NP-MRD: Showing NP-Card for 13-cycloheptyl-2-hydroxytridecanoic acid (NP0145140)

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Record Information

Version

2.0

Created at

2022-09-02 00:16:39 UTC

Updated at

2022-09-02 00:16:40 UTC

NP-MRD ID

NP0145140

Secondary Accession Numbers

None

Natural Product Identification

Common Name

13-cycloheptyl-2-hydroxytridecanoic acid

Description

13-Cycloheptyl-2-hydroxytridecanoic 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. 13-cycloheptyl-2-hydroxytridecanoic acid is found in Alicyclobacillus cycloheptanicus. 13-Cycloheptyl-2-hydroxytridecanoic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 61 61  0  0  0  0  0  0  0  0999 V2000
   -7.4395   -1.0859   -3.2390 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3146   -0.8557   -2.0189 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9588   -1.6882   -1.1412 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5083    0.2703   -1.5426 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.1431    1.0369   -2.6820 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1458   -0.2254   -1.0083 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3427   -1.0424    0.2016 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1354   -1.5695    0.8608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2197   -0.6564    1.5251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5743    0.4509    0.8016 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5769    1.1213    1.7709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9047    2.2671    1.0822 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1384    1.8223   -0.1261 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9254    0.8073    0.2957 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6625    0.4098   -0.9862 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7386   -0.5897   -0.7415 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8199   -0.1475    0.2052 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5463    1.0509   -0.2351 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7478    0.8957   -1.0628 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2181   -0.4664   -1.4066 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9309   -1.1551   -0.2625 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0619   -0.9721    0.9613 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6591   -1.3428    0.5348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9583   -1.8459   -1.2688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9940    0.8924   -0.7723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5746    1.9423   -2.6345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4508    0.6048   -0.9647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7218   -0.9380   -1.7983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0051   -1.9280   -0.1127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9848   -0.4615    0.9271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4362   -2.4140    1.5720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5000   -2.1775    0.1098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6867   -0.1780    2.4565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3764   -1.2593    2.0017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3063    1.2916    0.6174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1134    0.1795   -0.1219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1461    1.4411    2.6781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8558    0.3627    2.1208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6557    3.0440    0.7592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2118    2.7682    1.8114 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4418    2.6762   -0.5803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7450    1.3455   -0.9117 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6354    1.2638    0.9870 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4771   -0.1209    0.6804 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0470    1.2654   -1.5466 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8480   -0.0476   -1.6296 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1170   -0.9209   -1.7270 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2684   -1.5089   -0.2867 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2844    0.1147    1.1682 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8561    1.6455    0.6849 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8087    1.7479   -0.7157 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5846    1.4322   -2.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6431    1.4463   -0.6434 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4864   -1.1124   -1.9160 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0343   -0.3298   -2.1842 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9594   -0.7900   -0.1176 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9024   -2.2502   -0.4993 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1141    0.0649    1.3494 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4512   -1.6277    1.7654 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2151   -1.9091    1.3826 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6400   -2.0449   -0.3235 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
  4  2  1  0
  2  3  1  0
  2  1  2  0
 23 17  1  0
  5 26  1  0
  4 25  1  1
  6 27  1  0
  6 28  1  0
  7 29  1  0
  7 30  1  0
  8 31  1  0
  8 32  1  0
  9 33  1  0
  9 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 12 39  1  0
 12 40  1  0
 13 41  1  0
 13 42  1  0
 14 43  1  0
 14 44  1  0
 15 45  1  0
 15 46  1  0
 16 47  1  0
 16 48  1  0
 17 49  1  0
 18 50  1  0
 18 51  1  0
 19 52  1  0
 19 53  1  0
 20 54  1  0
 20 55  1  0
 21 56  1  0
 21 57  1  0
 22 58  1  0
 22 59  1  0
 23 60  1  0
 23 61  1  0
  3 24  1  0
M  END


  Mrv1533004161502542D          

 23 23  0  0  0  0            999 V2000
    8.3206   -0.0812    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3206   -0.9062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6061   -1.3187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8917   -0.9062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1772   -1.3187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4627   -0.9062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7483   -1.3187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0338   -0.9062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3193   -1.3187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048   -0.9062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8904   -1.3187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1759   -0.9062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4614   -1.3187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2530   -0.9062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9347   -1.3709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7230   -1.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0244   -0.3598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6119    0.3547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7962    0.4776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1914   -0.0835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0351   -1.3187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7496   -0.9062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0351   -2.1437    0.0000 O   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  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  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 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
 14 20  1  0  0  0  0
  2 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0145140

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC(CCCCCCCCCCCC1CCCCCC1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H38O3/c21-19(20(22)23)17-13-7-5-3-1-2-4-6-10-14-18-15-11-8-9-12-16-18/h18-19,21H,1-17H2,(H,22,23)

> <INCHI_KEY>
QMSDXTYLUVLIRZ-UHFFFAOYSA-N

> <FORMULA>
C20H38O3

> <MOLECULAR_WEIGHT>
326.521

> <EXACT_MASS>
326.282095084

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
41.83418048262562

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
13-cycloheptyl-2-hydroxytridecanoic acid

> <ALOGPS_LOGP>
7.07

> <JCHEM_LOGP>
6.542516045666667

> <ALOGPS_LOGS>
-5.87

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
14.284148890034412

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.255557640559995

> <JCHEM_PKA_STRONGEST_BASIC>
-3.797528712514443

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
95.12519999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.40e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
13-cycloheptyl-2-hydroxytridecanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  O   UNK     0      15.532  -0.152   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      15.532  -1.692   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      14.198  -2.462   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.864  -1.692   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.531  -2.462   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.197  -1.692   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.863  -2.462   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.530  -1.692   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.196  -2.462   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.862  -1.692   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.529  -2.462   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.195  -1.692   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.861  -2.462   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.472  -1.692   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.745  -2.559   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.216  -2.105   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.779  -0.672   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.009   0.662   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.486   0.892   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.357  -0.156   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      16.865  -2.462   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      18.199  -1.692   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      16.865  -4.002   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   21                                                  
CONECT    3    2    4                                                       
CONECT    4    3    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                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   20                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   14                                                       
CONECT   21    2   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   46    0
END

View in JSmol

Synonyms

Value	Source
13-Cycloheptyl-2-hydroxytridecanoate	Generator

Chemical Formula

C₂₀H₃₈O₃

Average Mass

326.5210 Da

Monoisotopic Mass

326.28210 Da

IUPAC Name

13-cycloheptyl-2-hydroxytridecanoic acid

Traditional Name

13-cycloheptyl-2-hydroxytridecanoic acid

CAS Registry Number

Not Available

SMILES

OC(CCCCCCCCCCCC1CCCCCC1)C(O)=O

InChI Identifier

InChI=1S/C20H38O3/c21-19(20(22)23)17-13-7-5-3-1-2-4-6-10-14-18-15-11-8-9-12-16-18/h18-19,21H,1-17H2,(H,22,23)

InChI Key

QMSDXTYLUVLIRZ-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, 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
Alicyclobacillus cycloheptanicus	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
Alpha-hydroxy acid
Hydroxy acid
Monosaccharide
Secondary alcohol
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Alcohol
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Organooxygen compound
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic 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	7.07	ALOGPS
logP	6.54	ChemAxon
logS	-5.9	ALOGPS
pKa (Strongest Acidic)	4.26	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	95.13 m³·mol⁻¹	ChemAxon
Polarizability	41.83 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

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

101921415

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 13-cycloheptyl-2-hydroxytridecanoic acid (NP0145140)

MOL for NP0145140 (13-cycloheptyl-2-hydroxytridecanoic acid)

3D MOL for NP0145140 (13-cycloheptyl-2-hydroxytridecanoic acid)

3D SDF for NP0145140 (13-cycloheptyl-2-hydroxytridecanoic acid)

3D-SDF for NP0145140 (13-cycloheptyl-2-hydroxytridecanoic acid)

PDB for NP0145140 (13-cycloheptyl-2-hydroxytridecanoic acid)

3D PDB for NP0145140 (13-cycloheptyl-2-hydroxytridecanoic acid)

SMILES for NP0145140 (13-cycloheptyl-2-hydroxytridecanoic acid)

INCHI for NP0145140 (13-cycloheptyl-2-hydroxytridecanoic acid)

Structure for NP0145140 (13-cycloheptyl-2-hydroxytridecanoic acid)

3D Structure for NP0145140 (13-cycloheptyl-2-hydroxytridecanoic acid)