NP-MRD: Showing NP-Card for 7,9-dihydroxy-1-(1-hydroxyethyl)-3,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-8-yl 3-methylbutanoate (NP0143968)

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Record Information

Version

2.0

Created at

2022-09-01 22:50:12 UTC

Updated at

2022-09-01 22:50:12 UTC

NP-MRD ID

NP0143968

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7,9-dihydroxy-1-(1-hydroxyethyl)-3,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-8-yl 3-methylbutanoate

Description

3,5-Dihydroxy-14-(1-hydroxyethyl)-2,6,6,12,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadeca-1(10),11-dien-4-yl 3-methylbutanoate belongs to the class of organic compounds known as steroid esters. Steroid esters are compounds containing a steroid moiety which bears a carboxylic acid ester group. 7,9-dihydroxy-1-(1-hydroxyethyl)-3,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-8-yl 3-methylbutanoate is found in Annona squamosa. 3,5-Dihydroxy-14-(1-hydroxyethyl)-2,6,6,12,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadeca-1(10),11-dien-4-yl 3-methylbutanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241500462D          

 34 37  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004241500462D          

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   -0.6168   -0.6798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3365    0.0961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1486   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8683    0.7268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  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
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 11 14  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  2  0  0  0  0
 18 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
 17 26  1  0  0  0  0
 21 26  1  0  0  0  0
 25 27  1  0  0  0  0
 23 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 18 31  1  0  0  0  0
 14 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
  8 33  1  0  0  0  0
 33 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0143968

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CC(=O)OC1C(O)C(C)(C)C2CCC3=C(CCC4(C)C(CC(C)=C34)C(C)O)C2(C)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C29H46O5/c1-15(2)13-22(31)34-24-25(32)27(5,6)21-10-9-18-19(29(21,8)26(24)33)11-12-28(7)20(17(4)30)14-16(3)23(18)28/h15,17,20-21,24-26,30,32-33H,9-14H2,1-8H3

> <INCHI_KEY>
BITGCGQAARSJKH-UHFFFAOYSA-N

> <FORMULA>
C29H46O5

> <MOLECULAR_WEIGHT>
474.682

> <EXACT_MASS>
474.334524581

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
55.83445693272308

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3,5-dihydroxy-14-(1-hydroxyethyl)-2,6,6,12,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(10),11-dien-4-yl 3-methylbutanoate

> <ALOGPS_LOGP>
4.06

> <JCHEM_LOGP>
3.7903045576666674

> <ALOGPS_LOGS>
-4.54

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.019617451669028

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.314675056405669

> <JCHEM_PKA_STRONGEST_BASIC>
-1.0017867642311553

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
134.01690000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.37e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,5-dihydroxy-14-(1-hydroxyethyl)-2,6,6,12,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(10),11-dien-4-yl 3-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -9.670   2.627   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.677   1.450   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -9.201   0.001   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.162   1.721   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.169   0.544   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -6.692  -0.905   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      -4.653   0.815   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -3.660  -0.363   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.183  -1.811   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -5.699  -2.082   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -3.191  -2.988   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.522  -3.762   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.660  -4.434   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.675  -2.717   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.682  -3.895   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.834  -3.624   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.357  -2.175   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.365  -0.998   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.888   0.451   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.404   0.722   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.396  -0.456   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.068   0.930   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.936  -0.506   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.364  -1.985   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.089  -2.849   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.873  -1.904   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.039  -4.388   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.881   0.710   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.301   2.137   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       7.406   0.499   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -1.151  -1.269   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -0.628   0.179   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -2.144  -0.092   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -1.621   1.357   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   33                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13   14                                             
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   11   15   31                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   26                                                  
CONECT   18   17   19   31                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23   26                                             
CONECT   22   21                                                            
CONECT   23   21   24   28                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25   17   21                                                  
CONECT   27   25                                                            
CONECT   28   23   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   18   14   32   33                                             
CONECT   32   31                                                            
CONECT   33   31    8   34                                                  
CONECT   34   33                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

View in JSmol

Synonyms

Value	Source
3,5-Dihydroxy-14-(1-hydroxyethyl)-2,6,6,12,15-pentamethyltetracyclo[8.7.0.0,.0,]heptadeca-1(10),11-dien-4-yl 3-methylbutanoic acid	Generator
3,5-Dihydroxy-14-(1-hydroxyethyl)-2,6,6,12,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(10),11-dien-4-yl 3-methylbutanoic acid	Generator

Chemical Formula

C₂₉H₄₆O₅

Average Mass

474.6820 Da

Monoisotopic Mass

474.33452 Da

IUPAC Name

3,5-dihydroxy-14-(1-hydroxyethyl)-2,6,6,12,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(10),11-dien-4-yl 3-methylbutanoate

Traditional Name

3,5-dihydroxy-14-(1-hydroxyethyl)-2,6,6,12,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(10),11-dien-4-yl 3-methylbutanoate

CAS Registry Number

Not Available

SMILES

CC(C)CC(=O)OC1C(O)C(C)(C)C2CCC3=C(CCC4(C)C(CC(C)=C34)C(C)O)C2(C)C1O

InChI Identifier

InChI=1S/C29H46O5/c1-15(2)13-22(31)34-24-25(32)27(5,6)21-10-9-18-19(29(21,8)26(24)33)11-12-28(7)20(17(4)30)14-16(3)23(18)28/h15,17,20-21,24-26,30,32-33H,9-14H2,1-8H3

InChI Key

BITGCGQAARSJKH-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
Annona squamosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroid esters. Steroid esters are compounds containing a steroid moiety which bears a carboxylic acid ester group.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid esters

Direct Parent

Steroid esters

Alternative Parents

Substituents

20-hydroxysteroid
Steroid ester
3-hydroxysteroid
1-hydroxysteroid
Hydroxysteroid
Fatty acid ester
Cyclitol or derivatives
Fatty acyl
Cyclic alcohol
Carboxylic acid ester
Secondary alcohol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Alcohol
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Organooxygen compound
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	4.06	ALOGPS
logP	3.79	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	13.31	ChemAxon
pKa (Strongest Basic)	-1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	134.02 m³·mol⁻¹	ChemAxon
Polarizability	55.83 Å³	ChemAxon
Number of Rings	4	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

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 7,9-dihydroxy-1-(1-hydroxyethyl)-3,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-8-yl 3-methylbutanoate (NP0143968)

MOL for NP0143968 (7,9-dihydroxy-1-(1-hydroxyethyl)-3,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-8-yl 3-methylbutanoate)

3D MOL for NP0143968 (7,9-dihydroxy-1-(1-hydroxyethyl)-3,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-8-yl 3-methylbutanoate)

3D SDF for NP0143968 (7,9-dihydroxy-1-(1-hydroxyethyl)-3,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-8-yl 3-methylbutanoate)

3D-SDF for NP0143968 (7,9-dihydroxy-1-(1-hydroxyethyl)-3,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-8-yl 3-methylbutanoate)

PDB for NP0143968 (7,9-dihydroxy-1-(1-hydroxyethyl)-3,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-8-yl 3-methylbutanoate)

3D PDB for NP0143968 (7,9-dihydroxy-1-(1-hydroxyethyl)-3,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-8-yl 3-methylbutanoate)

SMILES for NP0143968 (7,9-dihydroxy-1-(1-hydroxyethyl)-3,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-8-yl 3-methylbutanoate)

INCHI for NP0143968 (7,9-dihydroxy-1-(1-hydroxyethyl)-3,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-8-yl 3-methylbutanoate)

Structure for NP0143968 (7,9-dihydroxy-1-(1-hydroxyethyl)-3,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-8-yl 3-methylbutanoate)

3D Structure for NP0143968 (7,9-dihydroxy-1-(1-hydroxyethyl)-3,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-8-yl 3-methylbutanoate)