NP-MRD: Showing NP-Card for Camaranoic acid (NP0070986)

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Record Information

Version

1.0

Created at

2022-04-28 16:23:19 UTC

Updated at

2022-04-28 16:23:19 UTC

NP-MRD ID

NP0070986

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Camaranoic acid

Description

3Alpha-Hydroxy-11-oxo-3,25-epoxyurs-12-ene-28-oic acid belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Camaranoic acid is found in Lantana camara and Lantana camara LINN. . Based on a literature review very few articles have been published on 3alpha-Hydroxy-11-oxo-3,25-epoxyurs-12-ene-28-oic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282218232D          

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M  END

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M  END


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  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 12 10  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  4 16  1  0  0  0  0
 14 17  1  6  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 20 19  1  1  0  0  0
 20 21  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 20 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 24 28  1  0  0  0  0
 28 29  1  0  0  0  0
 21 29  1  0  0  0  0
 24 30  1  1  0  0  0
 13 31  1  1  0  0  0
  4 32  1  1  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
  1 35  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0070986

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1CC[C@@]2(CC[C@]3(C)C(=CC(=O)[C@H]4[C@@]3(C)CC[C@H]3C(C)(C)[C@]5(O)CC[C@]43CO5)[C@@H]2[C@H]1C)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H44O5/c1-17-7-10-28(24(32)33)12-11-26(5)19(22(28)18(17)2)15-20(31)23-27(26,6)9-8-21-25(3,4)30(34)14-13-29(21,23)16-35-30/h15,17-18,21-23,34H,7-14,16H2,1-6H3,(H,32,33)/t17-,18+,21+,22+,23+,26-,27-,28+,29-,30+/m1/s1

> <INCHI_KEY>
UWFTUXFLGQBKBJ-AZCUKQRLSA-N

> <FORMULA>
C30H44O5

> <MOLECULAR_WEIGHT>
484.677

> <EXACT_MASS>
484.318874517

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
55.126830384029304

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,6S,7S,8R,11S,14S,15R,18R,20S)-20-hydroxy-7,8,14,15,19,19-hexamethyl-3-oxo-21-oxahexacyclo[18.2.2.0^{1,18}.0^{2,15}.0^{5,14}.0^{6,11}]tetracos-4-ene-11-carboxylic acid

> <ALOGPS_LOGP>
4.56

> <JCHEM_LOGP>
5.480846920666665

> <ALOGPS_LOGS>
-5.50

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
11.684968968011562

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.4527533533013886

> <JCHEM_PKA_STRONGEST_BASIC>
-4.248794584472269

> <JCHEM_POLAR_SURFACE_AREA>
83.83

> <JCHEM_REFRACTIVITY>
134.18429999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.55e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,6S,7S,8R,11S,14S,15R,18R,20S)-20-hydroxy-7,8,14,15,19,19-hexamethyl-3-oxo-21-oxahexacyclo[18.2.2.0^{1,18}.0^{2,15}.0^{5,14}.0^{6,11}]tetracos-4-ene-11-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      13.473   1.350   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.396   0.116   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.789  -1.299   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.260  -1.481   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.337  -0.248   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.944   1.167   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.022   2.401   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.808  -0.430   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.886   0.803   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.357   0.621   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.434   1.854   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.750  -0.795   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.672  -2.028   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.201  -1.846   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.124  -3.079   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.653  -2.897   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.594  -3.261   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.747  -3.308   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.180  -3.216   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.463  -1.758   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.170  -0.274   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.115   1.197   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.618   1.633   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.222   0.123   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.888  -1.316   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.469  -1.913   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.525  -2.812   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       3.807   0.169   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       5.231   1.151   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       0.688  -0.013   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       8.005  -3.531   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      13.182  -2.714   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      12.575  -4.130   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      14.711  -2.532   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      14.080   2.765   0.000  0.00  0.00           C+0
CONECT    1    2    6   35                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   16   32                                             
CONECT    5    4    6    8                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6                                                            
CONECT    8    5    9   14                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   21                                                  
CONECT   13   12   14   18   31                                             
CONECT   14   13    8   15   17                                             
CONECT   15   14   16                                                       
CONECT   16   15    4                                                       
CONECT   17   14                                                            
CONECT   18   13   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   25                                                  
CONECT   21   20   12   22   29                                             
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   28   30                                             
CONECT   25   24   20   26   27                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   24   29                                                       
CONECT   29   28   21                                                       
CONECT   30   24                                                            
CONECT   31   13                                                            
CONECT   32    4   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35    1                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   80    0
END

View in JSmol

Synonyms

Value	Source
3a-Hydroxy-11-oxo-3,25-epoxyurs-12-ene-28-Oate	Generator
3a-Hydroxy-11-oxo-3,25-epoxyurs-12-ene-28-Oic acid	Generator
3alpha-Hydroxy-11-oxo-3,25-epoxyurs-12-ene-28-Oate	Generator
3Α-hydroxy-11-oxo-3,25-epoxyurs-12-ene-28-Oate	Generator
3Α-hydroxy-11-oxo-3,25-epoxyurs-12-ene-28-Oic acid	Generator

Chemical Formula

C₃₀H₄₄O₅

Average Mass

484.6770 Da

Monoisotopic Mass

484.31887 Da

IUPAC Name

(1R,2S,6S,7S,8R,11S,14S,15R,18R,20S)-20-hydroxy-7,8,14,15,19,19-hexamethyl-3-oxo-21-oxahexacyclo[18.2.2.0^{1,18}.0^{2,15}.0^{5,14}.0^{6,11}]tetracos-4-ene-11-carboxylic acid

Traditional Name

(1R,2S,6S,7S,8R,11S,14S,15R,18R,20S)-20-hydroxy-7,8,14,15,19,19-hexamethyl-3-oxo-21-oxahexacyclo[18.2.2.0^{1,18}.0^{2,15}.0^{5,14}.0^{6,11}]tetracos-4-ene-11-carboxylic acid

CAS Registry Number

Not Available

SMILES

C[C@@H]1CC[C@@]2(CC[C@]3(C)C(=CC(=O)[C@H]4[C@@]3(C)CC[C@H]3C(C)(C)[C@]5(O)CC[C@]43CO5)[C@@H]2[C@H]1C)C(O)=O

InChI Identifier

InChI=1S/C30H44O5/c1-17-7-10-28(24(32)33)12-11-26(5)19(22(28)18(17)2)15-20(31)23-27(26,6)9-8-21-25(3,4)30(34)14-13-29(21,23)16-35-30/h15,17-18,21-23,34H,7-14,16H2,1-6H3,(H,32,33)/t17-,18+,21+,22+,23+,26-,27-,28+,29-,30+/m1/s1

InChI Key

UWFTUXFLGQBKBJ-AZCUKQRLSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Lantana camara	LOTUS Database	35616633
Lantana camara LINN.	Plant	KNApSAcK

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
Naphthopyran
Naphthalene
Cyclohexenone
Pyran
Oxane
Cyclic alcohol
Hemiacetal
Ketone
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Oxacycle
Organoheterocyclic compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organic oxygen compound
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	4.56	ALOGPS
logP	5.48	ChemAxon
logS	-5.5	ALOGPS
pKa (Strongest Acidic)	4.45	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	134.18 m³·mol⁻¹	ChemAxon
Polarizability	55.13 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	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

102473742

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Camaranoic acid (NP0070986)

MOL for NP0070986 (Camaranoic acid)

3D MOL for NP0070986 (Camaranoic acid)

3D SDF for NP0070986 (Camaranoic acid)

3D-SDF for NP0070986 (Camaranoic acid)

PDB for NP0070986 (Camaranoic acid)

3D PDB for NP0070986 (Camaranoic acid)

SMILES for NP0070986 (Camaranoic acid)

INCHI for NP0070986 (Camaranoic acid)

Structure for NP0070986 (Camaranoic acid)

3D Structure for NP0070986 (Camaranoic acid)