NP-MRD: Showing NP-Card for (3s,4r,12s,13r,17r,20r)-18-[(2s,3r,4s)-3,4-dimethyl-5-oxooxolan-2-yl]-17-hydroxy-4,17-dimethyl-19,21-dioxahexacyclo[11.6.1.1¹,¹⁵.0³,¹².0⁴,⁹.0¹⁶,²⁰]henicosa-6,9-dien-5-one (NP0281269)

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Record Information

Version

2.0

Created at

2022-09-09 07:30:29 UTC

Updated at

2022-09-09 07:30:29 UTC

NP-MRD ID

NP0281269

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,4r,12s,13r,17r,20r)-18-[(2s,3r,4s)-3,4-dimethyl-5-oxooxolan-2-yl]-17-hydroxy-4,17-dimethyl-19,21-dioxahexacyclo[11.6.1.1¹,¹⁵.0³,¹².0⁴,⁹.0¹⁶,²⁰]henicosa-6,9-dien-5-one

Description

Subtrifloralactone A belongs to the class of organic compounds known as steroidal glycosides. These are sterol lipids containing a carbohydrate moiety glycosidically linked to the steroid skeleton. (3s,4r,12s,13r,17r,20r)-18-[(2s,3r,4s)-3,4-dimethyl-5-oxooxolan-2-yl]-17-hydroxy-4,17-dimethyl-19,21-dioxahexacyclo[11.6.1.1¹,¹⁵.0³,¹².0⁴,⁹.0¹⁶,²⁰]henicosa-6,9-dien-5-one is found in Deprea subtriflora. Based on a literature review very few articles have been published on Subtrifloralactone A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092209302D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309092209302D          

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M  END
> <DATABASE_ID>
NP0281269

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1[C@H](C)C(=O)O[C@@H]1C1OC23C[C@H]4[C@@H](CC=C5CC=CC(=O)[C@]45C)[C@H]4CC(O2)C([C@H]34)[C@@]1(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C27H34O6/c1-12-13(2)24(29)31-22(12)23-26(4,30)21-18-10-16-15-9-8-14-6-5-7-19(28)25(14,3)17(15)11-27(32-18,33-23)20(16)21/h5,7-8,12-13,15-18,20-23,30H,6,9-11H2,1-4H3/t12-,13+,15+,16-,17+,18?,20-,21?,22+,23?,25+,26-,27?/m1/s1

> <INCHI_KEY>
FACPJZWATGVLOU-DSAQLLTQSA-N

> <FORMULA>
C27H34O6

> <MOLECULAR_WEIGHT>
454.563

> <EXACT_MASS>
454.235538815

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
49.507105414750725

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,4R,12S,13R,17R,20R)-18-[(2S,3R,4S)-3,4-dimethyl-5-oxooxolan-2-yl]-17-hydroxy-4,17-dimethyl-19,21-dioxahexacyclo[11.6.1.1^{1,15}.0^{3,12}.0^{4,9}.0^{16,20}]henicosa-6,9-dien-5-one

> <JCHEM_LOGP>
3.1669998019999994

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.04841287478549

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.642996407838378

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3923526243343165

> <JCHEM_POLAR_SURFACE_AREA>
82.06

> <JCHEM_REFRACTIVITY>
121.11009999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4R,12S,13R,17R,20R)-18-[(2S,3R,4S)-3,4-dimethyl-5-oxooxolan-2-yl]-17-hydroxy-4,17-dimethyl-19,21-dioxahexacyclo[11.6.1.1^{1,15}.0^{3,12}.0^{4,9}.0^{16,20}]henicosa-6,9-dien-5-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.574   9.173   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.396   8.182   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.099   8.553   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       1.677   9.980   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       1.913   7.246   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       0.922   6.067   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.293   4.573   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       2.768   4.109   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       2.585   2.474   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.307   2.624   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.314   1.372   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.666  -0.025   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.552  -1.285   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.086  -1.147   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.734   0.250   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.267   0.387   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.915   1.784   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.029   3.044   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.495   2.906   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.609   4.166   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       6.848   1.509   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.962   2.769   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.082  -0.074   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.718  -0.749   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.694   0.451   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.372   1.845   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       1.072   2.117   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.475   1.347   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.217   3.485   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -1.194   2.868   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -1.024   4.396   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -0.505   6.646   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -1.812   5.831   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   32                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   32                                                  
CONECT    7    6    8   29                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   26   28                                             
CONECT   10    9   11                                                       
CONECT   11   10   12   21                                                  
CONECT   12   11   13   23                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   21                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   15   11   22                                             
CONECT   22   21                                                            
CONECT   23   12   24   28                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25    9                                                       
CONECT   27   25   28   29                                                  
CONECT   28   27   23    9                                                  
CONECT   29   27    7   30   31                                             
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32    6    2   33                                                  
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₄O₆

Average Mass

454.5630 Da

Monoisotopic Mass

454.23554 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H]1[C@H](C)C(=O)O[C@@H]1C1OC23C[C@H]4[C@@H](CC=C5CC=CC(=O)[C@]45C)[C@H]4CC(O2)C([C@H]34)[C@@]1(C)O

InChI Identifier

InChI=1S/C27H34O6/c1-12-13(2)24(29)31-22(12)23-26(4,30)21-18-10-16-15-9-8-14-6-5-7-19(28)25(14,3)17(15)11-27(32-18,33-23)20(16)21/h5,7-8,12-13,15-18,20-23,30H,6,9-11H2,1-4H3/t12-,13+,15+,16-,17+,18?,20-,21?,22+,23?,25+,26-,27?/m1/s1

InChI Key

FACPJZWATGVLOU-DSAQLLTQSA-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
Deprea subtriflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroidal glycosides. These are sterol lipids containing a carbohydrate moiety glycosidically linked to the steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal glycosides

Direct Parent

Steroidal glycosides

Alternative Parents

Substituents

Steroidal glycoside
Prostaglandin skeleton
Steroid lactone
Eicosanoid
20-hydroxysteroid
Hydroxysteroid
1-oxosteroid
Oxosteroid
Naphthopyran
Naphthofuran
C-glycosyl compound
Iridoid-skeleton
Glycosyl compound
Naphthalene
Ketal
1,3-dioxepane
Cyclohexenone
Dioxepane
Pyran
Oxane
Gamma butyrolactone
Fatty acyl
Tertiary alcohol
Oxolane
Carboxylic acid ester
Lactone
Ketone
Monocarboxylic acid or derivatives
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Acetal
Organooxygen compound
Organic oxygen compound
Organic oxide
Carbonyl group
Aldehyde
Hydrocarbon derivative
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

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

101236926

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,4r,12s,13r,17r,20r)-18-[(2s,3r,4s)-3,4-dimethyl-5-oxooxolan-2-yl]-17-hydroxy-4,17-dimethyl-19,21-dioxahexacyclo[11.6.1.1¹,¹⁵.0³,¹².0⁴,⁹.0¹⁶,²⁰]henicosa-6,9-dien-5-one (NP0281269)

MOL for NP0281269 ((3s,4r,12s,13r,17r,20r)-18-[(2s,3r,4s)-3,4-dimethyl-5-oxooxolan-2-yl]-17-hydroxy-4,17-dimethyl-19,21-dioxahexacyclo[11.6.1.1¹,¹⁵.0³,¹².0⁴,⁹.0¹⁶,²⁰]henicosa-6,9-dien-5-one)

3D MOL for NP0281269 ((3s,4r,12s,13r,17r,20r)-18-[(2s,3r,4s)-3,4-dimethyl-5-oxooxolan-2-yl]-17-hydroxy-4,17-dimethyl-19,21-dioxahexacyclo[11.6.1.1¹,¹⁵.0³,¹².0⁴,⁹.0¹⁶,²⁰]henicosa-6,9-dien-5-one)

3D SDF for NP0281269 ((3s,4r,12s,13r,17r,20r)-18-[(2s,3r,4s)-3,4-dimethyl-5-oxooxolan-2-yl]-17-hydroxy-4,17-dimethyl-19,21-dioxahexacyclo[11.6.1.1¹,¹⁵.0³,¹².0⁴,⁹.0¹⁶,²⁰]henicosa-6,9-dien-5-one)

3D-SDF for NP0281269 ((3s,4r,12s,13r,17r,20r)-18-[(2s,3r,4s)-3,4-dimethyl-5-oxooxolan-2-yl]-17-hydroxy-4,17-dimethyl-19,21-dioxahexacyclo[11.6.1.1¹,¹⁵.0³,¹².0⁴,⁹.0¹⁶,²⁰]henicosa-6,9-dien-5-one)

PDB for NP0281269 ((3s,4r,12s,13r,17r,20r)-18-[(2s,3r,4s)-3,4-dimethyl-5-oxooxolan-2-yl]-17-hydroxy-4,17-dimethyl-19,21-dioxahexacyclo[11.6.1.1¹,¹⁵.0³,¹².0⁴,⁹.0¹⁶,²⁰]henicosa-6,9-dien-5-one)

3D PDB for NP0281269 ((3s,4r,12s,13r,17r,20r)-18-[(2s,3r,4s)-3,4-dimethyl-5-oxooxolan-2-yl]-17-hydroxy-4,17-dimethyl-19,21-dioxahexacyclo[11.6.1.1¹,¹⁵.0³,¹².0⁴,⁹.0¹⁶,²⁰]henicosa-6,9-dien-5-one)

SMILES for NP0281269 ((3s,4r,12s,13r,17r,20r)-18-[(2s,3r,4s)-3,4-dimethyl-5-oxooxolan-2-yl]-17-hydroxy-4,17-dimethyl-19,21-dioxahexacyclo[11.6.1.1¹,¹⁵.0³,¹².0⁴,⁹.0¹⁶,²⁰]henicosa-6,9-dien-5-one)

INCHI for NP0281269 ((3s,4r,12s,13r,17r,20r)-18-[(2s,3r,4s)-3,4-dimethyl-5-oxooxolan-2-yl]-17-hydroxy-4,17-dimethyl-19,21-dioxahexacyclo[11.6.1.1¹,¹⁵.0³,¹².0⁴,⁹.0¹⁶,²⁰]henicosa-6,9-dien-5-one)

Structure for NP0281269 ((3s,4r,12s,13r,17r,20r)-18-[(2s,3r,4s)-3,4-dimethyl-5-oxooxolan-2-yl]-17-hydroxy-4,17-dimethyl-19,21-dioxahexacyclo[11.6.1.1¹,¹⁵.0³,¹².0⁴,⁹.0¹⁶,²⁰]henicosa-6,9-dien-5-one)

3D Structure for NP0281269 ((3s,4r,12s,13r,17r,20r)-18-[(2s,3r,4s)-3,4-dimethyl-5-oxooxolan-2-yl]-17-hydroxy-4,17-dimethyl-19,21-dioxahexacyclo[11.6.1.1¹,¹⁵.0³,¹².0⁴,⁹.0¹⁶,²⁰]henicosa-6,9-dien-5-one)