NP-MRD: Showing NP-Card for (1's,2r,2's,4's,7's,8'r,9's,12's,13'r,16's)-5,7',9',13',19'-pentamethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-ol (NP0281230)

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Record Information

Version

2.0

Created at

2022-09-09 07:26:55 UTC

Updated at

2022-09-09 07:26:56 UTC

NP-MRD ID

NP0281230

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1's,2r,2's,4's,7's,8'r,9's,12's,13'r,16's)-5,7',9',13',19'-pentamethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-ol

Description

6-Methyldiosgenin belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (1's,2r,2's,4's,7's,8'r,9's,12's,13'r,16's)-5,7',9',13',19'-pentamethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-ol is found in Balanites aegyptiaca and Trigonella foenum-graecum. (1's,2r,2's,4's,7's,8'r,9's,12's,13'r,16's)-5,7',9',13',19'-pentamethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-ol was first documented in 2002 (PMID: 12358471). Based on a literature review very few articles have been published on 6-Methyldiosgenin.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092209262D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309092209262D          

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 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 20 26  1  0  0  0  0
 20 27  1  0  0  0  0
 27 28  1  6  0  0  0
 29 27  1  1  0  0  0
 18 29  1  0  0  0  0
 14 29  1  0  0  0  0
 16 30  1  0  0  0  0
 11 30  1  0  0  0  0
 30 31  1  6  0  0  0
  2 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0281230

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1[C@H]2[C@H](C[C@H]3[C@@H]4CC(C)=C5C[C@@H](O)CC[C@]5(C)[C@H]4CC[C@]23C)O[C@]11CCC(C)CO1

> <INCHI_IDENTIFIER>
InChI=1S/C28H44O3/c1-16-6-11-28(30-15-16)18(3)25-24(31-28)14-23-20-12-17(2)22-13-19(29)7-9-26(22,4)21(20)8-10-27(23,25)5/h16,18-21,23-25,29H,6-15H2,1-5H3/t16?,18-,19-,20+,21-,23-,24-,25-,26+,27-,28+/m0/s1

> <INCHI_KEY>
RJQCTQMDJCNDGK-CYLZVYOHSA-N

> <FORMULA>
C28H44O3

> <MOLECULAR_WEIGHT>
428.657

> <EXACT_MASS>
428.329045277

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
52.81918931743945

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1'S,2R,2'S,4'S,7'S,8'R,9'S,12'S,13'R,16'S)-5,7',9',13',19'-pentamethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icosan]-18'-en-16'-ol

> <JCHEM_LOGP>
5.170666725666665

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.20109566448507

> <JCHEM_PKA_STRONGEST_BASIC>
-1.397671064542258

> <JCHEM_POLAR_SURFACE_AREA>
38.69

> <JCHEM_REFRACTIVITY>
124.5479

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,2R,2'S,4'S,7'S,8'R,9'S,12'S,13'R,16'S)-5,7',9',13',19'-pentamethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icosan]-18'-en-16'-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       2.335  -7.800   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.026  -6.423   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.180  -5.137   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.642  -5.226   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.204  -3.939   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -1.741  -4.029   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       0.487  -2.563   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.025  -2.474   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.871  -3.761   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.562  -2.384   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.408  -3.671   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.100  -2.295   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.637  -2.205   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.483  -3.492   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.315  -2.196   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.792  -4.868   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.887  -5.951   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.255  -5.244   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      10.778  -5.476   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      11.469  -4.100   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.013  -2.659   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      13.532  -2.409   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      14.508  -3.600   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      16.028  -3.351   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      13.965  -5.041   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      12.445  -5.291   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      10.374  -3.017   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.606  -1.495   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.006  -3.724   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.255  -4.958   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.563  -6.334   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   31                                                  
CONECT    3    2    4    9                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8    3   10   11                                             
CONECT   10    9                                                            
CONECT   11    9   12   30                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16   29                                             
CONECT   15   14                                                            
CONECT   16   14   17   30                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   29                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   26   27                                             
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   20                                                       
CONECT   27   20   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   18   14                                                  
CONECT   30   16   11   31                                                  
CONECT   31   30    2                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₄₄O₃

Average Mass

428.6570 Da

Monoisotopic Mass

428.32905 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H]1[C@H]2[C@H](C[C@H]3[C@@H]4CC(C)=C5C[C@@H](O)CC[C@]5(C)[C@H]4CC[C@]23C)O[C@]11CCC(C)CO1

InChI Identifier

InChI=1S/C28H44O3/c1-16-6-11-28(30-15-16)18(3)25-24(31-28)14-23-20-12-17(2)22-13-19(29)7-9-26(22,4)21(20)8-10-27(23,25)5/h16,18-21,23-25,29H,6-15H2,1-5H3/t16?,18-,19-,20+,21-,23-,24-,25-,26+,27-,28+/m0/s1

InChI Key

RJQCTQMDJCNDGK-CYLZVYOHSA-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
Balanites aegyptiaca	LOTUS Database	35616633
Trigonella foenum-graecum	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
Spirostane skeleton
3-beta-hydroxysteroid
3-beta-hydroxy-delta-5-steroid
Hydroxysteroid
3-hydroxysteroid
3-hydroxy-delta-5-steroid
Steroid
Delta-5-steroid
Ketal
Oxane
Tetrahydrofuran
Cyclic alcohol
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Acetal
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
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

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

29367466

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

91873636

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Taylor WG, Zulyniak HJ, Richards KW, Acharya SN, Bittman S, Elder JL: Variation in diosgenin levels among 10 accessions of fenugreek seeds produced in western Canada. J Agric Food Chem. 2002 Oct 9;50(21):5994-7. doi: 10.1021/jf020486y. [PubMed:12358471 ]
LOTUS database [Link]

Showing NP-Card for (1's,2r,2's,4's,7's,8'r,9's,12's,13'r,16's)-5,7',9',13',19'-pentamethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-ol (NP0281230)

MOL for NP0281230 ((1's,2r,2's,4's,7's,8'r,9's,12's,13'r,16's)-5,7',9',13',19'-pentamethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-ol)

3D MOL for NP0281230 ((1's,2r,2's,4's,7's,8'r,9's,12's,13'r,16's)-5,7',9',13',19'-pentamethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-ol)

3D SDF for NP0281230 ((1's,2r,2's,4's,7's,8'r,9's,12's,13'r,16's)-5,7',9',13',19'-pentamethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-ol)

3D-SDF for NP0281230 ((1's,2r,2's,4's,7's,8'r,9's,12's,13'r,16's)-5,7',9',13',19'-pentamethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-ol)

PDB for NP0281230 ((1's,2r,2's,4's,7's,8'r,9's,12's,13'r,16's)-5,7',9',13',19'-pentamethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-ol)

3D PDB for NP0281230 ((1's,2r,2's,4's,7's,8'r,9's,12's,13'r,16's)-5,7',9',13',19'-pentamethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-ol)

SMILES for NP0281230 ((1's,2r,2's,4's,7's,8'r,9's,12's,13'r,16's)-5,7',9',13',19'-pentamethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-ol)

INCHI for NP0281230 ((1's,2r,2's,4's,7's,8'r,9's,12's,13'r,16's)-5,7',9',13',19'-pentamethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-ol)

Structure for NP0281230 ((1's,2r,2's,4's,7's,8'r,9's,12's,13'r,16's)-5,7',9',13',19'-pentamethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-ol)

3D Structure for NP0281230 ((1's,2r,2's,4's,7's,8'r,9's,12's,13'r,16's)-5,7',9',13',19'-pentamethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-ol)