NP-MRD: Showing NP-Card for meliasenin m, (rel)- (NP0190186)

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Record Information

Version

2.0

Created at

2022-09-04 06:48:28 UTC

Updated at

2022-09-04 06:48:28 UTC

NP-MRD ID

NP0190186

Secondary Accession Numbers

None

Natural Product Identification

Common Name

meliasenin m, (rel)-

Description

Meliasenin M belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. meliasenin m, (rel)- is found in Melia azedarach. Based on a literature review very few articles have been published on Meliasenin M.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042208482D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309042208482D          

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 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 18 17  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 18 26  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
 28 15  1  1  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 13 31  1  0  0  0  0
 31 32  1  6  0  0  0
 33 31  1  6  0  0  0
 11 33  1  0  0  0  0
  7 33  1  0  0  0  0
  2 34  1  0  0  0  0
 34 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0190186

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)(OO)\C=C\C[C@@H]1[C@@H]2[C@H](C[C@]3(C)C4=CC[C@H]5C(C)(C)C(=O)CC[C@]5(C)[C@H]4CC[C@@]23C)OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H44O5/c1-26(2,35-33)14-8-9-18-24-21(34-25(18)32)17-30(7)20-10-11-22-27(3,4)23(31)13-15-28(22,5)19(20)12-16-29(24,30)6/h8,10,14,18-19,21-22,24,33H,9,11-13,15-17H2,1-7H3/b14-8+/t18-,19+,21+,22+,24-,28-,29+,30-/m1/s1

> <INCHI_KEY>
LQPSEQWINGOYLK-UHVZVPEASA-N

> <FORMULA>
C30H44O5

> <MOLECULAR_WEIGHT>
484.677

> <EXACT_MASS>
484.318874517

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
55.77565207084581

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,4S,7R,8S,9S,12R,13R,18R)-7-[(2E)-4-hydroperoxy-4-methylpent-2-en-1-yl]-2,9,13,17,17-pentamethyl-5-oxapentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icos-1(20)-ene-6,16-dione

> <JCHEM_LOGP>
5.783075772999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.911733340990317

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.700085349292454

> <JCHEM_PKA_STRONGEST_BASIC>
-4.242182667052647

> <JCHEM_POLAR_SURFACE_AREA>
72.83

> <JCHEM_REFRACTIVITY>
137.07950000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,4S,7R,8S,9S,12R,13R,18R)-7-[(2E)-4-hydroperoxy-4-methylpent-2-en-1-yl]-2,9,13,17,17-pentamethyl-5-oxapentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icos-1(20)-ene-6,16-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       9.637 -11.891   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.536 -10.640   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.434  -9.389   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.285  -9.742   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.437  -8.209   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.186  -7.311   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.338  -5.779   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.188  -4.755   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       5.684  -5.083   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       7.806  -3.344   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       9.339  -3.497   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.668  -2.719   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.818  -3.743   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.286  -2.276   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.349  -3.573   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.968  -2.163   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      15.498  -1.993   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      16.410  -3.234   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      17.941  -3.065   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      17.508  -1.587   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      19.321  -2.382   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      18.853  -4.305   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      20.384  -4.136   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      18.235  -5.716   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      16.704  -5.885   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      15.792  -4.645   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      15.173  -6.055   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      14.261  -4.814   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      13.643  -6.225   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      12.112  -6.394   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      11.200  -5.153   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      10.438  -6.491   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       9.668  -5.001   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      11.786 -11.538   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      13.190 -10.904   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   34                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   33                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   33                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15   31                                             
CONECT   14   13                                                            
CONECT   15   13   16   28                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   26                                                  
CONECT   19   18   20   21   22                                             
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   19   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   18   27   28                                             
CONECT   27   26                                                            
CONECT   28   26   15   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   13   32   33                                             
CONECT   32   31                                                            
CONECT   33   31   11    7                                                  
CONECT   34    2   35                                                       
CONECT   35   34                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₄O₅

Average Mass

484.6770 Da

Monoisotopic Mass

484.31887 Da

IUPAC Name

(2S,4S,7R,8S,9S,12R,13R,18R)-7-[(2E)-4-hydroperoxy-4-methylpent-2-en-1-yl]-2,9,13,17,17-pentamethyl-5-oxapentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icos-1(20)-ene-6,16-dione

Traditional Name

(2S,4S,7R,8S,9S,12R,13R,18R)-7-[(2E)-4-hydroperoxy-4-methylpent-2-en-1-yl]-2,9,13,17,17-pentamethyl-5-oxapentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icos-1(20)-ene-6,16-dione

CAS Registry Number

Not Available

SMILES

CC(C)(OO)\C=C\C[C@@H]1[C@@H]2[C@H](C[C@]3(C)C4=CC[C@H]5C(C)(C)C(=O)CC[C@]5(C)[C@H]4CC[C@@]23C)OC1=O

InChI Identifier

InChI=1S/C30H44O5/c1-26(2,35-33)14-8-9-18-24-21(34-25(18)32)17-30(7)20-10-11-22-27(3,4)23(31)13-15-28(22,5)19(20)12-16-29(24,30)6/h8,10,14,18-19,21-22,24,33H,9,11-13,15-17H2,1-7H3/b14-8+/t18-,19+,21+,22+,24-,28-,29+,30-/m1/s1

InChI Key

LQPSEQWINGOYLK-UHVZVPEASA-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
Melia azedarach	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
Steroid lactone
3-oxo-delta-7-steroid
3-oxosteroid
Oxosteroid
3-oxo-5-alpha-steroid
Delta-7-steroid
Steroid
Gamma butyrolactone
Tetrahydrofuran
Cyclic ketone
Carboxylic acid ester
Ketone
Lactone
Hydroperoxide
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Alkyl hydroperoxide
Peroxol
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Carbonyl group
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

triterpenoid (CHEBI:70521 )

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	5.78	ChemAxon
pKa (Strongest Acidic)	11.7	ChemAxon
pKa (Strongest Basic)	-4.2	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	4	ChemAxon
Refractivity	137.08 m³·mol⁻¹	ChemAxon
Polarizability	55.78 Å³	ChemAxon
Number of Rings	5	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

26377244

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

50900151

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for meliasenin m, (rel)- (NP0190186)

MOL for NP0190186 (meliasenin m, (rel)-)

3D MOL for NP0190186 (meliasenin m, (rel)-)

3D SDF for NP0190186 (meliasenin m, (rel)-)

3D-SDF for NP0190186 (meliasenin m, (rel)-)

PDB for NP0190186 (meliasenin m, (rel)-)

3D PDB for NP0190186 (meliasenin m, (rel)-)

SMILES for NP0190186 (meliasenin m, (rel)-)

INCHI for NP0190186 (meliasenin m, (rel)-)

Structure for NP0190186 (meliasenin m, (rel)-)

3D Structure for NP0190186 (meliasenin m, (rel)-)