NP-MRD: Showing NP-Card for (3beta,22E,24R)-5,8-Epidioxy-23-methylergosta-6,22-dien-3-ol (NP0047429)

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Record Information

Version

2.0

Created at

2022-03-17 20:40:03 UTC

Updated at

2022-03-17 20:40:03 UTC

NP-MRD ID

NP0047429

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3beta,22E,24R)-5,8-Epidioxy-23-methylergosta-6,22-dien-3-ol

Description

(3Beta,22E,24R)-5,8-Epidioxy-23-methylergosta-6,22-dien-3-ol 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 (3beta,22E,24R)-5,8-Epidioxy-23-methylergosta-6,22-dien-3-ol is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, (3beta,22E,24R)-5,8-epidioxy-23-methylergosta-6,22-dien-3-ol has been detected, but not quantified in, mushrooms. This could make (3beta,22E,24R)-5,8-epidioxy-23-methylergosta-6,22-dien-3-ol a potential biomarker for the consumption of these foods.

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 02241210522D          

 32 36  0  0  0  0            999 V2000
   -3.7069   -0.5711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7069   -1.3969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9926   -1.8098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2797   -1.3969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2797   -0.5711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9926   -0.1596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5655   -1.8098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8525   -1.3969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8525   -0.5711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5655   -0.1596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1411   -0.1596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1411    0.6620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8525    1.0721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5655    0.6620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6392   -0.4128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1195    0.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6392    0.9137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4540   -2.3121    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4713   -1.5496    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4225   -1.8098    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2797    0.1720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1411    1.4932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8952    1.6982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3433    2.3121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7030    1.8688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2549    1.2551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0628    1.4257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9989    0.4706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6147    0.8119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3189    2.2103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3587    0.0275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4225    0.9826    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
  2 20  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  7  1  0  0  0  0
  4 18  1  0  0  0  0
  5  6  1  0  0  0  0
  5 10  1  0  0  0  0
  5 21  1  0  0  0  0
  7  8  2  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 19  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
 12 13  1  0  0  0  0
 12 17  1  0  0  0  0
 12 22  1  0  0  0  0
 13 14  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 23  1  0  0  0  0
 18 19  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 27 29  1  0  0  0  0
 27 30  1  0  0  0  0
 29 31  1  0  0  0  0
 29 32  1  0  0  0  0
M  END


  Mrv0541 02241210522D          

 32 36  0  0  0  0            999 V2000
   -3.7069   -0.5711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7069   -1.3969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9926   -1.8098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2797   -1.3969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2797   -0.5711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9926   -0.1596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5655   -1.8098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8525   -1.3969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8525   -0.5711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5655   -0.1596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1411   -0.1596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1411    0.6620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8525    1.0721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5655    0.6620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6392   -0.4128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1195    0.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6392    0.9137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4540   -2.3121    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4713   -1.5496    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4225   -1.8098    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2797    0.1720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1411    1.4932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8952    1.6982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3433    2.3121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7030    1.8688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2549    1.2551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0628    1.4257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9989    0.4706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6147    0.8119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3189    2.2103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3587    0.0275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4225    0.9826    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
  2 20  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  7  1  0  0  0  0
  4 18  1  0  0  0  0
  5  6  1  0  0  0  0
  5 10  1  0  0  0  0
  5 21  1  0  0  0  0
  7  8  2  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 19  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
 12 13  1  0  0  0  0
 12 17  1  0  0  0  0
 12 22  1  0  0  0  0
 13 14  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 23  1  0  0  0  0
 18 19  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 27 29  1  0  0  0  0
 27 30  1  0  0  0  0
 29 31  1  0  0  0  0
 29 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0047429

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C(C)C(\C)=C\C(C)C1CCC2C1(C)CCC1C3(C)CCC(O)CC33OOC21C=C3

> <INCHI_IDENTIFIER>
InChI=1S/C29H46O3/c1-18(2)21(5)19(3)16-20(4)23-8-9-24-26(23,6)12-11-25-27(7)13-10-22(30)17-28(27)14-15-29(24,25)32-31-28/h14-16,18,20-25,30H,8-13,17H2,1-7H3/b19-16+

> <INCHI_KEY>
BEFYGZGLHDYVIF-KNTRCKAVSA-N

> <FORMULA>
C29H46O3

> <MOLECULAR_WEIGHT>
442.6737

> <EXACT_MASS>
442.344695338

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
53.550355132260485

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6,10-dimethyl-5-[(3E)-4,5,6-trimethylhept-3-en-2-yl]-16,17-dioxapentacyclo[13.2.2.0¹,⁹.0²,⁶.0¹⁰,¹⁵]nonadec-18-en-13-ol

> <ALOGPS_LOGP>
6.51

> <JCHEM_LOGP>
6.591300119333331

> <ALOGPS_LOGS>
-6.70

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.1490254826832

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7336162538743682

> <JCHEM_POLAR_SURFACE_AREA>
38.69

> <JCHEM_REFRACTIVITY>
131.10609999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.80e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6,10-dimethyl-5-[(3E)-4,5,6-trimethylhept-3-en-2-yl]-16,17-dioxapentacyclo[13.2.2.0¹,⁹.0²,⁶.0¹⁰,¹⁵]nonadec-18-en-13-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -6.920  -1.066   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.920  -2.608   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.586  -3.378   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.255  -2.608   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.255  -1.066   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.586  -0.298   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.922  -3.378   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.591  -2.608   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.591  -1.066   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.922  -0.298   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.263  -0.298   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.263   1.236   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.591   2.001   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.922   1.236   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.193  -0.771   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.090   0.470   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.193   1.706   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -2.714  -4.316   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -0.880  -2.893   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -8.255  -3.378   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -4.255   0.321   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.263   2.787   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.671   3.170   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.641   4.316   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.179   3.488   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.209   2.343   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.717   2.661   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.731   0.878   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.747   1.516   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.195   4.126   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.270   0.051   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.255   1.834   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   20                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    7   18                                             
CONECT    5    4    6   10   21                                             
CONECT    6    1    5                                                       
CONECT    7    4    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11   19                                             
CONECT   10    5    9   14                                                  
CONECT   11    9   12   15                                                  
CONECT   12   11   13   17   22                                             
CONECT   13   12   14                                                       
CONECT   14   10   13                                                       
CONECT   15   11   16                                                       
CONECT   16   15   17                                                       
CONECT   17   12   16   23                                                  
CONECT   18    4   19                                                       
CONECT   19    9   18                                                       
CONECT   20    2                                                            
CONECT   21    5                                                            
CONECT   22   12                                                            
CONECT   23   17   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26   29   30                                                  
CONECT   28   26                                                            
CONECT   29   27   31   32                                                  
CONECT   30   27                                                            
CONECT   31   29                                                            
CONECT   32   29                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

View in JSmol

Synonyms

Value	Source
(3b,22E,24R)-5,8-Epidioxy-23-methylergosta-6,22-dien-3-ol	Generator
(3Β,22E,24R)-5,8-epidioxy-23-methylergosta-6,22-dien-3-ol	Generator

Chemical Formula

C₂₉H₄₆O₃

Average Mass

442.6737 Da

Monoisotopic Mass

442.34470 Da

IUPAC Name

6,10-dimethyl-5-[(3E)-4,5,6-trimethylhept-3-en-2-yl]-16,17-dioxapentacyclo[13.2.2.0¹,⁹.0²,⁶.0¹⁰,¹⁵]nonadec-18-en-13-ol

Traditional Name

6,10-dimethyl-5-[(3E)-4,5,6-trimethylhept-3-en-2-yl]-16,17-dioxapentacyclo[13.2.2.0¹,⁹.0²,⁶.0¹⁰,¹⁵]nonadec-18-en-13-ol

CAS Registry Number

211486-11-2

SMILES

CC(C)C(C)C(\C)=C\C(C)C1CCC2C1(C)CCC1C3(C)CCC(O)CC33OOC21C=C3

InChI Identifier

InChI=1S/C29H46O3/c1-18(2)21(5)19(3)16-20(4)23-8-9-24-26(23,6)12-11-25-27(7)13-10-22(30)17-28(27)14-15-29(24,25)32-31-28/h14-16,18,20-25,30H,8-13,17H2,1-7H3/b19-16+

InChI Key

BEFYGZGLHDYVIF-KNTRCKAVSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Agaricus bisporus	FooDB	Shmuel Yannai Dictionary of Food Compounds with CD-ROM: Additives, Flavors, and Ingredients. Chap...
Pleurotus ostreatus	FooDB	Shmuel Yannai Dictionary of Food Compounds with CD-ROM: Additives, Flavors, and Ingredients. Chap...

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

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	6.51	ALOGPS
logP	6.59	ChemAxon
logS	-6.7	ALOGPS
pKa (Strongest Acidic)	15.15	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	38.69 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	131.11 m³·mol⁻¹	ChemAxon
Polarizability	53.55 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

HMDB0032668

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB010621

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

131751276

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for (3beta,22E,24R)-5,8-Epidioxy-23-methylergosta-6,22-dien-3-ol (NP0047429)

MOL for NP0047429 ((3beta,22E,24R)-5,8-Epidioxy-23-methylergosta-6,22-dien-3-ol)

3D MOL for NP0047429 ((3beta,22E,24R)-5,8-Epidioxy-23-methylergosta-6,22-dien-3-ol)

3D SDF for NP0047429 ((3beta,22E,24R)-5,8-Epidioxy-23-methylergosta-6,22-dien-3-ol)

3D-SDF for NP0047429 ((3beta,22E,24R)-5,8-Epidioxy-23-methylergosta-6,22-dien-3-ol)

PDB for NP0047429 ((3beta,22E,24R)-5,8-Epidioxy-23-methylergosta-6,22-dien-3-ol)

3D PDB for NP0047429 ((3beta,22E,24R)-5,8-Epidioxy-23-methylergosta-6,22-dien-3-ol)

SMILES for NP0047429 ((3beta,22E,24R)-5,8-Epidioxy-23-methylergosta-6,22-dien-3-ol)

INCHI for NP0047429 ((3beta,22E,24R)-5,8-Epidioxy-23-methylergosta-6,22-dien-3-ol)

Structure for NP0047429 ((3beta,22E,24R)-5,8-Epidioxy-23-methylergosta-6,22-dien-3-ol)

3D Structure for NP0047429 ((3beta,22E,24R)-5,8-Epidioxy-23-methylergosta-6,22-dien-3-ol)