NP-MRD: Showing NP-Card for Peniisocoumarin F (NP0018166)

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Record Information

Version

2.0

Created at

2021-01-06 02:45:24 UTC

Updated at

2021-07-15 17:27:28 UTC

NP-MRD ID

NP0018166

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Peniisocoumarin F

Provided By

NPAtlas

Description

Peniisocoumarin F is found in Penicillium and Penicillium commune. Based on a literature review very few articles have been published on Peniisocoumarin F.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242104313D          

 33 34  0  0  0  0            999 V2000
   -5.4995   -0.9978    0.0288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2006   -1.4588   -0.1918 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1109   -0.6284    0.0258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2529    0.6755    0.4645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1657    1.4895    0.6768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2691    2.7988    1.1154 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8983    0.9854    0.4436 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2190    1.7857    0.6498 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0933    2.9770    1.0504 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3912    1.2468    0.4100 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5840    0.0378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9541   -0.5220   -0.2570 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9420    0.5624    0.0499 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7569    1.0320    1.7498 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    5.3536    0.1974   -0.2978 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7689   -0.9301    0.4084 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.6526   -2.4561   -0.6553 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.5664   -0.4222    0.9757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2223   -1.8416    0.0408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2248    1.0837    0.6505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2112    3.1598    1.2842 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0414   -0.9385   -1.2724 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1204   -1.3639    0.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6617    1.4524   -0.5669 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0085    1.0293    0.0211 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4475    0.0963   -1.3817 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6340   -1.7089   -0.2133 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6461   -1.7935   -0.5566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4869   -3.0188   -0.7977 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
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 19 20  1  0  0  0  0
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  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  4 24  1  0  0  0  0
  6 25  1  0  0  0  0
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 13 28  1  6  0  0  0
 15 29  1  0  0  0  0
 15 30  1  0  0  0  0
 16 31  1  0  0  0  0
 17 32  1  0  0  0  0
 20 33  1  0  0  0  0
M  END

     RDKit          3D

 33 34  0  0  0  0  0  0  0  0999 V2000
   -5.4995   -0.9978    0.0288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2006   -1.4588   -0.1918 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1109   -0.6284    0.0258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2529    0.6755    0.4645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1657    1.4895    0.6768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2691    2.7988    1.1154 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8983    0.9854    0.4436 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2190    1.7857    0.6498 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0933    2.9770    1.0504 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3912    1.2468    0.4100 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5840    0.0378   -0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9541   -0.5220   -0.2570 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9420    0.5624    0.0499 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7569    1.0320    1.7498 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    5.3536    0.1974   -0.2978 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7689   -0.9301    0.4084 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5155   -0.7778   -0.2138 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7773   -0.3118    0.0081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8453   -1.1528   -0.2141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6526   -2.4561   -0.6553 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7541   -0.2869   -0.8068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5664   -0.4222    0.9757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2223   -1.8416    0.0408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2248    1.0837    0.6505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2112    3.1598    1.2842 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0414   -0.9385   -1.2724 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1204   -1.3639    0.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6617    1.4524   -0.5669 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0085    1.0293    0.0211 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4475    0.0963   -1.3817 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6340   -1.7089   -0.2133 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6461   -1.7935   -0.5566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4869   -3.0188   -0.7977 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
  5  6  1  0
  5  7  2  0
  7  8  1  0
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  8 10  1  0
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 19  3  1  0
 18  7  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
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 15 30  1  0
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 17 32  1  0
 20 33  1  0
M  END


  Mrv1652306242104313D          

 33 34  0  0  0  0            999 V2000
   -5.4995   -0.9978    0.0288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2006   -1.4588   -0.1918 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1109   -0.6284    0.0258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2529    0.6755    0.4645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1657    1.4895    0.6768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2691    2.7988    1.1154 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8983    0.9854    0.4436 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2190    1.7857    0.6498 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0933    2.9770    1.0504 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3912    1.2468    0.4100 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5840    0.0378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9541   -0.5220   -0.2570 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9420    0.5624    0.0499 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7569    1.0320    1.7498 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    5.3536    0.1974   -0.2978 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7689   -0.9301    0.4084 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5155   -0.7778   -0.2138 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7773   -0.3118    0.0081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8453   -1.1528   -0.2141 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.2248    1.0837    0.6505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2112    3.1598    1.2842 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0414   -0.9385   -1.2724 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1204   -1.3639    0.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6617    1.4524   -0.5669 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0085    1.0293    0.0211 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4475    0.0963   -1.3817 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6340   -1.7089   -0.2133 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6461   -1.7935   -0.5566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4869   -3.0188   -0.7977 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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
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  1 21  1  0  0  0  0
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 17 32  1  0  0  0  0
 20 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0018166

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C(=O)OC(=C([H])C2=C(O[H])C(OC([H])([H])[H])=C1[H])C([H])([H])[C@@]([H])(Cl)C([H])([H])O[H]

> <INCHI_IDENTIFIER>
InChI=1S/C13H13ClO6/c1-19-10-4-9(16)11-8(12(10)17)3-7(20-13(11)18)2-6(14)5-15/h3-4,6,15-17H,2,5H2,1H3/t6-/m1/s1

> <INCHI_KEY>
YQDKBMBOGVESDO-ZCFIWIBFSA-N

> <FORMULA>
C13H13ClO6

> <MOLECULAR_WEIGHT>
300.69

> <EXACT_MASS>
300.0400658

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
28.79780955117592

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-[(2R)-2-chloro-3-hydroxypropyl]-5,8-dihydroxy-6-methoxy-1H-isochromen-1-one

> <ALOGPS_LOGP>
1.77

> <JCHEM_LOGP>
1.8779678186666666

> <ALOGPS_LOGS>
-3.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.227955715493309

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.300257355975805

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0365403828222837

> <JCHEM_POLAR_SURFACE_AREA>
96.22000000000001

> <JCHEM_REFRACTIVITY>
73.1527

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.52e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-[(2R)-2-chloro-3-hydroxypropyl]-5,8-dihydroxy-6-methoxyisochromen-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 33 34  0  0  0  0  0  0  0  0999 V2000
   -5.4995   -0.9978    0.0288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2006   -1.4588   -0.1918 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1109   -0.6284    0.0258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2529    0.6755    0.4645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1657    1.4895    0.6768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2691    2.7988    1.1154 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8983    0.9854    0.4436 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2190    1.7857    0.6498 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0933    2.9770    1.0504 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3912    1.2468    0.4100 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5840    0.0378   -0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9541   -0.5220   -0.2570 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9420    0.5624    0.0499 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7569    1.0320    1.7498 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    5.3536    0.1974   -0.2978 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7689   -0.9301    0.4084 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5155   -0.7778   -0.2138 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7773   -0.3118    0.0081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8453   -1.1528   -0.2141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6526   -2.4561   -0.6553 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7541   -0.2869   -0.8068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5664   -0.4222    0.9757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2223   -1.8416    0.0408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2248    1.0837    0.6505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2112    3.1598    1.2842 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0414   -0.9385   -1.2724 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1204   -1.3639    0.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6617    1.4524   -0.5669 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0085    1.0293    0.0211 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4475    0.0963   -1.3817 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6340   -1.7089   -0.2133 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6461   -1.7935   -0.5566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4869   -3.0188   -0.7977 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
  5  6  1  0
  5  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 11 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 19  3  1  0
 18  7  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  4 24  1  0
  6 25  1  0
 12 26  1  0
 12 27  1  0
 13 28  1  6
 15 29  1  0
 15 30  1  0
 16 31  1  0
 17 32  1  0
 20 33  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      -5.500  -0.998   0.029  0.00  0.00           C+0
HETATM    2  O   UNK     0      -4.201  -1.459  -0.192  0.00  0.00           O+0
HETATM    3  C   UNK     0      -3.111  -0.628   0.026  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.253   0.676   0.465  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.166   1.490   0.677  0.00  0.00           C+0
HETATM    6  O   UNK     0      -2.269   2.799   1.115  0.00  0.00           O+0
HETATM    7  C   UNK     0      -0.898   0.985   0.444  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.219   1.786   0.650  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.093   2.977   1.050  0.00  0.00           O+0
HETATM   10  O   UNK     0       1.391   1.247   0.410  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.584   0.038   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.954  -0.522  -0.257  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.942   0.562   0.050  0.00  0.00           C+0
HETATM   14 Cl   UNK     0       3.757   1.032   1.750  0.00  0.00          Cl+0
HETATM   15  C   UNK     0       5.354   0.197  -0.298  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.769  -0.930   0.408  0.00  0.00           O+0
HETATM   17  C   UNK     0       0.516  -0.778  -0.214  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.777  -0.312   0.008  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.845  -1.153  -0.214  0.00  0.00           C+0
HETATM   20  O   UNK     0      -1.653  -2.456  -0.655  0.00  0.00           O+0
HETATM   21  H   UNK     0      -5.754  -0.287  -0.807  0.00  0.00           H+0
HETATM   22  H   UNK     0      -5.566  -0.422   0.976  0.00  0.00           H+0
HETATM   23  H   UNK     0      -6.222  -1.842   0.041  0.00  0.00           H+0
HETATM   24  H   UNK     0      -4.225   1.084   0.651  0.00  0.00           H+0
HETATM   25  H   UNK     0      -3.211   3.160   1.284  0.00  0.00           H+0
HETATM   26  H   UNK     0       3.041  -0.939  -1.272  0.00  0.00           H+0
HETATM   27  H   UNK     0       3.120  -1.364   0.453  0.00  0.00           H+0
HETATM   28  H   UNK     0       3.662   1.452  -0.567  0.00  0.00           H+0
HETATM   29  H   UNK     0       6.008   1.029   0.021  0.00  0.00           H+0
HETATM   30  H   UNK     0       5.447   0.096  -1.382  0.00  0.00           H+0
HETATM   31  H   UNK     0       5.634  -1.709  -0.213  0.00  0.00           H+0
HETATM   32  H   UNK     0       0.646  -1.794  -0.557  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.487  -3.019  -0.798  0.00  0.00           H+0
CONECT    1    2   21   22   23                                             
CONECT    2    1    3                                                       
CONECT    3    2    4   19                                                  
CONECT    4    3    5   24                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5   25                                                       
CONECT    7    5    8   18                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   17                                                  
CONECT   12   11   13   26   27                                             
CONECT   13   12   14   15   28                                             
CONECT   14   13                                                            
CONECT   15   13   16   29   30                                             
CONECT   16   15   31                                                       
CONECT   17   11   18   32                                                  
CONECT   18   17   19    7                                                  
CONECT   19   18   20    3                                                  
CONECT   20   19   33                                                       
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    4                                                            
CONECT   25    6                                                            
CONECT   26   12                                                            
CONECT   27   12                                                            
CONECT   28   13                                                            
CONECT   29   15                                                            
CONECT   30   15                                                            
CONECT   31   16                                                            
CONECT   32   17                                                            
CONECT   33   20                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   68    0
END

RDKit          3D

33 34  0  0  0  0  0  0  0  0999 V2000
   -5.4995   -0.9978    0.0288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2006   -1.4588   -0.1918 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1109   -0.6284    0.0258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2529    0.6755    0.4645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1657    1.4895    0.6768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2691    2.7988    1.1154 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8983    0.9854    0.4436 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2190    1.7857    0.6498 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0933    2.9770    1.0504 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3912    1.2468    0.4100 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5840    0.0378   -0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9541   -0.5220   -0.2570 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9420    0.5624    0.0499 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7569    1.0320    1.7498 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    5.3536    0.1974   -0.2978 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7689   -0.9301    0.4084 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5155   -0.7778   -0.2138 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7773   -0.3118    0.0081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8453   -1.1528   -0.2141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6526   -2.4561   -0.6553 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7541   -0.2869   -0.8068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5664   -0.4222    0.9757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2223   -1.8416    0.0408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2248    1.0837    0.6505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2112    3.1598    1.2842 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0414   -0.9385   -1.2724 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1204   -1.3639    0.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6617    1.4524   -0.5669 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0085    1.0293    0.0211 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4475    0.0963   -1.3817 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6340   -1.7089   -0.2133 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6461   -1.7935   -0.5566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4869   -3.0188   -0.7977 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
  5  6  1  0
  5  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 11 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 19  3  1  0
 18  7  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  4 24  1  0
  6 25  1  0
 12 26  1  0
 12 27  1  0
 13 28  1  6
 15 29  1  0
 15 30  1  0
 16 31  1  0
 17 32  1  0
 20 33  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₃H₁₃ClO₆

Average Mass

300.6900 Da

Monoisotopic Mass

300.04007 Da

IUPAC Name

3-[(2R)-2-chloro-3-hydroxypropyl]-5,8-dihydroxy-6-methoxy-1H-isochromen-1-one

Traditional Name

3-[(2R)-2-chloro-3-hydroxypropyl]-5,8-dihydroxy-6-methoxyisochromen-1-one

CAS Registry Number

Not Available

SMILES

COC1=C(O)C2=C(C(O)=C1)C(=O)OC(C[C@@H](Cl)CO)=C2

InChI Identifier

InChI=1S/C13H13ClO6/c1-19-10-4-9(16)11-8(12(10)17)3-7(20-13(11)18)2-6(14)5-15/h3-4,6,15-17H,2,5H2,1H3/t6-/m1/s1

InChI Key

YQDKBMBOGVESDO-ZCFIWIBFSA-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	NPAtlas	29792702
Penicillium commune	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	1.77	ALOGPS
logP	1.88	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	8.3	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	96.22 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	73.15 m³·mol⁻¹	ChemAxon
Polarizability	28.8 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA022678

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

71048952

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139590016

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Peniisocoumarin F (NP0018166)

MOL for NP0018166 (Peniisocoumarin F)

3D MOL for NP0018166 (Peniisocoumarin F)

3D SDF for NP0018166 (Peniisocoumarin F)

3D-SDF for NP0018166 (Peniisocoumarin F)

PDB for NP0018166 (Peniisocoumarin F)

3D PDB for NP0018166 (Peniisocoumarin F)

SMILES for NP0018166 (Peniisocoumarin F)

INCHI for NP0018166 (Peniisocoumarin F)

Structure for NP0018166 (Peniisocoumarin F)

3D Structure for NP0018166 (Peniisocoumarin F)