NP-MRD: Showing NP-Card for (2s,3s,3's,3'as,4as,5r,6's,6as,6br,7'ar,9r,11as,11br)-3',6',10,11b-tetramethyl-2,3,3'a,4,4',4a,5,5',6,6',6a,6b,7,7',7'a,8,11,11a-octadecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-2,3,5-triol (NP0327557)

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Record Information

Version

2.0

Created at

2022-09-12 10:14:23 UTC

Updated at

2022-09-12 10:14:23 UTC

NP-MRD ID

NP0327557

Secondary Accession Numbers

None

Natural Product Identification

Common Name

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

Description

(1'S,2R,2'R,3S,3aS,4'S,5'S,6S,7'S,7aR,8'R,10'S,11'R)-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'-ene-4',5',8'-triol 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. Based on a literature review very few articles have been published on (1'S,2R,2'R,3S,3aS,4'S,5'S,6S,7'S,7aR,8'R,10'S,11'R)-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'-ene-4',5',8'-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122212142D          

 32 37  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309122212142D          

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  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
  5 17  1  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  6  0  0  0
  6 19  1  0  0  0  0
 19  3  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  6  0  0  0
 24 23  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 30 29  1  1  0  0  0
 24 30  1  0  0  0  0
 30 31  1  0  0  0  0
 22 31  1  0  0  0  0
 31 32  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0327557

> <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]3C[C@@H](O)[C@H]4C[C@H](O)[C@@H](O)C[C@]4(C)[C@H]3CC2=C1C

> <INCHI_IDENTIFIER>
InChI=1S/C27H43NO4/c1-13-7-24-25(28-12-13)15(3)27(32-24)6-5-16-17(14(27)2)8-19-18(16)9-21(29)20-10-22(30)23(31)11-26(19,20)4/h13,15-16,18-25,28-31H,5-12H2,1-4H3/t13-,15-,16-,18+,19-,20+,21+,22-,23-,24+,25-,26+,27-/m0/s1

> <INCHI_KEY>
NOYZMBTXNXGBSR-YRXKMUBUSA-N

> <FORMULA>
C27H43NO4

> <MOLECULAR_WEIGHT>
445.644

> <EXACT_MASS>
445.319208869

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
52.41972776047041

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1'S,2R,2'R,3S,3aS,4'S,5'S,6S,7'S,7aR,8'R,10'S,11'R)-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}]heptadecan]-15'-ene-4',5',8'-triol

> <JCHEM_LOGP>
1.8183776876666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.81747959833033

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.853117259511155

> <JCHEM_PKA_STRONGEST_BASIC>
10.033960897687736

> <JCHEM_POLAR_SURFACE_AREA>
81.95

> <JCHEM_REFRACTIVITY>
124.27309999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,2R,2'R,3S,3aS,4'S,5'S,6S,7'S,7aR,8'R,10'S,11'R)-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}]heptadecan]-15'-ene-4',5',8'-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-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  C   UNK     0       9.973   0.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.411  -1.124   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.371  -2.328   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.894  -2.097   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      12.855  -3.301   0.000  0.00  0.00           O+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  O   UNK     0      14.142   3.637   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      12.058   1.974   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.495   0.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.535   1.744   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.873  -1.032   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.777  -2.113   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.292  -1.704   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.904  -0.214   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       3.700  -1.175   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.415  -0.327   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.925  -0.715   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.157   0.382   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.647  -0.006   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.253   1.867   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0       1.743   2.255   0.000  0.00  0.00           N+0
HETATM   30  C   UNK     0       2.824   1.158   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.362   1.228   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.772   2.712   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4   19                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   17                                                  
CONECT    6    5    7   19                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   17                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16    5   10   18                                             
CONECT   18   17                                                            
CONECT   19    6    3   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    2   23   31                                             
CONECT   23   22   24                                                       
CONECT   24   23   25   30                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   24   31                                                  
CONECT   31   30   22   32                                                  
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₄₃NO₄

Average Mass

445.6440 Da

Monoisotopic Mass

445.31921 Da

IUPAC Name

Traditional Name

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]3C[C@@H](O)[C@H]4C[C@H](O)[C@@H](O)C[C@]4(C)[C@H]3CC2=C1C

InChI Identifier

InChI=1S/C27H43NO4/c1-13-7-24-25(28-12-13)15(3)27(32-24)6-5-16-17(14(27)2)8-19-18(16)9-21(29)20-10-22(30)23(31)11-26(19,20)4/h13,15-16,18-25,28-31H,5-12H2,1-4H3/t13-,15-,16-,18+,19-,20+,21+,22-,23-,24+,25-,26+,27-/m0/s1

InChI Key

NOYZMBTXNXGBSR-YRXKMUBUSA-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

Not Available

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
Cyclic alcohol
Tetrahydrofuran
Secondary alcohol
Dialkyl ether
Secondary aliphatic amine
Ether
Polyol
Oxacycle
Secondary amine
Azacycle
Organoheterocyclic compound
Organopnictogen compound
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Organic nitrogen compound
Organic oxygen compound
Alcohol
Amine
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	1.82	ChemAxon
pKa (Strongest Acidic)	13.85	ChemAxon
pKa (Strongest Basic)	10.03	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	81.95 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	124.27 m³·mol⁻¹	ChemAxon
Polarizability	52.42 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

162955949

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,3s,3's,3'as,4as,5r,6's,6as,6br,7'ar,9r,11as,11br)-3',6',10,11b-tetramethyl-2,3,3'a,4,4',4a,5,5',6,6',6a,6b,7,7',7'a,8,11,11a-octadecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-2,3,5-triol (NP0327557)

MOL for NP0327557 ((2s,3s,3's,3'as,4as,5r,6's,6as,6br,7'ar,9r,11as,11br)-3',6',10,11b-tetramethyl-2,3,3'a,4,4',4a,5,5',6,6',6a,6b,7,7',7'a,8,11,11a-octadecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-2,3,5-triol)

3D MOL for NP0327557 ((2s,3s,3's,3'as,4as,5r,6's,6as,6br,7'ar,9r,11as,11br)-3',6',10,11b-tetramethyl-2,3,3'a,4,4',4a,5,5',6,6',6a,6b,7,7',7'a,8,11,11a-octadecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-2,3,5-triol)

3D SDF for NP0327557 ((2s,3s,3's,3'as,4as,5r,6's,6as,6br,7'ar,9r,11as,11br)-3',6',10,11b-tetramethyl-2,3,3'a,4,4',4a,5,5',6,6',6a,6b,7,7',7'a,8,11,11a-octadecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-2,3,5-triol)

3D-SDF for NP0327557 ((2s,3s,3's,3'as,4as,5r,6's,6as,6br,7'ar,9r,11as,11br)-3',6',10,11b-tetramethyl-2,3,3'a,4,4',4a,5,5',6,6',6a,6b,7,7',7'a,8,11,11a-octadecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-2,3,5-triol)

PDB for NP0327557 ((2s,3s,3's,3'as,4as,5r,6's,6as,6br,7'ar,9r,11as,11br)-3',6',10,11b-tetramethyl-2,3,3'a,4,4',4a,5,5',6,6',6a,6b,7,7',7'a,8,11,11a-octadecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-2,3,5-triol)

3D PDB for NP0327557 ((2s,3s,3's,3'as,4as,5r,6's,6as,6br,7'ar,9r,11as,11br)-3',6',10,11b-tetramethyl-2,3,3'a,4,4',4a,5,5',6,6',6a,6b,7,7',7'a,8,11,11a-octadecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-2,3,5-triol)

SMILES for NP0327557 ((2s,3s,3's,3'as,4as,5r,6's,6as,6br,7'ar,9r,11as,11br)-3',6',10,11b-tetramethyl-2,3,3'a,4,4',4a,5,5',6,6',6a,6b,7,7',7'a,8,11,11a-octadecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-2,3,5-triol)

INCHI for NP0327557 ((2s,3s,3's,3'as,4as,5r,6's,6as,6br,7'ar,9r,11as,11br)-3',6',10,11b-tetramethyl-2,3,3'a,4,4',4a,5,5',6,6',6a,6b,7,7',7'a,8,11,11a-octadecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-2,3,5-triol)

Structure for NP0327557 ((2s,3s,3's,3'as,4as,5r,6's,6as,6br,7'ar,9r,11as,11br)-3',6',10,11b-tetramethyl-2,3,3'a,4,4',4a,5,5',6,6',6a,6b,7,7',7'a,8,11,11a-octadecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-2,3,5-triol)

3D Structure for NP0327557 ((2s,3s,3's,3'as,4as,5r,6's,6as,6br,7'ar,9r,11as,11br)-3',6',10,11b-tetramethyl-2,3,3'a,4,4',4a,5,5',6,6',6a,6b,7,7',7'a,8,11,11a-octadecahydro-1h,3'h-spiro[cyclohexa[a]fluorene-9,2'-furo[3,2-b]pyridine]-2,3,5-triol)