NP-MRD: Showing NP-Card for chamilactone A (NP0341910)

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Record Information

Version

2.0

Created at

2024-10-22 03:45:17 UTC

Updated at

2025-06-11 05:35:07 UTC

NP-MRD ID

NP0341910

Natural Product DOI

https://doi.org/10.57994/3398

Secondary Accession Numbers

None

Natural Product Identification

Common Name

chamilactone A

Description

Based on a literature review very few articles have been published on chamilactone A.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 01192303562D          

 19 21  0  0  1  0            999 V2000
    3.8974    1.8646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425    1.0799    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1274    0.4125    0.0000 O   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
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   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
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8974   -1.0396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  9  8  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
  7 12  1  0  0  0  0
 12 13  2  0  0  0  0
  4 13  1  0  0  0  0
 13 14  1  0  0  0  0
 11 15  2  0  0  0  0
 10 16  1  1  0  0  0
  9 17  1  6  0  0  0
  5 18  1  0  0  0  0
  3 18  1  0  0  0  0
 18 19  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0341910

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1OC(=O)C2=C1C(O)=C1C(=O)[C@H](C)[C@@H](C)OC1=C2

> <INCHI_IDENTIFIER>
InChI=1S/C14H14O5/c1-5-6(2)18-9-4-8-10(7(3)19-14(8)17)13(16)11(9)12(5)15/h4-7,16H,1-3H3/t5-,6-,7+/m1/s1

> <INCHI_KEY>
RFYRHMABBGAAFK-QYNIQEEDSA-N

> <FORMULA>
C14H14O5

> <MOLECULAR_WEIGHT>
262.261

> <EXACT_MASS>
262.084123551

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
26.483621048589534

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4S,11R,12R)-2-hydroxy-4,11,12-trimethyl-5,10-dioxatricyclo[7.4.0.0^{3,7}]trideca-1,3(7),8-triene-6,13-dione

> <JCHEM_LOGP>
2.5888390993333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.178591683261951

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.496370034328803

> <JCHEM_PKA_STRONGEST_BASIC>
-4.922628949084574

> <JCHEM_POLAR_SURFACE_AREA>
72.83

> <JCHEM_REFRACTIVITY>
67.0372

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(4S,11R,12R)-2-hydroxy-4,11,12-trimethyl-5,10-dioxatricyclo[7.4.0.0^{3,7}]trideca-1,3(7),8-triene-6,13-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-JAN-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JAN-23         0                                  
HETATM    1  C   UNK     0       7.275   3.481   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.799   2.016   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       7.705   0.770   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.799  -0.476   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       7.275  -1.941   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2   18                                                       
CONECT    4    2    5   13                                                  
CONECT    5    4    6   18                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   17                                                  
CONECT   10    9   11   16                                                  
CONECT   11   10   12   15                                                  
CONECT   12   11    7   13                                                  
CONECT   13   12    4   14                                                  
CONECT   14   13                                                            
CONECT   15   11                                                            
CONECT   16   10                                                            
CONECT   17    9                                                            
CONECT   18    5    3   19                                                  
CONECT   19   18                                                            
MASTER        0    0    0    0    0    0    0    0   19    0   42    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₄H₁₄O₅

Average Mass

262.2610 Da

Monoisotopic Mass

262.08412 Da

IUPAC Name

(4S,11R,12R)-2-hydroxy-4,11,12-trimethyl-5,10-dioxatricyclo[7.4.0.0^{3,7}]trideca-1,3(7),8-triene-6,13-dione

Traditional Name

(4S,11R,12R)-2-hydroxy-4,11,12-trimethyl-5,10-dioxatricyclo[7.4.0.0^{3,7}]trideca-1,3(7),8-triene-6,13-dione

CAS Registry Number

Not Available

SMILES

C[C@@H]1OC(=O)C2=C1C(O)=C1C(=O)[C@H](C)[C@@H](C)OC1=C2

InChI Identifier

InChI=1S/C14H14O5/c1-5-6(2)18-9-4-8-10(7(3)19-14(8)17)13(16)11(9)12(5)15/h4-7,16H,1-3H3/t5-,6-,7+/m1/s1

InChI Key

RFYRHMABBGAAFK-QYNIQEEDSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
NOESY NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, CDCl3, experimental)	gang.li@qdu.edu.cn	Qingdao University	Gang Li	2024-10-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl3, experimental)	gang.li@qdu.edu.cn	Qingdao University	Gang Li	2024-10-22	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, CDCl3, experimental)	gang.li@qdu.edu.cn	Qingdao University	Gang Li	2024-10-22	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, CDCl3, experimental)	gang.li@qdu.edu.cn	Qingdao University	Gang Li	2024-10-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCl3, experimental)	gang.li@qdu.edu.cn	Qingdao University	Gang Li	2024-10-22	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, CDCl3, experimental)	gang.li@qdu.edu.cn	Qingdao University	Gang Li	2024-10-22	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Classification

Not classified

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	2.59	ChemAxon
pKa (Strongest Acidic)	7.5	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	67.04 m³·mol⁻¹	ChemAxon
Polarizability	26.48 Å³	ChemAxon
Number of Rings	3	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

Showing NP-Card for chamilactone A (NP0341910)

MOL for NP0341910 (chamilactone A)

3D MOL for NP0341910 (chamilactone A)

3D SDF for NP0341910 (chamilactone A)

3D-SDF for NP0341910 (chamilactone A)

PDB for NP0341910 (chamilactone A)

3D PDB for NP0341910 (chamilactone A)

SMILES for NP0341910 (chamilactone A)

INCHI for NP0341910 (chamilactone A)

Structure for NP0341910 (chamilactone A)

3D Structure for NP0341910 (chamilactone A)