NP-MRD: Showing NP-Card for (+)-Penigequinolone B (NP0083405)

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Record Information

Version

2.0

Created at

2022-04-29 04:27:54 UTC

Updated at

2022-04-29 04:27:54 UTC

NP-MRD ID

NP0083405

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Penigequinolone B

Description

Penigequinolone B belongs to the class of organic compounds known as phenylquinolines. These are heterocyclic compounds containing a quinoline moiety substituted with a phenyl group. (+)-Penigequinolone B is found in Penicillium cf. simplicissimum, Penicillium scabrosum, Penicillium sp. no.410 and Penicillium sp.NTC-47. Based on a literature review very few articles have been published on Penigequinolone B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292206272D          

 34 37  0  0  1  0            999 V2000
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8986    0.6320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0862    0.4887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4441    1.1207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1620    1.8960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6923    2.5279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4101    3.3032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6505    2.0392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1808    1.4072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9592    0.6320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9979   -0.7752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1855    0.6320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4676    1.4072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2801    1.5505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9979    2.3257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9946    1.9630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8104    0.9185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5282    0.1433    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 N   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  6  0  0  0
  4  5  1  0  0  0  0
  3  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  2  0  0  0  0
  7 14  1  0  0  0  0
  6 15  1  6  0  0  0
  6 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  1  0  0  0  0
 20 21  2  0  0  0  0
 22 21  1  1  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  1  0  0  0  0
 22 30  1  0  0  0  0
 19 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 16 33  1  0  0  0  0
 33 34  1  0  0  0  0
  2 34  1  0  0  0  0
M  END

     RDKit          3D

 67 70  0  0  0  0  0  0  0  0999 V2000
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   -4.0326    3.6913   -0.5350 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3654   -1.8269    0.2708 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4753   -0.8702    0.3040 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6821   -1.1173    0.7570 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7648   -0.0760    0.7545 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0486   -0.7469    1.1903 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9403    0.4269   -0.6618 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0884    1.4003   -0.7400 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0718    2.3159    0.4426 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3533    2.1648    1.2337 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0832    3.7490   -0.1079 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8506    2.1908    1.2883 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4911    0.9239    1.6496 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8442   -1.4174   -0.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0852   -0.1579   -0.7216 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8486   -4.5302    0.1758 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1036   -4.0923   -0.3318 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9779   -4.8681   -0.7807 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4166   -2.6177   -0.3379 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.4878   -2.3763   -1.1809 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5900   -1.8451   -0.5365 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5443    0.2111    0.4368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7468    1.5572    0.4992 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.3941   -0.0994   -2.9176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2366   -2.3390   -2.5333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4420   -5.0029    1.0533 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4597   -3.4232    1.1286 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3427    0.1522   -0.0675 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9097   -2.0907    1.1432 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8924   -1.8542    1.3520 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3812   -0.3859    2.2065 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8362   -0.6753    0.4331 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2136   -0.4552   -1.2782 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0008    0.8964   -0.9823 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9518    1.9500   -1.7178 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0699    0.8697   -0.8741 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0893    1.9058    2.2798 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9577    3.0935    1.2687 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9947    1.4010    0.7512 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.0462    4.0441   -0.2629 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6493    4.4304    0.5559 H   0  0  0  0  0  0  0  0  0  0  0  0
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 33  6  1  0
  9 10  1  0
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 34 67  1  0
 33 66  1  0
M  END


  Mrv1652304292206272D          

 34 37  0  0  1  0            999 V2000
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8986    0.6320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.1620    1.8960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4101    3.3032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6505    2.0392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1808    1.4072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9979   -0.7752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1855    0.6320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4676    1.4072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2801    1.5505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9979    2.3257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9946    1.9630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8104    0.9185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5282    0.1433    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 N   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  6  0  0  0
  4  5  1  0  0  0  0
  3  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
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  6 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  1  0  0  0  0
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 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  1  0  0  0  0
 22 30  1  0  0  0  0
 19 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 16 33  1  0  0  0  0
 33 34  1  0  0  0  0
  2 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0083405

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@H]1C(=O)NC2=CC=C(\C=C\[C@@]3(C)CCC(C)(C)CO3)C(O)=C2[C@]1(O)C1=CC=C(OC)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C27H33NO6/c1-25(2)14-15-26(3,34-16-25)13-12-17-6-11-20-21(22(17)29)27(31,23(33-5)24(30)28-20)18-7-9-19(32-4)10-8-18/h6-13,23,29,31H,14-16H2,1-5H3,(H,28,30)/b13-12+/t23-,26-,27+/m0/s1

> <INCHI_KEY>
CVWJKBJRSZXDIW-NURUMYOOSA-N

> <FORMULA>
C27H33NO6

> <MOLECULAR_WEIGHT>
467.562

> <EXACT_MASS>
467.230787787

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
51.30980067711464

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3R,4R)-4,5-dihydroxy-3-methoxy-4-(4-methoxyphenyl)-6-[(E)-2-[(2R)-2,5,5-trimethyloxan-2-yl]ethenyl]-1,2,3,4-tetrahydroquinolin-2-one

> <ALOGPS_LOGP>
4.22

> <JCHEM_LOGP>
3.837344882333333

> <ALOGPS_LOGS>
-5.01

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.81432405021162

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.273609138109922

> <JCHEM_PKA_STRONGEST_BASIC>
-3.853100526006742

> <JCHEM_POLAR_SURFACE_AREA>
97.25000000000001

> <JCHEM_REFRACTIVITY>
131.9899

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.60e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R,4R)-4,5-dihydroxy-3-methoxy-4-(4-methoxyphenyl)-6-[(E)-2-[(2R)-2,5,5-trimethyloxan-2-yl]ethenyl]-1,3-dihydroquinolin-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.677   1.180   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.161   0.912   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.829   2.092   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.302   3.539   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -1.292   4.719   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -0.766   6.166   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.214   3.807   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.204   2.627   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.657   1.180   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.669  -0.000   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.196  -1.447   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.680   1.180   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.206   2.627   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.723   2.894   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.196   4.341   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.057   3.664   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      12.713   1.715   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      12.186   0.267   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   34  N   UNK     0       2.667  -3.080   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3   34                                                  
CONECT    3    2    4    6                                                  
CONECT    4    3    5                                                       
CONECT    5    4                                                            
CONECT    6    3    7   15   16                                             
CONECT    7    6    8   14                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14                                                       
CONECT   14   13    7                                                       
CONECT   15    6                                                            
CONECT   16    6   17   33                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   31                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24   30                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28   29                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   26   30                                                       
CONECT   30   29   22                                                       
CONECT   31   19   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   16   34                                                  
CONECT   34   33    2                                                       
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

View in JSmol

Synonyms

Value	Source
Penigequinolone a	MeSH

Chemical Formula

C₂₇H₃₃NO₆

Average Mass

467.5620 Da

Monoisotopic Mass

467.23079 Da

IUPAC Name

(3R,4R)-4,5-dihydroxy-3-methoxy-4-(4-methoxyphenyl)-6-[(E)-2-[(2R)-2,5,5-trimethyloxan-2-yl]ethenyl]-1,2,3,4-tetrahydroquinolin-2-one

Traditional Name

(3R,4R)-4,5-dihydroxy-3-methoxy-4-(4-methoxyphenyl)-6-[(E)-2-[(2R)-2,5,5-trimethyloxan-2-yl]ethenyl]-1,3-dihydroquinolin-2-one

CAS Registry Number

Not Available

SMILES

CO[C@H]1C(=O)NC2=CC=C(\C=C\[C@@]3(C)CCC(C)(C)CO3)C(O)=C2[C@]1(O)C1=CC=C(OC)C=C1

InChI Identifier

InChI=1S/C27H33NO6/c1-25(2)14-15-26(3,34-16-25)13-12-17-6-11-20-21(22(17)29)27(31,23(33-5)24(30)28-20)18-7-9-19(32-4)10-8-18/h6-13,23,29,31H,14-16H2,1-5H3,(H,28,30)/b13-12+/t23-,26-,27+/m0/s1

InChI Key

CVWJKBJRSZXDIW-NURUMYOOSA-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 cf. simplicissimum	Fungi	KNApSAcK
Penicillium scabrosum	LOTUS Database	35616633
Penicillium sp. no.410	Fungi	KNApSAcK
Penicillium sp.NTC-47	Fungi	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenylquinolines. These are heterocyclic compounds containing a quinoline moiety substituted with a phenyl group.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Phenylquinolines

Direct Parent

Phenylquinolines

Alternative Parents

Substituents

Phenylquinoline
Tetrahydroquinolone
Quinolone
Tetrahydroquinoline
Anisole
Phenoxy compound
Phenol ether
Styrene
Methoxybenzene
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
Oxane
Tertiary alcohol
Carboxamide group
Secondary carboxylic acid amide
Lactam
Oxacycle
Ether
Dialkyl ether
Carboxylic acid derivative
Azacycle
Organonitrogen compound
Hydrocarbon derivative
Organic nitrogen compound
Organic oxide
Carbonyl group
Organooxygen compound
Organic oxygen compound
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	4.22	ALOGPS
logP	3.84	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	9.27	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	97.25 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	131.99 m³·mol⁻¹	ChemAxon
Polarizability	51.31 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00052086

Chemspider ID

62321916

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

38351019

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Penigequinolone B (NP0083405)

MOL for NP0083405 ((+)-Penigequinolone B)

3D MOL for NP0083405 ((+)-Penigequinolone B)

3D SDF for NP0083405 ((+)-Penigequinolone B)

3D-SDF for NP0083405 ((+)-Penigequinolone B)

PDB for NP0083405 ((+)-Penigequinolone B)

3D PDB for NP0083405 ((+)-Penigequinolone B)

SMILES for NP0083405 ((+)-Penigequinolone B)

INCHI for NP0083405 ((+)-Penigequinolone B)

Structure for NP0083405 ((+)-Penigequinolone B)

3D Structure for NP0083405 ((+)-Penigequinolone B)