

NP-MRD ID

NP0061612

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Furaquinocin H

Description

KO-3988H belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. (-)-Furaquinocin H is found in Streptomyces sp. KO-3988. Based on a literature review very few articles have been published on KO-3988H.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282208222D          

 30 32  0  0  1  0            999 V2000
    2.3637    0.3610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7983    1.0622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4083    1.7892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5837    1.8150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1491    1.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5391    0.3867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1045   -0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4944   -1.0415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2799   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1101    0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3245    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0655    1.8665    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9347    0.4640    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3247    1.1910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1547   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8429    2.4905    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5995    0.8656    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6601    0.0428    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8963   -0.2691    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3613   -0.3918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8869    1.6389    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7004    1.7766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9878    2.5499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8012    2.6877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0886    3.4610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5626    4.0965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3272    2.0521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1406    2.1898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3609    2.2745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4099    1.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  2  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
  9 15  1  0  0  0  0
  3 16  1  0  0  0  0
  2 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  1 19  1  0  0  0  0
 18 20  1  1  0  0  0
 17 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 24 27  1  0  0  0  0
 27 28  1  0  0  0  0
 21 29  1  6  0  0  0
 17 30  1  6  0  0  0
M  END

     RDKit          3D

 56 58  0  0  0  0  0  0  0  0999 V2000
   -6.8142   -2.1300   -0.2827 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1372   -1.9287    0.9599 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9168   -1.2768    0.9619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9049    0.0389    1.0615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1990    0.7551    1.1663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6646    0.8131    1.0720 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6677    2.0727    1.1678 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3800    0.1083    0.9684 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3638   -1.2667    0.8633 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1570   -1.9244    0.7672 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0568   -1.2555    0.7711 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2601   -1.9582    0.6751 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0610    0.1231    0.8742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1680    0.7741    0.9718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9382    2.1628    1.0712 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2903    2.3477    0.3286 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1038    2.2071   -1.1014 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0595    1.1919    0.9178 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1930    1.5527    2.4164 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3978    0.9617    0.4101 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1334    2.1669    0.6147 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5543    0.5376   -1.0323 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9977    0.3413   -1.3352 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5366   -0.7864   -1.7303 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8648   -2.0748   -1.9582 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3932   -3.0880   -1.1228 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0272   -0.7740   -1.9858 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5777    0.4765   -1.7471 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6520   -1.9843    0.8589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6421   -3.2292    0.7640 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0344   -1.1546   -0.7731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1066   -2.6635   -0.9827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6878   -2.7722   -0.1732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1333    1.4460    2.0327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4063    1.3926    0.2790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0377    0.0664    1.3409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1573   -3.0104    0.6852 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2217   -2.9557    0.6016 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7425    3.3271    0.5553 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4340    2.8997   -1.7840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1764    2.5774   -1.1860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1643    1.1691   -1.4345 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2763    0.5560    2.9298 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1334    2.0989    2.5977 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2884    2.0608    2.7527 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9282    0.2121    1.0246 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0882    2.0132    0.5974 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0142   -0.3614   -1.3211 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1797    1.3335   -1.7294 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6326    1.2130   -1.2122 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1814   -2.4053   -2.9935 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7860   -2.0810   -1.8690 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9047   -2.6881   -0.4009 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5132   -1.4874   -1.2863 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1861   -1.0289   -3.0427 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6993    0.9965   -2.5749 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  4  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  1
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  2  3
 24 25  1  0
 25 26  1  0
 24 27  1  0
 27 28  1  0
  9 29  1  0
 29 30  2  0
 29  3  1  0
 14  8  1  0
 18 13  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  5 34  1  0
  5 35  1  0
  5 36  1  0
 10 37  1  0
 12 38  1  0
 16 39  1  6
 17 40  1  0
 17 41  1  0
 17 42  1  0
 19 43  1  0
 19 44  1  0
 19 45  1  0
 20 46  1  1
 21 47  1  0
 22 48  1  0
 22 49  1  0
 23 50  1  0
 25 51  1  0
 25 52  1  0
 26 53  1  0
 27 54  1  0
 27 55  1  0
 28 56  1  0
M  END


  Mrv1652304282208222D          

 30 32  0  0  1  0            999 V2000
    2.3637    0.3610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7983    1.0622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4083    1.7892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5837    1.8150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1491    1.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5391    0.3867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1045   -0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4944   -1.0415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2799   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1101    0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3245    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0655    1.8665    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9347    0.4640    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3247    1.1910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1547   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8429    2.4905    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5995    0.8656    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6601    0.0428    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8963   -0.2691    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3613   -0.3918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8869    1.6389    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7004    1.7766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9878    2.5499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8012    2.6877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0886    3.4610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5626    4.0965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3272    2.0521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1406    2.1898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3609    2.2745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4099    1.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  2  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
  9 15  1  0  0  0  0
  3 16  1  0  0  0  0
  2 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  1 19  1  0  0  0  0
 18 20  1  1  0  0  0
 17 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 24 27  1  0  0  0  0
 27 28  1  0  0  0  0
 21 29  1  6  0  0  0
 17 30  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0061612

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(C)C(=O)C2=C(C=C(O)C3=C2O[C@H](C)[C@]3(C)[C@H](O)CC=C(CO)CO)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H26O8/c1-10-18(27)16-13(19(28)20(10)29-4)7-14(25)17-21(16)30-11(2)22(17,3)15(26)6-5-12(8-23)9-24/h5,7,11,15,23-26H,6,8-9H2,1-4H3/t11-,15-,22-/m1/s1

> <INCHI_KEY>
BELRYDYMOWPKNR-LKJSKEAUSA-N

> <FORMULA>
C22H26O8

> <MOLECULAR_WEIGHT>
418.442

> <EXACT_MASS>
418.162767797

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
44.083240862474845

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,3S)-3-[(1R)-1,5-dihydroxy-4-(hydroxymethyl)pent-3-en-1-yl]-4-hydroxy-7-methoxy-2,3,8-trimethyl-2H,3H,6H,9H-naphtho[1,2-b]furan-6,9-dione

> <ALOGPS_LOGP>
1.53

> <JCHEM_LOGP>
0.08959966266666697

> <ALOGPS_LOGS>
-3.66

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.259751403820054

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.730185874730242

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7567224577933827

> <JCHEM_POLAR_SURFACE_AREA>
133.52

> <JCHEM_REFRACTIVITY>
111.1686

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.19e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3S)-3-[(1R)-1,5-dihydroxy-4-(hydroxymethyl)pent-3-en-1-yl]-4-hydroxy-7-methoxy-2,3,8-trimethyl-2H-naphtho[1,2-b]furan-6,9-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       4.412   0.674   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.223   1.983   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.495   3.340   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.956   3.388   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.145   2.079   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.873   0.722   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.062  -0.587   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       2.790  -1.944   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       0.522  -0.539   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.206   0.818   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.606   2.127   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.122   3.484   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      -1.745   0.866   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -2.473   2.223   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.289  -1.848   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.307   4.649   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.719   1.616   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.832   0.080   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.406  -0.502   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.141  -0.731   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.256   3.059   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.774   3.316   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.311   4.760   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.829   5.017   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.365   6.460   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      10.384   7.647   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      11.811   3.831   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      13.329   4.088   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       6.274   4.246   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       8.232   1.905   0.000  0.00  0.00           C+0
CONECT    1    2    6   19                                                  
CONECT    2    1    3   17                                                  
CONECT    3    2    4   16                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   11                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   15                                                  
CONECT   10    9   11   13                                                  
CONECT   11   10    5   12                                                  
CONECT   12   11                                                            
CONECT   13   10   14                                                       
CONECT   14   13                                                            
CONECT   15    9                                                            
CONECT   16    3                                                            
CONECT   17    2   18   21   30                                             
CONECT   18   17   19   20                                                  
CONECT   19   18    1                                                       
CONECT   20   18                                                            
CONECT   21   17   22   29                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   24   28                                                       
CONECT   28   27                                                            
CONECT   29   21                                                            
CONECT   30   17                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₆O₈

Average Mass

418.4420 Da

Monoisotopic Mass

418.16277 Da

IUPAC Name

(2R,3S)-3-[(1R)-1,5-dihydroxy-4-(hydroxymethyl)pent-3-en-1-yl]-4-hydroxy-7-methoxy-2,3,8-trimethyl-2H,3H,6H,9H-naphtho[1,2-b]furan-6,9-dione

Traditional Name

(2R,3S)-3-[(1R)-1,5-dihydroxy-4-(hydroxymethyl)pent-3-en-1-yl]-4-hydroxy-7-methoxy-2,3,8-trimethyl-2H-naphtho[1,2-b]furan-6,9-dione

CAS Registry Number

Not Available

SMILES

COC1=C(C)C(=O)C2=C(C=C(O)C3=C2O[C@H](C)[C@]3(C)[C@H](O)CC=C(CO)CO)C1=O

InChI Identifier

InChI=1S/C22H26O8/c1-10-18(27)16-13(19(28)20(10)29-4)7-14(25)17-21(16)30-11(2)22(17,3)15(26)6-5-12(8-23)9-24/h5,7,11,15,23-26H,6,8-9H2,1-4H3/t11-,15-,22-/m1/s1

InChI Key

BELRYDYMOWPKNR-LKJSKEAUSA-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
Streptomyces sp. KO-3988	Bacteria	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthofurans

Sub Class

Not Available

Direct Parent

Naphthofurans

Alternative Parents

Substituents

Naphthofuran
Naphthoquinone
Naphthalene
Fatty alcohol
Coumaran
Quinone
Aryl ketone
Alkyl aryl ether
Phenol
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Fatty acyl
Vinylogous ester
Secondary alcohol
Ketone
Oxacycle
Ether
Alcohol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Primary alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	1.53	ALOGPS
logP	0.09	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	7.73	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	133.52 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	111.17 m³·mol⁻¹	ChemAxon
Polarizability	44.08 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	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9907224

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11732511

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Furaquinocin H (NP0061612)

MOL for NP0061612 ((-)-Furaquinocin H)

3D MOL for NP0061612 ((-)-Furaquinocin H)

3D SDF for NP0061612 ((-)-Furaquinocin H)

3D-SDF for NP0061612 ((-)-Furaquinocin H)

PDB for NP0061612 ((-)-Furaquinocin H)

3D PDB for NP0061612 ((-)-Furaquinocin H)

SMILES for NP0061612 ((-)-Furaquinocin H)

INCHI for NP0061612 ((-)-Furaquinocin H)

Structure for NP0061612 ((-)-Furaquinocin H)

3D Structure for NP0061612 ((-)-Furaquinocin H)