NP-MRD: Showing NP-Card for (-)-Salpichrolide M (NP0080869)

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Record Information

Version

2.0

Created at

2022-04-29 01:51:12 UTC

Updated at

2022-04-29 01:51:12 UTC

NP-MRD ID

NP0080869

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Salpichrolide M

Description

(1S,2R,7R,9S,11R)-2-methyl-15-[(1S)-1-[(2R,4R,5S,6S)-4,5,6-trihydroxy-4,5-dimethyloxan-2-yl]ethyl]-8-oxapentacyclo[9.8.0.0²,⁷.0⁷,⁹.0¹²,¹⁷]Nonadeca-4,12(17),13,15-tetraen-3-one belongs to the class of organic compounds known as phenanthrenes and derivatives. These are polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene. (-)-Salpichrolide M is found in Salpichroa origanifolia. Based on a literature review very few articles have been published on (1S,2R,7R,9S,11R)-2-methyl-15-[(1S)-1-[(2R,4R,5S,6S)-4,5,6-trihydroxy-4,5-dimethyloxan-2-yl]ethyl]-8-oxapentacyclo[9.8.0.0²,⁷.0⁷,⁹.0¹²,¹⁷]Nonadeca-4,12(17),13,15-tetraen-3-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292203512D          

 34 39  0  0  1  0            999 V2000
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  1 33  1  6  0  0  0
  1 34  1  1  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652304292203512D          

 34 39  0  0  1  0            999 V2000
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  2 32  1  1  0  0  0
  1 33  1  6  0  0  0
  1 34  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0080869

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]([C@H]1C[C@@](C)(O)[C@](C)(O)[C@@H](O)O1)C1=CC2=C(C=C1)[C@@H]1C[C@@H]3O[C@@]33CC=CC(=O)[C@]3(C)[C@H]1CC2

> <INCHI_IDENTIFIER>
InChI=1S/C28H36O6/c1-15(21-14-25(2,31)27(4,32)24(30)33-21)16-7-9-18-17(12-16)8-10-20-19(18)13-23-28(34-23)11-5-6-22(29)26(20,28)3/h5-7,9,12,15,19-21,23-24,30-32H,8,10-11,13-14H2,1-4H3/t15-,19-,20-,21+,23-,24-,25+,26-,27+,28-/m0/s1

> <INCHI_KEY>
UPOXIHOCSBWLNQ-QQQBEFQQSA-N

> <FORMULA>
C28H36O6

> <MOLECULAR_WEIGHT>
468.59

> <EXACT_MASS>
468.251188879

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
51.026952614801175

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2R,7R,9S,11R)-2-methyl-15-[(1S)-1-[(2R,4R,5S,6S)-4,5,6-trihydroxy-4,5-dimethyloxan-2-yl]ethyl]-8-oxapentacyclo[9.8.0.0^{2,7}.0^{7,9}.0^{12,17}]nonadeca-4,12(17),13,15-tetraen-3-one

> <ALOGPS_LOGP>
3.14

> <JCHEM_LOGP>
3.396358854999998

> <ALOGPS_LOGS>
-5.06

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.00574754841794

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.142241414348442

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3895724478213136

> <JCHEM_POLAR_SURFACE_AREA>
99.52000000000001

> <JCHEM_REFRACTIVITY>
127.76689999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.05e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,7R,9S,11R)-2-methyl-15-[(1S)-1-[(2R,4R,5S,6S)-4,5,6-trihydroxy-4,5-dimethyloxan-2-yl]ethyl]-8-oxapentacyclo[9.8.0.0^{2,7}.0^{7,9}.0^{12,17}]nonadeca-4,12(17),13,15-tetraen-3-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0      13.106   5.990   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.610   4.535   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.602   3.371   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.090   3.662   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      10.586   5.117   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      11.594   6.281   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      11.090   7.737   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      10.082   2.498   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.569   2.789   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.561   1.625   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.049   1.916   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.545   3.371   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.553   4.535   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.065   4.244   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.033   3.662   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.024   2.498   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.529   1.043   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.041   0.752   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.512   2.789   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.008   4.244   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.016   5.408   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.529   5.117   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.504   5.699   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -0.504   4.535   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.512   3.371   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.008   1.916   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.504   1.625   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.008   0.170   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.016   1.334   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.586   1.043   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      15.082   4.988   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      14.809   3.568   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      14.543   6.545   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      13.450   7.491   0.000  0.00  0.00           O+0
CONECT    1    2    6   33   34                                             
CONECT    2    1    3   31   32                                             
CONECT    3    2    4                                                       
CONECT    4    3    5    8                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6                                                            
CONECT    8    4    9   30                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   18                                                  
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13    9                                                       
CONECT   15   12   16   22                                                  
CONECT   16   15   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17   11                                                       
CONECT   19   16   20   27   29                                             
CONECT   20   19   21   23   24                                             
CONECT   21   20   22   23                                                  
CONECT   22   21   15                                                       
CONECT   23   21   20                                                       
CONECT   24   20   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   19   28                                                  
CONECT   28   27                                                            
CONECT   29   19                                                            
CONECT   30    8                                                            
CONECT   31    2                                                            
CONECT   32    2                                                            
CONECT   33    1                                                            
CONECT   34    1                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₃₆O₆

Average Mass

468.5900 Da

Monoisotopic Mass

468.25119 Da

IUPAC Name

(1S,2R,7R,9S,11R)-2-methyl-15-[(1S)-1-[(2R,4R,5S,6S)-4,5,6-trihydroxy-4,5-dimethyloxan-2-yl]ethyl]-8-oxapentacyclo[9.8.0.0^{2,7}.0^{7,9}.0^{12,17}]nonadeca-4,12(17),13,15-tetraen-3-one

Traditional Name

(1S,2R,7R,9S,11R)-2-methyl-15-[(1S)-1-[(2R,4R,5S,6S)-4,5,6-trihydroxy-4,5-dimethyloxan-2-yl]ethyl]-8-oxapentacyclo[9.8.0.0^{2,7}.0^{7,9}.0^{12,17}]nonadeca-4,12(17),13,15-tetraen-3-one

CAS Registry Number

Not Available

SMILES

C[C@H]([C@H]1C[C@@](C)(O)[C@](C)(O)[C@@H](O)O1)C1=CC2=C(C=C1)[C@@H]1C[C@@H]3O[C@@]33CC=CC(=O)[C@]3(C)[C@H]1CC2

InChI Identifier

InChI=1S/C28H36O6/c1-15(21-14-25(2,31)27(4,32)24(30)33-21)16-7-9-18-17(12-16)8-10-20-19(18)13-23-28(34-23)11-5-6-22(29)26(20,28)3/h5-7,9,12,15,19-21,23-24,30-32H,8,10-11,13-14H2,1-4H3/t15-,19-,20-,21+,23-,24-,25+,26-,27+,28-/m0/s1

InChI Key

UPOXIHOCSBWLNQ-QQQBEFQQSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Salpichroa origanifolia	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenanthrenes and derivatives. These are polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenanthrenes and derivatives

Sub Class

Not Available

Direct Parent

Phenanthrenes and derivatives

Alternative Parents

Substituents

Phenanthrene
Tetralin
Cyclohexenone
Oxepane
Oxane
Tertiary alcohol
Ketone
Hemiacetal
1,2-diol
Oxacycle
Organoheterocyclic compound
Polyol
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	3.14	ALOGPS
logP	3.4	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	11.14	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	99.52 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	127.77 m³·mol⁻¹	ChemAxon
Polarizability	51.03 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

162966529

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Salpichrolide M (NP0080869)

MOL for NP0080869 ((-)-Salpichrolide M)

3D MOL for NP0080869 ((-)-Salpichrolide M)

3D SDF for NP0080869 ((-)-Salpichrolide M)

3D-SDF for NP0080869 ((-)-Salpichrolide M)

PDB for NP0080869 ((-)-Salpichrolide M)

3D PDB for NP0080869 ((-)-Salpichrolide M)

SMILES for NP0080869 ((-)-Salpichrolide M)

INCHI for NP0080869 ((-)-Salpichrolide M)

Structure for NP0080869 ((-)-Salpichrolide M)

3D Structure for NP0080869 ((-)-Salpichrolide M)