NP-MRD: Showing NP-Card for jalapinolic acid (NP0179010)

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Record Information

Version

2.0

Created at

2022-09-03 17:07:24 UTC

Updated at

2022-09-03 17:07:24 UTC

NP-MRD ID

NP0179010

Secondary Accession Numbers

None

Natural Product Identification

Common Name

jalapinolic acid

Description

Jalapinolic acid, also known as jalapinolate, 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. jalapinolic acid is found in Cuscuta chinensis and Ipomoea stans. jalapinolic acid was first documented in 2016 (PMID: 25925631). Based on a literature review a small amount of articles have been published on jalapinolic acid (PMID: 28105860) (PMID: 31017778) (PMID: 27400121) (PMID: 27370528).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 50  0  0  0  0  0  0  0  0999 V2000
   -1.6695   -2.4282    0.2718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0747   -2.3555    0.8170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5642   -0.9284    0.8321 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5430   -0.4088   -0.5967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0179    1.0073   -0.6482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1789    1.9404    0.1681 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7268    3.2346    0.0384 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8002    2.0299   -0.4779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9287    2.9584    0.3146 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4269    3.0881   -0.3067 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0949    1.7236   -0.3433 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4785    1.8419   -0.9525 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1797    0.5222   -1.0351 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3565   -0.0658    0.3116 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0785   -1.3929    0.3066 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3918   -2.4536   -0.4791 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1986   -3.6884   -0.4040 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1931   -3.8012   -1.1488 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8871   -4.7132    0.4595 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2148   -3.4008    0.6037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0064   -1.6352    0.6467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6922   -2.4255   -0.8434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7493   -2.9197    0.1156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1155   -2.7980    1.8400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6271   -0.9323    1.1883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9741   -0.2934    1.5058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5425   -0.5758   -1.0031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2788   -1.0348   -1.1547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0474    1.0270   -0.2143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0299    1.3680   -1.6875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1359    1.7196    1.2335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8727    3.4395   -0.9355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3491    0.9973   -0.4991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9195    2.3658   -1.5084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4206    3.9614    0.4478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8684    2.5462    1.3591 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0581    3.8075    0.2423 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3695    3.4216   -1.3682 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5562    0.9889   -0.9659 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1543    1.3583    0.6805 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3679    2.3200   -1.9699 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0819    2.5991   -0.3769 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1304    0.7050   -1.5794 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5373   -0.1769   -1.6365 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3573   -0.1866    0.8031 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9425    0.6269    0.9494 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1193   -1.2868   -0.0361 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1291   -1.7308    1.3665 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3570   -2.6222   -0.0825 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3346   -2.1869   -1.5748 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5668   -5.1566    1.0622 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


  Mrv1652309032219072D          

 19 18  0  0  1  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
   10.0914    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
   11.5204    5.0013    0.0000 C   0  0  2  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
   12.2349    5.4138    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
   13.6638    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
   15.0927    5.4138    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
   16.5217    5.4138    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
   17.9506    5.4138    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
   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
  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  1  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  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  2  0  0  0  0
 17 19  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0179010

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCC[C@H](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)/t15-/m0/s1

> <INCHI_KEY>
YNQGVRJFSHTULP-HNNXBMFYSA-N

> <FORMULA>
C16H32O3

> <MOLECULAR_WEIGHT>
272.429

> <EXACT_MASS>
272.23514489

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
34.81408242793458

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(11S)-11-hydroxyhexadecanoic acid

> <JCHEM_LOGP>
4.869864250666666

> <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

> <JCHEM_TRADITIONAL_IUPAC>
jalapinolic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         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      18.837   9.336   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      20.171  10.106   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      21.505   9.336   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      21.505   7.796   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      22.838  10.106   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      24.172   9.336   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      25.506  10.106   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      26.839   9.336   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      28.173  10.106   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      29.507   9.336   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      30.840  10.106   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      32.174   9.336   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      33.508  10.106   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      34.842   9.336   0.000  0.00  0.00           C+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    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    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                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
MASTER        0    0    0    0    0    0    0    0   19    0   36    0
END

View in JSmol

Synonyms

Value	Source
(+)-Jalapinolic acid	ChEBI
(+)-Jalapinolate	Generator
Jalapinolate	Generator

Chemical Formula

C₁₆H₃₂O₃

Average Mass

272.4290 Da

Monoisotopic Mass

272.23514 Da

IUPAC Name

(11S)-11-hydroxyhexadecanoic acid

Traditional Name

jalapinolic acid

CAS Registry Number

Not Available

SMILES

CCCCC[C@H](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)/t15-/m0/s1

InChI Key

YNQGVRJFSHTULP-HNNXBMFYSA-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
Cuscuta chinensis	LOTUS Database	35616633
Ipomoea stans	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

hydroxypalmitic acid (CHEBI:75785 )
Hydroxy fatty acids (LMFA01050267 )

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	4.87	ChemAxon
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	34.81 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

C00044036

Chemspider ID

4472245

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5312820

PDB ID

Not Available

ChEBI ID

75785

Good Scents ID

rw1438971

References

General References

Ono M, Kanemaru Y, Yasuda S, Okawa M, Kinjo J, Miyashita H, Yokomizo K, Yoshimitsu H, Nohara T: A new resin glycoside from Calystegia soldanella and its antiviral activity towards herpes. Nat Prod Res. 2017 Nov;31(22):2660-2664. doi: 10.1080/14786419.2017.1280492. Epub 2017 Jan 20. [PubMed:28105860 ]
Sura MB, Ponnapalli MG, Annam SCVAR, Bobbili VVP: Ipomeolides A and B, Resin Glycosides from Ipomoea pes-caprae and Combination Therapy of Ipomeolide A with Doxorubicin. J Nat Prod. 2019 May 24;82(5):1292-1300. doi: 10.1021/acs.jnatprod.8b01100. Epub 2019 Apr 24. [PubMed:31017778 ]
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LOTUS database [Link]

Showing NP-Card for jalapinolic acid (NP0179010)

MOL for NP0179010 (jalapinolic acid)

3D MOL for NP0179010 (jalapinolic acid)

3D SDF for NP0179010 (jalapinolic acid)

3D-SDF for NP0179010 (jalapinolic acid)

PDB for NP0179010 (jalapinolic acid)

3D PDB for NP0179010 (jalapinolic acid)

SMILES for NP0179010 (jalapinolic acid)

INCHI for NP0179010 (jalapinolic acid)

Structure for NP0179010 (jalapinolic acid)

3D Structure for NP0179010 (jalapinolic acid)