NP-MRD: Showing NP-Card for 16-ethyl-3,6,8,9-tetrahydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-3,12,14-triene-20,28-dione (NP0197927)

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Record Information

Version

2.0

Created at

2022-09-04 16:17:10 UTC

Updated at

2022-09-04 16:17:10 UTC

NP-MRD ID

NP0197927

Secondary Accession Numbers

None

Natural Product Identification

Common Name

16-ethyl-3,6,8,9-tetrahydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-3,12,14-triene-20,28-dione

Description

16-Ethyl-3,6,8,9-tetrahydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-3,12,14-triene-20,28-dione belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. 16-ethyl-3,6,8,9-tetrahydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-3,12,14-triene-20,28-dione is found in Myxococcus virescens. 16-Ethyl-3,6,8,9-tetrahydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-3,12,14-triene-20,28-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004201506492D          

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M  END


  Mrv1533004201506492D          

 42 42  0  0  0  0            999 V2000
    5.2265    4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4043    4.8907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9345    4.2126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.4666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7567    4.1448    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5789    4.0770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0487    4.7551    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9312    3.3310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7535    3.2632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4614    2.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8138    1.9069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6360    1.8391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3440    1.2287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6963    0.4828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2265   -0.1954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5789   -0.9413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1090   -1.6195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.5517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4614   -2.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9916   -3.0436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3440   -3.7895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8741   -4.4677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2265   -5.2136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0487   -5.2815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0519   -4.3999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6995   -3.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8773   -3.5861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5250   -2.8401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7027   -2.7723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9948   -2.1620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6424   -1.4160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1122   -0.7379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9345   -0.8057    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7599    0.0081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9377    0.0759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2297    0.6862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8773    1.4322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0551    1.5000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3472    2.1103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9948    2.8563    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4646    3.5344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1122    4.2804    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  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 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
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 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
 25 22  1  4  0  0  0
 25 26  2  0  0  0  0
 27 26  1  4  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
  4 41  1  0  0  0  0
 41 42  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0197927

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC1OC(=O)C(C)CC(C)CCCCC(=O)CCCC(CC)C=CC=C(C)CCC(O)C(O)CC(O)CNC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C34H59NO7/c1-6-12-32-33(40)35-23-29(37)22-31(39)30(38)20-19-24(3)14-10-15-27(7-2)16-11-18-28(36)17-9-8-13-25(4)21-26(5)34(41)42-32/h10,14-15,25-27,29-32,37-39H,6-9,11-13,16-23H2,1-5H3,(H,35,40)

> <INCHI_KEY>
QTLCLULKZUFQLC-UHFFFAOYSA-N

> <FORMULA>
C34H59NO7

> <MOLECULAR_WEIGHT>
593.846

> <EXACT_MASS>
593.429153244

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
101

> <JCHEM_AVERAGE_POLARIZABILITY>
70.3690139633396

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
16-ethyl-6,8,9-trihydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-12,14-diene-3,20,28-trione

> <ALOGPS_LOGP>
4.80

> <JCHEM_LOGP>
5.764070290333332

> <ALOGPS_LOGS>
-5.23

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.388447410777232

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.714749149673278

> <JCHEM_PKA_STRONGEST_BASIC>
-2.890620012686944

> <JCHEM_POLAR_SURFACE_AREA>
133.16000000000003

> <JCHEM_REFRACTIVITY>
168.52870000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.52e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
16-ethyl-6,8,9-trihydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-12,14-diene-3,20,28-trione

> <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       9.756   9.003   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.221   9.129   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.344   7.863   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.002   6.471   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       8.879   7.737   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      10.414   7.610   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      11.291   8.876   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      11.072   6.218   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.606   6.091   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.195   4.952   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.852   3.560   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.387   3.433   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.975   2.294   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.633   0.901   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.756  -0.365   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.414  -1.757   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.537  -3.023   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       8.002  -2.896   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      10.195  -4.415   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.318  -5.681   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.975  -7.074   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.098  -8.340   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.756  -9.732   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      11.291  -9.859   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.564  -8.213   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.906  -6.821   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.371  -6.694   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.713  -5.302   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.178  -5.175   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.590  -4.036   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.932  -2.643   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.810  -1.377   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       7.344  -1.504   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       5.152   0.015   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       3.617   0.142   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       6.029   1.281   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       5.371   2.673   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       3.836   2.800   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       6.248   3.939   0.000  0.00  0.00           C+0
HETATM   40  N   UNK     0       5.590   5.332   0.000  0.00  0.00           N+0
HETATM   41  C   UNK     0       6.467   6.598   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       5.810   7.990   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   41                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40    4   42                                                  
CONECT   42   41                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₅₉NO₇

Average Mass

593.8460 Da

Monoisotopic Mass

593.42915 Da

IUPAC Name

16-ethyl-6,8,9-trihydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-12,14-diene-3,20,28-trione

Traditional Name

16-ethyl-6,8,9-trihydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-12,14-diene-3,20,28-trione

CAS Registry Number

Not Available

SMILES

CCCC1OC(=O)C(C)CC(C)CCCCC(=O)CCCC(CC)C=CC=C(C)CCC(O)C(O)CC(O)CNC1=O

InChI Identifier

InChI=1S/C34H59NO7/c1-6-12-32-33(40)35-23-29(37)22-31(39)30(38)20-19-24(3)14-10-15-27(7-2)16-11-18-28(36)17-9-8-13-25(4)21-26(5)34(41)42-32/h10,14-15,25-27,29-32,37-39H,6-9,11-13,16-23H2,1-5H3,(H,35,40)

InChI Key

QTLCLULKZUFQLC-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
Myxococcus virescens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Cyclic carboximidic acid
Carboxylic acid ester
Ketone
Lactone
Secondary alcohol
Cyclic ketone
Oxacycle
Azacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Polyol
Carboxylic acid derivative
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Hydrocarbon derivative
Organonitrogen compound
Organooxygen compound
Organic oxide
Alcohol
Carbonyl group
Organic nitrogen compound
Organic oxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	4.8	ALOGPS
logP	5.76	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	13.71	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	133.16 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	168.53 m³·mol⁻¹	ChemAxon
Polarizability	70.37 Å³	ChemAxon
Number of Rings	1	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

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

85155484

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 16-ethyl-3,6,8,9-tetrahydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-3,12,14-triene-20,28-dione (NP0197927)

MOL for NP0197927 (16-ethyl-3,6,8,9-tetrahydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-3,12,14-triene-20,28-dione)

3D MOL for NP0197927 (16-ethyl-3,6,8,9-tetrahydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-3,12,14-triene-20,28-dione)

3D SDF for NP0197927 (16-ethyl-3,6,8,9-tetrahydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-3,12,14-triene-20,28-dione)

3D-SDF for NP0197927 (16-ethyl-3,6,8,9-tetrahydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-3,12,14-triene-20,28-dione)

PDB for NP0197927 (16-ethyl-3,6,8,9-tetrahydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-3,12,14-triene-20,28-dione)

3D PDB for NP0197927 (16-ethyl-3,6,8,9-tetrahydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-3,12,14-triene-20,28-dione)

SMILES for NP0197927 (16-ethyl-3,6,8,9-tetrahydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-3,12,14-triene-20,28-dione)

INCHI for NP0197927 (16-ethyl-3,6,8,9-tetrahydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-3,12,14-triene-20,28-dione)

Structure for NP0197927 (16-ethyl-3,6,8,9-tetrahydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-3,12,14-triene-20,28-dione)

3D Structure for NP0197927 (16-ethyl-3,6,8,9-tetrahydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-3,12,14-triene-20,28-dione)