NP-MRD: Showing NP-Card for 1,4,7,10,13,16-hexahydroxy-18-(hydroxymethyl)-3-(1h-indol-3-ylmethyl)-15-isopropyl-6-methyl-9,12-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one (NP0217242)

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Record Information

Version

2.0

Created at

2022-09-05 17:31:39 UTC

Updated at

2022-09-05 17:31:39 UTC

NP-MRD ID

NP0217242

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,4,7,10,13,16-hexahydroxy-18-(hydroxymethyl)-3-(1h-indol-3-ylmethyl)-15-isopropyl-6-methyl-9,12-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one

Description

1,4,7,10,13,16-Hexahydroxy-18-(hydroxymethyl)-3-[(1H-indol-3-yl)methyl]-6-methyl-9,12-bis(2-methylpropyl)-15-(propan-2-yl)-3H,6H,9H,12H,15H,18H,19H,21H,22H,23H,23aH-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one belongs to the class of organic compounds known as cyclic peptides. Cyclic peptides are compounds containing a cyclic moiety bearing a peptide backbone. 1,4,7,10,13,16-hexahydroxy-18-(hydroxymethyl)-3-(1h-indol-3-ylmethyl)-15-isopropyl-6-methyl-9,12-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one is found in Jatropha integerrima. 1,4,7,10,13,16-Hexahydroxy-18-(hydroxymethyl)-3-[(1H-indol-3-yl)methyl]-6-methyl-9,12-bis(2-methylpropyl)-15-(propan-2-yl)-3H,6H,9H,12H,15H,18H,19H,21H,22H,23H,23aH-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241504552D          

 55 58  0  0  0  0            999 V2000
   10.6146   -2.0786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    9.1816   -1.2607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4651   -0.8517    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5841   -0.0353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3505    0.2699    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    6.6059    0.7727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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  9 10  1  0  0  0  0
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 23 24  2  0  0  0  0
 16 24  1  0  0  0  0
 19 24  1  0  0  0  0
 14 25  1  0  0  0  0
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M  END

     RDKit          3D

113116  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1533004241504552D          

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 41 53  1  0  0  0  0
 53 54  1  0  0  0  0
 53 55  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0217242

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CC1NC(=O)C(C)NC(=O)C(CC2=CNC3=CC=CC=C23)NC(=O)C2CCCN2C(=O)C(CO)NC(=O)C(NC(=O)C(CC(C)C)NC1=O)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C39H58N8O8/c1-20(2)15-27-35(51)43-28(16-21(3)4)36(52)46-32(22(5)6)38(54)45-30(19-48)39(55)47-14-10-13-31(47)37(53)44-29(34(50)41-23(7)33(49)42-27)17-24-18-40-26-12-9-8-11-25(24)26/h8-9,11-12,18,20-23,27-32,40,48H,10,13-17,19H2,1-7H3,(H,41,50)(H,42,49)(H,43,51)(H,44,53)(H,45,54)(H,46,52)

> <INCHI_KEY>
WFQBWZPTVRKYLS-UHFFFAOYSA-N

> <FORMULA>
C39H58N8O8

> <MOLECULAR_WEIGHT>
766.941

> <EXACT_MASS>
766.43776086

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
113

> <JCHEM_AVERAGE_POLARIZABILITY>
82.23172705285063

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
18-(hydroxymethyl)-3-[(1H-indol-3-yl)methyl]-6-methyl-9,12-bis(2-methylpropyl)-15-(propan-2-yl)-docosahydro-1H-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosane-1,4,7,10,13,16,19-heptone

> <ALOGPS_LOGP>
1.41

> <JCHEM_LOGP>
0.6209265243333317

> <ALOGPS_LOGS>
-3.93

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.933884194676747

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.539113583225905

> <JCHEM_PKA_STRONGEST_BASIC>
-2.844587194963144

> <JCHEM_POLAR_SURFACE_AREA>
230.92999999999998

> <JCHEM_REFRACTIVITY>
202.36290000000014

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.91e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
18-(hydroxymethyl)-3-(1H-indol-3-ylmethyl)-15-isopropyl-6-methyl-9,12-bis(2-methylpropyl)-hexadecahydropyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosane-1,4,7,10,13,16,19-heptone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      19.814  -3.880   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      19.806  -2.340   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      21.136  -1.564   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      18.469  -1.577   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      17.139  -2.353   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      15.802  -1.590   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      16.024  -0.066   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      17.454   0.504   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      14.815   0.888   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      15.037   2.412   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      13.384   0.319   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      12.331   1.442   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      12.778   2.916   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      10.831   1.092   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.778   2.216   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.225   3.690   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.680   4.195   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0      11.649   5.734   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0      10.176   6.181   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.521   7.575   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.987   7.706   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.107   6.442   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.761   5.048   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.295   4.917   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0      10.385  -0.382   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0       8.850  -0.504   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.976   0.764   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       8.188  -1.895   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.712  -2.334   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.674  -3.874   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.477  -4.462   0.000  0.00  0.00           C+0
HETATM   32  N   UNK     0       9.062  -3.163   0.000  0.00  0.00           N+0
HETATM   33  C   UNK     0       8.201  -4.440   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       6.707  -4.812   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       8.876  -5.824   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       8.015  -7.101   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       6.478  -6.993   0.000  0.00  0.00           O+0
HETATM   38  N   UNK     0      10.412  -5.931   0.000  0.00  0.00           N+0
HETATM   39  C   UNK     0      10.873  -7.401   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       9.831  -8.535   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      12.376  -7.736   0.000  0.00  0.00           C+0
HETATM   42  N   UNK     0      13.418  -6.602   0.000  0.00  0.00           N+0
HETATM   43  C   UNK     0      14.854  -7.158   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      15.091  -8.679   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0      16.054  -6.191   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      17.490  -6.747   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      17.727  -8.269   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      19.163  -8.824   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      16.528  -9.235   0.000  0.00  0.00           C+0
HETATM   50  N   UNK     0      15.817  -4.670   0.000  0.00  0.00           N+0
HETATM   51  C   UNK     0      17.147  -3.893   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      18.484  -4.657   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0      12.837  -9.205   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      14.340  -9.541   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      11.796 -10.339   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   51                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   25                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   24                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   16   19                                                  
CONECT   25   14   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   32                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   28   33                                                  
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36   38                                                  
CONECT   36   35   37                                                       
CONECT   37   36                                                            
CONECT   38   35   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42   53                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   46   50                                                  
CONECT   46   45   47                                                       
CONECT   47   46   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47                                                            
CONECT   50   45   51                                                       
CONECT   51   50    5   52                                                  
CONECT   52   51                                                            
CONECT   53   41   54   55                                                  
CONECT   54   53                                                            
CONECT   55   53                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  116    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₉H₅₈N₈O₈

Average Mass

766.9410 Da

Monoisotopic Mass

766.43776 Da

IUPAC Name

18-(hydroxymethyl)-3-[(1H-indol-3-yl)methyl]-6-methyl-9,12-bis(2-methylpropyl)-15-(propan-2-yl)-docosahydro-1H-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosane-1,4,7,10,13,16,19-heptone

Traditional Name

18-(hydroxymethyl)-3-(1H-indol-3-ylmethyl)-15-isopropyl-6-methyl-9,12-bis(2-methylpropyl)-hexadecahydropyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosane-1,4,7,10,13,16,19-heptone

CAS Registry Number

Not Available

SMILES

CC(C)CC1NC(=O)C(C)NC(=O)C(CC2=CNC3=CC=CC=C23)NC(=O)C2CCCN2C(=O)C(CO)NC(=O)C(NC(=O)C(CC(C)C)NC1=O)C(C)C

InChI Identifier

InChI=1S/C39H58N8O8/c1-20(2)15-27-35(51)43-28(16-21(3)4)36(52)46-32(22(5)6)38(54)45-30(19-48)39(55)47-14-10-13-31(47)37(53)44-29(34(50)41-23(7)33(49)42-27)17-24-18-40-26-12-9-8-11-25(24)26/h8-9,11-12,18,20-23,27-32,40,48H,10,13-17,19H2,1-7H3,(H,41,50)(H,42,49)(H,43,51)(H,44,53)(H,45,54)(H,46,52)

InChI Key

WFQBWZPTVRKYLS-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
Jatropha integerrima	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclic peptides. Cyclic peptides are compounds containing a cyclic moiety bearing a peptide backbone.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Cyclic peptides

Alternative Parents

Substituents

Cyclic alpha peptide
Alpha-amino acid or derivatives
3-alkylindole
Indole
Indole or derivatives
Substituted pyrrole
Benzenoid
Pyrrole
Pyrrolidine
Heteroaromatic compound
Tertiary carboxylic acid amide
Cyclic carboximidic acid
Carboxamide group
Lactam
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Organoheterocyclic compound
Azacycle
Polyol
Organonitrogen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
Carbonyl group
Primary alcohol
Alcohol
Organic nitrogen compound
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	1.41	ALOGPS
logP	0.62	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	11.54	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	230.93 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	202.36 m³·mol⁻¹	ChemAxon
Polarizability	82.23 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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 1,4,7,10,13,16-hexahydroxy-18-(hydroxymethyl)-3-(1h-indol-3-ylmethyl)-15-isopropyl-6-methyl-9,12-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one (NP0217242)

MOL for NP0217242 (1,4,7,10,13,16-hexahydroxy-18-(hydroxymethyl)-3-(1h-indol-3-ylmethyl)-15-isopropyl-6-methyl-9,12-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one)

3D MOL for NP0217242 (1,4,7,10,13,16-hexahydroxy-18-(hydroxymethyl)-3-(1h-indol-3-ylmethyl)-15-isopropyl-6-methyl-9,12-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one)

3D SDF for NP0217242 (1,4,7,10,13,16-hexahydroxy-18-(hydroxymethyl)-3-(1h-indol-3-ylmethyl)-15-isopropyl-6-methyl-9,12-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one)

3D-SDF for NP0217242 (1,4,7,10,13,16-hexahydroxy-18-(hydroxymethyl)-3-(1h-indol-3-ylmethyl)-15-isopropyl-6-methyl-9,12-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one)

PDB for NP0217242 (1,4,7,10,13,16-hexahydroxy-18-(hydroxymethyl)-3-(1h-indol-3-ylmethyl)-15-isopropyl-6-methyl-9,12-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one)

3D PDB for NP0217242 (1,4,7,10,13,16-hexahydroxy-18-(hydroxymethyl)-3-(1h-indol-3-ylmethyl)-15-isopropyl-6-methyl-9,12-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one)

SMILES for NP0217242 (1,4,7,10,13,16-hexahydroxy-18-(hydroxymethyl)-3-(1h-indol-3-ylmethyl)-15-isopropyl-6-methyl-9,12-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one)

INCHI for NP0217242 (1,4,7,10,13,16-hexahydroxy-18-(hydroxymethyl)-3-(1h-indol-3-ylmethyl)-15-isopropyl-6-methyl-9,12-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one)

Structure for NP0217242 (1,4,7,10,13,16-hexahydroxy-18-(hydroxymethyl)-3-(1h-indol-3-ylmethyl)-15-isopropyl-6-methyl-9,12-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one)

3D Structure for NP0217242 (1,4,7,10,13,16-hexahydroxy-18-(hydroxymethyl)-3-(1h-indol-3-ylmethyl)-15-isopropyl-6-methyl-9,12-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one)