NP-MRD: Showing NP-Card for builic acid (NP0182716)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-03 21:29:36 UTC

Updated at

2022-09-03 21:29:36 UTC

NP-MRD ID

NP0182716

Secondary Accession Numbers

None

Natural Product Identification

Common Name

builic acid

Description

11-Hydroxy palmitic 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. builic acid is found in Ipomoea muricata. 11-Hydroxy palmitic acid is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 50  0  0  0  0  0  0  0  0999 V2000
   -7.1985    0.9149    0.0977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7338    1.2859   -0.0709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1157    0.3992   -1.1321 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6567    0.7471   -1.3267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8584    0.5727   -0.0620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8784   -0.8345    0.4808 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3573   -1.7657   -0.3975 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1747   -0.8872    1.7859 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7540   -0.4535    1.7195 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1031   -1.2789    0.7998 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5032   -0.6966    0.8984 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5047   -1.3948    0.0277 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8354   -0.6340    0.2900 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9306   -1.1969   -0.5153 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2460   -0.5506   -0.2975 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3913    0.8878   -0.5540 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7208    1.8590    0.2883 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1612    1.7373    1.3817 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6961    3.1873   -0.2255 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8047    1.8557    0.0407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5107    0.1792   -0.6462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3105    0.4348    1.1085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6182    2.3284   -0.3803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1769    1.0867    0.8659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1957   -0.6705   -0.9189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6867    0.5680   -2.0816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2106    0.2125   -2.1744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5759    1.8404   -1.5871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7889    0.7773   -0.3186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1717    1.2972    0.6880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9571   -1.1407    0.6666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4108   -1.4410   -1.3105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1887   -1.9219    2.2347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7379   -0.2676    2.5261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3102   -0.5121    2.7605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6404    0.6275    1.4617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2217   -1.0362   -0.2558 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0707   -2.3440    0.9895 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8943   -0.7373    1.9422 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5091    0.3795    0.5978 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6828   -2.4317    0.3930 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2693   -1.4269   -1.0324 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5986    0.3806   -0.1390 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0133   -0.6507    1.3536 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6809   -1.2271   -1.6159 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0492   -2.2875   -0.1817 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4662   -0.6856    0.8238 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0371   -1.1634   -0.8253 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5118    1.1114   -0.4794 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2038    1.1093   -1.6619 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1651    3.8575    0.3936 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
  6  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 19  1  0
 17 18  2  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  0
  2 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  0
  5 30  1  0
  6 31  1  1
  7 32  1  0
  8 33  1  0
  8 34  1  0
  9 35  1  0
  9 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 13 44  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 16 49  1  0
 16 50  1  0
 19 51  1  0
M  END


  Mrv1652309081718372D          

 19 18  0  0  0  0            999 V2000
    7.9480    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6625    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3770    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0927    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3783    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8072    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6638    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5217    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0914    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9493    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2362    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8059    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2349    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9506    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5204    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6651    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5204    4.1763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.3796    5.4138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.6651    4.1763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  5  4  1  0  0  0  0
  6  4  1  0  0  0  0
  7  5  1  0  0  0  0
  8  6  1  0  0  0  0
  9  3  1  0  0  0  0
 10  7  1  0  0  0  0
 11  8  1  0  0  0  0
 12  9  1  0  0  0  0
 13 10  1  0  0  0  0
 14 11  1  0  0  0  0
 15 12  1  0  0  0  0
 15 13  1  0  0  0  0
 16 14  1  0  0  0  0
 17 15  1  0  0  0  0
 18 16  2  0  0  0  0
 19 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0182716

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCC(O)CCCCCCCCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H32O3/c1-2-3-9-12-15(17)13-10-7-5-4-6-8-11-14-16(18)19/h15,17H,2-14H2,1H3,(H,18,19)

> <INCHI_KEY>
YNQGVRJFSHTULP-UHFFFAOYSA-N

> <FORMULA>
C16H32O3

> <MOLECULAR_WEIGHT>
272.429

> <EXACT_MASS>
272.23514489

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
34.84780917882715

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
11-hydroxyhexadecanoic acid

> <ALOGPS_LOGP>
5.66

> <JCHEM_LOGP>
4.869864250666666

> <ALOGPS_LOGS>
-4.33

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
18.48417303718234

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.952019912826163

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2748229711340455

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
78.75309999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.28e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
builic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-17   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-17         0                                  
HETATM    1  C   UNK     0      14.836  10.106   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      16.170   9.336   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      17.504  10.106   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      28.173  10.106   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      26.839   9.336   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      29.507   9.336   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      25.506  10.106   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      30.840  10.106   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      18.837   9.336   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      24.172   9.336   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      32.174   9.336   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      20.171  10.106   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      22.838  10.106   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      33.508  10.106   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      21.505   9.336   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      34.842   9.336   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      21.505   7.796   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      36.175  10.106   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      34.842   7.796   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    9                                                       
CONECT    4    5    6                                                       
CONECT    5    4    7                                                       
CONECT    6    4    8                                                       
CONECT    7    5   10                                                       
CONECT    8    6   11                                                       
CONECT    9    3   12                                                       
CONECT   10    7   13                                                       
CONECT   11    8   14                                                       
CONECT   12    9   15                                                       
CONECT   13   10   15                                                       
CONECT   14   11   16                                                       
CONECT   15   12   13   17                                                  
CONECT   16   14   18   19                                                  
CONECT   17   15                                                            
CONECT   18   16                                                            
CONECT   19   16                                                            
MASTER        0    0    0    0    0    0    0    0   19    0   36    0
END

View in JSmol

Synonyms

Value	Source
11-Hydroxy palmitate	Generator
16:0(11-OH)	SMPDB, HMDB
11-hydroxypalmitic acid	SMPDB, HMDB
11-hydroxyhexadecanoic acid	SMPDB
11-Hydroxyhexadecanoate	Generator

Chemical Formula

C₁₆H₃₂O₃

Average Mass

272.4290 Da

Monoisotopic Mass

272.23514 Da

IUPAC Name

11-hydroxyhexadecanoic acid

Traditional Name

builic acid

CAS Registry Number

Not Available

SMILES

CCCCCC(O)CCCCCCCCCC(O)=O

InChI Identifier

InChI=1S/C16H32O3/c1-2-3-9-12-15(17)13-10-7-5-4-6-8-11-14-16(18)19/h15,17H,2-14H2,1H3,(H,18,19)

InChI Key

YNQGVRJFSHTULP-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
Ipomoea muricata	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
Secondary alcohol
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Hydroxy fatty acids (LMFA01050049 )

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	5.66	ALOGPS
logP	4.87	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	4.95	ChemAxon
pKa (Strongest Basic)	-1.3	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	14	ChemAxon
Refractivity	78.75 m³·mol⁻¹	ChemAxon
Polarizability	34.85 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

HMDB0112189

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

3013895

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for builic acid (NP0182716)

MOL for NP0182716 (builic acid)

3D MOL for NP0182716 (builic acid)

3D SDF for NP0182716 (builic acid)

3D-SDF for NP0182716 (builic acid)

PDB for NP0182716 (builic acid)

3D PDB for NP0182716 (builic acid)

SMILES for NP0182716 (builic acid)

INCHI for NP0182716 (builic acid)

Structure for NP0182716 (builic acid)

3D Structure for NP0182716 (builic acid)