NP-MRD: Showing NP-Card for (1z,4s,5r,14r,19z)-14-hydroxy-5-(hydroxymethyl)-6,6,21,21-tetramethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0³,¹⁶.0⁴,⁷.0⁴,¹⁴.0⁸,¹³.0²²,³⁰.0²⁴,²⁹]hentriaconta-1(31),8,10,12,15,19,22(30),24,26,28-decaene-2,17-dione (NP0227245)

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Record Information

Version

2.0

Created at

2022-09-06 06:30:34 UTC

Updated at

2022-09-06 06:30:34 UTC

NP-MRD ID

NP0227245

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1z,4s,5r,14r,19z)-14-hydroxy-5-(hydroxymethyl)-6,6,21,21-tetramethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0³,¹⁶.0⁴,⁷.0⁴,¹⁴.0⁸,¹³.0²²,³⁰.0²⁴,²⁹]hentriaconta-1(31),8,10,12,15,19,22(30),24,26,28-decaene-2,17-dione

Description

Okaramine F belongs to the class of organic compounds known as pyrroloindoles. Pyrroloindoles are compounds containing a pyrroloindole moiety, which is a tricyclic heterocycle which consists of a pyrrole ring fused to an indole. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Indole is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. (1z,4s,5r,14r,19z)-14-hydroxy-5-(hydroxymethyl)-6,6,21,21-tetramethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0³,¹⁶.0⁴,⁷.0⁴,¹⁴.0⁸,¹³.0²²,³⁰.0²⁴,²⁹]hentriaconta-1(31),8,10,12,15,19,22(30),24,26,28-decaene-2,17-dione is found in Penicillium simplicissimum. Based on a literature review very few articles have been published on Okaramine F.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062208302D          

 40 47  0  0  1  0            999 V2000
    6.1686    5.0873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8844    4.2467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7611    4.3916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1721    4.6630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3741    4.4537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9578    3.7415    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1621    3.9592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8529    4.7763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5756    3.3789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7849    2.5809    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5031    2.4503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5096    1.5048    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1671    2.9434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8794    2.5272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6774    2.7364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0937    3.4487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4149    1.0517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7520    3.4265    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
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  4  5  2  0  0  0  0
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  9 10  1  0  0  0  0
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  6 13  1  0  0  0  0
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 14 15  1  0  0  0  0
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  2 16  1  0  0  0  0
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 24 38  1  0  0  0  0
 38 39  1  1  0  0  0
 38 40  1  0  0  0  0
  9 40  2  0  0  0  0
M  END

     RDKit          3D

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  4 47  1  0
  5 48  1  0
M  END


  Mrv1652309062208302D          

 40 47  0  0  1  0            999 V2000
    6.1686    5.0873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9673    1.4142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3808    0.8340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4149    1.0517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6242    1.8497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0378    2.4300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7580    2.2122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4523    2.6579    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8017    3.2594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7520    3.4265    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
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
  2 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 15 23  1  0  0  0  0
 18 23  1  0  0  0  0
 10 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 25 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 28 31  1  0  0  0  0
 24 31  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 32 37  1  0  0  0  0
 37 38  1  0  0  0  0
 24 38  1  0  0  0  0
 38 39  1  1  0  0  0
 38 40  1  0  0  0  0
  9 40  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0227245

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)[C@@H](CO)[C@@]23N1C1=CC=CC=C1[C@]2(O)C=C1N3C(=O)\C2=C\C3=C(NC4=CC=CC=C34)C(C)(C)\C=C/N2C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C32H30N4O4/c1-29(2)13-14-34-23(15-19-18-9-5-7-11-21(18)33-26(19)29)28(39)35-24(27(34)38)16-31(40)20-10-6-8-12-22(20)36-30(3,4)25(17-37)32(31,35)36/h5-16,25,33,37,40H,17H2,1-4H3/b14-13-,23-15-/t25-,31-,32-/m1/s1

> <INCHI_KEY>
IBPSBAXFAWXHPO-VJZIPGSUSA-N

> <FORMULA>
C32H30N4O4

> <MOLECULAR_WEIGHT>
534.616

> <EXACT_MASS>
534.226705462

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
58.107877043084905

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4S,5R,14R,19Z)-14-hydroxy-5-(hydroxymethyl)-6,6,21,21-tetramethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0^{3,16}.0^{4,7}.0^{4,14}.0^{8,13}.0^{22,30}.0^{24,29}]hentriaconta-1(31),8,10,12,15,19,22(30),24,26,28-decaene-2,17-dione

> <JCHEM_LOGP>
3.8691268013333353

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.97349296481666

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.418212358550512

> <JCHEM_PKA_STRONGEST_BASIC>
-2.665813995264653

> <JCHEM_POLAR_SURFACE_AREA>
100.11

> <JCHEM_REFRACTIVITY>
153.88020000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(4S,5R,14R,19Z)-14-hydroxy-5-(hydroxymethyl)-6,6,21,21-tetramethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0^{3,16}.0^{4,7}.0^{4,14}.0^{8,13}.0^{22,30}.0^{24,29}]hentriaconta-1(31),8,10,12,15,19,22(30),24,26,28-decaene-2,17-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      11.515   9.496   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.984   7.927   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.621   8.198   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.655   8.704   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.165   8.314   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0       7.388   6.984   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       5.903   7.391   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       5.325   8.916   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.808   6.307   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       5.199   4.818   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       6.539   4.574   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.551   2.809   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       7.779   5.494   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.108   4.717   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.598   5.108   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.375   6.438   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0      12.879   6.109   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0      13.032   4.577   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      14.273   3.665   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      14.104   2.135   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.694   1.516   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.453   2.427   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.622   3.958   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.903   3.986   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.337   3.426   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.970   3.819   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.338   3.023   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       4.778   1.992   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.992   0.785   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.198   0.455   0.000  0.00  0.00           C+0
HETATM   31  N   UNK     0       3.343   2.551   0.000  0.00  0.00           N+0
HETATM   32  C   UNK     0       1.806   2.640   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       0.711   1.557   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.775   1.963   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -1.165   3.453   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -0.070   4.536   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       1.415   4.129   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       2.711   4.961   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       1.497   6.084   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       3.270   6.396   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4   16                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   13                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   40                                                  
CONECT   10    9   11   24                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    6   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   23                                                  
CONECT   16   15    2   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   15   18                                                  
CONECT   24   10   25   31   38                                             
CONECT   25   24   26   28                                                  
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   25   29   30   31                                             
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   28   24   32                                                  
CONECT   32   31   33   37                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   32   38                                                  
CONECT   38   37   24   39   40                                             
CONECT   39   38                                                            
CONECT   40   38    9                                                       
MASTER        0    0    0    0    0    0    0    0   40    0   94    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₃₀N₄O₄

Average Mass

534.6160 Da

Monoisotopic Mass

534.22671 Da

IUPAC Name

(4S,5R,14R,19Z)-14-hydroxy-5-(hydroxymethyl)-6,6,21,21-tetramethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0^{3,16}.0^{4,7}.0^{4,14}.0^{8,13}.0^{22,30}.0^{24,29}]hentriaconta-1(31),8,10,12,15,19,22(30),24,26,28-decaene-2,17-dione

Traditional Name

CAS Registry Number

Not Available

SMILES

CC1(C)[C@@H](CO)[C@@]23N1C1=CC=CC=C1[C@]2(O)C=C1N3C(=O)\C2=C\C3=C(NC4=CC=CC=C34)C(C)(C)\C=C/N2C1=O

InChI Identifier

InChI=1S/C32H30N4O4/c1-29(2)13-14-34-23(15-19-18-9-5-7-11-21(18)33-26(19)29)28(39)35-24(27(34)38)16-31(40)20-10-6-8-12-22(20)36-30(3,4)25(17-37)32(31,35)36/h5-16,25,33,37,40H,17H2,1-4H3/b14-13-,23-15-/t25-,31-,32-/m1/s1

InChI Key

IBPSBAXFAWXHPO-VJZIPGSUSA-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
Penicillium simplicissimum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrroloindoles. Pyrroloindoles are compounds containing a pyrroloindole moiety, which is a tricyclic heterocycle which consists of a pyrrole ring fused to an indole. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Indole is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Pyrroloindoles

Direct Parent

Pyrroloindoles

Alternative Parents

Substituents

Pyrroloindole
Benzazepine
Indole
Pyrrolopyrazine
Dialkylarylamine
Azepine
Pyrazine
Benzenoid
Pyrrole
Heteroaromatic compound
Tertiary alcohol
Lactam
Azetidine
Azacycle
Alcohol
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Organonitrogen compound
Organic oxide
Organic oxygen compound
Organic nitrogen compound
Amine
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	3.87	ChemAxon
pKa (Strongest Acidic)	12.42	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	100.11 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	153.88 m³·mol⁻¹	ChemAxon
Polarizability	58.11 Å³	ChemAxon
Number of Rings	8	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

101678045

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1z,4s,5r,14r,19z)-14-hydroxy-5-(hydroxymethyl)-6,6,21,21-tetramethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0³,¹⁶.0⁴,⁷.0⁴,¹⁴.0⁸,¹³.0²²,³⁰.0²⁴,²⁹]hentriaconta-1(31),8,10,12,15,19,22(30),24,26,28-decaene-2,17-dione (NP0227245)

MOL for NP0227245 ((1z,4s,5r,14r,19z)-14-hydroxy-5-(hydroxymethyl)-6,6,21,21-tetramethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0³,¹⁶.0⁴,⁷.0⁴,¹⁴.0⁸,¹³.0²²,³⁰.0²⁴,²⁹]hentriaconta-1(31),8,10,12,15,19,22(30),24,26,28-decaene-2,17-dione)

3D MOL for NP0227245 ((1z,4s,5r,14r,19z)-14-hydroxy-5-(hydroxymethyl)-6,6,21,21-tetramethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0³,¹⁶.0⁴,⁷.0⁴,¹⁴.0⁸,¹³.0²²,³⁰.0²⁴,²⁹]hentriaconta-1(31),8,10,12,15,19,22(30),24,26,28-decaene-2,17-dione)

3D SDF for NP0227245 ((1z,4s,5r,14r,19z)-14-hydroxy-5-(hydroxymethyl)-6,6,21,21-tetramethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0³,¹⁶.0⁴,⁷.0⁴,¹⁴.0⁸,¹³.0²²,³⁰.0²⁴,²⁹]hentriaconta-1(31),8,10,12,15,19,22(30),24,26,28-decaene-2,17-dione)

3D-SDF for NP0227245 ((1z,4s,5r,14r,19z)-14-hydroxy-5-(hydroxymethyl)-6,6,21,21-tetramethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0³,¹⁶.0⁴,⁷.0⁴,¹⁴.0⁸,¹³.0²²,³⁰.0²⁴,²⁹]hentriaconta-1(31),8,10,12,15,19,22(30),24,26,28-decaene-2,17-dione)

PDB for NP0227245 ((1z,4s,5r,14r,19z)-14-hydroxy-5-(hydroxymethyl)-6,6,21,21-tetramethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0³,¹⁶.0⁴,⁷.0⁴,¹⁴.0⁸,¹³.0²²,³⁰.0²⁴,²⁹]hentriaconta-1(31),8,10,12,15,19,22(30),24,26,28-decaene-2,17-dione)

3D PDB for NP0227245 ((1z,4s,5r,14r,19z)-14-hydroxy-5-(hydroxymethyl)-6,6,21,21-tetramethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0³,¹⁶.0⁴,⁷.0⁴,¹⁴.0⁸,¹³.0²²,³⁰.0²⁴,²⁹]hentriaconta-1(31),8,10,12,15,19,22(30),24,26,28-decaene-2,17-dione)

SMILES for NP0227245 ((1z,4s,5r,14r,19z)-14-hydroxy-5-(hydroxymethyl)-6,6,21,21-tetramethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0³,¹⁶.0⁴,⁷.0⁴,¹⁴.0⁸,¹³.0²²,³⁰.0²⁴,²⁹]hentriaconta-1(31),8,10,12,15,19,22(30),24,26,28-decaene-2,17-dione)

INCHI for NP0227245 ((1z,4s,5r,14r,19z)-14-hydroxy-5-(hydroxymethyl)-6,6,21,21-tetramethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0³,¹⁶.0⁴,⁷.0⁴,¹⁴.0⁸,¹³.0²²,³⁰.0²⁴,²⁹]hentriaconta-1(31),8,10,12,15,19,22(30),24,26,28-decaene-2,17-dione)

Structure for NP0227245 ((1z,4s,5r,14r,19z)-14-hydroxy-5-(hydroxymethyl)-6,6,21,21-tetramethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0³,¹⁶.0⁴,⁷.0⁴,¹⁴.0⁸,¹³.0²²,³⁰.0²⁴,²⁹]hentriaconta-1(31),8,10,12,15,19,22(30),24,26,28-decaene-2,17-dione)

3D Structure for NP0227245 ((1z,4s,5r,14r,19z)-14-hydroxy-5-(hydroxymethyl)-6,6,21,21-tetramethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0³,¹⁶.0⁴,⁷.0⁴,¹⁴.0⁸,¹³.0²²,³⁰.0²⁴,²⁹]hentriaconta-1(31),8,10,12,15,19,22(30),24,26,28-decaene-2,17-dione)