NP-MRD: Showing NP-Card for (1's,2s,3's,4'r,10's,15'r)-3'-ethyl-12'-hydroxy-4'-methoxy-4-methyl-15'-[(2r,4r)-4-methyl-5-oxooxolan-2-yl]-13'-oxa-9',11'-diazaspiro[furan-2,2'-tetracyclo[7.4.2.0¹,¹⁰.0⁴,¹⁰]pentadecane]-5',11'-dien-5-one (NP0245046)

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Record Information

Version

2.0

Created at

2022-09-07 05:58:53 UTC

Updated at

2022-09-07 05:58:53 UTC

NP-MRD ID

NP0245046

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1's,2s,3's,4'r,10's,15'r)-3'-ethyl-12'-hydroxy-4'-methoxy-4-methyl-15'-[(2r,4r)-4-methyl-5-oxooxolan-2-yl]-13'-oxa-9',11'-diazaspiro[furan-2,2'-tetracyclo[7.4.2.0¹,¹⁰.0⁴,¹⁰]pentadecane]-5',11'-dien-5-one

Description

(1'S,2S,3'S,4'R,10'S,15'R)-3'-ethyl-12'-hydroxy-4'-methoxy-4-methyl-15'-[(2R,4R)-4-methyl-5-oxooxolan-2-yl]-5H-13'-oxa-9',11'-diazaspiro[furan-2,2'-tetracyclo[7.4.2.0¹,¹⁰.0⁴,¹⁰]Pentadecane]-5',11'-dien-5-one belongs to the class of organic compounds known as stichoneurine-type alkaloids. These are stemona alkaloids with a structure that typically contains a 3-methyloxolan-2-one and a 5-propyloxolan-2-one moieties that are attached to the characteristic pyrrolo[1,2-a]azepine skeleton at the C3 and C9 position, respectively. (1's,2s,3's,4'r,10's,15'r)-3'-ethyl-12'-hydroxy-4'-methoxy-4-methyl-15'-[(2r,4r)-4-methyl-5-oxooxolan-2-yl]-13'-oxa-9',11'-diazaspiro[furan-2,2'-tetracyclo[7.4.2.0¹,¹⁰.0⁴,¹⁰]pentadecane]-5',11'-dien-5-one is found in Stemona sessilifolia. Based on a literature review very few articles have been published on (1'S,2S,3'S,4'R,10'S,15'R)-3'-ethyl-12'-hydroxy-4'-methoxy-4-methyl-15'-[(2R,4R)-4-methyl-5-oxooxolan-2-yl]-5H-13'-oxa-9',11'-diazaspiro[furan-2,2'-tetracyclo[7.4.2.0¹,¹⁰.0⁴,¹⁰]Pentadecane]-5',11'-dien-5-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072207582D          

 33 38  0  0  1  0            999 V2000
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    4.3042    1.7721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309072207582D          

 33 38  0  0  1  0            999 V2000
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M  END
> <DATABASE_ID>
NP0245046

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@H]1[C@]2(OC(=O)C(C)=C2)[C@]23C[C@H]([C@H]4C[C@@H](C)C(=O)O4)N4CCC=C[C@]1(OC)[C@]24N=C(O)O3

> <INCHI_IDENTIFIER>
InChI=1S/C24H30N2O7/c1-5-17-21(30-4)8-6-7-9-26-15(16-10-13(2)18(27)31-16)12-23(24(21,26)25-20(29)33-23)22(17)11-14(3)19(28)32-22/h6,8,11,13,15-17H,5,7,9-10,12H2,1-4H3,(H,25,29)/t13-,15-,16-,17+,21-,22+,23-,24-/m1/s1

> <INCHI_KEY>
RCEVGJPPQYQRPU-WRBWIVIWSA-N

> <FORMULA>
C24H30N2O7

> <MOLECULAR_WEIGHT>
458.511

> <EXACT_MASS>
458.205301314

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
46.93538855237282

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1'S,2S,3'S,4'R,10'S,15'R)-3'-ethyl-12'-hydroxy-4'-methoxy-4-methyl-15'-[(2R,4R)-4-methyl-5-oxooxolan-2-yl]-5H-13'-oxa-9',11'-diazaspiro[furan-2,2'-tetracyclo[7.4.2.0^{1,10}.0^{4,10}]pentadecane]-5',11'-dien-5-one

> <JCHEM_LOGP>
1.811845668961369

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.5068139567354253

> <JCHEM_PKA_STRONGEST_BASIC>
5.618128981987646

> <JCHEM_POLAR_SURFACE_AREA>
106.89000000000001

> <JCHEM_REFRACTIVITY>
116.19930000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,2S,3'S,4'R,10'S,15'R)-3'-ethyl-12'-hydroxy-4'-methoxy-4-methyl-15'-[(2R,4R)-4-methyl-5-oxooxolan-2-yl]-13'-oxa-9',11'-diazaspiro[furan-2,2'-tetracyclo[7.4.2.0^{1,10}.0^{4,10}]pentadecane]-5',11'-dien-5-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       1.886   4.734   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.643   5.088   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.605   3.569   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.774   2.113   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.478   3.483   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.998   3.236   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.627   3.699   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.233   1.714   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       9.870   1.390   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       6.859   1.020   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       6.062   0.521   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.591  -0.945   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.051  -0.950   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.150  -2.199   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.631  -3.662   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.389  -4.572   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.394  -6.112   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.140  -3.671   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.323  -4.152   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       1.610  -2.205   0.000  0.00  0.00           O+0
HETATM   21  N   UNK     0       3.570   0.513   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       2.084   0.917   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.474   2.331   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.199   3.690   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.559   3.815   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.166   3.504   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.407   5.622   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       5.563   7.296   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.813   1.422   0.000  0.00  0.00           C+0
HETATM   30  N   UNK     0       5.283   2.889   0.000  0.00  0.00           N+0
HETATM   31  C   UNK     0       6.823   2.894   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       8.014   4.333   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       7.304   1.431   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   26                                                  
CONECT    4    3    5   10   11                                             
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8    4                                                       
CONECT   11    4   12   29   33                                             
CONECT   12   11   13                                                       
CONECT   13   12   14   21                                                  
CONECT   14   13   15   20                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   14                                                       
CONECT   21   13   22   29                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25    3   27   29                                             
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29   26   21   11   30                                             
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   11                                                       
MASTER        0    0    0    0    0    0    0    0   33    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₀N₂O₇

Average Mass

458.5110 Da

Monoisotopic Mass

458.20530 Da

IUPAC Name

Traditional Name

(1'S,2S,3'S,4'R,10'S,15'R)-3'-ethyl-12'-hydroxy-4'-methoxy-4-methyl-15'-[(2R,4R)-4-methyl-5-oxooxolan-2-yl]-13'-oxa-9',11'-diazaspiro[furan-2,2'-tetracyclo[7.4.2.0^{1,10}.0^{4,10}]pentadecane]-5',11'-dien-5-one

CAS Registry Number

Not Available

SMILES

CC[C@@H]1[C@]2(OC(=O)C(C)=C2)[C@]23C[C@H]([C@H]4C[C@@H](C)C(=O)O4)N4CCC=C[C@]1(OC)[C@]24N=C(O)O3

InChI Identifier

InChI=1S/C24H30N2O7/c1-5-17-21(30-4)8-6-7-9-26-15(16-10-13(2)18(27)31-16)12-23(24(21,26)25-20(29)33-23)22(17)11-14(3)19(28)32-22/h6,8,11,13,15-17H,5,7,9-10,12H2,1-4H3,(H,25,29)/t13-,15-,16-,17+,21-,22+,23-,24-/m1/s1

InChI Key

RCEVGJPPQYQRPU-WRBWIVIWSA-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
Stemona sessilifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as stichoneurine-type alkaloids. These are stemona alkaloids with a structure that typically contains a 3-methyloxolan-2-one and a 5-propyloxolan-2-one moieties that are attached to the characteristic pyrrolo[1,2-a]azepine skeleton at the C3 and C9 position, respectively.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Stemona alkaloids

Sub Class

Stemoamide-type alkaloids

Direct Parent

Stichoneurine-type alkaloids

Alternative Parents

Substituents

Stichoneurine-type alkaloid
Azepine
2-furanone
Dicarboxylic acid or derivatives
Gamma butyrolactone
N-alkylpyrrolidine
Dihydrofuran
Oxazoline
Pyrrolidine
Tetrahydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Lactone
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Oxacycle
Carboxylic acid derivative
Dialkyl ether
Ether
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organonitrogen compound
Organooxygen compound
Organic nitrogen compound
Organic oxygen compound
Carbonyl group
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	1.81	ChemAxon
pKa (Strongest Acidic)	3.51	ChemAxon
pKa (Strongest Basic)	5.62	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	106.89 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	116.2 m³·mol⁻¹	ChemAxon
Polarizability	46.94 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

162923033

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1's,2s,3's,4'r,10's,15'r)-3'-ethyl-12'-hydroxy-4'-methoxy-4-methyl-15'-[(2r,4r)-4-methyl-5-oxooxolan-2-yl]-13'-oxa-9',11'-diazaspiro[furan-2,2'-tetracyclo[7.4.2.0¹,¹⁰.0⁴,¹⁰]pentadecane]-5',11'-dien-5-one (NP0245046)

MOL for NP0245046 ((1's,2s,3's,4'r,10's,15'r)-3'-ethyl-12'-hydroxy-4'-methoxy-4-methyl-15'-[(2r,4r)-4-methyl-5-oxooxolan-2-yl]-13'-oxa-9',11'-diazaspiro[furan-2,2'-tetracyclo[7.4.2.0¹,¹⁰.0⁴,¹⁰]pentadecane]-5',11'-dien-5-one)

3D MOL for NP0245046 ((1's,2s,3's,4'r,10's,15'r)-3'-ethyl-12'-hydroxy-4'-methoxy-4-methyl-15'-[(2r,4r)-4-methyl-5-oxooxolan-2-yl]-13'-oxa-9',11'-diazaspiro[furan-2,2'-tetracyclo[7.4.2.0¹,¹⁰.0⁴,¹⁰]pentadecane]-5',11'-dien-5-one)

3D SDF for NP0245046 ((1's,2s,3's,4'r,10's,15'r)-3'-ethyl-12'-hydroxy-4'-methoxy-4-methyl-15'-[(2r,4r)-4-methyl-5-oxooxolan-2-yl]-13'-oxa-9',11'-diazaspiro[furan-2,2'-tetracyclo[7.4.2.0¹,¹⁰.0⁴,¹⁰]pentadecane]-5',11'-dien-5-one)

3D-SDF for NP0245046 ((1's,2s,3's,4'r,10's,15'r)-3'-ethyl-12'-hydroxy-4'-methoxy-4-methyl-15'-[(2r,4r)-4-methyl-5-oxooxolan-2-yl]-13'-oxa-9',11'-diazaspiro[furan-2,2'-tetracyclo[7.4.2.0¹,¹⁰.0⁴,¹⁰]pentadecane]-5',11'-dien-5-one)

PDB for NP0245046 ((1's,2s,3's,4'r,10's,15'r)-3'-ethyl-12'-hydroxy-4'-methoxy-4-methyl-15'-[(2r,4r)-4-methyl-5-oxooxolan-2-yl]-13'-oxa-9',11'-diazaspiro[furan-2,2'-tetracyclo[7.4.2.0¹,¹⁰.0⁴,¹⁰]pentadecane]-5',11'-dien-5-one)

3D PDB for NP0245046 ((1's,2s,3's,4'r,10's,15'r)-3'-ethyl-12'-hydroxy-4'-methoxy-4-methyl-15'-[(2r,4r)-4-methyl-5-oxooxolan-2-yl]-13'-oxa-9',11'-diazaspiro[furan-2,2'-tetracyclo[7.4.2.0¹,¹⁰.0⁴,¹⁰]pentadecane]-5',11'-dien-5-one)

SMILES for NP0245046 ((1's,2s,3's,4'r,10's,15'r)-3'-ethyl-12'-hydroxy-4'-methoxy-4-methyl-15'-[(2r,4r)-4-methyl-5-oxooxolan-2-yl]-13'-oxa-9',11'-diazaspiro[furan-2,2'-tetracyclo[7.4.2.0¹,¹⁰.0⁴,¹⁰]pentadecane]-5',11'-dien-5-one)

INCHI for NP0245046 ((1's,2s,3's,4'r,10's,15'r)-3'-ethyl-12'-hydroxy-4'-methoxy-4-methyl-15'-[(2r,4r)-4-methyl-5-oxooxolan-2-yl]-13'-oxa-9',11'-diazaspiro[furan-2,2'-tetracyclo[7.4.2.0¹,¹⁰.0⁴,¹⁰]pentadecane]-5',11'-dien-5-one)

Structure for NP0245046 ((1's,2s,3's,4'r,10's,15'r)-3'-ethyl-12'-hydroxy-4'-methoxy-4-methyl-15'-[(2r,4r)-4-methyl-5-oxooxolan-2-yl]-13'-oxa-9',11'-diazaspiro[furan-2,2'-tetracyclo[7.4.2.0¹,¹⁰.0⁴,¹⁰]pentadecane]-5',11'-dien-5-one)

3D Structure for NP0245046 ((1's,2s,3's,4'r,10's,15'r)-3'-ethyl-12'-hydroxy-4'-methoxy-4-methyl-15'-[(2r,4r)-4-methyl-5-oxooxolan-2-yl]-13'-oxa-9',11'-diazaspiro[furan-2,2'-tetracyclo[7.4.2.0¹,¹⁰.0⁴,¹⁰]pentadecane]-5',11'-dien-5-one)