NP-MRD: Showing NP-Card for (2s,7s,9s)-15-(5,6-dimethylhept-3-en-2-yl)-5,12-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-en-10-one (NP0199322)

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Record Information

Version

2.0

Created at

2022-09-04 17:57:00 UTC

Updated at

2022-09-04 17:57:00 UTC

NP-MRD ID

NP0199322

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,7s,9s)-15-(5,6-dimethylhept-3-en-2-yl)-5,12-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-en-10-one

Description

Gargalol C belongs to the class of organic compounds known as ergostane steroids. These are steroids with a structure based on the ergostane skeleton, which arises from the methylation of cholestane at the 24-position. (2s,7s,9s)-15-(5,6-dimethylhept-3-en-2-yl)-5,12-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-en-10-one is found in Grifola gargal. Based on a literature review very few articles have been published on Gargalol C.

Structure

MOL 3D MOL SDF PDB SMILES InChI

  Mrv1652309042219572D          

 32 36  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END

  Mrv1652309042219572D          

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M  END
> <DATABASE_ID>
NP0199322

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C(C)C=CC(C)C1CCC2(O)C3=C(CCC12C)[C@]1(C)CCC(O)C[C@]11O[C@@H]1C3=O

> <INCHI_IDENTIFIER>
InChI=1S/C28H42O4/c1-16(2)17(3)7-8-18(4)20-11-14-27(31)22-21(10-13-25(20,27)5)26(6)12-9-19(29)15-28(26)24(32-28)23(22)30/h7-8,16-20,24,29,31H,9-15H2,1-6H3/t17?,18?,19?,20?,24-,25?,26+,27?,28-/m1/s1

> <INCHI_KEY>
OEDKYCMBXKTOPW-RBVIVZJYSA-N

> <FORMULA>
C28H42O4

> <MOLECULAR_WEIGHT>
442.64

> <EXACT_MASS>
442.308309832

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
52.238955111024225

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,7S,9S)-15-(5,6-dimethylhept-3-en-2-yl)-5,12-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.0^{2,7}.0^{7,9}.0^{12,16}]octadec-1(11)-en-10-one

> <JCHEM_LOGP>
4.694011779999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.168945876166127

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.582905574135651

> <JCHEM_PKA_STRONGEST_BASIC>
-2.729131121161056

> <JCHEM_POLAR_SURFACE_AREA>
70.06

> <JCHEM_REFRACTIVITY>
127.24099999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S,7S,9S)-15-(5,6-dimethylhept-3-en-2-yl)-5,12-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.0^{2,7}.0^{7,9}.0^{12,16}]octadec-1(11)-en-10-one

> <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      15.015  -0.970   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.490  -1.180   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.909  -2.607   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.544   0.035   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.125   1.462   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.019  -0.175   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.074   1.041   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.548   0.830   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.968  -0.597   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.603   2.046   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.031   3.525   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.756   4.389   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.541   3.444   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.172   4.939   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       4.025   3.715   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.032   2.538   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.555   1.089   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.071   0.818   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.064   1.996   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.736   0.610   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.516   2.809   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.039   1.361   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.523   1.632   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.993   1.903   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.516   3.351   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -3.032   3.622   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -0.523   4.528   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.993   4.257   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       0.470   5.706   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       1.985   5.435   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.501   5.164   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       4.494   6.341   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   19                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15   19                                             
CONECT   14   13                                                            
CONECT   15   13   16   31                                                  
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   10   13   20                                             
CONECT   20   19                                                            
CONECT   21   16   22   23   28                                             
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   21   29   30                                             
CONECT   29   28   30                                                       
CONECT   30   29   28   31                                                  
CONECT   31   30   15   32                                                  
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₄₂O₄

Average Mass

442.6400 Da

Monoisotopic Mass

442.30831 Da

IUPAC Name

(2S,7S,9S)-15-(5,6-dimethylhept-3-en-2-yl)-5,12-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.0^{2,7}.0^{7,9}.0^{12,16}]octadec-1(11)-en-10-one

Traditional Name

(2S,7S,9S)-15-(5,6-dimethylhept-3-en-2-yl)-5,12-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.0^{2,7}.0^{7,9}.0^{12,16}]octadec-1(11)-en-10-one

CAS Registry Number

Not Available

SMILES

CC(C)C(C)C=CC(C)C1CCC2(O)C3=C(CCC12C)[C@]1(C)CCC(O)C[C@]11O[C@@H]1C3=O

InChI Identifier

InChI=1S/C28H42O4/c1-16(2)17(3)7-8-18(4)20-11-14-27(31)22-21(10-13-25(20,27)5)26(6)12-9-19(29)15-28(26)24(32-28)23(22)30/h7-8,16-20,24,29,31H,9-15H2,1-6H3/t17?,18?,19?,20?,24-,25?,26+,27?,28-/m1/s1

InChI Key

OEDKYCMBXKTOPW-RBVIVZJYSA-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
Grifola gargal	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ergostane steroids. These are steroids with a structure based on the ergostane skeleton, which arises from the methylation of cholestane at the 24-position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Ergostane steroids

Direct Parent

Ergostane steroids

Alternative Parents

Substituents

Ergostane-skeleton
5,6-epoxysteroid
Cyclohexenone
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Ketone
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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
logP	4.69	ChemAxon
pKa (Strongest Acidic)	13.58	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	70.06 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	127.24 m³·mol⁻¹	ChemAxon
Polarizability	52.24 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

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

139587305

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,7s,9s)-15-(5,6-dimethylhept-3-en-2-yl)-5,12-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-en-10-one (NP0199322)

MOL for NP0199322 ((2s,7s,9s)-15-(5,6-dimethylhept-3-en-2-yl)-5,12-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-en-10-one)

3D MOL for NP0199322 ((2s,7s,9s)-15-(5,6-dimethylhept-3-en-2-yl)-5,12-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-en-10-one)

3D SDF for NP0199322 ((2s,7s,9s)-15-(5,6-dimethylhept-3-en-2-yl)-5,12-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-en-10-one)

3D-SDF for NP0199322 ((2s,7s,9s)-15-(5,6-dimethylhept-3-en-2-yl)-5,12-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-en-10-one)

PDB for NP0199322 ((2s,7s,9s)-15-(5,6-dimethylhept-3-en-2-yl)-5,12-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-en-10-one)

3D PDB for NP0199322 ((2s,7s,9s)-15-(5,6-dimethylhept-3-en-2-yl)-5,12-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-en-10-one)

SMILES for NP0199322 ((2s,7s,9s)-15-(5,6-dimethylhept-3-en-2-yl)-5,12-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-en-10-one)

INCHI for NP0199322 ((2s,7s,9s)-15-(5,6-dimethylhept-3-en-2-yl)-5,12-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-en-10-one)

Structure for NP0199322 ((2s,7s,9s)-15-(5,6-dimethylhept-3-en-2-yl)-5,12-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-en-10-one)

3D Structure for NP0199322 ((2s,7s,9s)-15-(5,6-dimethylhept-3-en-2-yl)-5,12-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-en-10-one)