NP-MRD: Showing NP-Card for Coronalolic acid (NP0140730)

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Record Information

Version

2.0

Created at

2022-06-29 21:49:07 UTC

Updated at

2022-06-29 21:49:07 UTC

NP-MRD ID

NP0140730

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Coronalolic acid

Description

Coronalolic acid, also known as coronalolate, belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Coronalolic acid is found in Gardenia coronaria. Coronalolic acid was first documented in 2014 (PMID: 24695677). Based on a literature review very few articles have been published on Coronalolic acid (PMID: 35532362).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652306292223492D          

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M  END

     RDKit          3D

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M  END


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 13 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 17 23  1  1  0  0  0
 22 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 21 29  1  1  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 14 33  1  1  0  0  0
 13 34  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0140730

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](CC\C=C(/C)C=O)[C@H]1CC[C@@]2(C)[C@@H]3CC[C@@H](C(=C)CO)[C@@]4(CCC(O)=O)C[C@@]34CC[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C30H46O4/c1-20(17-31)7-6-8-21(2)23-11-13-28(5)25-10-9-24(22(3)18-32)29(14-12-26(33)34)19-30(25,29)16-15-27(23,28)4/h7,17,21,23-25,32H,3,6,8-16,18-19H2,1-2,4-5H3,(H,33,34)/b20-7+/t21-,23-,24+,25+,27-,28+,29-,30+/m1/s1

> <INCHI_KEY>
IOFXIXOKOAYADV-ICQJXUMVSA-N

> <FORMULA>
C30H46O4

> <MOLECULAR_WEIGHT>
470.694

> <EXACT_MASS>
470.339609961

$$$$

HEADER    PROTEIN                                 29-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-JUN-22         0                                  
HETATM    1  C   UNK     0       7.389   3.057   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.218   1.759   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.756   1.827   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.466   3.193   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.005   3.261   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.833   1.963   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.123   0.596   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      14.372   2.031   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      15.200   0.732   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       7.507   0.392   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.195  -0.986   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.097  -2.066   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.731  -1.355   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.984   0.164   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.795   1.143   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.353   0.603   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.100  -0.916   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.289  -1.895   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.035  -3.414   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.593  -3.954   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.404  -2.975   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.658  -1.456   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.911   0.063   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.139  -1.203   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.401   0.239   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.577   1.428   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       0.037   2.870   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       2.096   1.175   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -0.038  -3.515   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -0.291  -5.034   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -1.227  -2.537   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -2.669  -3.077   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       6.395   1.648   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.638  -2.892   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   10                                                  
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                                                            
CONECT   10    2   11   14                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   18   34                                             
CONECT   14   13   10   15   33                                             
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   22   23                                             
CONECT   18   17   13   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   29                                                  
CONECT   22   21   17   23   24                                             
CONECT   23   22   17                                                       
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   21   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31                                                            
CONECT   33   14                                                            
CONECT   34   13                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

View in JSmol

Synonyms

Value	Source
Coronalolate	Generator

Chemical Formula

C₃₀H₄₆O₄

Average Mass

470.6940 Da

Monoisotopic Mass

470.33961 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H](CC\C=C(/C)C=O)[C@H]1CC[C@@]2(C)[C@@H]3CC[C@@H](C(=C)CO)[C@@]4(CCC(O)=O)C[C@@]34CC[C@]12C

InChI Identifier

InChI=1S/C30H46O4/c1-20(17-31)7-6-8-21(2)23-11-13-28(5)25-10-9-24(22(3)18-32)29(14-12-26(33)34)19-30(25,29)16-15-27(23,28)4/h7,17,21,23-25,32H,3,6,8-16,18-19H2,1-2,4-5H3,(H,33,34)/b20-7+/t21-,23-,24+,25+,27-,28+,29-,30+/m1/s1

InChI Key

IOFXIXOKOAYADV-ICQJXUMVSA-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
Gardenia coronaria	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Carbocyclic fatty acid
Hydroxy fatty acid
Fatty acyl
Enal
Alpha,beta-unsaturated aldehyde
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxygen compound
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
Aldehyde
Organic oxide
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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

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

8823421

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10648063

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Khac Hung N, Quang DN, Quang LD, Minh TT, Dung TN, Duong PQ, Tung NH, Hoang VD: New cycloartane coronalyl acetate and other terpenoids with anti-inflammatory activity from the leaves of Vietnamese Gardenia philastrei. Nat Prod Res. 2022 May 9:1-5. doi: 10.1080/14786419.2022.2074004. [PubMed:35532362 ]
Chowdhury A, Azam S, Jainul MA, Faruq KO, Islam A: Antibacterial Activities and In Vitro Anti-Inflammatory (Membrane Stability) Properties of Methanolic Extracts of Gardenia coronaria Leaves. Int J Microbiol. 2014;2014:410935. doi: 10.1155/2014/410935. Epub 2014 Feb 19. [PubMed:24695677 ]

Showing NP-Card for Coronalolic acid (NP0140730)

MOL for NP0140730 (Coronalolic acid)

3D MOL for NP0140730 (Coronalolic acid)

3D SDF for NP0140730 (Coronalolic acid)

3D-SDF for NP0140730 (Coronalolic acid)

PDB for NP0140730 (Coronalolic acid)

3D PDB for NP0140730 (Coronalolic acid)

SMILES for NP0140730 (Coronalolic acid)

INCHI for NP0140730 (Coronalolic acid)

Structure for NP0140730 (Coronalolic acid)

3D Structure for NP0140730 (Coronalolic acid)