NP-MRD: Showing NP-Card for Punctaporonin C (NP0064924)

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Record Information

Version

2.0

Created at

2022-04-28 09:13:35 UTC

Updated at

2022-04-28 09:13:35 UTC

NP-MRD ID

NP0064924

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Punctaporonin C

Description

4-{[(1S,4R,5R,6R,7R,8R,9R,13S)-6,9-dihydroxy-2,2,9-trimethyl-12-oxatetracyclo[6.3.2.0¹,⁴.0⁵,¹³]Tridecan-7-yl]oxy}-4-oxobutanoic acid belongs to the class of organic compounds known as oxepanes. Oxepanes are compounds containing an oxepane ring, which is a seven-member saturated aliphatic heterocycle with one oxygen and six carbon atoms. Punctaporonin C is found in Poronia punctata. Based on a literature review very few articles have been published on 4-{[(1S,4R,5R,6R,7R,8R,9R,13S)-6,9-dihydroxy-2,2,9-trimethyl-12-oxatetracyclo[6.3.2.0¹,⁴.0⁵,¹³]Tridecan-7-yl]oxy}-4-oxobutanoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282211132D          

 26 29  0  0  1  0            999 V2000
   -0.7346   -1.6641    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8261   -0.8064    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6207   -0.8338    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1408   -1.3926    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5147   -2.0100    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6629   -2.8216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8328   -0.8097    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6208    0.0914    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0984   -0.1718    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4461    0.1945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6230   -0.6220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5097    1.0171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2012    0.5270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9334    0.7472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0276    0.7343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5528    0.0053    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1290    0.4698    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2234   -0.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0201   -2.0766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6943   -1.6641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6943   -0.8391    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4088   -2.0766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1233   -1.6641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8377   -2.0766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5522   -1.6641    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8377   -2.9016    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  1  5  1  0  0  0  0
  5  6  1  6  0  0  0
  4  7  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  3  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
  7 11  1  1  0  0  0
 10 12  1  0  0  0  0
 10 13  1  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  2 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  6  0  0  0
  1 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
M  END

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
   -4.5621   -0.8190    1.3739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7605   -1.2802    0.1773 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6666   -1.8927   -0.8552 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6434   -2.2819    0.5886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9803   -1.8356   -0.6697 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7155   -1.3685   -0.9050 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6355   -0.3713    0.2711 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7954   -0.1914    0.8390 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6457   -0.4861   -0.2600 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5773    0.6945   -1.0488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9583    1.9482   -0.4041 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4657    1.8656   -0.0794 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2384    3.1214   -0.6112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3498    1.9541    1.3245 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0353    0.6714   -0.5844 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2514   -0.0942   -0.7279 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0719   -0.0579    0.4115 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4305    0.2113    0.3738 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9348    0.4320   -0.7520 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2875    0.2475    1.5795 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6972    0.5680    1.1613 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6317    0.6270    2.2965 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2227    0.4216    3.4522 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9574    0.9096    2.0766 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6884   -1.5574   -0.9244 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2485   -2.1244   -2.0480 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0253   -1.7336    1.8408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4035   -0.2252    0.9903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9507   -0.2823    2.1186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4404   -1.4949   -1.8721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5149   -2.9924   -0.9237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7475   -1.6590   -0.6749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1137   -1.9783    1.5033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0679   -3.2918    0.5763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5501   -2.3105   -1.5264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8701   -0.8298   -1.9092 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0608   -0.7389    1.0649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6546    1.0642   -1.1716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2859    0.6125   -2.1386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1593    2.8145   -1.0744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5637    2.1235    0.5108 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0830    3.3663    0.0804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4594    3.9879   -0.5516 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6421    2.9653   -1.6131 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4902    2.3737    1.5811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3296    0.6976   -1.6679 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8485    0.1212   -1.6385 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -0.7256    2.1068 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9712    1.0475    2.2927 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0892   -0.2260    0.4636 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7612    1.5587    0.6395 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2463    1.3934    1.2336 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0523   -2.1472   -0.0486 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6361   -2.8022   -2.3937 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6 25  1  0
 25 26  1  0
 25 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 24  1  0
 22 23  2  0
 16 15  1  0
 15  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  6
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  1
  9  2  1  0
  9  5  1  0
  7  6  1  0
 12 15  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  3 31  1  0
  3 32  1  0
  4 33  1  0
  4 34  1  0
  5 35  1  6
  6 36  1  6
 25 53  1  1
 26 54  1  0
 16 47  1  6
 20 48  1  0
 20 49  1  0
 21 50  1  0
 21 51  1  0
 24 52  1  0
 15 46  1  6
  7 37  1  1
 10 38  1  0
 10 39  1  0
 11 40  1  0
 11 41  1  0
 13 42  1  0
 13 43  1  0
 13 44  1  0
 14 45  1  0
M  END


  Mrv1652304282211132D          

 26 29  0  0  1  0            999 V2000
   -0.7346   -1.6641    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8261   -0.8064    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6207   -0.8338    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1408   -1.3926    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5147   -2.0100    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6629   -2.8216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8328   -0.8097    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6208    0.0914    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0984   -0.1718    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4461    0.1945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6230   -0.6220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5097    1.0171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2012    0.5270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9334    0.7472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0276    0.7343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5528    0.0053    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1290    0.4698    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2234   -0.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0201   -2.0766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6943   -1.6641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6943   -0.8391    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4088   -2.0766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1233   -1.6641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8377   -2.0766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5522   -1.6641    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8377   -2.9016    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  1  5  1  0  0  0  0
  5  6  1  6  0  0  0
  4  7  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  3  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
  7 11  1  1  0  0  0
 10 12  1  0  0  0  0
 10 13  1  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  2 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  6  0  0  0
  1 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0064924

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)C[C@@H]2[C@@H]3[C@@H](O)[C@H](OC(=O)CCC(O)=O)[C@H]4[C@H]3O[C@]12CC[C@@]4(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C19H28O7/c1-17(2)8-9-12-14(23)16(25-11(22)5-4-10(20)21)13-15(12)26-19(9,17)7-6-18(13,3)24/h9,12-16,23-24H,4-8H2,1-3H3,(H,20,21)/t9-,12-,13-,14-,15+,16-,18-,19+/m1/s1

> <INCHI_KEY>
ZGMOCGJWZDFJFJ-WMELFTEMSA-N

> <FORMULA>
C19H28O7

> <MOLECULAR_WEIGHT>
368.426

> <EXACT_MASS>
368.183503242

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
39.12727679187273

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-{[(1S,4R,5R,6R,7R,8R,9R,13S)-6,9-dihydroxy-2,2,9-trimethyl-12-oxatetracyclo[6.3.2.0^{1,4}.0^{5,13}]tridecan-7-yl]oxy}-4-oxobutanoic acid

> <ALOGPS_LOGP>
0.95

> <JCHEM_LOGP>
0.256203356333333

> <ALOGPS_LOGS>
-1.97

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.752506990868032

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.922104642240522

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9671031741634986

> <JCHEM_POLAR_SURFACE_AREA>
113.29

> <JCHEM_REFRACTIVITY>
88.70329999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.99e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-{[(1S,4R,5R,6R,7R,8R,9R,13S)-6,9-dihydroxy-2,2,9-trimethyl-12-oxatetracyclo[6.3.2.0^{1,4}.0^{5,13}]tridecan-7-yl]oxy}-4-oxobutanoic acid

> <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      -1.371  -3.106   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.542  -1.505   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.025  -1.556   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.996  -2.599   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.828  -3.752   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -3.104  -5.267   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -5.288  -1.511   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.892   0.171   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -3.917  -0.321   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -6.433   0.363   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -6.763  -1.161   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -6.552   1.899   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -7.842   0.984   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.609   1.395   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.918   1.371   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.032   0.010   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.241   0.877   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.417  -0.512   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.038  -3.876   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.296  -3.106   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.296  -1.566   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.630  -3.876   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.963  -3.106   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.297  -3.876   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       6.631  -3.106   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       5.297  -5.416   0.000  0.00  0.00           O+0
CONECT    1    2    5   19                                                  
CONECT    2    1    3   16                                                  
CONECT    3    2    4    9                                                  
CONECT    4    3    5    7                                                  
CONECT    5    4    1    6                                                  
CONECT    6    5                                                            
CONECT    7    4    8   11                                                  
CONECT    8    7    9   10   14                                             
CONECT    9    8    3                                                       
CONECT   10    8   11   12   13                                             
CONECT   11   10    7                                                       
CONECT   12   10                                                            
CONECT   13   10                                                            
CONECT   14    8   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15    2   17   18                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19    1   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Value	Source
4-{[(1S,4R,5R,6R,7R,8R,9R,13S)-6,9-dihydroxy-2,2,9-trimethyl-12-oxatetracyclo[6.3.2.0,.0,]tridecan-7-yl]oxy}-4-oxobutanoate	Generator

Chemical Formula

C₁₉H₂₈O₇

Average Mass

368.4260 Da

Monoisotopic Mass

368.18350 Da

IUPAC Name

4-{[(1S,4R,5R,6R,7R,8R,9R,13S)-6,9-dihydroxy-2,2,9-trimethyl-12-oxatetracyclo[6.3.2.0^{1,4}.0^{5,13}]tridecan-7-yl]oxy}-4-oxobutanoic acid

Traditional Name

4-{[(1S,4R,5R,6R,7R,8R,9R,13S)-6,9-dihydroxy-2,2,9-trimethyl-12-oxatetracyclo[6.3.2.0^{1,4}.0^{5,13}]tridecan-7-yl]oxy}-4-oxobutanoic acid

CAS Registry Number

Not Available

SMILES

CC1(C)C[C@@H]2[C@@H]3[C@@H](O)[C@H](OC(=O)CCC(O)=O)[C@H]4[C@H]3O[C@]12CC[C@@]4(C)O

InChI Identifier

InChI=1S/C19H28O7/c1-17(2)8-9-12-14(23)16(25-11(22)5-4-10(20)21)13-15(12)26-19(9,17)7-6-18(13,3)24/h9,12-16,23-24H,4-8H2,1-3H3,(H,20,21)/t9-,12-,13-,14-,15+,16-,18-,19+/m1/s1

InChI Key

ZGMOCGJWZDFJFJ-WMELFTEMSA-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
Poronia punctata	Fungi	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxepanes. Oxepanes are compounds containing an oxepane ring, which is a seven-member saturated aliphatic heterocycle with one oxygen and six carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Oxepanes

Sub Class

Not Available

Direct Parent

Oxepanes

Alternative Parents

Substituents

Oxepane
Hydroxy fatty acid
Heterocyclic fatty acid
Fatty acid ester
Fatty acyl
Dicarboxylic acid or derivatives
Tetrahydrofuran
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Oxacycle
Ether
Dialkyl ether
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	0.95	ALOGPS
logP	0.26	ChemAxon
logS	-2	ALOGPS
pKa (Strongest Acidic)	3.92	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	113.29 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	88.7 m³·mol⁻¹	ChemAxon
Polarizability	39.13 Å³	ChemAxon
Number of Rings	4	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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163077941

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Punctaporonin C (NP0064924)

MOL for NP0064924 (Punctaporonin C)

3D MOL for NP0064924 (Punctaporonin C)

3D SDF for NP0064924 (Punctaporonin C)

3D-SDF for NP0064924 (Punctaporonin C)

PDB for NP0064924 (Punctaporonin C)

3D PDB for NP0064924 (Punctaporonin C)

SMILES for NP0064924 (Punctaporonin C)

INCHI for NP0064924 (Punctaporonin C)

Structure for NP0064924 (Punctaporonin C)

3D Structure for NP0064924 (Punctaporonin C)