NP-MRD: Showing NP-Card for Mangiferoleanone (NP0337224)

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Record Information

Version

2.0

Created at

2024-09-11 09:54:08 UTC

Updated at

2024-09-11 09:54:09 UTC

NP-MRD ID

NP0337224

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Mangiferoleanone

Description

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

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 05262312262D          

 31 35  0  0  0  0            999 V2000
   -2.8557   -0.8572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8557   -1.6840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1404   -2.0977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4263   -1.6840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4263   -0.8572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1404   -0.4452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7111   -2.0977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0027   -1.6840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0027   -0.8572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7111   -0.4452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7152   -0.4452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7152    0.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0027    0.7883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7111    0.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4277   -0.8557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1389   -0.4452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1389    0.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4277    0.7870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8488    0.7870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8488    1.6070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1389    2.0148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4277    1.6070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5539   -2.8143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7269   -2.8143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4263    0.7911    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4263   -0.0302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0027   -0.0302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7152   -1.2720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9253    2.8143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3526    2.8143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8557   -0.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3 23  1  0  0  0  0
  3 24  1  0  0  0  0
  4  5  1  0  0  0  0
  4  7  1  0  0  0  0
  5  6  1  0  0  0  0
  5 10  1  0  0  0  0
  5 26  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 27  1  0  0  0  0
 10 14  1  0  0  0  0
 11 12  1  0  0  0  0
 11 15  1  0  0  0  0
 11 28  1  0  0  0  0
 12 13  1  0  0  0  0
 12 18  2  0  0  0  0
 13 14  1  0  0  0  0
 14 25  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 31  1  0  0  0  0
 18 22  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 29  1  0  0  0  0
 21 30  1  0  0  0  0
M  END


  Mrv2104 05262312262D          

 31 35  0  0  0  0            999 V2000
   -2.8557   -0.8572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8557   -1.6840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1404   -2.0977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4263   -1.6840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4263   -0.8572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1404   -0.4452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7111   -2.0977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0027   -1.6840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0027   -0.8572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7111   -0.4452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7152   -0.4452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7152    0.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0027    0.7883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7111    0.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4277   -0.8557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1389   -0.4452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1389    0.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4277    0.7870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8488    0.7870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8488    1.6070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1389    2.0148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4277    1.6070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5539   -2.8143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7269   -2.8143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4263    0.7911    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4263   -0.0302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0027   -0.0302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7152   -1.2720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9253    2.8143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3526    2.8143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8557   -0.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3 23  1  0  0  0  0
  3 24  1  0  0  0  0
  4  5  1  0  0  0  0
  4  7  1  0  0  0  0
  5  6  1  0  0  0  0
  5 10  1  0  0  0  0
  5 26  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 27  1  0  0  0  0
 10 14  1  0  0  0  0
 11 12  1  0  0  0  0
 11 15  1  0  0  0  0
 11 28  1  0  0  0  0
 12 13  1  0  0  0  0
 12 18  2  0  0  0  0
 13 14  1  0  0  0  0
 14 25  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 31  1  0  0  0  0
 18 22  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 29  1  0  0  0  0
 21 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0337224

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)CCC2(C)CCC3(C)C(CC(=O)C4C5(C)CCCC(C)(C)C5CCC34C)=C2C1

> <INCHI_IDENTIFIER>
InChI=1/C30H48O/c1-25(2)14-15-27(5)16-17-29(7)20(21(27)19-25)18-22(31)24-28(6)12-9-11-26(3,4)23(28)10-13-30(24,29)8/h23-24H,9-19H2,1-8H3

> <INCHI_KEY>
MQILTVJSXIHHGW-UHFFFAOYNA-N

> <FORMULA>
C30H48O

> <MOLECULAR_WEIGHT>
424.713

> <EXACT_MASS>
424.370516166

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
53.0290559219426

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2,2,4a,6a,6b,9,9,12a-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14-icosahydropicen-13-one

> <JCHEM_LOGP>
7.667043533333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.841401928709997

> <JCHEM_PKA_STRONGEST_BASIC>
-7.514772176408651

> <JCHEM_POLAR_SURFACE_AREA>
17.07

> <JCHEM_REFRACTIVITY>
130.7925

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2,2,4a,6a,6b,9,9,12a-octamethyl-3,4,5,6,7,8,8a,10,11,12,12b,14-dodecahydro-1H-picen-13-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 26-MAY-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-MAY-23         0                                  
HETATM    1  C   UNK     0      -5.331  -1.600   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.331  -3.143   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.995  -3.916   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.662  -3.143   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.662  -1.600   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.995  -0.831   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.327  -3.916   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.005  -3.143   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.005  -1.600   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.327  -0.831   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.335  -0.831   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.335   0.705   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.005   1.471   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.327   0.705   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.665  -1.597   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.993  -0.831   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.993   0.705   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.665   1.469   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.318   1.469   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.318   3.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.993   3.761   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.665   3.000   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.767  -5.253   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.224  -5.253   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -2.662   1.477   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -2.662  -0.056   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.005  -0.056   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.335  -2.374   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.594   5.253   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.392   5.253   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.331  -0.067   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   23   24                                             
CONECT    4    3    5    7                                                  
CONECT    5    4    6   10   26                                             
CONECT    6    1    5                                                       
CONECT    7    4    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11   27                                             
CONECT   10    5    9   14                                                  
CONECT   11    9   12   15   28                                             
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   10   13   25                                                  
CONECT   15   11   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19   31                                             
CONECT   18   12   17   22                                                  
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   29   30                                             
CONECT   22   18   21                                                       
CONECT   23    3                                                            
CONECT   24    3                                                            
CONECT   25   14                                                            
CONECT   26    5                                                            
CONECT   27    9                                                            
CONECT   28   11                                                            
CONECT   29   21                                                            
CONECT   30   21                                                            
CONECT   31   17                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₈O

Average Mass

424.7130 Da

Monoisotopic Mass

424.37052 Da

IUPAC Name

2,2,4a,6a,6b,9,9,12a-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14-icosahydropicen-13-one

Traditional Name

2,2,4a,6a,6b,9,9,12a-octamethyl-3,4,5,6,7,8,8a,10,11,12,12b,14-dodecahydro-1H-picen-13-one

CAS Registry Number

Not Available

SMILES

CC1(C)CCC2(C)CCC3(C)C(CC(=O)C4C5(C)CCCC(C)(C)C5CCC34C)=C2C1

InChI Identifier

InChI=1/C30H48O/c1-25(2)14-15-27(5)16-17-29(7)20(21(27)19-25)18-22(31)24-28(6)12-9-11-26(3,4)23(28)10-13-30(24,29)8/h23-24H,9-19H2,1-8H3

InChI Key

MQILTVJSXIHHGW-UHFFFAOYNA-N

Experimental Spectra

Not Available

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	7.67	ChemAxon
pKa (Strongest Acidic)	15.84	ChemAxon
pKa (Strongest Basic)	-7.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	17.07 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	130.79 m³·mol⁻¹	ChemAxon
Polarizability	53.03 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	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

Not Available

Showing NP-Card for Mangiferoleanone (NP0337224)

MOL for NP0337224 (Mangiferoleanone)

3D MOL for NP0337224 (Mangiferoleanone)

3D SDF for NP0337224 (Mangiferoleanone)

3D-SDF for NP0337224 (Mangiferoleanone)

PDB for NP0337224 (Mangiferoleanone)

3D PDB for NP0337224 (Mangiferoleanone)

SMILES for NP0337224 (Mangiferoleanone)

INCHI for NP0337224 (Mangiferoleanone)

Structure for NP0337224 (Mangiferoleanone)

3D Structure for NP0337224 (Mangiferoleanone)