NP-MRD: Showing NP-Card for isophloionolic acid (NP0280599)

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Record Information

Version

2.0

Created at

2022-09-09 06:28:52 UTC

Updated at

2022-09-09 06:28:52 UTC

NP-MRD ID

NP0280599

Secondary Accession Numbers

None

Natural Product Identification

Common Name

isophloionolic acid

Description

9R,10s,18-trihydroxy-stearic acid belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms. isophloionolic acid is found in Pinus radiata. Based on a literature review very few articles have been published on 9r,10s,18-trihydroxy-stearic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 59 58  0  0  0  0  0  0  0  0999 V2000
    7.1057   -1.8087    2.1893 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7731   -2.0086    1.0070 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1697   -3.1369    0.3497 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9113   -0.9307    0.3568 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5917   -1.2934   -1.0355 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8709   -0.3334   -1.8524 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5470    0.1334   -1.4507 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3510    0.9562   -0.2360 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8370    1.2640   -0.1832 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5077    2.0951    1.0069 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0265    2.3844    1.0273 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3396    3.2272    0.0021 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7294    1.0855    1.0932 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1642    0.2980    2.1462 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1336    1.3507    1.5752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9100    2.1343    0.5875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0173    1.5427   -0.7450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6974    0.2741   -0.9880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2365   -0.9915   -0.3839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1484   -2.1029   -0.9612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5842   -1.9042   -0.6480 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8251   -1.8680    0.8606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2137   -1.6840    1.0478 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0802   -3.5428    0.3315 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9464   -1.0143    0.9524 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4127    0.0082    0.5155 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0183   -2.2748   -1.0440 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5367   -1.5895   -1.6124 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7645   -0.7751   -2.9240 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5598    0.5887   -2.0467 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0990    0.6710   -2.3705 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8335   -0.7730   -1.3994 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8293    1.9603   -0.3966 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6376    0.5791    0.7135 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6328    1.8469   -1.1002 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3192    0.2921   -0.1277 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7573    1.5803    1.9720 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0611    3.0569    1.0420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2026    2.9918    1.9728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0784    2.8659   -0.8674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6299    0.5365    0.1776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4810   -0.6305    1.9363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9509    2.0359    2.5151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5929    0.4387    1.9449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4698    3.1745    0.5290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9578    2.3626    1.0148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5318    2.3103   -1.4328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9811    1.4880   -1.2623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7406    0.1307   -2.1250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7907    0.4031   -0.6561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2001   -1.2810   -0.6620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3677   -1.1007    0.7067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9500   -2.0773   -2.0489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8071   -3.0731   -0.5842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0780   -1.0377   -1.0795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1396   -2.7930   -1.0749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2941   -0.9864    1.2846 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5427   -2.8160    1.3193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3939   -0.7136    1.1210 H   0  0  0  0  0  0  0  0  0  0  0  0
 23 22  1  0
 22 21  1  0
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17 16  1  0
 16 15  1  0
 15 13  1  0
 13 14  1  0
 13 11  1  0
 11 12  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  3  1  0
  2  1  2  0
 23 59  1  0
 22 57  1  0
 22 58  1  0
 21 55  1  0
 21 56  1  0
 20 53  1  0
 20 54  1  0
 19 51  1  0
 19 52  1  0
 18 49  1  0
 18 50  1  0
 17 47  1  0
 17 48  1  0
 16 45  1  0
 16 46  1  0
 15 43  1  0
 15 44  1  0
 13 41  1  6
 14 42  1  0
 11 39  1  1
 12 40  1  0
 10 37  1  0
 10 38  1  0
  9 35  1  0
  9 36  1  0
  8 33  1  0
  8 34  1  0
  7 31  1  0
  7 32  1  0
  6 29  1  0
  6 30  1  0
  5 27  1  0
  5 28  1  0
  4 25  1  0
  4 26  1  0
  3 24  1  0
M  END

  Mrv1652309092208282D          

 23 22  0  0  1  0            999 V2000
    8.4711    5.7158    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1855    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1855    6.9533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9000    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6145    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3289    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0434    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7579    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4724    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1868    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9013    6.1283    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.9013    6.9533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.6158    5.7158    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.6158    4.8908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.3302    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0447    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7592    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4737    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1881    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.9026    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6171    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.3315    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.0460    6.1283    0.0000 O   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0280599

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OCCCCCCCC[C@H](O)[C@H](O)CCCCCCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H36O5/c19-15-11-7-2-1-4-8-12-16(20)17(21)13-9-5-3-6-10-14-18(22)23/h16-17,19-21H,1-15H2,(H,22,23)/t16-,17+/m0/s1

> <INCHI_KEY>
OISFHODBOQNZAG-DLBZAZTESA-N

> <FORMULA>
C18H36O5

> <MOLECULAR_WEIGHT>
332.481

> <EXACT_MASS>
332.256274259

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
40.458369643998424

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(9R,10S)-9,10,18-trihydroxyoctadecanoic acid

> <JCHEM_LOGP>
3.247419356999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.909717016038122

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.6153254581459935

> <JCHEM_PKA_STRONGEST_BASIC>
-1.9922595168618003

> <JCHEM_POLAR_SURFACE_AREA>
97.99000000000001

> <JCHEM_REFRACTIVITY>
91.24529999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
17

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(9R,10S)-9,10,18-trihydroxyoctadecanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  O   UNK     0      15.813  10.669   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      17.146  11.439   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      17.146  12.979   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      18.480  10.669   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      19.814  11.439   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      21.147  10.669   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      22.481  11.439   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      23.815  10.669   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      25.148  11.439   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      26.482  10.669   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      27.816  11.439   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      27.816  12.979   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      29.149  10.669   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      29.149   9.129   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      30.483  11.439   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      31.817  10.669   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      33.150  11.439   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      34.484  10.669   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      35.818  11.439   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      37.152  10.669   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      38.485  11.439   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      39.819  10.669   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      41.153  11.439   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   44    0
END

View in JSmol

Synonyms

Value	Source
9R,10S,18-Trihydroxy-stearate	Generator

Chemical Formula

C₁₈H₃₆O₅

Average Mass

332.4810 Da

Monoisotopic Mass

332.25627 Da

IUPAC Name

(9R,10S)-9,10,18-trihydroxyoctadecanoic acid

Traditional Name

(9R,10S)-9,10,18-trihydroxyoctadecanoic acid

CAS Registry Number

Not Available

SMILES

OCCCCCCCC[C@H](O)[C@H](O)CCCCCCCC(O)=O

InChI Identifier

InChI=1S/C18H36O5/c19-15-11-7-2-1-4-8-12-16(20)17(21)13-9-5-3-6-10-14-18(22)23/h16-17,19-21H,1-15H2,(H,22,23)/t16-,17+/m0/s1

InChI Key

OISFHODBOQNZAG-DLBZAZTESA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Pinus radiata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Long-chain fatty acids

Alternative Parents

Substituents

Long-chain fatty acid
Hydroxy fatty acid
1,2-diol
Secondary alcohol
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Polyol
Hydrocarbon derivative
Organic oxide
Alcohol
Organic oxygen compound
Organooxygen compound
Carbonyl group
Primary alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Other Octadecanoids (LMFA02000006 )

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	3.25	ChemAxon
pKa (Strongest Acidic)	4.62	ChemAxon
pKa (Strongest Basic)	-2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	97.99 Å²	ChemAxon
Rotatable Bond Count	17	ChemAxon
Refractivity	91.25 m³·mol⁻¹	ChemAxon
Polarizability	40.46 Å³	ChemAxon
Number of Rings	0	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

12311165

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for isophloionolic acid (NP0280599)

MOL for NP0280599 (isophloionolic acid)

3D MOL for NP0280599 (isophloionolic acid)

3D SDF for NP0280599 (isophloionolic acid)

3D-SDF for NP0280599 (isophloionolic acid)

PDB for NP0280599 (isophloionolic acid)

3D PDB for NP0280599 (isophloionolic acid)

SMILES for NP0280599 (isophloionolic acid)

INCHI for NP0280599 (isophloionolic acid)

Structure for NP0280599 (isophloionolic acid)

3D Structure for NP0280599 (isophloionolic acid)