NP-MRD: Showing NP-Card for 2-[(2-{[2-(dimethylamino)-1-hydroxy-3-phenylpropylidene]amino}-1-hydroxy-3-(indol-1-yl)-4-methylpentylidene)amino]-3-methylpentanoic acid (NP0190174)

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Record Information

Version

2.0

Created at

2022-09-04 06:47:40 UTC

Updated at

2022-09-04 06:47:40 UTC

NP-MRD ID

NP0190174

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(2-{[2-(dimethylamino)-1-hydroxy-3-phenylpropylidene]amino}-1-hydroxy-3-(indol-1-yl)-4-methylpentylidene)amino]-3-methylpentanoic acid

Description

2-[(2-{[2-(Dimethylamino)-1-hydroxy-3-phenylpropylidene]amino}-1-hydroxy-3-(1H-indol-1-yl)-4-methylpentylidene)amino]-3-methylpentanoic acid belongs to the class of organic compounds known as peptides. Peptides are compounds containing an amide derived from two or more amino carboxylic acid molecules (the same or different) by formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another. 2-[(2-{[2-(dimethylamino)-1-hydroxy-3-phenylpropylidene]amino}-1-hydroxy-3-(indol-1-yl)-4-methylpentylidene)amino]-3-methylpentanoic acid is found in Ixora coccinea. 2-[(2-{[2-(Dimethylamino)-1-hydroxy-3-phenylpropylidene]amino}-1-hydroxy-3-(1H-indol-1-yl)-4-methylpentylidene)amino]-3-methylpentanoic acid is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004261504422D          

 39 41  0  0  0  0            999 V2000
    5.0389   -0.9413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.1992   -2.8122    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.4693   -3.5917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9292   -4.2154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   11.0260   -5.9861    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
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
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  7  9  1  0  0  0  0
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 15 20  1  0  0  0  0
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  9 24  1  0  0  0  0
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 28 36  1  0  0  0  0
 31 36  1  0  0  0  0
  5 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1533004261504422D          

 39 41  0  0  0  0            999 V2000
    5.0389   -0.9413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.2794   -5.9304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1992   -4.9949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3596   -4.6831    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.9619   -4.1194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6842   -4.5180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5283   -5.3281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0260   -5.9861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7051   -6.7461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8864   -6.8481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3887   -6.1902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7096   -5.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8490   -3.2799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1190   -4.0595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0389   -3.1240    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
  3  5  1  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
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
  9 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 24 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 28 36  1  0  0  0  0
 31 36  1  0  0  0  0
  5 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0190174

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)C(NC(=O)C(NC(=O)C(CC1=CC=CC=C1)N(C)C)C(C(C)C)N1C=CC2=CC=CC=C12)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C31H42N4O4/c1-7-21(4)26(31(38)39)32-30(37)27(28(20(2)3)35-18-17-23-15-11-12-16-24(23)35)33-29(36)25(34(5)6)19-22-13-9-8-10-14-22/h8-18,20-21,25-28H,7,19H2,1-6H3,(H,32,37)(H,33,36)(H,38,39)

> <INCHI_KEY>
DPHRDZLCFBXNED-UHFFFAOYSA-N

> <FORMULA>
C31H42N4O4

> <MOLECULAR_WEIGHT>
534.701

> <EXACT_MASS>
534.320605848

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
59.002552394545326

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-{2-[2-(dimethylamino)-3-phenylpropanamido]-3-(1H-indol-1-yl)-4-methylpentanamido}-3-methylpentanoic acid

> <ALOGPS_LOGP>
4.07

> <JCHEM_LOGP>
2.5340678623306934

> <ALOGPS_LOGS>
-4.97

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.574116604567745

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.6888413867706045

> <JCHEM_PKA_STRONGEST_BASIC>
7.241680413527636

> <JCHEM_POLAR_SURFACE_AREA>
103.67

> <JCHEM_REFRACTIVITY>
152.115

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.71e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-{2-[2-(dimethylamino)-3-phenylpropanamido]-3-(indol-1-yl)-4-methylpentanamido}-3-methylpentanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-15         0                                  
HETATM    1  C   UNK     0       9.406  -1.757   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.910  -3.212   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.422  -3.503   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.430  -2.339   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.926  -4.958   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      13.439  -5.249   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      13.943  -6.705   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      12.934  -7.869   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      15.455  -6.996   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0      16.463  -5.831   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      15.959  -4.376   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      14.447  -4.085   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      16.967  -3.212   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      16.463  -1.757   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      17.471  -0.593   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      16.967   0.862   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      17.975   2.026   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      19.488   1.735   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      19.992   0.280   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      18.983  -0.884   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0      18.479  -3.503   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0      19.488  -2.339   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      18.983  -4.958   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      15.959  -8.451   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      14.951  -9.615   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      15.455 -11.070   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      13.439  -9.324   0.000  0.00  0.00           C+0
HETATM   28  N   UNK     0      17.471  -8.742   0.000  0.00  0.00           N+0
HETATM   29  C   UNK     0      18.596  -7.689   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      19.944  -8.434   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      19.653  -9.946   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      20.582 -11.174   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      19.983 -12.593   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      18.455 -12.783   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      17.526 -11.555   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      18.125 -10.136   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      10.918  -6.123   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      11.422  -7.578   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       9.406  -5.831   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   37                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   24                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   21                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   15                                                       
CONECT   21   13   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24    9   25   28                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   24   29   36                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   28   31                                                  
CONECT   37    5   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   82    0
END

View in JSmol

Synonyms

Value	Source
2-[(2-{[2-(dimethylamino)-1-hydroxy-3-phenylpropylidene]amino}-1-hydroxy-3-(1H-indol-1-yl)-4-methylpentylidene)amino]-3-methylpentanoate	Generator

Chemical Formula

C₃₁H₄₂N₄O₄

Average Mass

534.7010 Da

Monoisotopic Mass

534.32061 Da

IUPAC Name

2-{2-[2-(dimethylamino)-3-phenylpropanamido]-3-(1H-indol-1-yl)-4-methylpentanamido}-3-methylpentanoic acid

Traditional Name

2-{2-[2-(dimethylamino)-3-phenylpropanamido]-3-(indol-1-yl)-4-methylpentanamido}-3-methylpentanoic acid

CAS Registry Number

Not Available

SMILES

CCC(C)C(NC(=O)C(NC(=O)C(CC1=CC=CC=C1)N(C)C)C(C(C)C)N1C=CC2=CC=CC=C12)C(O)=O

InChI Identifier

InChI=1S/C31H42N4O4/c1-7-21(4)26(31(38)39)32-30(37)27(28(20(2)3)35-18-17-23-15-11-12-16-24(23)35)33-29(36)25(34(5)6)19-22-13-9-8-10-14-22/h8-18,20-21,25-28H,7,19H2,1-6H3,(H,32,37)(H,33,36)(H,38,39)

InChI Key

DPHRDZLCFBXNED-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
Ixora coccinea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as peptides. Peptides are compounds containing an amide derived from two or more amino carboxylic acid molecules (the same or different) by formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Peptides

Alternative Parents

Substituents

Alpha peptide
Isoleucine or derivatives
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
Alpha-amino acid or derivatives
Amphetamine or derivatives
N-alkylindole
Indole
Indole or derivatives
Aralkylamine
Monocyclic benzene moiety
Benzenoid
Substituted pyrrole
Pyrrole
Heteroaromatic compound
Tertiary amine
Tertiary aliphatic amine
Amino acid
Amino acid or derivatives
Carboximidic acid
Carboximidic acid derivative
Carboxylic acid
Azacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Amine
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organic nitrogen compound
Organonitrogen compound
Organooxygen 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	4.07	ALOGPS
logP	2.53	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	3.69	ChemAxon
pKa (Strongest Basic)	7.24	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	103.67 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	152.12 m³·mol⁻¹	ChemAxon
Polarizability	59 Å³	ChemAxon
Number of Rings	3	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

75583337

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[(2-{[2-(dimethylamino)-1-hydroxy-3-phenylpropylidene]amino}-1-hydroxy-3-(indol-1-yl)-4-methylpentylidene)amino]-3-methylpentanoic acid (NP0190174)

MOL for NP0190174 (2-[(2-{[2-(dimethylamino)-1-hydroxy-3-phenylpropylidene]amino}-1-hydroxy-3-(indol-1-yl)-4-methylpentylidene)amino]-3-methylpentanoic acid)

3D MOL for NP0190174 (2-[(2-{[2-(dimethylamino)-1-hydroxy-3-phenylpropylidene]amino}-1-hydroxy-3-(indol-1-yl)-4-methylpentylidene)amino]-3-methylpentanoic acid)

3D SDF for NP0190174 (2-[(2-{[2-(dimethylamino)-1-hydroxy-3-phenylpropylidene]amino}-1-hydroxy-3-(indol-1-yl)-4-methylpentylidene)amino]-3-methylpentanoic acid)

3D-SDF for NP0190174 (2-[(2-{[2-(dimethylamino)-1-hydroxy-3-phenylpropylidene]amino}-1-hydroxy-3-(indol-1-yl)-4-methylpentylidene)amino]-3-methylpentanoic acid)

PDB for NP0190174 (2-[(2-{[2-(dimethylamino)-1-hydroxy-3-phenylpropylidene]amino}-1-hydroxy-3-(indol-1-yl)-4-methylpentylidene)amino]-3-methylpentanoic acid)

3D PDB for NP0190174 (2-[(2-{[2-(dimethylamino)-1-hydroxy-3-phenylpropylidene]amino}-1-hydroxy-3-(indol-1-yl)-4-methylpentylidene)amino]-3-methylpentanoic acid)

SMILES for NP0190174 (2-[(2-{[2-(dimethylamino)-1-hydroxy-3-phenylpropylidene]amino}-1-hydroxy-3-(indol-1-yl)-4-methylpentylidene)amino]-3-methylpentanoic acid)

INCHI for NP0190174 (2-[(2-{[2-(dimethylamino)-1-hydroxy-3-phenylpropylidene]amino}-1-hydroxy-3-(indol-1-yl)-4-methylpentylidene)amino]-3-methylpentanoic acid)

Structure for NP0190174 (2-[(2-{[2-(dimethylamino)-1-hydroxy-3-phenylpropylidene]amino}-1-hydroxy-3-(indol-1-yl)-4-methylpentylidene)amino]-3-methylpentanoic acid)

3D Structure for NP0190174 (2-[(2-{[2-(dimethylamino)-1-hydroxy-3-phenylpropylidene]amino}-1-hydroxy-3-(indol-1-yl)-4-methylpentylidene)amino]-3-methylpentanoic acid)