NP-MRD: Showing NP-Card for 22-hydroxy-6-{[(2z)-3-hydroxybut-2-en-2-yl]amino}-21,24-dimethoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1,4(9),7,10,17(29),18(27),20(25)-heptaene-3,5,26,28-tetrone (NP0311021)

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Record Information

Version

2.0

Created at

2022-09-11 06:44:01 UTC

Updated at

2022-09-11 06:44:01 UTC

NP-MRD ID

NP0311021

Secondary Accession Numbers

None

Natural Product Identification

Common Name

22-hydroxy-6-{[(2z)-3-hydroxybut-2-en-2-yl]amino}-21,24-dimethoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1,4(9),7,10,17(29),18(27),20(25)-heptaene-3,5,26,28-tetrone

Description

Not Available

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112208442D          

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M  END

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M  END


  Mrv1652309112208442D          

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   11.4401    3.0768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1288    3.6446    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.4566    4.4016    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.9649    5.0641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1453    4.9694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2927    5.8212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8010    6.4836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1123    5.9158    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3092    3.5499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8175    4.2124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1453    1.3734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3258    1.2787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9979    0.5217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1784    0.4270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8506   -0.3301    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0310   -0.4247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5393    0.2377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8671    0.9948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6867    1.0895    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 10 16  2  0  0  0  0
  3 16  1  0  0  0  0
 13 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 28 35  1  0  0  0  0
 23 35  1  0  0  0  0
 35 36  2  0  0  0  0
 24 37  1  0  0  0  0
 37 38  2  0  0  0  0
 20 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 12 44  1  0  0  0  0
 44 45  2  0  0  0  0
 19 45  1  0  0  0  0
 40 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0311021

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1CC(O)C(OC)C2=C1C(=O)C1=C(O2)C2=C3C(CC4=CC5=C(C(=O)N(N\C(C)=C(\C)O)C(C)=C5)C(=O)C4=C3C1=O)OCO2

> <INCHI_IDENTIFIER>
InChI=1S/C32H30N2O11/c1-11-6-14-7-15-8-18-21-23(19(15)25(37)20(14)32(40)34(11)33-12(2)13(3)35)27(39)24-26(38)22-17(41-4)9-16(36)28(42-5)30(22)45-31(24)29(21)44-10-43-18/h6-7,16-18,28,33,35-36H,8-10H2,1-5H3/b13-12-

> <INCHI_KEY>
WGPBBJROUQQTBF-SEYXRHQNSA-N

> <FORMULA>
C32H30N2O11

> <MOLECULAR_WEIGHT>
618.595

> <EXACT_MASS>
618.184959794

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
63.66754707488849

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
22-hydroxy-6-{[(2Z)-3-hydroxybut-2-en-2-yl]amino}-21,24-dimethoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0^{2,11}.0^{4,9}.0^{13,29}.0^{18,27}.0^{20,25}]nonacosa-1,4(9),7,10,17(29),18(27),20(25)-heptaene-3,5,26,28-tetrone

> <JCHEM_LOGP>
-1.3954317816666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.95866896637446

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.476735509202602

> <JCHEM_PKA_STRONGEST_BASIC>
1.1335548935314033

> <JCHEM_POLAR_SURFACE_AREA>
170.15999999999997

> <JCHEM_REFRACTIVITY>
175.41190000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
22-hydroxy-6-{[(2Z)-3-hydroxybut-2-en-2-yl]amino}-21,24-dimethoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0^{2,11}.0^{4,9}.0^{13,29}.0^{18,27}.0^{20,25}]nonacosa-1,4(9),7,10,17(29),18(27),20(25)-heptaene-3,5,26,28-tetrone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       9.422   8.393   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.892   8.216   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.280   6.803   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.750   6.627   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.139   5.213   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       3.609   5.037   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       6.056   3.977   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       5.445   2.564   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       6.362   1.327   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.586   4.153   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.504   2.917   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      10.034   3.094   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.646   4.507   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.728   5.743   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      10.340   7.157   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.198   5.567   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.176   4.683   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      12.788   6.097   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      13.094   3.447   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      14.624   3.623   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      15.235   5.037   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      14.318   6.273   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      16.765   5.213   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      17.683   3.977   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      19.213   4.153   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      19.825   5.567   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      21.355   5.743   0.000  0.00  0.00           C+0
HETATM   28  N   UNK     0      18.907   6.803   0.000  0.00  0.00           N+0
HETATM   29  N   UNK     0      19.519   8.216   0.000  0.00  0.00           N+0
HETATM   30  C   UNK     0      18.601   9.453   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      17.071   9.276   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      19.213  10.866   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      18.295  12.103   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      20.743  11.043   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      17.377   6.627   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      16.459   7.863   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      17.071   2.564   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      15.541   2.387   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      14.930   0.974   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      13.400   0.797   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      12.788  -0.616   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      11.258  -0.793   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      10.340   0.444   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      10.952   1.857   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      12.482   2.034   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   16                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   44                                                  
CONECT   13   12   14   17                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   10    3                                                  
CONECT   17   13   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   45                                                  
CONECT   20   19   21   38                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   35                                                  
CONECT   24   23   25   37                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   35                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35   28   23   36                                                  
CONECT   36   35                                                            
CONECT   37   24   38                                                       
CONECT   38   37   20   39                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41   45                                                  
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   12   45                                                  
CONECT   45   44   19   40                                                  
MASTER        0    0    0    0    0    0    0    0   45    0  102    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₃₀N₂O₁₁

Average Mass

618.5950 Da

Monoisotopic Mass

618.18496 Da

IUPAC Name

22-hydroxy-6-{[(2Z)-3-hydroxybut-2-en-2-yl]amino}-21,24-dimethoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0^{2,11}.0^{4,9}.0^{13,29}.0^{18,27}.0^{20,25}]nonacosa-1,4(9),7,10,17(29),18(27),20(25)-heptaene-3,5,26,28-tetrone

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1CC(O)C(OC)C2=C1C(=O)C1=C(O2)C2=C3C(CC4=CC5=C(C(=O)N(N\C(C)=C(\C)O)C(C)=C5)C(=O)C4=C3C1=O)OCO2

InChI Identifier

InChI=1S/C32H30N2O11/c1-11-6-14-7-15-8-18-21-23(19(15)25(37)20(14)32(40)34(11)33-12(2)13(3)35)27(39)24-26(38)22-17(41-4)9-16(36)28(42-5)30(22)45-31(24)29(21)44-10-43-18/h6-7,16-18,28,33,35-36H,8-10H2,1-5H3/b13-12-

InChI Key

WGPBBJROUQQTBF-SEYXRHQNSA-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

Not Available

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	-1.4	ChemAxon
pKa (Strongest Acidic)	10.48	ChemAxon
pKa (Strongest Basic)	1.13	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	170.16 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	175.41 m³·mol⁻¹	ChemAxon
Polarizability	63.67 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 22-hydroxy-6-{[(2z)-3-hydroxybut-2-en-2-yl]amino}-21,24-dimethoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1,4(9),7,10,17(29),18(27),20(25)-heptaene-3,5,26,28-tetrone (NP0311021)

MOL for NP0311021 (22-hydroxy-6-{[(2z)-3-hydroxybut-2-en-2-yl]amino}-21,24-dimethoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1,4(9),7,10,17(29),18(27),20(25)-heptaene-3,5,26,28-tetrone)

3D MOL for NP0311021 (22-hydroxy-6-{[(2z)-3-hydroxybut-2-en-2-yl]amino}-21,24-dimethoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1,4(9),7,10,17(29),18(27),20(25)-heptaene-3,5,26,28-tetrone)

3D SDF for NP0311021 (22-hydroxy-6-{[(2z)-3-hydroxybut-2-en-2-yl]amino}-21,24-dimethoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1,4(9),7,10,17(29),18(27),20(25)-heptaene-3,5,26,28-tetrone)

3D-SDF for NP0311021 (22-hydroxy-6-{[(2z)-3-hydroxybut-2-en-2-yl]amino}-21,24-dimethoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1,4(9),7,10,17(29),18(27),20(25)-heptaene-3,5,26,28-tetrone)

PDB for NP0311021 (22-hydroxy-6-{[(2z)-3-hydroxybut-2-en-2-yl]amino}-21,24-dimethoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1,4(9),7,10,17(29),18(27),20(25)-heptaene-3,5,26,28-tetrone)

3D PDB for NP0311021 (22-hydroxy-6-{[(2z)-3-hydroxybut-2-en-2-yl]amino}-21,24-dimethoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1,4(9),7,10,17(29),18(27),20(25)-heptaene-3,5,26,28-tetrone)

SMILES for NP0311021 (22-hydroxy-6-{[(2z)-3-hydroxybut-2-en-2-yl]amino}-21,24-dimethoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1,4(9),7,10,17(29),18(27),20(25)-heptaene-3,5,26,28-tetrone)

INCHI for NP0311021 (22-hydroxy-6-{[(2z)-3-hydroxybut-2-en-2-yl]amino}-21,24-dimethoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1,4(9),7,10,17(29),18(27),20(25)-heptaene-3,5,26,28-tetrone)

Structure for NP0311021 (22-hydroxy-6-{[(2z)-3-hydroxybut-2-en-2-yl]amino}-21,24-dimethoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1,4(9),7,10,17(29),18(27),20(25)-heptaene-3,5,26,28-tetrone)

3D Structure for NP0311021 (22-hydroxy-6-{[(2z)-3-hydroxybut-2-en-2-yl]amino}-21,24-dimethoxy-7-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.0²,¹¹.0⁴,⁹.0¹³,²⁹.0¹⁸,²⁷.0²⁰,²⁵]nonacosa-1,4(9),7,10,17(29),18(27),20(25)-heptaene-3,5,26,28-tetrone)