NP-MRD: Showing NP-Card for 14-ethyl-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosane-2,3-diol (NP0199258)

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Record Information

Version

2.0

Created at

2022-09-04 17:51:52 UTC

Updated at

2022-09-04 17:51:52 UTC

NP-MRD ID

NP0199258

Secondary Accession Numbers

None

Natural Product Identification

Common Name

14-ethyl-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosane-2,3-diol

Description

14-Ethyl-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]Docosane-2,3-diol belongs to the class of organic compounds known as aconitane-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the hexacyclic aconitane skeleton. These compounds have no oxygen functionality at the C7 atom. 14-ethyl-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosane-2,3-diol is found in Delphinium taliense. Based on a literature review very few articles have been published on 14-ethyl-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]Docosane-2,3-diol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042219512D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309042219512D          

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    4.1443    0.1487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8786    0.7559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6351    1.2101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8991   -1.4305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  5  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
  5 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 17 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 14 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 21 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 26 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 17 35  1  0  0  0  0
  3 35  1  0  0  0  0
 14 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0199258

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCN1CC2(COC)CCC(OC)C34C2CC2(OCOC22CC(OC)C5CC3(O)C2(O)C5OC)C14

> <INCHI_IDENTIFIER>
InChI=1S/C26H41NO8/c1-6-27-12-21(13-30-2)8-7-18(32-4)25-17(21)11-22(20(25)27)24(35-14-34-22)10-16(31-3)15-9-23(25,28)26(24,29)19(15)33-5/h15-20,28-29H,6-14H2,1-5H3

> <INCHI_KEY>
VQCHSLAMMAZPAA-UHFFFAOYSA-N

> <FORMULA>
C26H41NO8

> <MOLECULAR_WEIGHT>
495.613

> <EXACT_MASS>
495.283217284

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
53.1820370714178

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
14-ethyl-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.1^{2,5}.0^{1,13}.0^{3,8}.0^{8,12}.0^{16,20}]docosane-2,3-diol

> <JCHEM_LOGP>
-0.8718039266666663

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
13.787717783463844

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.691009048859893

> <JCHEM_PKA_STRONGEST_BASIC>
9.181544022801196

> <JCHEM_POLAR_SURFACE_AREA>
99.08000000000001

> <JCHEM_REFRACTIVITY>
123.83539999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
14-ethyl-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.1^{2,5}.0^{1,13}.0^{3,8}.0^{8,12}.0^{16,20}]docosane-2,3-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.395  -5.156   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.982  -4.358   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0       1.777  -2.869   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0       0.923  -1.494   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.572  -0.020   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.049   0.695   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -0.553   2.178   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -2.078   2.390   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.049   1.529   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.561   1.954   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.524   0.742   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.292   2.578   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.873   4.130   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.129  -0.860   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.879  -0.688   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.739  -2.355   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.627  -3.110   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.658  -4.728   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       6.067  -5.359   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       7.029  -4.179   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       6.380  -2.712   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.984  -2.915   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.143  -1.838   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      10.821  -1.933   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      11.856  -3.163   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.586  -0.295   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.013   0.960   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.644  -0.108   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.928   1.592   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       6.540  -1.118   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       7.865  -2.195   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       7.736   0.278   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       9.107   1.411   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      10.519   2.259   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       3.545  -2.670   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   35                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    9   15                                             
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    5   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11   15   28   35                                             
CONECT   15   14    5   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   21   35                                             
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   17   22   30                                             
CONECT   22   21   23                                                       
CONECT   23   22   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   27   32                                                  
CONECT   27   26   28                                                       
CONECT   28   27   14   29   30                                             
CONECT   29   28                                                            
CONECT   30   28   21   31   32                                             
CONECT   31   30                                                            
CONECT   32   30   26   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33                                                            
CONECT   35   17    3   14                                                  
MASTER        0    0    0    0    0    0    0    0   35    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₄₁NO₈

Average Mass

495.6130 Da

Monoisotopic Mass

495.28322 Da

IUPAC Name

14-ethyl-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.1^{2,5}.0^{1,13}.0^{3,8}.0^{8,12}.0^{16,20}]docosane-2,3-diol

Traditional Name

14-ethyl-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.1^{2,5}.0^{1,13}.0^{3,8}.0^{8,12}.0^{16,20}]docosane-2,3-diol

CAS Registry Number

Not Available

SMILES

CCN1CC2(COC)CCC(OC)C34C2CC2(OCOC22CC(OC)C5CC3(O)C2(O)C5OC)C14

InChI Identifier

InChI=1S/C26H41NO8/c1-6-27-12-21(13-30-2)8-7-18(32-4)25-17(21)11-22(20(25)27)24(35-14-34-22)10-16(31-3)15-9-23(25,28)26(24,29)19(15)33-5/h15-20,28-29H,6-14H2,1-5H3

InChI Key

VQCHSLAMMAZPAA-UHFFFAOYSA-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
Delphinium taliense	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aconitane-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the hexacyclic aconitane skeleton. These compounds have no oxygen functionality at the C7 atom.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Aconitane-type diterpenoid alkaloids

Alternative Parents

Substituents

Aconitane-type diterpenoid alkaloid
Quinolidine
Alkaloid or derivatives
Azepane
Piperidine
Meta-dioxolane
Tertiary alcohol
Cyclic alcohol
1,2-diol
Tertiary aliphatic amine
Tertiary amine
Oxacycle
Azacycle
Organoheterocyclic compound
Acetal
Dialkyl ether
Ether
Hydrocarbon derivative
Organonitrogen compound
Organooxygen compound
Organic nitrogen compound
Amine
Alcohol
Organic oxygen compound
Organopnictogen 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	-0.87	ChemAxon
pKa (Strongest Acidic)	11.69	ChemAxon
pKa (Strongest Basic)	9.18	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	99.08 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	123.84 m³·mol⁻¹	ChemAxon
Polarizability	53.18 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

13891353

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 14-ethyl-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosane-2,3-diol (NP0199258)

MOL for NP0199258 (14-ethyl-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosane-2,3-diol)

3D MOL for NP0199258 (14-ethyl-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosane-2,3-diol)

3D SDF for NP0199258 (14-ethyl-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosane-2,3-diol)

3D-SDF for NP0199258 (14-ethyl-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosane-2,3-diol)

PDB for NP0199258 (14-ethyl-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosane-2,3-diol)

3D PDB for NP0199258 (14-ethyl-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosane-2,3-diol)

SMILES for NP0199258 (14-ethyl-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosane-2,3-diol)

INCHI for NP0199258 (14-ethyl-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosane-2,3-diol)

Structure for NP0199258 (14-ethyl-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosane-2,3-diol)

3D Structure for NP0199258 (14-ethyl-4,6,19-trimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosane-2,3-diol)