NP-MRD: Showing NP-Card for methyl 3-{15-hydroxy-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadec-3-en-2-yl}propanoate (NP0219664)

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Record Information

Version

2.0

Created at

2022-09-05 20:44:08 UTC

Updated at

2022-09-05 20:44:08 UTC

NP-MRD ID

NP0219664

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 3-{15-hydroxy-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadec-3-en-2-yl}propanoate

Description

Methyl 3-[15-hydroxy-1-methyl-14-(propan-2-yl)-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]Hexadec-3-en-2-yl]propanoate belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. methyl 3-{15-hydroxy-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadec-3-en-2-yl}propanoate is found in Daphniphyllum calycinum. Methyl 3-[15-hydroxy-1-methyl-14-(propan-2-yl)-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]Hexadec-3-en-2-yl]propanoate is a very strong basic compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004171521282D          

 27 30  0  0  0  0            999 V2000
    2.5962    4.4960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7948    4.3002    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5590    3.4923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3777    3.5946    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2214    2.6921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4511    1.7893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5736    0.7499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2328   -0.1291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9365   -0.4606    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2354    0.2632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7119    1.2197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0226    2.1072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8621    1.9897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1501    1.2220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9070    0.8938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8287    0.0725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0234   -0.1069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6040    0.6036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0836    1.2797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4668    1.9515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2608    1.1882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0227    0.4045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8873    0.2584    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4539   -0.2711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0895   -1.0633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3126   -1.9065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6261   -1.5629    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  2  0  0  0  0
  3  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
  8  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
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
  7 18  1  0  0  0  0
 14 18  1  0  0  0  0
 11 19  1  0  0  0  0
  7 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
  8 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
M  END


  Mrv1533004171521282D          

 27 30  0  0  0  0            999 V2000
    2.5962    4.4960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7948    4.3002    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5590    3.4923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3777    3.5946    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2214    2.6921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4511    1.7893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5736    0.7499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2328   -0.1291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9365   -0.4606    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2354    0.2632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7119    1.2197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0226    2.1072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8621    1.9897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1501    1.2220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9070    0.8938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8287    0.0725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0234   -0.1069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6040    0.6036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0836    1.2797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4668    1.9515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2608    1.1882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0227    0.4045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8873    0.2584    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4539   -0.2711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0895   -1.0633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3126   -1.9065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6261   -1.5629    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  2  0  0  0  0
  3  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
  8  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
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
  7 18  1  0  0  0  0
 14 18  1  0  0  0  0
 11 19  1  0  0  0  0
  7 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
  8 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0219664

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)CCC12C3NCC(CCC4CCC=C14)C2(C)CC(O)C3C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C23H37NO3/c1-14(2)20-18(25)12-22(3)16-9-8-15-6-5-7-17(15)23(22,21(20)24-13-16)11-10-19(26)27-4/h7,14-16,18,20-21,24-25H,5-6,8-13H2,1-4H3

> <INCHI_KEY>
IIHXSJJFQSDLJE-UHFFFAOYSA-N

> <FORMULA>
C23H37NO3

> <MOLECULAR_WEIGHT>
375.553

> <EXACT_MASS>
375.277344055

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
43.357376826608146

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 3-[15-hydroxy-1-methyl-14-(propan-2-yl)-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadec-3-en-2-yl]propanoate

> <ALOGPS_LOGP>
3.45

> <JCHEM_LOGP>
2.868773205666668

> <ALOGPS_LOGS>
-4.59

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.873346548909986

> <JCHEM_PKA_STRONGEST_BASIC>
10.566324686601153

> <JCHEM_POLAR_SURFACE_AREA>
58.56

> <JCHEM_REFRACTIVITY>
107.31519999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.62e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 3-{15-hydroxy-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadec-3-en-2-yl}propanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       4.846   8.393   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       3.350   8.027   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.910   6.519   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       4.438   6.710   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.280   5.025   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.709   3.340   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.937   1.400   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.301  -0.241   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       3.615  -0.860   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       4.173   0.491   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.195   2.277   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.775   3.933   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.343   3.714   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.880   2.281   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.293   1.668   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.147   0.135   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.644  -0.199   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.861   1.127   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.023   2.389   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.871   3.643   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.487   2.218   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.042   0.755   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.656   0.482   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       0.847  -0.506   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.167  -1.985   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.583  -3.559   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.169  -2.917   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                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   18   19                                             
CONECT    8    7    9   24                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   19                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   18                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17    7   14                                                  
CONECT   19   11    7   20   21                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22    8   25                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Value	Source
Methyl 3-[15-hydroxy-1-methyl-14-(propan-2-yl)-12-azatetracyclo[8.6.0.0,.0,]hexadec-3-en-2-yl]propanoic acid	Generator
Methyl 3-[15-hydroxy-1-methyl-14-(propan-2-yl)-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadec-3-en-2-yl]propanoic acid	Generator

Chemical Formula

C₂₃H₃₇NO₃

Average Mass

375.5530 Da

Monoisotopic Mass

375.27734 Da

IUPAC Name

methyl 3-[15-hydroxy-1-methyl-14-(propan-2-yl)-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadec-3-en-2-yl]propanoate

Traditional Name

methyl 3-{15-hydroxy-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadec-3-en-2-yl}propanoate

CAS Registry Number

Not Available

SMILES

COC(=O)CCC12C3NCC(CCC4CCC=C14)C2(C)CC(O)C3C(C)C

InChI Identifier

InChI=1S/C23H37NO3/c1-14(2)20-18(25)12-22(3)16-9-8-15-6-5-7-17(15)23(22,21(20)24-13-16)11-10-19(26)27-4/h7,14-16,18,20-21,24-25H,5-6,8-13H2,1-4H3

InChI Key

IIHXSJJFQSDLJE-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 calycinum	LOTUS Database	35616633

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
Delta amino acid or derivatives
Fatty acid ester
Piperidine
Fatty acyl
Cyclic alcohol
Methyl ester
Amino acid or derivatives
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Secondary aliphatic amine
Monocarboxylic acid or derivatives
Azacycle
Organoheterocyclic compound
Secondary amine
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Amine
Organonitrogen compound
Organooxygen compound
Organic nitrogen compound
Carbonyl group
Alcohol
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	3.45	ALOGPS
logP	2.87	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	14.87	ChemAxon
pKa (Strongest Basic)	10.57	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	58.56 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	107.32 m³·mol⁻¹	ChemAxon
Polarizability	43.36 Å³	ChemAxon
Number of Rings	4	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

74392194

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 3-{15-hydroxy-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadec-3-en-2-yl}propanoate (NP0219664)

MOL for NP0219664 (methyl 3-{15-hydroxy-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadec-3-en-2-yl}propanoate)

3D MOL for NP0219664 (methyl 3-{15-hydroxy-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadec-3-en-2-yl}propanoate)

3D SDF for NP0219664 (methyl 3-{15-hydroxy-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadec-3-en-2-yl}propanoate)

3D-SDF for NP0219664 (methyl 3-{15-hydroxy-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadec-3-en-2-yl}propanoate)

PDB for NP0219664 (methyl 3-{15-hydroxy-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadec-3-en-2-yl}propanoate)

3D PDB for NP0219664 (methyl 3-{15-hydroxy-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadec-3-en-2-yl}propanoate)

SMILES for NP0219664 (methyl 3-{15-hydroxy-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadec-3-en-2-yl}propanoate)

INCHI for NP0219664 (methyl 3-{15-hydroxy-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadec-3-en-2-yl}propanoate)

Structure for NP0219664 (methyl 3-{15-hydroxy-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadec-3-en-2-yl}propanoate)

3D Structure for NP0219664 (methyl 3-{15-hydroxy-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadec-3-en-2-yl}propanoate)