NP-MRD: Showing NP-Card for 6-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecan-15-ol (NP0174475)

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Record Information

Version

2.0

Created at

2022-09-03 11:44:13 UTC

Updated at

2022-09-03 11:44:13 UTC

NP-MRD ID

NP0174475

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecan-15-ol

Description

(3AlphaOH,20S,24S)-3,19:20,24-Diepoxydammarane-3,25-diol belongs to the class of organic compounds known as triterpene saponins. These are glycosylated derivatives of triterpene sapogenins. The sapogenin moiety backbone is usually based on the oleanane, ursane, taraxastane, bauerane, lanostane, lupeol, lupane, dammarane, cycloartane, friedelane, hopane, 9b,19-cyclo-lanostane, cycloartane, or cycloartanol skeleton (3alphaOH,20S,24S)-3,19:20,24-Diepoxydammarane-3,25-diol is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, (3alphaoh,20S,24S)-3,19:20,24-Diepoxydammarane-3,25-diol has been detected, but not quantified in, green vegetables. 6-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecan-15-ol is found in Cleome africana and Gynandropsis gynandra. This could make (3alphaoh,20S,24S)-3,19:20,24-Diepoxydammarane-3,25-diol a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 05061308002D          

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M  END

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M  END


  Mrv0541 05061308002D          

 34 39  0  0  0  0            999 V2000
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   -2.3660   -1.2194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3662    1.8595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1739    1.6911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9288    1.3585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4785    1.9737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0632    2.6866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2569    2.5119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7284    4.1965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3958    3.4416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6408    3.7742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1508    3.1089    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0173   -0.8400    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  7  1  0  0  0  0
  1 18  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4 10  1  0  0  0  0
  4 17  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7 21  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 14  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 25  1  0  0  0  0
 14 15  1  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
 18 19  1  0  0  0  0
 18 23  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
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 29  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 31  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 23 34  1  0  0  0  0
 21 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0174475

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)(O)C1CCC(C)(O1)C1CCC2(C)C1CCC1C2(C)CCC2C(C)(C)C3(O)CCC12CO3

> <INCHI_IDENTIFIER>
InChI=1S/C30H50O4/c1-24(2)21-11-14-27(6)22(29(21)16-17-30(24,32)33-18-29)9-8-19-20(10-13-26(19,27)5)28(7)15-12-23(34-28)25(3,4)31/h19-23,31-32H,8-18H2,1-7H3

> <INCHI_KEY>
VQVGNVXQGAGQRV-UHFFFAOYSA-N

> <FORMULA>
C30H50O4

> <MOLECULAR_WEIGHT>
474.7156

> <EXACT_MASS>
474.370910088

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
56.418619834328446

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecan-15-ol

> <ALOGPS_LOGP>
4.56

> <JCHEM_LOGP>
5.324514271666665

> <ALOGPS_LOGS>
-6.59

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.326321841385937

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.684017866917213

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0939011853446026

> <JCHEM_POLAR_SURFACE_AREA>
58.92

> <JCHEM_REFRACTIVITY>
134.32319999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.22e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecan-15-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      -3.728  -2.657   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.391  -3.422   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.060  -2.647   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.066  -1.107   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.050   0.274   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.064  -4.608   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.058  -3.432   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -6.044  -4.616   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.431  -1.862   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.264  -0.331   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.731  -0.802   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.631   0.448   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.721   1.690   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.258   1.209   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.078   1.973   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.409   1.198   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.403  -0.342   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.734  -1.117   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -5.070  -0.352   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -6.401  -1.127   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -6.395  -2.667   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -7.726  -3.443   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -4.417  -2.276   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.684   3.471   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.191   3.157   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.600   2.536   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.627   3.684   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.851   5.015   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       2.346   4.689   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       5.093   7.833   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.472   6.424   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.063   7.045   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       5.881   5.803   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      -5.632  -1.568   0.000  0.00  0.00           O+0
CONECT    1    2    7   18                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   10   17                                             
CONECT    5    4                                                            
CONECT    6    7                                                            
CONECT    7    1    6    8   21                                             
CONECT    8    7                                                            
CONECT    9   10                                                            
CONECT   10    4    9   11   14                                             
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   25                                                  
CONECT   14   10   13   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17    4   16   18                                                  
CONECT   18    1   17   19   23                                             
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21    7   20   22   34                                             
CONECT   22   21                                                            
CONECT   23   18   34                                                       
CONECT   24   25                                                            
CONECT   25   13   24   26   29                                             
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   31                                                  
CONECT   29   25   28                                                       
CONECT   30   31                                                            
CONECT   31   28   30   32   33                                             
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   23   21                                                       
MASTER        0    0    0    0    0    0    0    0   34    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₅₀O₄

Average Mass

474.7156 Da

Monoisotopic Mass

474.37091 Da

IUPAC Name

6-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecan-15-ol

Traditional Name

6-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecan-15-ol

CAS Registry Number

Not Available

SMILES

CC(C)(O)C1CCC(C)(O1)C1CCC2(C)C1CCC1C2(C)CCC2C(C)(C)C3(O)CCC12CO3

InChI Identifier

InChI=1S/C30H50O4/c1-24(2)21-11-14-27(6)22(29(21)16-17-30(24,32)33-18-29)9-8-19-20(10-13-26(19,27)5)28(7)15-12-23(34-28)25(3,4)31/h19-23,31-32H,8-18H2,1-7H3

InChI Key

VQVGNVXQGAGQRV-UHFFFAOYSA-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
Cleome africana	LOTUS Database	35616633
Cleome gynandra	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpene saponins. These are glycosylated derivatives of triterpene sapogenins. The sapogenin moiety backbone is usually based on the oleanane, ursane, taraxastane, bauerane, lanostane, lupeol, lupane, dammarane, cycloartane, friedelane, hopane, 9b,19-cyclo-lanostane, cycloartane, or cycloartanol skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Triterpene saponins

Alternative Parents

Not Available

Substituents

Not Available

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	5.32	ChemAxon
logS	-6.6	ALOGPS
pKa (Strongest Acidic)	11.68	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	58.92 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	134.32 m³·mol⁻¹	ChemAxon
Polarizability	56.42 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

HMDB0034683

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB013212

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

73804808

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecan-15-ol (NP0174475)

MOL for NP0174475 (6-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecan-15-ol)

3D MOL for NP0174475 (6-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecan-15-ol)

3D SDF for NP0174475 (6-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecan-15-ol)

3D-SDF for NP0174475 (6-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecan-15-ol)

PDB for NP0174475 (6-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecan-15-ol)

3D PDB for NP0174475 (6-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecan-15-ol)

SMILES for NP0174475 (6-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecan-15-ol)

INCHI for NP0174475 (6-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecan-15-ol)

Structure for NP0174475 (6-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecan-15-ol)

3D Structure for NP0174475 (6-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecan-15-ol)