NP-MRD: Showing NP-Card for (3'r,3'as,6's,6as,7'ar,9r,11br)-3',6',10,11b-tetramethyl-2,3'a,4',5,5',6,6',6a,6b,7,7',7'a,8,11a-tetradecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-3,11-dione (NP0210492)

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Record Information

Version

2.0

Created at

2022-09-05 08:19:58 UTC

Updated at

2022-09-05 08:19:58 UTC

NP-MRD ID

NP0210492

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3'r,3'as,6's,6as,7'ar,9r,11br)-3',6',10,11b-tetramethyl-2,3'a,4',5,5',6,6',6a,6b,7,7',7'a,8,11a-tetradecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-3,11-dione

Description

(+)-Jervinone belongs to the class of organic compounds known as jerveratrum-type alkaloids. These are steroidal alkaloids with a structure that is based on the jervane ring system. Jerveratrum alkaloids have alkamines with 1-3 oxygen atoms, and occur as such or as monoglycosides. (3'r,3'as,6's,6as,7'ar,9r,11br)-3',6',10,11b-tetramethyl-2,3'a,4',5,5',6,6',6a,6b,7,7',7'a,8,11a-tetradecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-3,11-dione is found in Veratrum album. Based on a literature review very few articles have been published on (+)-Jervinone.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052210192D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309052210192D          

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M  END
> <DATABASE_ID>
NP0210492

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1[C@@H]2NC[C@@H](C)C[C@H]2O[C@]11CCC2[C@@H]3CCC4=CC(=O)CC[C@]4(C)C3C(=O)C2=C1C

> <INCHI_IDENTIFIER>
InChI=1S/C27H37NO3/c1-14-11-21-24(28-13-14)16(3)27(31-21)10-8-19-20-6-5-17-12-18(29)7-9-26(17,4)23(20)25(30)22(19)15(27)2/h12,14,16,19-21,23-24,28H,5-11,13H2,1-4H3/t14-,16+,19?,20-,21+,23?,24-,26-,27-/m0/s1

> <INCHI_KEY>
KLTPAUQDYRELPI-QCZICOGXSA-N

> <FORMULA>
C27H37NO3

> <MOLECULAR_WEIGHT>
423.597

> <EXACT_MASS>
423.277344055

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
48.27608458709382

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,2'R,3R,3aS,6S,7aR,10'S)-2',3,6,15'-tetramethyl-3a,4,5,6,7,7a-hexahydro-3H-spiro[furo[3,2-b]pyridine-2,14'-tetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadecane]-6',15'-diene-5',17'-dione

> <JCHEM_LOGP>
3.952396378999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.87010550683734

> <JCHEM_PKA_STRONGEST_BASIC>
9.934018075890675

> <JCHEM_POLAR_SURFACE_AREA>
55.400000000000006

> <JCHEM_REFRACTIVITY>
121.83679999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R,2'R,3R,3aS,6S,7aR,10'S)-2',3,6,15'-tetramethyl-3a,4,5,6,7,7a-hexahydro-3H-spiro[furo[3,2-b]pyridine-2,14'-tetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadecane]-6',15'-diene-5',17'-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       5.613   2.357   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.001   0.867   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.485   0.458   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.783   1.288   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       8.874   2.825   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       9.973   0.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.411  -1.124   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.371  -2.328   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.894  -2.097   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.456  -0.664   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.979  -0.434   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.541   1.000   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      16.064   1.230   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      13.580   2.204   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.058   1.974   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.495   0.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.535   1.744   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.873  -1.032   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.777  -2.113   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.292  -1.704   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.904  -0.214   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.700  -1.175   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.415  -0.327   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.925  -0.715   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.157   0.382   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.647  -0.006   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.253   1.867   0.000  0.00  0.00           C+0
HETATM   28  N   UNK     0       1.743   2.255   0.000  0.00  0.00           N+0
HETATM   29  C   UNK     0       2.824   1.158   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.362   1.228   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.772   2.712   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   21                                                  
CONECT    3    2    4   18                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   16                                                  
CONECT    7    6    8   18                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   10    6   17                                             
CONECT   17   16                                                            
CONECT   18    7    3   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20    2   22   30                                             
CONECT   22   21   23                                                       
CONECT   23   22   24   29                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   23   30                                                  
CONECT   30   29   21   31                                                  
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₇NO₃

Average Mass

423.5970 Da

Monoisotopic Mass

423.27734 Da

IUPAC Name

(2R,2'R,3R,3aS,6S,7aR,10'S)-2',3,6,15'-tetramethyl-3a,4,5,6,7,7a-hexahydro-3H-spiro[furo[3,2-b]pyridine-2,14'-tetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadecane]-6',15'-diene-5',17'-dione

Traditional Name

(2R,2'R,3R,3aS,6S,7aR,10'S)-2',3,6,15'-tetramethyl-3a,4,5,6,7,7a-hexahydro-3H-spiro[furo[3,2-b]pyridine-2,14'-tetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadecane]-6',15'-diene-5',17'-dione

CAS Registry Number

Not Available

SMILES

C[C@@H]1[C@@H]2NC[C@@H](C)C[C@H]2O[C@]11CCC2[C@@H]3CCC4=CC(=O)CC[C@]4(C)C3C(=O)C2=C1C

InChI Identifier

InChI=1S/C27H37NO3/c1-14-11-21-24(28-13-14)16(3)27(31-21)10-8-19-20-6-5-17-12-18(29)7-9-26(17,4)23(20)25(30)22(19)15(27)2/h12,14,16,19-21,23-24,28H,5-11,13H2,1-4H3/t14-,16+,19?,20-,21+,23?,24-,26-,27-/m0/s1

InChI Key

KLTPAUQDYRELPI-QCZICOGXSA-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
Veratrum album	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as jerveratrum-type alkaloids. These are steroidal alkaloids with a structure that is based on the jervane ring system. Jerveratrum alkaloids have alkamines with 1-3 oxygen atoms, and occur as such or as monoglycosides.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal alkaloids

Direct Parent

Jerveratrum-type alkaloids

Alternative Parents

Substituents

Jerveratrum-type alkaloid
Azasteroid
Alkaloid or derivatives
Cyclohexenone
Piperidine
Oxolane
Ketone
Cyclic ketone
Dialkyl ether
Secondary aliphatic amine
Ether
Oxacycle
Secondary amine
Azacycle
Organoheterocyclic compound
Organic oxide
Organic oxygen compound
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Carbonyl group
Amine
Organic nitrogen compound
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
logP	3.95	ChemAxon
pKa (Strongest Acidic)	18.87	ChemAxon
pKa (Strongest Basic)	9.93	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	55.4 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	121.84 m³·mol⁻¹	ChemAxon
Polarizability	48.28 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

5144169

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6712079

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3'r,3'as,6's,6as,7'ar,9r,11br)-3',6',10,11b-tetramethyl-2,3'a,4',5,5',6,6',6a,6b,7,7',7'a,8,11a-tetradecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-3,11-dione (NP0210492)

MOL for NP0210492 ((3'r,3'as,6's,6as,7'ar,9r,11br)-3',6',10,11b-tetramethyl-2,3'a,4',5,5',6,6',6a,6b,7,7',7'a,8,11a-tetradecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-3,11-dione)

3D MOL for NP0210492 ((3'r,3'as,6's,6as,7'ar,9r,11br)-3',6',10,11b-tetramethyl-2,3'a,4',5,5',6,6',6a,6b,7,7',7'a,8,11a-tetradecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-3,11-dione)

3D SDF for NP0210492 ((3'r,3'as,6's,6as,7'ar,9r,11br)-3',6',10,11b-tetramethyl-2,3'a,4',5,5',6,6',6a,6b,7,7',7'a,8,11a-tetradecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-3,11-dione)

3D-SDF for NP0210492 ((3'r,3'as,6's,6as,7'ar,9r,11br)-3',6',10,11b-tetramethyl-2,3'a,4',5,5',6,6',6a,6b,7,7',7'a,8,11a-tetradecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-3,11-dione)

PDB for NP0210492 ((3'r,3'as,6's,6as,7'ar,9r,11br)-3',6',10,11b-tetramethyl-2,3'a,4',5,5',6,6',6a,6b,7,7',7'a,8,11a-tetradecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-3,11-dione)

3D PDB for NP0210492 ((3'r,3'as,6's,6as,7'ar,9r,11br)-3',6',10,11b-tetramethyl-2,3'a,4',5,5',6,6',6a,6b,7,7',7'a,8,11a-tetradecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-3,11-dione)

SMILES for NP0210492 ((3'r,3'as,6's,6as,7'ar,9r,11br)-3',6',10,11b-tetramethyl-2,3'a,4',5,5',6,6',6a,6b,7,7',7'a,8,11a-tetradecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-3,11-dione)

INCHI for NP0210492 ((3'r,3'as,6's,6as,7'ar,9r,11br)-3',6',10,11b-tetramethyl-2,3'a,4',5,5',6,6',6a,6b,7,7',7'a,8,11a-tetradecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-3,11-dione)

Structure for NP0210492 ((3'r,3'as,6's,6as,7'ar,9r,11br)-3',6',10,11b-tetramethyl-2,3'a,4',5,5',6,6',6a,6b,7,7',7'a,8,11a-tetradecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-3,11-dione)

3D Structure for NP0210492 ((3'r,3'as,6's,6as,7'ar,9r,11br)-3',6',10,11b-tetramethyl-2,3'a,4',5,5',6,6',6a,6b,7,7',7'a,8,11a-tetradecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-3,11-dione)