NP-MRD: Showing NP-Card for Melanocin C (NP0005188)

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Record Information

Version

2.0

Created at

2020-12-09 02:30:30 UTC

Updated at

2021-07-15 16:51:17 UTC

NP-MRD ID

NP0005188

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Melanocin C

Provided By

NPAtlas

Description

Melanocin C belongs to the class of organic compounds known as naphthols and derivatives. These are naphthalene derivatives carrying one or more hydroxyl (-OH) groups at any ring position. Melanocin C is found in Penicillium miczynskii and Penicillium shearii. Based on a literature review very few articles have been published on Melanocin C.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118173D          

 40 42  0  0  0  0            999 V2000
   -2.2215   -5.6496   -1.2953 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3254   -4.8003   -0.9394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3628   -3.4951   -0.7336 N   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4020   -2.1329   -0.5188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4842   -1.3063   -0.4536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3607    0.0646   -0.1752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5040    0.8542   -0.1160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3714    2.2061    0.1655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5005    3.0100    0.2286 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1271    2.7566    0.3826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0059    4.0914    0.6617 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0238    1.9615    0.3179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1288    0.6176    0.0403 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0094   -0.1897   -0.0179 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2790    0.4674    0.2091 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9541    1.0653   -0.8313 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1700    1.7095   -0.6821 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7255    1.7466    0.5878 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9409    2.3890    0.7430 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0464    1.1457    1.6341 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6633    1.2203    2.8916 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8348    0.5090    1.4625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1368   -1.5088   -0.2872 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9917   -2.3481   -0.3613 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6160   -2.4789   -1.6572 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1866   -1.8798   -2.6765 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3435   -5.3934   -0.8014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6625   -3.5136   -1.1790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5067   -1.6449   -0.6103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4665    0.4109   -0.2875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4339    2.6589    0.0879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1184    4.5406    0.8294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0046    2.3634    0.4844 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5735    1.0736   -1.8570 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6772    2.1714   -1.5264 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3591    2.4237    1.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1992    0.7962    3.6599 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3689    0.0623    2.3417 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4091   -2.8690    0.4164 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4866   -3.1054   -1.7985 H   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  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  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  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 14 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 23  4  1  0  0  0  0
 13  6  1  0  0  0  0
 22 15  1  0  0  0  0
  2 27  1  0  0  0  0
  3 28  1  0  0  0  0
  5 29  1  0  0  0  0
  7 30  1  0  0  0  0
  9 31  1  0  0  0  0
 11 32  1  0  0  0  0
 12 33  1  0  0  0  0
 16 34  1  0  0  0  0
 17 35  1  0  0  0  0
 19 36  1  0  0  0  0
 21 37  1  0  0  0  0
 22 38  1  0  0  0  0
 24 39  1  0  0  0  0
 25 40  1  0  0  0  0
M  END

     RDKit          3D

 40 42  0  0  0  0  0  0  0  0999 V2000
   -2.2215   -5.6496   -1.2953 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3254   -4.8003   -0.9394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3628   -3.4951   -0.7336 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4020   -2.1329   -0.5188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4842   -1.3063   -0.4536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3607    0.0646   -0.1752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5040    0.8542   -0.1160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3714    2.2061    0.1655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5005    3.0100    0.2286 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1271    2.7566    0.3826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0059    4.0914    0.6617 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0238    1.9615    0.3179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1288    0.6176    0.0403 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0094   -0.1897   -0.0179 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2790    0.4674    0.2091 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9541    1.0653   -0.8313 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1700    1.7095   -0.6821 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7255    1.7466    0.5878 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9409    2.3890    0.7430 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0464    1.1457    1.6341 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6633    1.2203    2.8916 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8348    0.5090    1.4625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1368   -1.5088   -0.2872 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9917   -2.3481   -0.3613 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6160   -2.4789   -1.6572 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1866   -1.8798   -2.6765 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3435   -5.3934   -0.8014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6625   -3.5136   -1.1790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5067   -1.6449   -0.6103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4665    0.4109   -0.2875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4339    2.6589    0.0879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1184    4.5406    0.8294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0046    2.3634    0.4844 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5735    1.0736   -1.8570 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6772    2.1714   -1.5264 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3591    2.4237    1.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1992    0.7962    3.6599 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3689    0.0623    2.3417 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4091   -2.8690    0.4164 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4866   -3.1054   -1.7985 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  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  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  2  0
 14 23  2  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
 23  4  1  0
 13  6  1  0
 22 15  1  0
  2 27  1  0
  3 28  1  0
  5 29  1  0
  7 30  1  0
  9 31  1  0
 11 32  1  0
 12 33  1  0
 16 34  1  0
 17 35  1  0
 19 36  1  0
 21 37  1  0
 22 38  1  0
 24 39  1  0
 25 40  1  0
M  END


  Mrv1652306242118173D          

 40 42  0  0  0  0            999 V2000
   -2.2215   -5.6496   -1.2953 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3254   -4.8003   -0.9394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3628   -3.4951   -0.7336 N   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4020   -2.1329   -0.5188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4842   -1.3063   -0.4536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3607    0.0646   -0.1752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5040    0.8542   -0.1160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3714    2.2061    0.1655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5005    3.0100    0.2286 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1271    2.7566    0.3826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0059    4.0914    0.6617 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0238    1.9615    0.3179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1288    0.6176    0.0403 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0094   -0.1897   -0.0179 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2790    0.4674    0.2091 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9541    1.0653   -0.8313 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1700    1.7095   -0.6821 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7255    1.7466    0.5878 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9409    2.3890    0.7430 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0464    1.1457    1.6341 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6633    1.2203    2.8916 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8348    0.5090    1.4625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1368   -1.5088   -0.2872 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9917   -2.3481   -0.3613 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6160   -2.4789   -1.6572 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1866   -1.8798   -2.6765 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3435   -5.3934   -0.8014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6625   -3.5136   -1.1790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5067   -1.6449   -0.6103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4665    0.4109   -0.2875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4339    2.6589    0.0879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1184    4.5406    0.8294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0046    2.3634    0.4844 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5735    1.0736   -1.8570 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6772    2.1714   -1.5264 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3591    2.4237    1.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1992    0.7962    3.6599 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3689    0.0623    2.3417 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4091   -2.8690    0.4164 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4866   -3.1054   -1.7985 H   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  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  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  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 14 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 23  4  1  0  0  0  0
 13  6  1  0  0  0  0
 22 15  1  0  0  0  0
  2 27  1  0  0  0  0
  3 28  1  0  0  0  0
  5 29  1  0  0  0  0
  7 30  1  0  0  0  0
  9 31  1  0  0  0  0
 11 32  1  0  0  0  0
 12 33  1  0  0  0  0
 16 34  1  0  0  0  0
 17 35  1  0  0  0  0
 19 36  1  0  0  0  0
 21 37  1  0  0  0  0
 22 38  1  0  0  0  0
 24 39  1  0  0  0  0
 25 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0005188

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C([H])=C(C([H])=C1O[H])C1=C(N([H])C([H])=O)C(N([H])C([H])=O)=C([H])C2=C([H])C(O[H])=C(O[H])C([H])=C12

> <INCHI_IDENTIFIER>
InChI=1S/C18H14N2O6/c21-7-19-12-3-10-5-15(25)16(26)6-11(10)17(18(12)20-8-22)9-1-2-13(23)14(24)4-9/h1-8,23-26H,(H,19,21)(H,20,22)

> <INCHI_KEY>
JIBJFCGHEWXKFO-UHFFFAOYSA-N

> <FORMULA>
C18H14N2O6

> <MOLECULAR_WEIGHT>
354.318

> <EXACT_MASS>
354.085186179

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
35.199674904176554

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-[1-(3,4-dihydroxyphenyl)-3-formamido-6,7-dihydroxynaphthalen-2-yl]formamide

> <ALOGPS_LOGP>
1.80

> <JCHEM_LOGP>
1.7737099666666665

> <ALOGPS_LOGS>
-3.41

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.3740350791072

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.770732828212202

> <JCHEM_PKA_STRONGEST_BASIC>
-4.236705006070567

> <JCHEM_POLAR_SURFACE_AREA>
139.12

> <JCHEM_REFRACTIVITY>
96.31299999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.38e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-[1-(3,4-dihydroxyphenyl)-3-formamido-6,7-dihydroxynaphthalen-2-yl]formamide

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 40 42  0  0  0  0  0  0  0  0999 V2000
   -2.2215   -5.6496   -1.2953 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3254   -4.8003   -0.9394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3628   -3.4951   -0.7336 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4020   -2.1329   -0.5188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4842   -1.3063   -0.4536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3607    0.0646   -0.1752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5040    0.8542   -0.1160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3714    2.2061    0.1655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5005    3.0100    0.2286 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1271    2.7566    0.3826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0059    4.0914    0.6617 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0238    1.9615    0.3179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1288    0.6176    0.0403 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0094   -0.1897   -0.0179 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2790    0.4674    0.2091 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9541    1.0653   -0.8313 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1700    1.7095   -0.6821 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7255    1.7466    0.5878 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9409    2.3890    0.7430 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0464    1.1457    1.6341 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6633    1.2203    2.8916 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8348    0.5090    1.4625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1368   -1.5088   -0.2872 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9917   -2.3481   -0.3613 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6160   -2.4789   -1.6572 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1866   -1.8798   -2.6765 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.6625   -3.5136   -1.1790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5067   -1.6449   -0.6103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4665    0.4109   -0.2875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4339    2.6589    0.0879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1184    4.5406    0.8294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0046    2.3634    0.4844 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5735    1.0736   -1.8570 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6772    2.1714   -1.5264 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3591    2.4237    1.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1992    0.7962    3.6599 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  2  0
  2  3  1  0
  3  4  1  0
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 13  6  1  0
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 16 34  1  0
 17 35  1  0
 19 36  1  0
 21 37  1  0
 22 38  1  0
 24 39  1  0
 25 40  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  O   UNK     0      -2.221  -5.650  -1.295  0.00  0.00           O+0
HETATM    2  C   UNK     0      -1.325  -4.800  -0.939  0.00  0.00           C+0
HETATM    3  N   UNK     0      -1.363  -3.495  -0.734  0.00  0.00           N+0
HETATM    4  C   UNK     0      -1.402  -2.133  -0.519  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.484  -1.306  -0.454  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.361   0.065  -0.175  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.504   0.854  -0.116  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.371   2.206   0.166  0.00  0.00           C+0
HETATM    9  O   UNK     0      -4.500   3.010   0.229  0.00  0.00           O+0
HETATM   10  C   UNK     0      -2.127   2.757   0.383  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.006   4.091   0.662  0.00  0.00           O+0
HETATM   12  C   UNK     0      -1.024   1.962   0.318  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.129   0.618   0.040  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.009  -0.190  -0.018  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.279   0.467   0.209  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.954   1.065  -0.831  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.170   1.710  -0.682  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.725   1.747   0.588  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.941   2.389   0.743  0.00  0.00           O+0
HETATM   20  C   UNK     0       3.046   1.146   1.634  0.00  0.00           C+0
HETATM   21  O   UNK     0       3.663   1.220   2.892  0.00  0.00           O+0
HETATM   22  C   UNK     0       1.835   0.509   1.462  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.137  -1.509  -0.287  0.00  0.00           C+0
HETATM   24  N   UNK     0       0.992  -2.348  -0.361  0.00  0.00           N+0
HETATM   25  C   UNK     0       1.616  -2.479  -1.657  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.187  -1.880  -2.676  0.00  0.00           O+0
HETATM   27  H   UNK     0      -0.344  -5.393  -0.801  0.00  0.00           H+0
HETATM   28  H   UNK     0      -2.663  -3.514  -1.179  0.00  0.00           H+0
HETATM   29  H   UNK     0      -3.507  -1.645  -0.610  0.00  0.00           H+0
HETATM   30  H   UNK     0      -4.466   0.411  -0.288  0.00  0.00           H+0
HETATM   31  H   UNK     0      -5.434   2.659   0.088  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.118   4.541   0.829  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.005   2.363   0.484  0.00  0.00           H+0
HETATM   34  H   UNK     0       1.573   1.074  -1.857  0.00  0.00           H+0
HETATM   35  H   UNK     0       3.677   2.171  -1.526  0.00  0.00           H+0
HETATM   36  H   UNK     0       5.359   2.424   1.661  0.00  0.00           H+0
HETATM   37  H   UNK     0       3.199   0.796   3.660  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.369   0.062   2.342  0.00  0.00           H+0
HETATM   39  H   UNK     0       1.409  -2.869   0.416  0.00  0.00           H+0
HETATM   40  H   UNK     0       2.487  -3.105  -1.799  0.00  0.00           H+0
CONECT    1    2                                                            
CONECT    2    1    3   27                                                  
CONECT    3    2    4   28                                                  
CONECT    4    3    5   23                                                  
CONECT    5    4    6   29                                                  
CONECT    6    5    7   13                                                  
CONECT    7    6    8   30                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8   31                                                       
CONECT   10    8   11   12                                                  
CONECT   11   10   32                                                       
CONECT   12   10   13   33                                                  
CONECT   13   12   14    6                                                  
CONECT   14   13   15   23                                                  
CONECT   15   14   16   22                                                  
CONECT   16   15   17   34                                                  
CONECT   17   16   18   35                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18   36                                                       
CONECT   20   18   21   22                                                  
CONECT   21   20   37                                                       
CONECT   22   20   15   38                                                  
CONECT   23   14   24    4                                                  
CONECT   24   23   25   39                                                  
CONECT   25   24   26   40                                                  
CONECT   26   25                                                            
CONECT   27    2                                                            
CONECT   28    3                                                            
CONECT   29    5                                                            
CONECT   30    7                                                            
CONECT   31    9                                                            
CONECT   32   11                                                            
CONECT   33   12                                                            
CONECT   34   16                                                            
CONECT   35   17                                                            
CONECT   36   19                                                            
CONECT   37   21                                                            
CONECT   38   22                                                            
CONECT   39   24                                                            
CONECT   40   25                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   84    0
END

RDKit          3D

40 42  0  0  0  0  0  0  0  0999 V2000
   -2.2215   -5.6496   -1.2953 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3254   -4.8003   -0.9394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3628   -3.4951   -0.7336 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4020   -2.1329   -0.5188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4842   -1.3063   -0.4536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3607    0.0646   -0.1752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5040    0.8542   -0.1160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3714    2.2061    0.1655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5005    3.0100    0.2286 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1271    2.7566    0.3826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0059    4.0914    0.6617 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0238    1.9615    0.3179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1288    0.6176    0.0403 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0094   -0.1897   -0.0179 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2790    0.4674    0.2091 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9541    1.0653   -0.8313 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1700    1.7095   -0.6821 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7255    1.7466    0.5878 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9409    2.3890    0.7430 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0464    1.1457    1.6341 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6633    1.2203    2.8916 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8348    0.5090    1.4625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1368   -1.5088   -0.2872 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9917   -2.3481   -0.3613 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6160   -2.4789   -1.6572 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1866   -1.8798   -2.6765 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3435   -5.3934   -0.8014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6625   -3.5136   -1.1790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5067   -1.6449   -0.6103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4665    0.4109   -0.2875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4339    2.6589    0.0879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1184    4.5406    0.8294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0046    2.3634    0.4844 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5735    1.0736   -1.8570 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6772    2.1714   -1.5264 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3591    2.4237    1.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1992    0.7962    3.6599 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3689    0.0623    2.3417 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4091   -2.8690    0.4164 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4866   -3.1054   -1.7985 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
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 14 23  2  0
 23 24  1  0
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 23  4  1  0
 13  6  1  0
 22 15  1  0
  2 27  1  0
  3 28  1  0
  5 29  1  0
  7 30  1  0
  9 31  1  0
 11 32  1  0
 12 33  1  0
 16 34  1  0
 17 35  1  0
 19 36  1  0
 21 37  1  0
 22 38  1  0
 24 39  1  0
 25 40  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
N-[4-(3,4-Dihydroxyphenyl)-6,7-dihydroxy-3-[(hydroxymethylidene)amino]naphthalen-2-yl]carboximidate	Generator

Chemical Formula

C₁₈H₁₄N₂O₆

Average Mass

354.3180 Da

Monoisotopic Mass

354.08519 Da

IUPAC Name

N-[1-(3,4-dihydroxyphenyl)-3-formamido-6,7-dihydroxynaphthalen-2-yl]formamide

Traditional Name

N-[1-(3,4-dihydroxyphenyl)-3-formamido-6,7-dihydroxynaphthalen-2-yl]formamide

CAS Registry Number

Not Available

SMILES

OC1=C(O)C=C(C=C1)C1=C(NC=O)C(NC=O)=CC2=CC(O)=C(O)C=C12

InChI Identifier

InChI=1S/C18H14N2O6/c21-7-19-12-3-10-5-15(25)16(26)6-11(10)17(18(12)20-8-22)9-1-2-13(23)14(24)4-9/h1-8,23-26H,(H,19,21)(H,20,22)

InChI Key

JIBJFCGHEWXKFO-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
Penicillium miczynskii	LOTUS Database	35616633
Penicillium shearii	NPAtlas	15015725

Species Where Detected

Species Name	Source	Reference
Eupenicillium shearii F80695	KNApSAcK Database	22123792

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthols and derivatives. These are naphthalene derivatives carrying one or more hydroxyl (-OH) groups at any ring position.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Naphthalenes

Sub Class

Naphthols and derivatives

Direct Parent

Naphthols and derivatives

Alternative Parents

Substituents

2-naphthol
Catechol
N-arylamide
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Carboxamide group
Secondary carboxylic acid amide
Carboxylic acid derivative
Organonitrogen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Organic nitrogen compound
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	1.8	ALOGPS
logP	1.77	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	8.77	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	139.12 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	96.31 m³·mol⁻¹	ChemAxon
Polarizability	35.2 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA016863

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00015021

Chemspider ID

8648709

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10473298

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Melanocin C (NP0005188)

MOL for NP0005188 (Melanocin C)

3D MOL for NP0005188 (Melanocin C)

3D SDF for NP0005188 (Melanocin C)

3D-SDF for NP0005188 (Melanocin C)

PDB for NP0005188 (Melanocin C)

3D PDB for NP0005188 (Melanocin C)

SMILES for NP0005188 (Melanocin C)

INCHI for NP0005188 (Melanocin C)

Structure for NP0005188 (Melanocin C)

3D Structure for NP0005188 (Melanocin C)