NP-MRD: Showing NP-Card for 14-[3-(acetyloxy)-5-hydroxy-6-methyloxan-2-yl]-4,9,14,20-tetramethyl-5,15-dioxo-21,22,23,24-tetraazapentacyclo[16.2.1.1³,⁶.1⁸,¹¹.1¹³,¹⁶]tetracosa-1(20),2,6(24),7,9,11,13(22),16,18-nonaen-4-yl acetate (NP0200210)

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Record Information

Version

2.0

Created at

2022-09-04 19:00:14 UTC

Updated at

2022-09-04 19:00:15 UTC

NP-MRD ID

NP0200210

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Description

14-[3-(acetyloxy)-5-hydroxy-6-methyloxan-2-yl]-4,9,14,20-tetramethyl-5,15-dioxo-21,22,23,24-tetraazapentacyclo[16.2.1.1³,⁶.1⁸,¹¹.1¹³,¹⁶]tetracosa-1(20),2,6(24),7,9,11,13(22),16,18-nonaen-4-yl acetate is found in Tolypothrix nodosa. 14-[3-(Acetyloxy)-5-hydroxy-6-methyloxan-2-yl]-4,9,14,20-tetramethyl-5,15-dioxo-21,22,23,24-tetraazapentacyclo[16.2.1.1³,⁶.1⁸,¹¹.1¹³,¹⁶]Tetracosa-1(20),2,6(24),7,9,11,13(22),16,18-nonaen-4-yl acetate is a moderately basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004201501552D          

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M  END

     RDKit          3D

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M  END


  Mrv1533004201501552D          

 46 51  0  0  0  0            999 V2000
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   -1.4819   -2.0624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1145   -2.5920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7243   -1.6459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8480   -0.8857    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6690   -0.7465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0558   -0.0472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6818    0.7174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0393    1.4169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4588    2.0076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6046    2.8196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7239    1.6627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0047    2.0496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7107    1.6752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8643    0.8567    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6265    0.7462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0427    0.0179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6683   -0.6881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8501   -0.8709    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7106   -1.6627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0112   -2.0494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5044   -2.0364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0558   -1.4752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8703   -1.6063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0297    1.5110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8449    1.6379    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4686    2.0624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9773    2.7119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1779    2.8345    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7013    3.4723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5152    3.3380    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4106    4.2444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8926    0.8706    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0430   -1.5110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8562   -1.6502    0.0000 O   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
  2  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  2  0  0  0  0
 10 12  1  0  0  0  0
  4 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  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
 15 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 29 34  1  0  0  0  0
 34 35  1  0  0  0  0
 27 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 25 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 41 43  1  0  0  0  0
 23 44  1  0  0  0  0
 19 44  1  0  0  0  0
 17 45  1  0  0  0  0
 13 45  1  0  0  0  0
 45 46  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0200210

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC(C(CC1O)OC(C)=O)C1(C)C(=O)\C2=C\C3=CC(C)=C(N3)\C=C3/N=C(/C=C4\N\C(\C=C4C)=C/C1=N2)C(=O)C3(C)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C34H36N4O8/c1-15-9-21-11-28-33(6,32-27(45-18(4)39)14-26(41)17(3)44-32)30(42)24(37-28)10-20-8-16(2)23(35-20)13-29-34(7,46-19(5)40)31(43)25(38-29)12-22(15)36-21/h8-13,17,26-27,32,35-36,41H,14H2,1-7H3/b20-10-,21-11-,22-12-,23-13-,24-10-,25-12-,28-11-,29-13-

> <INCHI_KEY>
ORIYDESLCYSDRU-IVSKNRDKSA-N

> <FORMULA>
C34H36N4O8

> <MOLECULAR_WEIGHT>
628.682

> <EXACT_MASS>
628.253314135

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
82

> <JCHEM_AVERAGE_POLARIZABILITY>
66.7268381881913

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
14-[3-(acetyloxy)-5-hydroxy-6-methyloxan-2-yl]-4,9,14,20-tetramethyl-5,15-dioxo-21,22,23,24-tetraazapentacyclo[16.2.1.1³,⁶.1⁸,¹¹.1¹³,¹⁶]tetracosa-1(20),2,6(24),7,9,11,13(22),16,18-nonaen-4-yl acetate

> <ALOGPS_LOGP>
3.34

> <JCHEM_LOGP>
3.998269922333334

> <ALOGPS_LOGS>
-4.75

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.341847943461861

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.092247552876017

> <JCHEM_PKA_STRONGEST_BASIC>
1.145600664101085

> <JCHEM_POLAR_SURFACE_AREA>
173.56

> <JCHEM_REFRACTIVITY>
164.01030000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.12e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
14-[3-(acetyloxy)-5-hydroxy-6-methyloxan-2-yl]-4,9,14,20-tetramethyl-5,15-dioxo-21,22,23,24-tetraazapentacyclo[16.2.1.1³,⁶.1⁸,¹¹.1¹³,¹⁶]tetracosa-1(20),2,6(24),7,9,11,13(22),16,18-nonaen-4-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  C   UNK     0       2.043  -6.158   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.508  -6.275   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -0.361  -5.004   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -1.897  -5.121   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.563  -6.509   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.694  -7.781   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.158  -7.663   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       0.711  -8.935   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      -4.099  -6.627   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -4.968  -5.356   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -4.302  -3.967   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -6.503  -5.473   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.766  -3.850   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.947  -4.838   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.352  -3.072   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0      -1.583  -1.653   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0      -3.115  -1.393   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.837  -0.088   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -3.139   1.339   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -3.807   2.645   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.723   3.748   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.995   5.263   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.351   3.104   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.009   3.826   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.327   3.127   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0       1.613   1.599   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0       3.036   1.393   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.813   0.033   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.114  -1.284   0.000  0.00  0.00           C+0
HETATM   30  N   UNK     0       1.587  -1.626   0.000  0.00  0.00           N+0
HETATM   31  C   UNK     0       1.326  -3.104   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.021  -3.826   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.808  -3.801   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       3.837  -2.754   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.358  -2.998   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.789   2.821   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       5.310   3.057   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       2.741   3.850   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       3.691   5.062   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       2.199   5.291   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       3.176   6.482   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       4.695   6.231   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       2.633   7.923   0.000  0.00  0.00           C+0
HETATM   44  N   UNK     0      -1.666   1.625   0.000  0.00  0.00           N+0
HETATM   45  C   UNK     0      -3.814  -2.821   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0      -5.332  -3.080   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   13                                                  
CONECT    5    4    6    9                                                  
CONECT    6    5    7                                                       
CONECT    7    6    2    8                                                  
CONECT    8    7                                                            
CONECT    9    5   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    4   14   15   45                                             
CONECT   14   13                                                            
CONECT   15   13   16   32                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   45                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   44                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   44                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   38                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   36                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31   15                                                       
CONECT   33   31   34                                                       
CONECT   34   33   29   35                                                  
CONECT   35   34                                                            
CONECT   36   27   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   25   39   40                                             
CONECT   39   38                                                            
CONECT   40   38   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41                                                            
CONECT   44   23   19                                                       
CONECT   45   17   13   46                                                  
CONECT   46   45                                                            
MASTER        0    0    0    0    0    0    0    0   46    0  102    0
END

View in JSmol

Synonyms

Value	Source
14-[3-(Acetyloxy)-5-hydroxy-6-methyloxan-2-yl]-4,9,14,20-tetramethyl-5,15-dioxo-21,22,23,24-tetraazapentacyclo[16.2.1.1,.1,.1,]tetracosa-1(20),2,6(24),7,9,11,13(22),16,18-nonaen-4-yl acetic acid	Generator
14-[3-(Acetyloxy)-5-hydroxy-6-methyloxan-2-yl]-4,9,14,20-tetramethyl-5,15-dioxo-21,22,23,24-tetraazapentacyclo[16.2.1.1³,⁶.1⁸,¹¹.1¹³,¹⁶]tetracosa-1(20),2,6(24),7,9,11,13(22),16,18-nonaen-4-yl acetic acid	Generator

Chemical Formula

C₃₄H₃₆N₄O₈

Average Mass

628.6820 Da

Monoisotopic Mass

628.25331 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CC1OC(C(CC1O)OC(C)=O)C1(C)C(=O)\C2=C\C3=CC(C)=C(N3)\C=C3/N=C(/C=C4\N\C(\C=C4C)=C/C1=N2)C(=O)C3(C)OC(C)=O

InChI Identifier

InChI=1S/C34H36N4O8/c1-15-9-21-11-28-33(6,32-27(45-18(4)39)14-26(41)17(3)44-32)30(42)24(37-28)10-20-8-16(2)23(35-20)13-29-34(7,46-19(5)40)31(43)25(38-29)12-22(15)36-21/h8-13,17,26-27,32,35-36,41H,14H2,1-7H3/b20-10-,21-11-,22-12-,23-13-,24-10-,25-12-,28-11-,29-13-

InChI Key

ORIYDESLCYSDRU-IVSKNRDKSA-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
Tolypothrix nodosa	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	3.34	ALOGPS
logP	4	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	14.09	ChemAxon
pKa (Strongest Basic)	1.15	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	173.56 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	164.01 m³·mol⁻¹	ChemAxon
Polarizability	66.73 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 14-[3-(acetyloxy)-5-hydroxy-6-methyloxan-2-yl]-4,9,14,20-tetramethyl-5,15-dioxo-21,22,23,24-tetraazapentacyclo[16.2.1.1³,⁶.1⁸,¹¹.1¹³,¹⁶]tetracosa-1(20),2,6(24),7,9,11,13(22),16,18-nonaen-4-yl acetate (NP0200210)

MOL for NP0200210 (14-[3-(acetyloxy)-5-hydroxy-6-methyloxan-2-yl]-4,9,14,20-tetramethyl-5,15-dioxo-21,22,23,24-tetraazapentacyclo[16.2.1.1³,⁶.1⁸,¹¹.1¹³,¹⁶]tetracosa-1(20),2,6(24),7,9,11,13(22),16,18-nonaen-4-yl acetate)

3D MOL for NP0200210 (14-[3-(acetyloxy)-5-hydroxy-6-methyloxan-2-yl]-4,9,14,20-tetramethyl-5,15-dioxo-21,22,23,24-tetraazapentacyclo[16.2.1.1³,⁶.1⁸,¹¹.1¹³,¹⁶]tetracosa-1(20),2,6(24),7,9,11,13(22),16,18-nonaen-4-yl acetate)

3D SDF for NP0200210 (14-[3-(acetyloxy)-5-hydroxy-6-methyloxan-2-yl]-4,9,14,20-tetramethyl-5,15-dioxo-21,22,23,24-tetraazapentacyclo[16.2.1.1³,⁶.1⁸,¹¹.1¹³,¹⁶]tetracosa-1(20),2,6(24),7,9,11,13(22),16,18-nonaen-4-yl acetate)

3D-SDF for NP0200210 (14-[3-(acetyloxy)-5-hydroxy-6-methyloxan-2-yl]-4,9,14,20-tetramethyl-5,15-dioxo-21,22,23,24-tetraazapentacyclo[16.2.1.1³,⁶.1⁸,¹¹.1¹³,¹⁶]tetracosa-1(20),2,6(24),7,9,11,13(22),16,18-nonaen-4-yl acetate)

PDB for NP0200210 (14-[3-(acetyloxy)-5-hydroxy-6-methyloxan-2-yl]-4,9,14,20-tetramethyl-5,15-dioxo-21,22,23,24-tetraazapentacyclo[16.2.1.1³,⁶.1⁸,¹¹.1¹³,¹⁶]tetracosa-1(20),2,6(24),7,9,11,13(22),16,18-nonaen-4-yl acetate)

3D PDB for NP0200210 (14-[3-(acetyloxy)-5-hydroxy-6-methyloxan-2-yl]-4,9,14,20-tetramethyl-5,15-dioxo-21,22,23,24-tetraazapentacyclo[16.2.1.1³,⁶.1⁸,¹¹.1¹³,¹⁶]tetracosa-1(20),2,6(24),7,9,11,13(22),16,18-nonaen-4-yl acetate)

SMILES for NP0200210 (14-[3-(acetyloxy)-5-hydroxy-6-methyloxan-2-yl]-4,9,14,20-tetramethyl-5,15-dioxo-21,22,23,24-tetraazapentacyclo[16.2.1.1³,⁶.1⁸,¹¹.1¹³,¹⁶]tetracosa-1(20),2,6(24),7,9,11,13(22),16,18-nonaen-4-yl acetate)

INCHI for NP0200210 (14-[3-(acetyloxy)-5-hydroxy-6-methyloxan-2-yl]-4,9,14,20-tetramethyl-5,15-dioxo-21,22,23,24-tetraazapentacyclo[16.2.1.1³,⁶.1⁸,¹¹.1¹³,¹⁶]tetracosa-1(20),2,6(24),7,9,11,13(22),16,18-nonaen-4-yl acetate)

Structure for NP0200210 (14-[3-(acetyloxy)-5-hydroxy-6-methyloxan-2-yl]-4,9,14,20-tetramethyl-5,15-dioxo-21,22,23,24-tetraazapentacyclo[16.2.1.1³,⁶.1⁸,¹¹.1¹³,¹⁶]tetracosa-1(20),2,6(24),7,9,11,13(22),16,18-nonaen-4-yl acetate)

3D Structure for NP0200210 (14-[3-(acetyloxy)-5-hydroxy-6-methyloxan-2-yl]-4,9,14,20-tetramethyl-5,15-dioxo-21,22,23,24-tetraazapentacyclo[16.2.1.1³,⁶.1⁸,¹¹.1¹³,¹⁶]tetracosa-1(20),2,6(24),7,9,11,13(22),16,18-nonaen-4-yl acetate)