NP-MRD: Showing NP-Card for 3-hydroxy-12-(5-hydroxy-6-methylpiperidin-2-yl)dodecanoic acid (NP0229551)

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Record Information

Version

2.0

Created at

2022-09-06 09:40:03 UTC

Updated at

2022-09-06 09:40:04 UTC

NP-MRD ID

NP0229551

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-hydroxy-12-(5-hydroxy-6-methylpiperidin-2-yl)dodecanoic acid

Description

3-Hydroxy-12-(5-hydroxy-6-methylpiperidin-2-yl)dodecanoic 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. 3-hydroxy-12-(5-hydroxy-6-methylpiperidin-2-yl)dodecanoic acid is found in Morus alba. 3-Hydroxy-12-(5-hydroxy-6-methylpiperidin-2-yl)dodecanoic acid is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 58 58  0  0  0  0  0  0  0  0999 V2000
   -6.7184    0.9253   -0.9261 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8544   -0.1567   -0.3550 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5873   -0.2731   -1.0674 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7859    0.8851   -0.7284 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7262    1.2538   -1.6557 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6393    0.3470   -2.0102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7150   -0.1191   -0.9169 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2958   -1.0314   -1.6374 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3349   -1.5880   -0.7234 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1227   -0.4445   -0.1275 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1754   -1.0649    0.7968 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0102    0.0396    1.4002 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7509    0.8628    0.4210 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7881    0.2193   -0.4174 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2513   -0.8317   -1.1701 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0111   -0.2489    0.2936 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8358   -1.2814    1.3105 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1600   -2.3286    1.1534 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4566   -1.1166    2.5672 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4022    0.9461    0.7072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7291    1.1630    1.4819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6084    0.0059    1.1347 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.8375    0.0477    1.7914 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2554    1.2035   -1.9098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8116    1.8089   -0.2630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7209    0.5133   -1.1484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3750   -1.1269   -0.4835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1595   -1.1683   -0.7476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5696    1.7429   -0.8269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2303    2.1952   -1.2240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2096    1.6844   -2.5911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9594    0.8886   -2.7434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9325   -0.5719   -2.5635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2396    0.7092   -0.3977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2583   -0.8289   -0.2444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3244   -1.8949   -1.9921 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6863   -0.4995   -2.5197 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8545   -2.2148    0.0359 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0204   -2.2149   -1.3662 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5974    0.1424   -0.9154 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4760    0.2293    0.4824 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6384   -1.5733    1.6155 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7150   -1.7977    0.2195 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2927    0.7211    1.9392 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6700   -0.3810    2.1520 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0705    1.4368   -0.2715 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2498    1.6998    1.0103 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1670    0.9951   -1.1840 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9758   -1.4163   -1.5141 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7124   -0.6231   -0.5206 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5677    0.6394    0.6976 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7844   -0.1841    2.8592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8311    1.8853    0.8775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9175    0.0481    1.1204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1513    2.1194    1.1234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5384    1.1374    2.5610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1140   -0.9221    1.4845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4688   -0.5929    1.4185 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  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
 14 16  1  0
 16 17  1  0
 17 19  1  0
 17 18  2  0
  4 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22  2  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  1
  3 28  1  0
  4 29  1  1
  5 30  1  0
  5 31  1  0
  6 32  1  0
  6 33  1  0
  7 34  1  0
  7 35  1  0
  8 36  1  0
  8 37  1  0
  9 38  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  0
 11 43  1  0
 12 44  1  0
 12 45  1  0
 13 46  1  0
 13 47  1  0
 14 48  1  6
 15 49  1  0
 16 50  1  0
 16 51  1  0
 19 52  1  0
 20 53  1  0
 20 54  1  0
 21 55  1  0
 21 56  1  0
 22 57  1  1
 23 58  1  0
M  END


  Mrv1533004201501522D          

 23 23  0  0  0  0            999 V2000
   -4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.8250    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
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  4 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0229551

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1NC(CCCCCCCCCC(O)CC(O)=O)CCC1O

> <INCHI_IDENTIFIER>
InChI=1S/C18H35NO4/c1-14-17(21)12-11-15(19-14)9-7-5-3-2-4-6-8-10-16(20)13-18(22)23/h14-17,19-21H,2-13H2,1H3,(H,22,23)

> <INCHI_KEY>
OPRYWCSVGFCHJA-UHFFFAOYSA-N

> <FORMULA>
C18H35NO4

> <MOLECULAR_WEIGHT>
329.481

> <EXACT_MASS>
329.256608611

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
39.960937275575844

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-hydroxy-12-(5-hydroxy-6-methylpiperidin-2-yl)dodecanoic acid

> <ALOGPS_LOGP>
1.74

> <JCHEM_LOGP>
0.36047298381508586

> <ALOGPS_LOGS>
-3.88

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.527590923789592

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.371849290779984

> <JCHEM_PKA_STRONGEST_BASIC>
10.066993831645002

> <JCHEM_POLAR_SURFACE_AREA>
89.79

> <JCHEM_REFRACTIVITY>
90.74939999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.37e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-hydroxy-12-(5-hydroxy-6-methylpiperidin-2-yl)dodecanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  C   UNK     0      -8.002   4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.668   3.850   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0      -5.335   4.620   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0      -4.001   3.850   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       9.336   2.310   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      10.669   4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.003   3.850   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      13.337   4.620   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      12.003   2.310   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -5.335   1.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -6.668   2.310   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -8.002   1.540   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   20                                                  
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   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20    4   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    2   23                                                  
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   46    0
END

View in JSmol

Synonyms

Value	Source
3-Hydroxy-12-(5-hydroxy-6-methylpiperidin-2-yl)dodecanoate	Generator

Chemical Formula

C₁₈H₃₅NO₄

Average Mass

329.4810 Da

Monoisotopic Mass

329.25661 Da

IUPAC Name

3-hydroxy-12-(5-hydroxy-6-methylpiperidin-2-yl)dodecanoic acid

Traditional Name

3-hydroxy-12-(5-hydroxy-6-methylpiperidin-2-yl)dodecanoic acid

CAS Registry Number

Not Available

SMILES

CC1NC(CCCCCCCCCC(O)CC(O)=O)CCC1O

InChI Identifier

InChI=1S/C18H35NO4/c1-14-17(21)12-11-15(19-14)9-7-5-3-2-4-6-8-10-16(20)13-18(22)23/h14-17,19-21H,2-13H2,1H3,(H,22,23)

InChI Key

OPRYWCSVGFCHJA-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
Morus alba	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
Alkaloid or derivatives
Amino fatty acid
Beta-hydroxy acid
Heterocyclic fatty acid
Hydroxy fatty acid
Hydroxy acid
Piperidine
1,2-aminoalcohol
Amino acid or derivatives
Amino acid
Secondary alcohol
Carboxylic acid derivative
Carboxylic acid
Secondary aliphatic amine
Azacycle
Organoheterocyclic compound
Secondary amine
Monocarboxylic acid or derivatives
Alcohol
Organic nitrogen compound
Carbonyl group
Amine
Organic oxygen compound
Organic oxide
Organooxygen compound
Hydrocarbon derivative
Organonitrogen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	1.74	ALOGPS
logP	0.36	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	4.37	ChemAxon
pKa (Strongest Basic)	10.07	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	89.79 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	90.75 m³·mol⁻¹	ChemAxon
Polarizability	39.96 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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-hydroxy-12-(5-hydroxy-6-methylpiperidin-2-yl)dodecanoic acid (NP0229551)

MOL for NP0229551 (3-hydroxy-12-(5-hydroxy-6-methylpiperidin-2-yl)dodecanoic acid)

3D MOL for NP0229551 (3-hydroxy-12-(5-hydroxy-6-methylpiperidin-2-yl)dodecanoic acid)

3D SDF for NP0229551 (3-hydroxy-12-(5-hydroxy-6-methylpiperidin-2-yl)dodecanoic acid)

3D-SDF for NP0229551 (3-hydroxy-12-(5-hydroxy-6-methylpiperidin-2-yl)dodecanoic acid)

PDB for NP0229551 (3-hydroxy-12-(5-hydroxy-6-methylpiperidin-2-yl)dodecanoic acid)

3D PDB for NP0229551 (3-hydroxy-12-(5-hydroxy-6-methylpiperidin-2-yl)dodecanoic acid)

SMILES for NP0229551 (3-hydroxy-12-(5-hydroxy-6-methylpiperidin-2-yl)dodecanoic acid)

INCHI for NP0229551 (3-hydroxy-12-(5-hydroxy-6-methylpiperidin-2-yl)dodecanoic acid)

Structure for NP0229551 (3-hydroxy-12-(5-hydroxy-6-methylpiperidin-2-yl)dodecanoic acid)

3D Structure for NP0229551 (3-hydroxy-12-(5-hydroxy-6-methylpiperidin-2-yl)dodecanoic acid)