NP-MRD: Showing NP-Card for (3s,6s,9s,12s,15r,18r,21r)-15-[(2s)-butan-2-yl]-8,17,20-trihydroxy-18-[(1r)-1-hydroxy-2-methylpropyl]-1,3,4,10,12,13,21-heptamethyl-6,9-bis(2-methylpropyl)-1,4,7,10,13,16,19-heptaazacyclohenicosa-7,16,19-triene-2,5,11,14-tetrone (NP0312676)

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Record Information

Version

2.0

Created at

2022-09-11 09:39:52 UTC

Updated at

2022-09-11 09:39:52 UTC

NP-MRD ID

NP0312676

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,6s,9s,12s,15r,18r,21r)-15-[(2s)-butan-2-yl]-8,17,20-trihydroxy-18-[(1r)-1-hydroxy-2-methylpropyl]-1,3,4,10,12,13,21-heptamethyl-6,9-bis(2-methylpropyl)-1,4,7,10,13,16,19-heptaazacyclohenicosa-7,16,19-triene-2,5,11,14-tetrone

Description

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652305221920452D          

 61 61  0  0  1  0            999 V2000
    3.1391   -6.1880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 22  8  1  1  0  0  0
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 30 21  1  0  0  0  0
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M  END

     RDKit          3D

119119  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652305221920452D          

 61 61  0  0  1  0            999 V2000
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 19  2  1  0  0  0  0
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 21  6  1  0  0  0  0
 21  7  1  0  0  0  0
 22  8  1  1  0  0  0
 22 16  1  0  0  0  0
 23  9  1  6  0  0  0
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 36 26  1  0  0  0  0
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 44 27  1  0  0  0  0
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 30 45  1  1  0  0  0
 31 46  1  4  0  0  0
 32 47  1  4  0  0  0
 33 48  1  4  0  0  0
 49 34  2  0  0  0  0
 50 35  2  0  0  0  0
 51 36  2  0  0  0  0
 52 37  2  0  0  0  0
 22 53  1  6  0  0  0
 23 54  1  1  0  0  0
 24 55  1  6  0  0  0
 25 56  1  6  0  0  0
 26 57  1  6  0  0  0
 27 58  1  6  0  0  0
 28 59  1  1  0  0  0
 29 60  1  1  0  0  0
 30 61  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0312676

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@](C)(CC)[C@@]1([H])N=C(O)[C@]([H])(N=C(O)[C@@]([H])(C)N(C)C(=O)[C@]([H])(C)N(C)C(=O)[C@]([H])(CC(C)C)N=C(O)[C@]([H])(CC(C)C)N(C)C(=O)[C@]([H])(C)N(C)C1=O)[C@]([H])(O)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C37H67N7O8/c1-16-22(8)28-37(52)43(14)25(11)35(50)44(15)27(18-20(4)5)32(47)38-26(17-19(2)3)36(51)42(13)24(10)34(49)41(12)23(9)31(46)40-29(33(48)39-28)30(45)21(6)7/h19-30,45H,16-18H2,1-15H3,(H,38,47)(H,39,48)(H,40,46)/t22-,23+,24-,25-,26-,27-,28+,29+,30+/m0/s1

> <INCHI_KEY>
ZMFVAIFXJWEOMH-PTPSPKLBSA-N

> <FORMULA>
C37H67N7O8

> <MOLECULAR_WEIGHT>
737.97

> <EXACT_MASS>
737.505112155

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
119

> <JCHEM_AVERAGE_POLARIZABILITY>
80.81118814021863

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,6S,9S,12S,15R,18R,21R)-15-[(2S)-butan-2-yl]-8,17,20-trihydroxy-18-[(1R)-1-hydroxy-2-methylpropyl]-1,3,4,10,12,13,21-heptamethyl-6,9-bis(2-methylpropyl)-1,4,7,10,13,16,19-heptaazacyclohenicosa-7,16,19-triene-2,5,11,14-tetrone

> <ALOGPS_LOGP>
3.16

> <JCHEM_LOGP>
3.6953281406666667

> <ALOGPS_LOGS>
-4.33

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
4.393545025837686

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.5080688794015473

> <JCHEM_PKA_STRONGEST_BASIC>
1.5354063469188666

> <JCHEM_POLAR_SURFACE_AREA>
199.23999999999998

> <JCHEM_REFRACTIVITY>
198.1356000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.45e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,6S,9S,12S,15R,18R,21R)-15-[(2S)-butan-2-yl]-8,17,20-trihydroxy-18-[(1R)-1-hydroxy-2-methylpropyl]-1,3,4,10,12,13,21-heptamethyl-6,9-bis(2-methylpropyl)-1,4,7,10,13,16,19-heptaazacyclohenicosa-7,16,19-triene-2,5,11,14-tetrone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 22-MAY-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   22-MAY-19         0                                  
HETATM    1  C   UNK     0       5.860 -11.551   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.861  -0.416   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.378   0.559   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.206  -7.932   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.420  -5.383   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.617  -6.884   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.431  -4.929   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.090  -8.480   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.395   0.329   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.770   1.334   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.387 -10.484   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.642  -2.721   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.102  -2.721   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.770  -6.541   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.801  -5.784   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.587 -10.683   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.776  -2.079   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.605  -7.338   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -5.338  -0.645   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -6.077  -6.884   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.960  -5.383   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.702  -9.148   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.833  -1.104   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.502  -8.948   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -3.253  -2.308   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -3.477  -6.291   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.430  -8.280   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.359  -4.789   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.831  -4.335   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.793  -2.308   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -3.819  -4.789   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.017  -6.291   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       1.540   0.000   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -1.890  -8.280   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -2.293  -1.104   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.042  -8.948   0.000  0.00  0.00           C+0
HETATM   38  N   UNK     0      -2.690  -3.742   0.000  0.00  0.00           N+0
HETATM   39  N   UNK     0       3.545  -6.744   0.000  0.00  0.00           N+0
HETATM   40  N   UNK     0       4.230  -3.742   0.000  0.00  0.00           N+0
HETATM   41  N   UNK     0       2.310  -1.334   0.000  0.00  0.00           N+0
HETATM   42  N   UNK     0      -0.770  -1.334   0.000  0.00  0.00           N+0
HETATM   43  N   UNK     0       0.770  -8.081   0.000  0.00  0.00           N+0
HETATM   44  N   UNK     0      -2.005  -6.744   0.000  0.00  0.00           N+0
HETATM   45  O   UNK     0       7.174  -2.834   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0       6.316  -2.079   0.000  0.00  0.00           O+0
HETATM   47  O   UNK     0      -5.291  -4.335   0.000  0.00  0.00           O+0
HETATM   48  O   UNK     0       6.145  -7.338   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0       2.310   1.334   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0      -3.162  -9.148   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0      -2.855   0.329   0.000  0.00  0.00           O+0
HETATM   52  O   UNK     0       1.927 -10.484   0.000  0.00  0.00           O+0
HETATM   53  H   UNK     0       5.975 -10.015   0.000  0.00  0.00           H+0
HETATM   54  H   UNK     0       5.356  -0.875   0.000  0.00  0.00           H+0
HETATM   55  H   UNK     0      -1.540  -0.000   0.000  0.00  0.00           H+0
HETATM   56  H   UNK     0       0.885  -9.617   0.000  0.00  0.00           H+0
HETATM   57  H   UNK     0      -4.213  -3.512   0.000  0.00  0.00           H+0
HETATM   58  H   UNK     0      -3.134  -7.792   0.000  0.00  0.00           H+0
HETATM   59  H   UNK     0       4.817  -7.612   0.000  0.00  0.00           H+0
HETATM   60  H   UNK     0       5.702  -3.288   0.000  0.00  0.00           H+0
HETATM   61  H   UNK     0       6.488  -5.837   0.000  0.00  0.00           H+0
CONECT    1   16                                                            
CONECT    2   19                                                            
CONECT    3   19                                                            
CONECT    4   20                                                            
CONECT    5   20                                                            
CONECT    6   21                                                            
CONECT    7   21                                                            
CONECT    8   22                                                            
CONECT    9   23                                                            
CONECT   10   24                                                            
CONECT   11   25                                                            
CONECT   12   41                                                            
CONECT   13   42                                                            
CONECT   14   43                                                            
CONECT   15   44                                                            
CONECT   16    1   22                                                       
CONECT   17   19   26                                                       
CONECT   18   20   27                                                       
CONECT   19    2    3   17                                                  
CONECT   20    4    5   18                                                  
CONECT   21    6    7   30                                                  
CONECT   22    8   16   28   53                                             
CONECT   23    9   31   41   54                                             
CONECT   24   10   34   42   55                                             
CONECT   25   11   35   43   56                                             
CONECT   26   17   36   38   57                                             
CONECT   27   18   32   44   58                                             
CONECT   28   22   37   39   59                                             
CONECT   29   30   33   40   60                                             
CONECT   30   21   29   45   61                                             
CONECT   31   23   40   46                                                  
CONECT   32   27   38   47                                                  
CONECT   33   29   39   48                                                  
CONECT   34   24   41   49                                                  
CONECT   35   25   44   50                                                  
CONECT   36   26   42   51                                                  
CONECT   37   28   43   52                                                  
CONECT   38   26   32                                                       
CONECT   39   28   33                                                       
CONECT   40   29   31                                                       
CONECT   41   12   23   34                                                  
CONECT   42   13   24   36                                                  
CONECT   43   14   25   37                                                  
CONECT   44   15   27   35                                                  
CONECT   45   30                                                            
CONECT   46   31                                                            
CONECT   47   32                                                            
CONECT   48   33                                                            
CONECT   49   34                                                            
CONECT   50   35                                                            
CONECT   51   36                                                            
CONECT   52   37                                                            
CONECT   53   22                                                            
CONECT   54   23                                                            
CONECT   55   24                                                            
CONECT   56   25                                                            
CONECT   57   26                                                            
CONECT   58   27                                                            
CONECT   59   28                                                            
CONECT   60   29                                                            
CONECT   61   30                                                            
MASTER        0    0    0    0    0    0    0    0   61    0  122    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₆₇N₇O₈

Average Mass

737.9700 Da

Monoisotopic Mass

737.50511 Da

IUPAC Name

(3S,6S,9S,12S,15R,18R,21R)-15-[(2S)-butan-2-yl]-8,17,20-trihydroxy-18-[(1R)-1-hydroxy-2-methylpropyl]-1,3,4,10,12,13,21-heptamethyl-6,9-bis(2-methylpropyl)-1,4,7,10,13,16,19-heptaazacyclohenicosa-7,16,19-triene-2,5,11,14-tetrone

Traditional Name

CAS Registry Number

Not Available

SMILES

[H][C@](C)(CC)[C@@]1([H])N=C(O)[C@]([H])(N=C(O)[C@@]([H])(C)N(C)C(=O)[C@]([H])(C)N(C)C(=O)[C@]([H])(CC(C)C)N=C(O)[C@]([H])(CC(C)C)N(C)C(=O)[C@]([H])(C)N(C)C1=O)[C@]([H])(O)C(C)C

InChI Identifier

InChI=1S/C37H67N7O8/c1-16-22(8)28-37(52)43(14)25(11)35(50)44(15)27(18-20(4)5)32(47)38-26(17-19(2)3)36(51)42(13)24(10)34(49)41(12)23(9)31(46)40-29(33(48)39-28)30(45)21(6)7/h19-30,45H,16-18H2,1-15H3,(H,38,47)(H,39,48)(H,40,46)/t22-,23+,24-,25-,26-,27-,28+,29+,30+/m0/s1

InChI Key

ZMFVAIFXJWEOMH-PTPSPKLBSA-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
Trametes Versicolor	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Oligopeptides

Alternative Parents

Substituents

Alpha-oligopeptide
Macrolactam
Alpha-amino acid or derivatives
Tertiary carboxylic acid amide
Carboxamide group
Lactam
Secondary alcohol
Secondary carboxylic acid amide
Organoheterocyclic compound
Azacycle
Organopnictogen compound
Carbonyl group
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
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	3.16	ALOGPS
logP	3.7	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	3.51	ChemAxon
pKa (Strongest Basic)	1.54	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	199.24 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	198.14 m³·mol⁻¹	ChemAxon
Polarizability	80.81 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

FDB020851

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Ternatin heptapeptide

METLIN ID

Not Available

PubChem Compound

11707536

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,6s,9s,12s,15r,18r,21r)-15-[(2s)-butan-2-yl]-8,17,20-trihydroxy-18-[(1r)-1-hydroxy-2-methylpropyl]-1,3,4,10,12,13,21-heptamethyl-6,9-bis(2-methylpropyl)-1,4,7,10,13,16,19-heptaazacyclohenicosa-7,16,19-triene-2,5,11,14-tetrone (NP0312676)

MOL for NP0312676 ((3s,6s,9s,12s,15r,18r,21r)-15-[(2s)-butan-2-yl]-8,17,20-trihydroxy-18-[(1r)-1-hydroxy-2-methylpropyl]-1,3,4,10,12,13,21-heptamethyl-6,9-bis(2-methylpropyl)-1,4,7,10,13,16,19-heptaazacyclohenicosa-7,16,19-triene-2,5,11,14-tetrone)

3D MOL for NP0312676 ((3s,6s,9s,12s,15r,18r,21r)-15-[(2s)-butan-2-yl]-8,17,20-trihydroxy-18-[(1r)-1-hydroxy-2-methylpropyl]-1,3,4,10,12,13,21-heptamethyl-6,9-bis(2-methylpropyl)-1,4,7,10,13,16,19-heptaazacyclohenicosa-7,16,19-triene-2,5,11,14-tetrone)

3D SDF for NP0312676 ((3s,6s,9s,12s,15r,18r,21r)-15-[(2s)-butan-2-yl]-8,17,20-trihydroxy-18-[(1r)-1-hydroxy-2-methylpropyl]-1,3,4,10,12,13,21-heptamethyl-6,9-bis(2-methylpropyl)-1,4,7,10,13,16,19-heptaazacyclohenicosa-7,16,19-triene-2,5,11,14-tetrone)

3D-SDF for NP0312676 ((3s,6s,9s,12s,15r,18r,21r)-15-[(2s)-butan-2-yl]-8,17,20-trihydroxy-18-[(1r)-1-hydroxy-2-methylpropyl]-1,3,4,10,12,13,21-heptamethyl-6,9-bis(2-methylpropyl)-1,4,7,10,13,16,19-heptaazacyclohenicosa-7,16,19-triene-2,5,11,14-tetrone)

PDB for NP0312676 ((3s,6s,9s,12s,15r,18r,21r)-15-[(2s)-butan-2-yl]-8,17,20-trihydroxy-18-[(1r)-1-hydroxy-2-methylpropyl]-1,3,4,10,12,13,21-heptamethyl-6,9-bis(2-methylpropyl)-1,4,7,10,13,16,19-heptaazacyclohenicosa-7,16,19-triene-2,5,11,14-tetrone)

3D PDB for NP0312676 ((3s,6s,9s,12s,15r,18r,21r)-15-[(2s)-butan-2-yl]-8,17,20-trihydroxy-18-[(1r)-1-hydroxy-2-methylpropyl]-1,3,4,10,12,13,21-heptamethyl-6,9-bis(2-methylpropyl)-1,4,7,10,13,16,19-heptaazacyclohenicosa-7,16,19-triene-2,5,11,14-tetrone)

SMILES for NP0312676 ((3s,6s,9s,12s,15r,18r,21r)-15-[(2s)-butan-2-yl]-8,17,20-trihydroxy-18-[(1r)-1-hydroxy-2-methylpropyl]-1,3,4,10,12,13,21-heptamethyl-6,9-bis(2-methylpropyl)-1,4,7,10,13,16,19-heptaazacyclohenicosa-7,16,19-triene-2,5,11,14-tetrone)

INCHI for NP0312676 ((3s,6s,9s,12s,15r,18r,21r)-15-[(2s)-butan-2-yl]-8,17,20-trihydroxy-18-[(1r)-1-hydroxy-2-methylpropyl]-1,3,4,10,12,13,21-heptamethyl-6,9-bis(2-methylpropyl)-1,4,7,10,13,16,19-heptaazacyclohenicosa-7,16,19-triene-2,5,11,14-tetrone)

Structure for NP0312676 ((3s,6s,9s,12s,15r,18r,21r)-15-[(2s)-butan-2-yl]-8,17,20-trihydroxy-18-[(1r)-1-hydroxy-2-methylpropyl]-1,3,4,10,12,13,21-heptamethyl-6,9-bis(2-methylpropyl)-1,4,7,10,13,16,19-heptaazacyclohenicosa-7,16,19-triene-2,5,11,14-tetrone)

3D Structure for NP0312676 ((3s,6s,9s,12s,15r,18r,21r)-15-[(2s)-butan-2-yl]-8,17,20-trihydroxy-18-[(1r)-1-hydroxy-2-methylpropyl]-1,3,4,10,12,13,21-heptamethyl-6,9-bis(2-methylpropyl)-1,4,7,10,13,16,19-heptaazacyclohenicosa-7,16,19-triene-2,5,11,14-tetrone)