NP-MRD: Showing NP-Card for (1r,2s,3s,5r,7s,10r,11s,12s,13s,14r,16s,17r,18s,19r)-4-ethyl-10-(hydroxymethyl)-12,16,18-trimethoxy-6-oxa-4-azaheptacyclo[15.2.1.0²,⁷.0²,¹¹.0³,¹³.0⁵,¹⁰.0¹⁴,¹⁹]icosane-13,14-diol (NP0299158)

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Record Information

Version

2.0

Created at

2022-09-10 10:49:38 UTC

Updated at

2022-09-10 10:49:38 UTC

NP-MRD ID

NP0299158

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,3s,5r,7s,10r,11s,12s,13s,14r,16s,17r,18s,19r)-4-ethyl-10-(hydroxymethyl)-12,16,18-trimethoxy-6-oxa-4-azaheptacyclo[15.2.1.0²,⁷.0²,¹¹.0³,¹³.0⁵,¹⁰.0¹⁴,¹⁹]icosane-13,14-diol

Description

(1R,2S,3S,5R,7S,10R,11S,12S,13S,14R,16S,17R,18S,19R)-4-ethyl-10-(hydroxymethyl)-12,16,18-trimethoxy-6-oxa-4-azaheptacyclo[15.2.1.0²,⁷.0²,¹¹.0³,¹³.0⁵,¹⁰.0¹⁴,¹⁹]Icosane-13,14-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. (1r,2s,3s,5r,7s,10r,11s,12s,13s,14r,16s,17r,18s,19r)-4-ethyl-10-(hydroxymethyl)-12,16,18-trimethoxy-6-oxa-4-azaheptacyclo[15.2.1.0²,⁷.0²,¹¹.0³,¹³.0⁵,¹⁰.0¹⁴,¹⁹]icosane-13,14-diol is found in Consolida orientalis and Delphinium carduchorum. Based on a literature review very few articles have been published on (1R,2S,3S,5R,7S,10R,11S,12S,13S,14R,16S,17R,18S,19R)-4-ethyl-10-(hydroxymethyl)-12,16,18-trimethoxy-6-oxa-4-azaheptacyclo[15.2.1.0²,⁷.0²,¹¹.0³,¹³.0⁵,¹⁰.0¹⁴,¹⁹]Icosane-13,14-diol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102212492D          

 32 38  0  0  1  0            999 V2000
   -1.0631   -2.9095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  6 32  1  1  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309102212492D          

 32 38  0  0  1  0            999 V2000
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 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  6  0  0  0
 26 25  1  6  0  0  0
  5 26  1  0  0  0  0
 27 26  1  6  0  0  0
 18 27  1  0  0  0  0
 27 28  1  0  0  0  0
 24 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
  9 31  1  0  0  0  0
 31  3  1  6  0  0  0
 31 32  1  0  0  0  0
  6 32  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0299158

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCN1[C@@H]2[C@]3(O)[C@@H](OC)[C@H]4[C@]2([C@@H]2C[C@H]5[C@H](OC)[C@@H]2[C@]3(O)C[C@@H]5OC)[C@@H]2CC[C@@]4(CO)[C@H]1O2

> <INCHI_IDENTIFIER>
InChI=1S/C24H37NO7/c1-5-25-19-23-12-8-11-13(29-2)9-22(27,15(12)16(11)30-3)24(19,28)18(31-4)17(23)21(10-26)7-6-14(23)32-20(21)25/h11-20,26-28H,5-10H2,1-4H3/t11-,12-,13+,14+,15-,16+,17-,18+,19+,20-,21+,22-,23+,24-/m1/s1

> <INCHI_KEY>
ZYBCAXDRBVBGGT-IEDUYXJUSA-N

> <FORMULA>
C24H37NO7

> <MOLECULAR_WEIGHT>
451.56

> <EXACT_MASS>
451.257002535

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
47.88309607965938

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,3S,5R,7S,10R,11S,12S,13S,14R,16S,17R,18S,19R)-4-ethyl-10-(hydroxymethyl)-12,16,18-trimethoxy-6-oxa-4-azaheptacyclo[15.2.1.0^{2,7}.0^{2,11}.0^{3,13}.0^{5,10}.0^{14,19}]icosane-13,14-diol

> <JCHEM_LOGP>
-1.2806569960000018

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.951033259052998

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.198980415530968

> <JCHEM_PKA_STRONGEST_BASIC>
5.491486946616566

> <JCHEM_POLAR_SURFACE_AREA>
100.85000000000002

> <JCHEM_REFRACTIVITY>
113.0836

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,3S,5R,7S,10R,11S,12S,13S,14R,16S,17R,18S,19R)-4-ethyl-10-(hydroxymethyl)-12,16,18-trimethoxy-6-oxa-4-azaheptacyclo[15.2.1.0^{2,7}.0^{2,11}.0^{3,13}.0^{5,10}.0^{14,19}]icosane-13,14-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.985  -5.431   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.531  -4.922   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0      -0.245  -3.409   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0       1.214  -2.808   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.509  -0.948   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.304   0.006   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.143   1.095   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.389   1.210   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.933  -0.618   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.415  -0.201   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.795   1.292   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.508  -0.973   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.351  -2.491   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -0.954  -3.308   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -2.314  -2.587   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.226  -3.173   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.121  -4.709   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       3.873  -2.818   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       3.781  -4.355   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.352  -3.327   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.559  -2.309   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       8.039  -2.734   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       8.411  -4.229   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.052  -0.730   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.564   0.662   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.108  -0.235   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.048  -1.261   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.354   0.030   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       5.391   1.570   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       6.743   2.307   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -1.385  -2.317   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -1.744  -0.941   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   31                                                  
CONECT    4    3    5   16                                                  
CONECT    5    4    6   12   26                                             
CONECT    6    5    7   32                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   12   31                                             
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    9    5   13                                                  
CONECT   13   12   14   16                                                  
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16   13    4   17   18                                             
CONECT   17   16                                                            
CONECT   18   16   19   20   27                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21   25   28                                                  
CONECT   25   24   26                                                       
CONECT   26   25    5   27                                                  
CONECT   27   26   18   28                                                  
CONECT   28   27   24   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29                                                            
CONECT   31    9    3   32                                                  
CONECT   32   31    6                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₇NO₇

Average Mass

451.5600 Da

Monoisotopic Mass

451.25700 Da

IUPAC Name

(1R,2S,3S,5R,7S,10R,11S,12S,13S,14R,16S,17R,18S,19R)-4-ethyl-10-(hydroxymethyl)-12,16,18-trimethoxy-6-oxa-4-azaheptacyclo[15.2.1.0^{2,7}.0^{2,11}.0^{3,13}.0^{5,10}.0^{14,19}]icosane-13,14-diol

Traditional Name

(1R,2S,3S,5R,7S,10R,11S,12S,13S,14R,16S,17R,18S,19R)-4-ethyl-10-(hydroxymethyl)-12,16,18-trimethoxy-6-oxa-4-azaheptacyclo[15.2.1.0^{2,7}.0^{2,11}.0^{3,13}.0^{5,10}.0^{14,19}]icosane-13,14-diol

CAS Registry Number

Not Available

SMILES

CCN1[C@@H]2[C@]3(O)[C@@H](OC)[C@H]4[C@]2([C@@H]2C[C@H]5[C@H](OC)[C@@H]2[C@]3(O)C[C@@H]5OC)[C@@H]2CC[C@@]4(CO)[C@H]1O2

InChI Identifier

InChI=1S/C24H37NO7/c1-5-25-19-23-12-8-11-13(29-2)9-22(27,15(12)16(11)30-3)24(19,28)18(31-4)17(23)21(10-26)7-6-14(23)32-20(21)25/h11-20,26-28H,5-10H2,1-4H3/t11-,12-,13+,14+,15-,16+,17-,18+,19+,20-,21+,22-,23+,24-/m1/s1

InChI Key

ZYBCAXDRBVBGGT-IEDUYXJUSA-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
Consolida orientalis	LOTUS Database	35616633
Delphinium carduchorum	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
1,3-oxazinane
Oxane
Oxazinane
Piperidine
Tertiary alcohol
Cyclic alcohol
Hemiaminal
Oxacycle
Azacycle
Organoheterocyclic compound
Dialkyl ether
Ether
Organopnictogen compound
Organonitrogen compound
Organooxygen compound
Alcohol
Organic nitrogen compound
Primary alcohol
Hydrocarbon derivative
Organic oxygen 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	-1.3	ChemAxon
pKa (Strongest Acidic)	12.2	ChemAxon
pKa (Strongest Basic)	5.49	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	100.85 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	113.08 m³·mol⁻¹	ChemAxon
Polarizability	47.88 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	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

162950946

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2s,3s,5r,7s,10r,11s,12s,13s,14r,16s,17r,18s,19r)-4-ethyl-10-(hydroxymethyl)-12,16,18-trimethoxy-6-oxa-4-azaheptacyclo[15.2.1.0²,⁷.0²,¹¹.0³,¹³.0⁵,¹⁰.0¹⁴,¹⁹]icosane-13,14-diol (NP0299158)

MOL for NP0299158 ((1r,2s,3s,5r,7s,10r,11s,12s,13s,14r,16s,17r,18s,19r)-4-ethyl-10-(hydroxymethyl)-12,16,18-trimethoxy-6-oxa-4-azaheptacyclo[15.2.1.0²,⁷.0²,¹¹.0³,¹³.0⁵,¹⁰.0¹⁴,¹⁹]icosane-13,14-diol)

3D MOL for NP0299158 ((1r,2s,3s,5r,7s,10r,11s,12s,13s,14r,16s,17r,18s,19r)-4-ethyl-10-(hydroxymethyl)-12,16,18-trimethoxy-6-oxa-4-azaheptacyclo[15.2.1.0²,⁷.0²,¹¹.0³,¹³.0⁵,¹⁰.0¹⁴,¹⁹]icosane-13,14-diol)

3D SDF for NP0299158 ((1r,2s,3s,5r,7s,10r,11s,12s,13s,14r,16s,17r,18s,19r)-4-ethyl-10-(hydroxymethyl)-12,16,18-trimethoxy-6-oxa-4-azaheptacyclo[15.2.1.0²,⁷.0²,¹¹.0³,¹³.0⁵,¹⁰.0¹⁴,¹⁹]icosane-13,14-diol)

3D-SDF for NP0299158 ((1r,2s,3s,5r,7s,10r,11s,12s,13s,14r,16s,17r,18s,19r)-4-ethyl-10-(hydroxymethyl)-12,16,18-trimethoxy-6-oxa-4-azaheptacyclo[15.2.1.0²,⁷.0²,¹¹.0³,¹³.0⁵,¹⁰.0¹⁴,¹⁹]icosane-13,14-diol)

PDB for NP0299158 ((1r,2s,3s,5r,7s,10r,11s,12s,13s,14r,16s,17r,18s,19r)-4-ethyl-10-(hydroxymethyl)-12,16,18-trimethoxy-6-oxa-4-azaheptacyclo[15.2.1.0²,⁷.0²,¹¹.0³,¹³.0⁵,¹⁰.0¹⁴,¹⁹]icosane-13,14-diol)

3D PDB for NP0299158 ((1r,2s,3s,5r,7s,10r,11s,12s,13s,14r,16s,17r,18s,19r)-4-ethyl-10-(hydroxymethyl)-12,16,18-trimethoxy-6-oxa-4-azaheptacyclo[15.2.1.0²,⁷.0²,¹¹.0³,¹³.0⁵,¹⁰.0¹⁴,¹⁹]icosane-13,14-diol)

SMILES for NP0299158 ((1r,2s,3s,5r,7s,10r,11s,12s,13s,14r,16s,17r,18s,19r)-4-ethyl-10-(hydroxymethyl)-12,16,18-trimethoxy-6-oxa-4-azaheptacyclo[15.2.1.0²,⁷.0²,¹¹.0³,¹³.0⁵,¹⁰.0¹⁴,¹⁹]icosane-13,14-diol)

INCHI for NP0299158 ((1r,2s,3s,5r,7s,10r,11s,12s,13s,14r,16s,17r,18s,19r)-4-ethyl-10-(hydroxymethyl)-12,16,18-trimethoxy-6-oxa-4-azaheptacyclo[15.2.1.0²,⁷.0²,¹¹.0³,¹³.0⁵,¹⁰.0¹⁴,¹⁹]icosane-13,14-diol)

Structure for NP0299158 ((1r,2s,3s,5r,7s,10r,11s,12s,13s,14r,16s,17r,18s,19r)-4-ethyl-10-(hydroxymethyl)-12,16,18-trimethoxy-6-oxa-4-azaheptacyclo[15.2.1.0²,⁷.0²,¹¹.0³,¹³.0⁵,¹⁰.0¹⁴,¹⁹]icosane-13,14-diol)

3D Structure for NP0299158 ((1r,2s,3s,5r,7s,10r,11s,12s,13s,14r,16s,17r,18s,19r)-4-ethyl-10-(hydroxymethyl)-12,16,18-trimethoxy-6-oxa-4-azaheptacyclo[15.2.1.0²,⁷.0²,¹¹.0³,¹³.0⁵,¹⁰.0¹⁴,¹⁹]icosane-13,14-diol)