NP-MRD: Showing NP-Card for 11-hydroxy-1-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-3a,3b,9a-trimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-one (NP0146719)

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Record Information

Version

2.0

Created at

2022-09-02 02:10:10 UTC

Updated at

2022-09-02 02:10:10 UTC

NP-MRD ID

NP0146719

Secondary Accession Numbers

None

Natural Product Identification

Common Name

11-hydroxy-1-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-3a,3b,9a-trimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-one

Description

16-Hydroxy-14-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-2,10,11-trimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecan-5-one belongs to the class of organic compounds known as oxosteroids. These are steroid derivatives carrying a C=O group attached to steroid skeleton. 11-hydroxy-1-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-3a,3b,9a-trimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-one is found in Alnus serrulatoides. 16-Hydroxy-14-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-2,10,11-trimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecan-5-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191514212D          

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M  END

     RDKit          3D

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M  END


  Mrv1533004191514212D          

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 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  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
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 21 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 14 31  1  0  0  0  0
 20 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0146719

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C(=C)CCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(=O)CC3CCC21C

> <INCHI_IDENTIFIER>
InChI=1S/C29H48O3/c1-18(2)19(3)8-15-29(7,32)22-11-14-28(6)25(22)23(31)17-24-26(4)12-10-21(30)16-20(26)9-13-27(24,28)5/h18,20,22-25,31-32H,3,8-17H2,1-2,4-7H3

> <INCHI_KEY>
DGZFYYWNLNMHDT-UHFFFAOYSA-N

> <FORMULA>
C29H48O3

> <MOLECULAR_WEIGHT>
444.7

> <EXACT_MASS>
444.360345406

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
53.74554627578364

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
16-hydroxy-14-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-2,10,11-trimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-one

> <ALOGPS_LOGP>
4.94

> <JCHEM_LOGP>
5.341417696999999

> <ALOGPS_LOGS>
-5.71

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.149928276566698

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.530114128575711

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8388984669757322

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
130.81419999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.58e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
16-hydroxy-14-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-2,10,11-trimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0      -5.105  -0.447   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.160  -1.662   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.741  -3.089   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.635  -1.452   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.054  -0.025   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.690  -2.668   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.164  -2.457   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.781  -3.673   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.435  -4.618   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.997  -2.728   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.726  -4.889   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.298  -6.368   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.573  -7.232   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.789  -6.287   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.158  -7.782   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.266  -4.839   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.258  -3.661   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.735  -2.213   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.774  -3.932   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.297  -5.381   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.813  -5.652   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.290  -4.203   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.806  -4.474   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.322  -4.746   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.845  -6.194   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      12.361  -6.465   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       9.853  -7.371   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.337  -7.100   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.344  -8.277   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.828  -8.006   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.305  -6.558   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.724  -7.984   0.000  0.00  0.00           C+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   11                                             
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    8   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16   31                                             
CONECT   15   14                                                            
CONECT   16   14   11   17                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   31                                                  
CONECT   21   20   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                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   14   20   32                                             
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₄₈O₃

Average Mass

444.7000 Da

Monoisotopic Mass

444.36035 Da

IUPAC Name

16-hydroxy-14-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-2,10,11-trimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-one

Traditional Name

16-hydroxy-14-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-2,10,11-trimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-one

CAS Registry Number

Not Available

SMILES

CC(C)C(=C)CCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(=O)CC3CCC21C

InChI Identifier

InChI=1S/C29H48O3/c1-18(2)19(3)8-15-29(7,32)22-11-14-28(6)25(22)23(31)17-24-26(4)12-10-21(30)16-20(26)9-13-27(24,28)5/h18,20,22-25,31-32H,3,8-17H2,1-2,4-7H3

InChI Key

DGZFYYWNLNMHDT-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
Alnus serrulatoides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxosteroids. These are steroid derivatives carrying a C=O group attached to steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Oxosteroids

Direct Parent

Oxosteroids

Alternative Parents

Substituents

20-hydroxysteroid
3-oxosteroid
12-hydroxysteroid
Hydroxysteroid
Oxosteroid
Cyclic alcohol
Tertiary alcohol
Ketone
Cyclic ketone
Secondary alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	4.94	ALOGPS
logP	5.34	ChemAxon
logS	-5.7	ALOGPS
pKa (Strongest Acidic)	14.53	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	130.81 m³·mol⁻¹	ChemAxon
Polarizability	53.75 Å³	ChemAxon
Number of Rings	4	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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 11-hydroxy-1-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-3a,3b,9a-trimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-one (NP0146719)

MOL for NP0146719 (11-hydroxy-1-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-3a,3b,9a-trimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-one)

3D MOL for NP0146719 (11-hydroxy-1-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-3a,3b,9a-trimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-one)

3D SDF for NP0146719 (11-hydroxy-1-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-3a,3b,9a-trimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-one)

3D-SDF for NP0146719 (11-hydroxy-1-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-3a,3b,9a-trimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-one)

PDB for NP0146719 (11-hydroxy-1-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-3a,3b,9a-trimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-one)

3D PDB for NP0146719 (11-hydroxy-1-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-3a,3b,9a-trimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-one)

SMILES for NP0146719 (11-hydroxy-1-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-3a,3b,9a-trimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-one)

INCHI for NP0146719 (11-hydroxy-1-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-3a,3b,9a-trimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-one)

Structure for NP0146719 (11-hydroxy-1-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-3a,3b,9a-trimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-one)

3D Structure for NP0146719 (11-hydroxy-1-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-3a,3b,9a-trimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-one)