NP-MRD: Showing NP-Card for methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0⁷,²⁰]icosa-7(20),10-diene-3-carboxylate (NP0252396)

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Record Information

Version

2.0

Created at

2022-09-07 15:53:48 UTC

Updated at

2022-09-07 15:53:48 UTC

NP-MRD ID

NP0252396

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0⁷,²⁰]icosa-7(20),10-diene-3-carboxylate

Description

Methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0⁷,²⁰]Icosa-7(20),10-diene-3-carboxylate belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0⁷,²⁰]icosa-7(20),10-diene-3-carboxylate is found in Daphniphyllum macropodum. Methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0⁷,²⁰]Icosa-7(20),10-diene-3-carboxylate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251504402D          

 35 39  0  0  0  0            999 V2000
    1.2344   -4.5742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4520   -3.7362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0208   -2.9468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4525   -3.6137    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.4183   -1.2734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8825   -0.6606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.5680   -2.1636    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0843   -1.6863    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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 31 35  1  0  0  0  0
M  END

     RDKit          3D

 70 74  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1533004251504402D          

 35 39  0  0  0  0            999 V2000
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 16 21  1  0  0  0  0
  7 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  2  0  0  0  0
 24 26  1  0  0  0  0
 21 27  1  0  0  0  0
 27 28  2  0  0  0  0
 10 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
  7 32  1  0  0  0  0
 32 33  1  0  0  0  0
  5 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 31 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0252396

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1CC23C4=C(CCC14)CCC1=CN(CC(C)CCC(OC(C)=O)C21COC(C)=O)C3=O

> <INCHI_IDENTIFIER>
InChI=1S/C27H35NO7/c1-15-5-10-22(35-17(3)30)27(14-34-16(2)29)19-8-6-18-7-9-20-21(24(31)33-4)11-26(27,23(18)20)25(32)28(12-15)13-19/h13,15,20-22H,5-12,14H2,1-4H3

> <INCHI_KEY>
XCEBFXVRSJEDEA-UHFFFAOYSA-N

> <FORMULA>
C27H35NO7

> <MOLECULAR_WEIGHT>
485.577

> <EXACT_MASS>
485.241352471

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
51.46732058024328

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0⁷,²⁰]icosa-7(20),10-diene-3-carboxylate

> <ALOGPS_LOGP>
2.61

> <JCHEM_LOGP>
1.3488439203333331

> <ALOGPS_LOGS>
-3.94

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7185572073182813

> <JCHEM_POLAR_SURFACE_AREA>
99.21000000000001

> <JCHEM_REFRACTIVITY>
126.00069999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.57e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0⁷,²⁰]icosa-7(20),10-diene-3-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       2.304  -8.538   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.710  -6.974   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.905  -5.501   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       0.845  -6.745   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.979  -3.693   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.781  -2.377   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.647  -1.233   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.600  -2.656   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.927  -4.039   0.000  0.00  0.00           O+0
HETATM   10  N   UNK     0       0.157  -3.148   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      -1.151  -4.060   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.521  -3.333   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.921  -4.658   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.059  -1.886   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.543  -0.417   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.210   0.405   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.530   2.055   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -2.719   3.180   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -4.311   2.989   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -2.483   4.751   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.282  -0.184   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.641  -2.050   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -2.392  -2.465   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -3.745  -3.643   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -3.004  -5.300   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -5.474  -3.474   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.749   0.559   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.440  -1.223   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.076   1.629   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.618   1.103   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.119  -0.414   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.111  -1.512   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       3.449  -3.013   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.029  -2.881   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.428  -1.353   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   33                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   21   32                                             
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   28                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   16    7   22   27                                             
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   21   28   29                                                  
CONECT   28   27   10                                                       
CONECT   29   27   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   35                                                  
CONECT   32   31    7   33                                                  
CONECT   33   32    5   34                                                  
CONECT   34   33   35                                                       
CONECT   35   34   31                                                       
MASTER        0    0    0    0    0    0    0    0   35    0   78    0
END

View in JSmol

Synonyms

Value	Source
Methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1,.0,.0,]icosa-7(20),10-diene-3-carboxylic acid	Generator
Methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0⁷,²⁰]icosa-7(20),10-diene-3-carboxylic acid	Generator

Chemical Formula

C₂₇H₃₅NO₇

Average Mass

485.5770 Da

Monoisotopic Mass

485.24135 Da

IUPAC Name

methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0⁷,²⁰]icosa-7(20),10-diene-3-carboxylate

Traditional Name

methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0⁷,²⁰]icosa-7(20),10-diene-3-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1CC23C4=C(CCC14)CCC1=CN(CC(C)CCC(OC(C)=O)C21COC(C)=O)C3=O

InChI Identifier

InChI=1S/C27H35NO7/c1-15-5-10-22(35-17(3)30)27(14-34-16(2)29)19-8-6-18-7-9-20-21(24(31)33-4)11-26(27,23(18)20)25(32)28(12-15)13-19/h13,15,20-22H,5-12,14H2,1-4H3

InChI Key

XCEBFXVRSJEDEA-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
Daphniphyllum macropodum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tricarboxylic acids and derivatives

Direct Parent

Tricarboxylic acids and derivatives

Alternative Parents

Substituents

Tricarboxylic acid or derivatives
Tetrahydropyridine
Tertiary carboxylic acid amide
Methyl ester
Carboxamide group
Carboxylic acid ester
Lactam
Organoheterocyclic compound
Azacycle
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Carbonyl group
Hydrocarbon derivative
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	2.61	ALOGPS
logP	1.35	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	99.21 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	126 m³·mol⁻¹	ChemAxon
Polarizability	51.47 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	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

85110075

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0⁷,²⁰]icosa-7(20),10-diene-3-carboxylate (NP0252396)

MOL for NP0252396 (methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0⁷,²⁰]icosa-7(20),10-diene-3-carboxylate)

3D MOL for NP0252396 (methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0⁷,²⁰]icosa-7(20),10-diene-3-carboxylate)

3D SDF for NP0252396 (methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0⁷,²⁰]icosa-7(20),10-diene-3-carboxylate)

3D-SDF for NP0252396 (methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0⁷,²⁰]icosa-7(20),10-diene-3-carboxylate)

PDB for NP0252396 (methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0⁷,²⁰]icosa-7(20),10-diene-3-carboxylate)

3D PDB for NP0252396 (methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0⁷,²⁰]icosa-7(20),10-diene-3-carboxylate)

SMILES for NP0252396 (methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0⁷,²⁰]icosa-7(20),10-diene-3-carboxylate)

INCHI for NP0252396 (methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0⁷,²⁰]icosa-7(20),10-diene-3-carboxylate)

Structure for NP0252396 (methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0⁷,²⁰]icosa-7(20),10-diene-3-carboxylate)

3D Structure for NP0252396 (methyl 17-(acetyloxy)-18-[(acetyloxy)methyl]-14-methyl-19-oxo-12-azapentacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0⁷,²⁰]icosa-7(20),10-diene-3-carboxylate)