NP-MRD: Showing NP-Card for Sporovexin B (NP0001621)

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Record Information

Version

2.0

Created at

2020-09-23 01:58:58 UTC

Updated at

2021-08-10 02:55:45 UTC

NP-MRD ID

NP0001621

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Sporovexin B

Provided By

NPAtlas

Description

4-(3-Carboxy-2-hydroxy-3-methylpropoxy)benzoic acid belongs to the class of organic compounds known as benzoic acids. These are organic Compounds containing a benzene ring which bears at least one carboxyl group. Sporovexin B is found in Sporormiella vexans. Based on a literature review very few articles have been published on 4-(3-carboxy-2-hydroxy-3-methylpropoxy)benzoic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242117443D          

 32 32  0  0  0  0            999 V2000
   -3.2220    0.9608   -0.9759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2463   -0.0703    0.1083 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7656   -1.3660   -0.3815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4053   -1.4878   -1.5690 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7084   -2.4539    0.4623 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5041    0.3982    1.3417 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1364    1.5633    1.7907 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0638    0.7221    1.0449 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3944   -0.4378    0.5875 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9509   -0.3877    0.2486 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7143    0.7562    0.3282 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0480    0.8035   -0.0083 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6571   -0.3552   -0.4496 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0668   -0.3353   -0.8127 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6445   -1.3759   -1.2170 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8237    0.8152   -0.7299 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9206   -1.5119   -0.5393 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5759   -1.5446   -0.1964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0750    1.9508   -0.5008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2065    0.9658   -1.4815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4637    0.7507   -1.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3130   -0.2184    0.4343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4453   -2.5184    1.1742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5497   -0.3483    2.1333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4358    2.1546    2.1765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5971    1.0358    2.0014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9539    1.5736    0.3421 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2348    1.6572    0.6729 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6613    1.6921    0.0481 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7194    1.4961    0.0047 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4247   -2.4049   -0.8884 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0443   -2.4795   -0.2855 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
  3  5  1  0  0  0  0
  2  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 13 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 10  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  2 22  1  1  0  0  0
  5 23  1  0  0  0  0
  6 24  1  1  0  0  0
  7 25  1  0  0  0  0
  8 26  1  0  0  0  0
  8 27  1  0  0  0  0
 11 28  1  0  0  0  0
 12 29  1  0  0  0  0
 16 30  1  0  0  0  0
 17 31  1  0  0  0  0
 18 32  1  0  0  0  0
M  END

     RDKit          3D

 32 32  0  0  0  0  0  0  0  0999 V2000
   -3.2220    0.9608   -0.9759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2463   -0.0703    0.1083 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7656   -1.3660   -0.3815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4053   -1.4878   -1.5690 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7084   -2.4539    0.4623 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5041    0.3982    1.3417 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1364    1.5633    1.7907 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0638    0.7221    1.0449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3944   -0.4378    0.5875 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9509   -0.3877    0.2486 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7143    0.7562    0.3282 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0480    0.8035   -0.0083 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6571   -0.3552   -0.4496 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0668   -0.3353   -0.8127 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6445   -1.3759   -1.2170 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8237    0.8152   -0.7299 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9206   -1.5119   -0.5393 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5759   -1.5446   -0.1964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0750    1.9508   -0.5008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2065    0.9658   -1.4815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4637    0.7507   -1.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3130   -0.2184    0.4343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4453   -2.5184    1.1742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5497   -0.3483    2.1333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4358    2.1546    2.1765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5971    1.0358    2.0014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9539    1.5736    0.3421 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2348    1.6572    0.6729 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6613    1.6921    0.0481 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7194    1.4961    0.0047 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4247   -2.4049   -0.8884 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0443   -2.4795   -0.2855 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
  3  5  1  0
  2  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 13 17  1  0
 17 18  2  0
 18 10  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  1
  5 23  1  0
  6 24  1  1
  7 25  1  0
  8 26  1  0
  8 27  1  0
 11 28  1  0
 12 29  1  0
 16 30  1  0
 17 31  1  0
 18 32  1  0
M  END


  Mrv1652306242117443D          

 32 32  0  0  0  0            999 V2000
   -3.2220    0.9608   -0.9759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2463   -0.0703    0.1083 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7656   -1.3660   -0.3815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4053   -1.4878   -1.5690 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7084   -2.4539    0.4623 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5041    0.3982    1.3417 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1364    1.5633    1.7907 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0638    0.7221    1.0449 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3944   -0.4378    0.5875 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9509   -0.3877    0.2486 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7143    0.7562    0.3282 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0480    0.8035   -0.0083 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6571   -0.3552   -0.4496 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0668   -0.3353   -0.8127 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6445   -1.3759   -1.2170 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8237    0.8152   -0.7299 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9206   -1.5119   -0.5393 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5759   -1.5446   -0.1964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0750    1.9508   -0.5008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2065    0.9658   -1.4815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4637    0.7507   -1.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3130   -0.2184    0.4343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4453   -2.5184    1.1742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5497   -0.3483    2.1333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4358    2.1546    2.1765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5971    1.0358    2.0014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9539    1.5736    0.3421 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2348    1.6572    0.6729 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6613    1.6921    0.0481 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7194    1.4961    0.0047 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4247   -2.4049   -0.8884 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0443   -2.4795   -0.2855 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
  3  5  1  0  0  0  0
  2  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 13 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 10  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  2 22  1  1  0  0  0
  5 23  1  0  0  0  0
  6 24  1  1  0  0  0
  7 25  1  0  0  0  0
  8 26  1  0  0  0  0
  8 27  1  0  0  0  0
 11 28  1  0  0  0  0
 12 29  1  0  0  0  0
 16 30  1  0  0  0  0
 17 31  1  0  0  0  0
 18 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0001621

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)C1=C([H])C([H])=C(OC([H])([H])[C@@]([H])(O[H])[C@]([H])(C(=O)O[H])C([H])([H])[H])C([H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C12H14O6/c1-7(11(14)15)10(13)6-18-9-4-2-8(3-5-9)12(16)17/h2-5,7,10,13H,6H2,1H3,(H,14,15)(H,16,17)/t7-,10-/m1/s1

> <INCHI_KEY>
ZWLHAEAWGFIHEL-UHFFFAOYSA-N

> <FORMULA>
C12H14O6

> <MOLECULAR_WEIGHT>
254.238

> <EXACT_MASS>
254.079038171

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
24.453276676231567

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-[(2S,3R)-3-carboxy-2-hydroxy-3-methylpropoxy]benzoic acid

> <ALOGPS_LOGP>
1.05

> <JCHEM_LOGP>
1.1008048393333338

> <ALOGPS_LOGS>
-2.19

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
4.454974811492728

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.6566371300502585

> <JCHEM_PKA_STRONGEST_BASIC>
-3.277700732194617

> <JCHEM_POLAR_SURFACE_AREA>
104.06000000000002

> <JCHEM_REFRACTIVITY>
61.09840000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.65e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-[(2S,3R)-3-carboxy-2-hydroxy-3-methylpropoxy]benzoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 32 32  0  0  0  0  0  0  0  0999 V2000
   -3.2220    0.9608   -0.9759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2463   -0.0703    0.1083 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7656   -1.3660   -0.3815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4053   -1.4878   -1.5690 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7084   -2.4539    0.4623 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5041    0.3982    1.3417 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1364    1.5633    1.7907 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0638    0.7221    1.0449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3944   -0.4378    0.5875 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9509   -0.3877    0.2486 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7143    0.7562    0.3282 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0480    0.8035   -0.0083 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6571   -0.3552   -0.4496 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0668   -0.3353   -0.8127 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6445   -1.3759   -1.2170 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8237    0.8152   -0.7299 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9206   -1.5119   -0.5393 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5759   -1.5446   -0.1964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0750    1.9508   -0.5008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2065    0.9658   -1.4815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4637    0.7507   -1.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3130   -0.2184    0.4343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4453   -2.5184    1.1742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5497   -0.3483    2.1333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4358    2.1546    2.1765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5971    1.0358    2.0014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9539    1.5736    0.3421 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2348    1.6572    0.6729 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6613    1.6921    0.0481 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7194    1.4961    0.0047 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4247   -2.4049   -0.8884 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0443   -2.4795   -0.2855 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
  3  5  1  0
  2  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 13 17  1  0
 17 18  2  0
 18 10  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  1
  5 23  1  0
  6 24  1  1
  7 25  1  0
  8 26  1  0
  8 27  1  0
 11 28  1  0
 12 29  1  0
 16 30  1  0
 17 31  1  0
 18 32  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      -3.222   0.961  -0.976  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.246  -0.070   0.108  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.766  -1.366  -0.382  0.00  0.00           C+0
HETATM    4  O   UNK     0      -2.405  -1.488  -1.569  0.00  0.00           O+0
HETATM    5  O   UNK     0      -2.708  -2.454   0.462  0.00  0.00           O+0
HETATM    6  C   UNK     0      -2.504   0.398   1.342  0.00  0.00           C+0
HETATM    7  O   UNK     0      -3.136   1.563   1.791  0.00  0.00           O+0
HETATM    8  C   UNK     0      -1.064   0.722   1.045  0.00  0.00           C+0
HETATM    9  O   UNK     0      -0.394  -0.438   0.588  0.00  0.00           O+0
HETATM   10  C   UNK     0       0.951  -0.388   0.249  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.714   0.756   0.328  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.048   0.804  -0.008  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.657  -0.355  -0.450  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.067  -0.335  -0.813  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.644  -1.376  -1.217  0.00  0.00           O+0
HETATM   16  O   UNK     0       5.824   0.815  -0.730  0.00  0.00           O+0
HETATM   17  C   UNK     0       2.921  -1.512  -0.539  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.576  -1.545  -0.196  0.00  0.00           C+0
HETATM   19  H   UNK     0      -3.075   1.951  -0.501  0.00  0.00           H+0
HETATM   20  H   UNK     0      -4.207   0.966  -1.482  0.00  0.00           H+0
HETATM   21  H   UNK     0      -2.464   0.751  -1.761  0.00  0.00           H+0
HETATM   22  H   UNK     0      -4.313  -0.218   0.434  0.00  0.00           H+0
HETATM   23  H   UNK     0      -3.445  -2.518   1.174  0.00  0.00           H+0
HETATM   24  H   UNK     0      -2.550  -0.348   2.133  0.00  0.00           H+0
HETATM   25  H   UNK     0      -2.436   2.155   2.176  0.00  0.00           H+0
HETATM   26  H   UNK     0      -0.597   1.036   2.001  0.00  0.00           H+0
HETATM   27  H   UNK     0      -0.954   1.574   0.342  0.00  0.00           H+0
HETATM   28  H   UNK     0       1.235   1.657   0.673  0.00  0.00           H+0
HETATM   29  H   UNK     0       3.661   1.692   0.048  0.00  0.00           H+0
HETATM   30  H   UNK     0       5.719   1.496   0.005  0.00  0.00           H+0
HETATM   31  H   UNK     0       3.425  -2.405  -0.888  0.00  0.00           H+0
HETATM   32  H   UNK     0       1.044  -2.479  -0.286  0.00  0.00           H+0
CONECT    1    2   19   20   21                                             
CONECT    2    1    3    6   22                                             
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3   23                                                       
CONECT    6    2    7    8   24                                             
CONECT    7    6   25                                                       
CONECT    8    6    9   26   27                                             
CONECT    9    8   10                                                       
CONECT   10    9   11   18                                                  
CONECT   11   10   12   28                                                  
CONECT   12   11   13   29                                                  
CONECT   13   12   14   17                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   30                                                       
CONECT   17   13   18   31                                                  
CONECT   18   17   10   32                                                  
CONECT   19    1                                                            
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    2                                                            
CONECT   23    5                                                            
CONECT   24    6                                                            
CONECT   25    7                                                            
CONECT   26    8                                                            
CONECT   27    8                                                            
CONECT   28   11                                                            
CONECT   29   12                                                            
CONECT   30   16                                                            
CONECT   31   17                                                            
CONECT   32   18                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   64    0
END

RDKit          3D

32 32  0  0  0  0  0  0  0  0999 V2000
   -3.2220    0.9608   -0.9759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2463   -0.0703    0.1083 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7656   -1.3660   -0.3815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4053   -1.4878   -1.5690 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7084   -2.4539    0.4623 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5041    0.3982    1.3417 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1364    1.5633    1.7907 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0638    0.7221    1.0449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3944   -0.4378    0.5875 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9509   -0.3877    0.2486 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7143    0.7562    0.3282 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0480    0.8035   -0.0083 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6571   -0.3552   -0.4496 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0668   -0.3353   -0.8127 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6445   -1.3759   -1.2170 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8237    0.8152   -0.7299 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9206   -1.5119   -0.5393 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5759   -1.5446   -0.1964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0750    1.9508   -0.5008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2065    0.9658   -1.4815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4637    0.7507   -1.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3130   -0.2184    0.4343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4453   -2.5184    1.1742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5497   -0.3483    2.1333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4358    2.1546    2.1765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5971    1.0358    2.0014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9539    1.5736    0.3421 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2348    1.6572    0.6729 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6613    1.6921    0.0481 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7194    1.4961    0.0047 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4247   -2.4049   -0.8884 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0443   -2.4795   -0.2855 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
  3  5  1  0
  2  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 13 17  1  0
 17 18  2  0
 18 10  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  1
  5 23  1  0
  6 24  1  1
  7 25  1  0
  8 26  1  0
  8 27  1  0
 11 28  1  0
 12 29  1  0
 16 30  1  0
 17 31  1  0
 18 32  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
4-(3-Carboxy-2-hydroxy-3-methylpropoxy)benzoate	Generator

Chemical Formula

C₁₂H₁₄O₆

Average Mass

254.2380 Da

Monoisotopic Mass

254.07904 Da

IUPAC Name

4-[(2S,3R)-3-carboxy-2-hydroxy-3-methylpropoxy]benzoic acid

Traditional Name

4-[(2S,3R)-3-carboxy-2-hydroxy-3-methylpropoxy]benzoic acid

CAS Registry Number

Not Available

SMILES

[H]OC(=O)C1=C([H])C([H])=C(OC([H])([H])[C@@]([H])(O[H])[C@]([H])(C(=O)O[H])C([H])([H])[H])C([H])=C1[H]

InChI Identifier

InChI=1S/C12H14O6/c1-7(11(14)15)10(13)6-18-9-4-2-8(3-5-9)12(16)17/h2-5,7,10,13H,6H2,1H3,(H,14,15)(H,16,17)/t7-,10-/m1/s1

InChI Key

ZWLHAEAWGFIHEL-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Sporormiella vexans	NPAtlas	10217738

Species Where Detected

Species Name	Source	Reference
Sporormiella vexans JS306	KNApSAcK Database	22123792

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzoic acids. These are organic Compounds containing a benzene ring which bears at least one carboxyl group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Benzoic acids

Alternative Parents

Substituents

Benzoic acid
Phenoxy compound
Benzoyl
Phenol ether
Beta-hydroxy acid
Alkyl aryl ether
Hydroxy acid
Dicarboxylic acid or derivatives
Secondary alcohol
Ether
Carboxylic acid
Carboxylic acid derivative
Organooxygen compound
Carbonyl group
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	1.05	ALOGPS
logP	1.1	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	3.66	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	104.06 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	61.1 m³·mol⁻¹	ChemAxon
Polarizability	24.45 Å³	ChemAxon
Number of Rings	1	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

NPA010435

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

417690

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

475768

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Sporovexin B (NP0001621)

MOL for NP0001621 (Sporovexin B)

3D MOL for NP0001621 (Sporovexin B)

3D SDF for NP0001621 (Sporovexin B)

3D-SDF for NP0001621 (Sporovexin B)

PDB for NP0001621 (Sporovexin B)

3D PDB for NP0001621 (Sporovexin B)

SMILES for NP0001621 (Sporovexin B)

INCHI for NP0001621 (Sporovexin B)

Structure for NP0001621 (Sporovexin B)

3D Structure for NP0001621 (Sporovexin B)