NP-MRD: Showing NP-Card for Nb-Formyl-Nb-nor-(+)-harappamine (NP0067725)

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Record Information

Version

2.0

Created at

2022-04-28 12:34:22 UTC

Updated at

2022-04-28 12:34:22 UTC

NP-MRD ID

NP0067725

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Nb-Formyl-Nb-nor-(+)-harappamine

Description

N-[(1S)-1-[(6R,7S,10S,11R,14R,15R,20S)-6,10,15,19-tetramethyl-17-oxa-19-azapentacyclo[12.8.0.0³,¹¹.0⁶,¹⁰.0¹⁵,²⁰]Docosa-1,3-dien-7-yl]ethyl]carboximidic acid belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. Nb-Formyl-Nb-nor-(+)-harappamine is found in Buxus papillosa and Buxus papilosa. Based on a literature review very few articles have been published on N-[(1S)-1-[(6R,7S,10S,11R,14R,15R,20S)-6,10,15,19-tetramethyl-17-oxa-19-azapentacyclo[12.8.0.0³,¹¹.0⁶,¹⁰.0¹⁵,²⁰]Docosa-1,3-dien-7-yl]ethyl]carboximidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282214342D          

 31 35  0  0  1  0            999 V2000
    7.2188    3.2175    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0529    4.0257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1 31  1  1  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652304282214342D          

 31 35  0  0  1  0            999 V2000
    7.2188    3.2175    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    8.7784    3.9502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   10.1065    2.9711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.0456    2.0605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0067725

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](NC=O)[C@H]1CC[C@@]2(C)[C@@H]3CC[C@@H]4C(CC[C@@H]5N(C)COC[C@]45C)=CC3=CC[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C27H42N2O2/c1-18(28-16-30)21-11-13-27(4)23-8-7-22-19(14-20(23)10-12-26(21,27)3)6-9-24-25(22,2)15-31-17-29(24)5/h10,14,16,18,21-24H,6-9,11-13,15,17H2,1-5H3,(H,28,30)/t18-,21+,22+,23+,24-,25+,26+,27-/m0/s1

> <INCHI_KEY>
YWURLTOLHCNEKH-NFJXPMKSSA-N

> <FORMULA>
C27H42N2O2

> <MOLECULAR_WEIGHT>
426.645

> <EXACT_MASS>
426.3246286

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
51.81866269899988

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-[(1S)-1-[(6R,7S,10S,11R,14R,15R,20S)-6,10,15,19-tetramethyl-17-oxa-19-azapentacyclo[12.8.0.0^{3,11}.0^{6,10}.0^{15,20}]docosa-1,3-dien-7-yl]ethyl]formamide

> <ALOGPS_LOGP>
4.59

> <JCHEM_LOGP>
3.828764489666666

> <ALOGPS_LOGS>
-5.26

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.076651213721135

> <JCHEM_PKA_STRONGEST_BASIC>
7.354378902372229

> <JCHEM_POLAR_SURFACE_AREA>
41.57

> <JCHEM_REFRACTIVITY>
126.80949999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.33e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-[(1S)-1-[(6R,7S,10S,11R,14R,15R,20S)-6,10,15,19-tetramethyl-17-oxa-19-azapentacyclo[12.8.0.0^{3,11}.0^{6,10}.0^{15,20}]docosa-1,3-dien-7-yl]ethyl]formamide

> <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      13.475   6.006   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.165   7.515   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.704   8.001   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.553   6.978   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.862   5.470   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.324   4.984   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.940   3.572   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      14.473   3.723   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.803   5.227   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      16.215   5.843   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      16.386   7.374   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0      17.454   4.930   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0      18.865   5.546   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      20.105   4.632   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      11.285   3.846   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.876   4.287   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.336   4.321   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.403   5.545   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.778   7.039   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.180   7.677   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.673   8.111   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.191   7.689   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.816   6.196   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.922   5.124   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.027   4.052   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.546   3.630   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       4.065   3.209   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       2.959   4.281   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0       3.335   5.774   0.000  0.00  0.00           N+0
HETATM   30  C   UNK     0       2.229   6.846   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      14.727   6.903   0.000  0.00  0.00           C+0
CONECT    1    2    6    9   31                                             
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   20                                                  
CONECT    5    4    6   16                                                  
CONECT    6    5    1    7   15                                             
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8    1   10                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15    6                                                            
CONECT   16    5   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   24                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19    4                                                       
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   29                                                  
CONECT   24   23   18   25   26                                             
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   23   30                                                  
CONECT   30   29                                                            
CONECT   31    1                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

View in JSmol

Synonyms

Value	Source
N-[(1S)-1-[(6R,7S,10S,11R,14R,15R,20S)-6,10,15,19-Tetramethyl-17-oxa-19-azapentacyclo[12.8.0.0,.0,.0,]docosa-1,3-dien-7-yl]ethyl]carboximidate	Generator

Chemical Formula

C₂₇H₄₂N₂O₂

Average Mass

426.6450 Da

Monoisotopic Mass

426.32463 Da

IUPAC Name

N-[(1S)-1-[(6R,7S,10S,11R,14R,15R,20S)-6,10,15,19-tetramethyl-17-oxa-19-azapentacyclo[12.8.0.0^{3,11}.0^{6,10}.0^{15,20}]docosa-1,3-dien-7-yl]ethyl]formamide

Traditional Name

N-[(1S)-1-[(6R,7S,10S,11R,14R,15R,20S)-6,10,15,19-tetramethyl-17-oxa-19-azapentacyclo[12.8.0.0^{3,11}.0^{6,10}.0^{15,20}]docosa-1,3-dien-7-yl]ethyl]formamide

CAS Registry Number

Not Available

SMILES

C[C@H](NC=O)[C@H]1CC[C@@]2(C)[C@@H]3CC[C@@H]4C(CC[C@@H]5N(C)COC[C@]45C)=CC3=CC[C@]12C

InChI Identifier

InChI=1S/C27H42N2O2/c1-18(28-16-30)21-11-13-27(4)23-8-7-22-19(14-20(23)10-12-26(21,27)3)6-9-24-25(22,2)15-31-17-29(24)5/h10,14,16,18,21-24H,6-9,11-13,15,17H2,1-5H3,(H,28,30)/t18-,21+,22+,23+,24-,25+,26+,27-/m0/s1

InChI Key

YWURLTOLHCNEKH-NFJXPMKSSA-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
Buxus papillosa	LOTUS Database	35616633
Buxus papilosa	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Pinguisane sesquiterpenoid
1,3-oxazinane
Oxazinane
Hemiaminal
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Carboximidic acid derivative
Carboximidic acid
Oxacycle
Hydrocarbon derivative
Organopnictogen compound
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Organic nitrogen 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	4.59	ALOGPS
logP	3.83	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	16.08	ChemAxon
pKa (Strongest Basic)	7.35	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	41.57 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	126.81 m³·mol⁻¹	ChemAxon
Polarizability	51.82 Å³	ChemAxon
Number of Rings	5	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

162911839

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Nb-Formyl-Nb-nor-(+)-harappamine (NP0067725)

MOL for NP0067725 (Nb-Formyl-Nb-nor-(+)-harappamine)

3D MOL for NP0067725 (Nb-Formyl-Nb-nor-(+)-harappamine)

3D SDF for NP0067725 (Nb-Formyl-Nb-nor-(+)-harappamine)

3D-SDF for NP0067725 (Nb-Formyl-Nb-nor-(+)-harappamine)

PDB for NP0067725 (Nb-Formyl-Nb-nor-(+)-harappamine)

3D PDB for NP0067725 (Nb-Formyl-Nb-nor-(+)-harappamine)

SMILES for NP0067725 (Nb-Formyl-Nb-nor-(+)-harappamine)

INCHI for NP0067725 (Nb-Formyl-Nb-nor-(+)-harappamine)

Structure for NP0067725 (Nb-Formyl-Nb-nor-(+)-harappamine)

3D Structure for NP0067725 (Nb-Formyl-Nb-nor-(+)-harappamine)