NP-MRD: Showing NP-Card for (-)-Tortifolisine (NP0070544)

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Record Information

Version

2.0

Created at

2022-04-28 15:56:01 UTC

Updated at

2022-04-28 15:56:01 UTC

NP-MRD ID

NP0070544

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Tortifolisine

Description

(1'S,2R,2'R,3R,3aS,5'S,6R,7'S,7aR,10'R,11'S)-5'-hydroxy-2',3,6,15'-tetramethyl-3a,4,5,6,7,7a-hexahydro-3H-spiro[furo[3,2-b]pyridine-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]Heptadecan]-15'-en-8'-one 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. (-)-Tortifolisine is found in Fritillaria tortifolia and Fritillaria yuminensis L.. Based on a literature review very few articles have been published on (1'S,2R,2'R,3R,3aS,5'S,6R,7'S,7aR,10'R,11'S)-5'-hydroxy-2',3,6,15'-tetramethyl-3a,4,5,6,7,7a-hexahydro-3H-spiro[furo[3,2-b]pyridine-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]Heptadecan]-15'-en-8'-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282217562D          

 31 36  0  0  1  0            999 V2000
    7.2752   -0.3556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7898    0.2892    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4886    1.0573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6729    1.1806    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1583    0.5358    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4594   -0.2323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3425    0.6590    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0414    1.4271    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5560    2.0719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3718    1.9487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8864    2.5935    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2179    1.3780    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0100    0.5796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2147    0.3604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6272    0.9396    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8350    1.7380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  7 29  1  1  0  0  0
  5 30  1  1  0  0  0
  2 31  1  1  0  0  0
M  END

     RDKit          3D

 72 77  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652304282217562D          

 31 36  0  0  1  0            999 V2000
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M  END
> <DATABASE_ID>
NP0070544

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1[C@@H]2NC[C@H](C)C[C@H]2O[C@]11CC[C@H]2[C@@H]3CC(=O)[C@H]4C[C@@H](O)CC[C@]4(C)[C@H]3CC2=C1C

> <INCHI_IDENTIFIER>
InChI=1S/C27H41NO3/c1-14-9-24-25(28-13-14)16(3)27(31-24)8-6-18-19(15(27)2)11-21-20(18)12-23(30)22-10-17(29)5-7-26(21,22)4/h14,16-18,20-22,24-25,28-29H,5-13H2,1-4H3/t14-,16-,17+,18-,20+,21+,22-,24-,25+,26-,27+/m1/s1

> <INCHI_KEY>
KYELXPJVGNZIGC-ZAVURYGYSA-N

> <FORMULA>
C27H41NO3

> <MOLECULAR_WEIGHT>
427.629

> <EXACT_MASS>
427.308644184

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
72

> <JCHEM_AVERAGE_POLARIZABILITY>
51.34658067940365

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,3'R,3'aS,4aS,6'R,6aR,6bS,7'aR,9R,11aS,11bR)-3-hydroxy-3',6',10,11b-tetramethyl-1,2,3,3'a,4,4',4a,5,5',6,6',6a,6b,7,7',7'a,8,11,11a,11b-icosahydro-3'H-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-5-one

> <ALOGPS_LOGP>
3.28

> <JCHEM_LOGP>
3.2787955483333335

> <ALOGPS_LOGS>
-4.83

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
19.418424241734304

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.234279099870616

> <JCHEM_PKA_STRONGEST_BASIC>
9.934024597163146

> <JCHEM_POLAR_SURFACE_AREA>
58.56

> <JCHEM_REFRACTIVITY>
121.98639999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.33e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,3'R,3'aS,4aS,6'R,6aR,6bS,7'aR,9R,11aS,11bR)-3-hydroxy-3',6',10,11b-tetramethyl-1,2,3,3'a,4,4',4a,5',6,6',6a,6b,7,7',7'a,8,11,11a-octadecahydro-3'H-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-5-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      13.580  -0.664   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.541   0.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.979   1.974   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.456   2.204   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.495   1.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.058  -0.434   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.973   1.230   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.411   2.664   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.371   3.868   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.894   3.637   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      12.855   4.841   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.873   2.572   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.485   1.082   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.001   0.673   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.904   1.754   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.292   3.244   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.777   3.653   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.700   2.715   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.415   1.867   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.824   0.382   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.362   0.312   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.210  -0.973   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0       1.743  -0.715   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0       0.253  -0.327   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.157   1.158   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.925   2.255   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.647   1.546   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.092  -0.864   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.783   0.252   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.535  -0.204   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      16.064   0.310   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   31                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7   30                                             
CONECT    6    5    1                                                       
CONECT    7    5    8   29                                                  
CONECT    8    7    9   12                                                  
CONECT    9    8   10                                                       
CONECT   10    9    4   11                                                  
CONECT   11   10                                                            
CONECT   12    8   13   17                                                  
CONECT   13   12   14   29                                                  
CONECT   14   13   15   28                                                  
CONECT   15   14   16   18   21                                             
CONECT   16   15   17                                                       
CONECT   17   16   12                                                       
CONECT   18   15   19                                                       
CONECT   19   18   20   26                                                  
CONECT   20   19   21   23                                                  
CONECT   21   20   15   22                                                  
CONECT   22   21                                                            
CONECT   23   20   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25   19                                                       
CONECT   27   25                                                            
CONECT   28   14                                                            
CONECT   29   13    7                                                       
CONECT   30    5                                                            
CONECT   31    2                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₄₁NO₃

Average Mass

427.6290 Da

Monoisotopic Mass

427.30864 Da

IUPAC Name

(3S,3'R,3'aS,4aS,6'R,6aR,6bS,7'aR,9R,11aS,11bR)-3-hydroxy-3',6',10,11b-tetramethyl-1,2,3,3'a,4,4',4a,5,5',6,6',6a,6b,7,7',7'a,8,11,11a,11b-icosahydro-3'H-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-5-one

Traditional Name

(3S,3'R,3'aS,4aS,6'R,6aR,6bS,7'aR,9R,11aS,11bR)-3-hydroxy-3',6',10,11b-tetramethyl-1,2,3,3'a,4,4',4a,5',6,6',6a,6b,7,7',7'a,8,11,11a-octadecahydro-3'H-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-5-one

CAS Registry Number

Not Available

SMILES

C[C@@H]1[C@@H]2NC[C@H](C)C[C@H]2O[C@]11CC[C@H]2[C@@H]3CC(=O)[C@H]4C[C@@H](O)CC[C@]4(C)[C@H]3CC2=C1C

InChI Identifier

InChI=1S/C27H41NO3/c1-14-9-24-25(28-13-14)16(3)27(31-24)8-6-18-19(15(27)2)11-21-20(18)12-23(30)22-10-17(29)5-7-26(21,22)4/h14,16-18,20-22,24-25,28-29H,5-13H2,1-4H3/t14-,16-,17+,18-,20+,21+,22-,24-,25+,26-,27+/m1/s1

InChI Key

KYELXPJVGNZIGC-ZAVURYGYSA-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
Fritillaria tortifolia	Plant	KNApSAcK
Fritillaria yuminensis L.	Plant	KNApSAcK

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
Piperidine
Tetrahydrofuran
Cyclic alcohol
Secondary alcohol
Ketone
Oxacycle
Azacycle
Organoheterocyclic compound
Secondary amine
Ether
Secondary aliphatic amine
Dialkyl ether
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
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
logP	3.28	ALOGPS
logP	3.28	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	15.23	ChemAxon
pKa (Strongest Basic)	9.93	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	58.56 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	121.99 m³·mol⁻¹	ChemAxon
Polarizability	51.35 Å³	ChemAxon
Number of Rings	6	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

163028299

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Tortifolisine (NP0070544)

MOL for NP0070544 ((-)-Tortifolisine)

3D MOL for NP0070544 ((-)-Tortifolisine)

3D SDF for NP0070544 ((-)-Tortifolisine)

3D-SDF for NP0070544 ((-)-Tortifolisine)

PDB for NP0070544 ((-)-Tortifolisine)

3D PDB for NP0070544 ((-)-Tortifolisine)

SMILES for NP0070544 ((-)-Tortifolisine)

INCHI for NP0070544 ((-)-Tortifolisine)

Structure for NP0070544 ((-)-Tortifolisine)

3D Structure for NP0070544 ((-)-Tortifolisine)