NP-MRD: Showing NP-Card for (1s,3s)-6-hydroxy-1-(3h-imidazol-4-ylmethyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indole-3-carboxylic acid (NP0252459)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 15:58:43 UTC

Updated at

2022-09-07 15:58:43 UTC

NP-MRD ID

NP0252459

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3s)-6-hydroxy-1-(3h-imidazol-4-ylmethyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indole-3-carboxylic acid

Description

Hyrtioreticulin B belongs to the class of organic compounds known as harmala alkaloids. Harmala alkaloids are compounds with a structure based on harmaline, harmine, harmalol, harman or a derivative of those parents. These parents are beta-carbolines, consisting of a pyrimidine fused to the pyrrole moiety of an indole to form a pyrido[3,4-b]indole. (1s,3s)-6-hydroxy-1-(3h-imidazol-4-ylmethyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indole-3-carboxylic acid is found in Hyrtios reticulatus. Based on a literature review very few articles have been published on Hyrtioreticulin B.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 42  0  0  0  0  0  0  0  0999 V2000
    1.7706    3.7263   -0.1263 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5705    3.7489   -0.2940 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0110    4.8591   -0.9705 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3945    2.7113    0.1425 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3299    1.7256    1.0143 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7045    0.4243    0.3785 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2417   -0.1311   -0.4800 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2530   -1.2849   -0.8935 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4377   -1.4670   -0.3490 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3820   -2.4914   -0.4739 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5617   -2.3913    0.1979 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8636   -1.3356    0.9994 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0860   -1.2624    1.6789 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9425   -0.3582    1.1349 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7649   -0.4095    0.4663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3866    0.7516   -0.6466 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5957    0.1921   -1.3199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0439   -0.9758   -0.5140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0736   -2.2906   -0.8420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4218   -2.9928    0.2513 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6280   -2.1490    1.2680 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3977   -0.9128    0.8117 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9044    2.0061   -1.0725 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2138    4.7490   -2.0067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2193    3.1802    0.6585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1303    1.5894    2.0198 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3246    2.2061    1.2719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2813   -1.8951   -1.5901 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1338   -3.3073   -1.0966 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3207   -3.1935    0.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7516   -2.0143    1.6249 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1237    0.5225    1.7925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7804    0.9590    0.4260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3147   -0.1450   -2.3569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4173    0.9359   -1.3498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8532   -2.7503   -1.8247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9071   -2.3994    2.2711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4573    0.0130    1.3170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0753    1.8569   -1.6739 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0
  2  1  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  2  0
  7 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 16 23  1  0
 23  4  1  0
 15  6  1  0
 22 18  1  0
 15  9  1  0
  3 24  1  0
  4 25  1  1
  5 26  1  0
  5 27  1  0
  8 28  1  0
 10 29  1  0
 11 30  1  0
 13 31  1  0
 14 32  1  0
 16 33  1  1
 17 34  1  0
 17 35  1  0
 19 36  1  0
 21 37  1  0
 22 38  1  0
 23 39  1  0
M  END


  Mrv1652309072217582D          

 23 26  0  0  1  0            999 V2000
    5.0645    1.4672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2575    1.6387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0025    2.4233    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7054    1.0256    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8985    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3464    0.5840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6014   -0.2006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9339   -0.6855    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2665   -0.2006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4595   -0.3721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0925    0.2410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1624    1.0256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3896    1.6387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9694    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5214    0.5840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4084   -0.3721    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6633   -1.1567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1113   -1.7698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2828   -2.5768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5683   -2.9893    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9552   -2.4373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2908   -1.6836    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9604    0.2410    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  4  2  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
  6 15  1  0  0  0  0
  9 15  1  0  0  0  0
  7 16  1  0  0  0  0
 16 17  1  1  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
 18 22  1  0  0  0  0
 16 23  1  0  0  0  0
  4 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0252459

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC(=O)[C@@H]1CC2=C(NC3=CC=C(O)C=C23)[C@H](CC2=CN=CN2)N1

> <INCHI_IDENTIFIER>
InChI=1S/C16H16N4O3/c21-9-1-2-12-10(4-9)11-5-14(16(22)23)19-13(15(11)20-12)3-8-6-17-7-18-8/h1-2,4,6-7,13-14,19-21H,3,5H2,(H,17,18)(H,22,23)/t13-,14-/m0/s1

> <INCHI_KEY>
VXURZHPEJYLPGK-KBPBESRZSA-N

> <FORMULA>
C16H16N4O3

> <MOLECULAR_WEIGHT>
312.329

> <EXACT_MASS>
312.122240391

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
32.51208411013485

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3S)-6-hydroxy-1-[(1H-imidazol-5-yl)methyl]-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-3-carboxylic acid

> <JCHEM_LOGP>
-1.7016586465794403

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
9.674390391803357

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.521027527248596

> <JCHEM_PKA_STRONGEST_BASIC>
8.935525478348364

> <JCHEM_POLAR_SURFACE_AREA>
114.03

> <JCHEM_REFRACTIVITY>
83.37089999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3S)-6-hydroxy-1-(3H-imidazol-4-ylmethyl)-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-3-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  O   UNK     0       9.454   2.739   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       7.947   3.059   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       7.471   4.524   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       6.917   1.914   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.410   2.235   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.380   1.090   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.856  -0.374   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       3.610  -1.280   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       2.364  -0.374   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.858  -0.695   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.173   0.450   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.303   1.914   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.727   3.059   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.810   2.235   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.840   1.090   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.362  -0.695   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.838  -2.159   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.808  -3.304   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.128  -4.810   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       4.794  -5.580   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       3.650  -4.550   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0       4.276  -3.143   0.000  0.00  0.00           N+0
HETATM   23  N   UNK     0       7.393   0.450   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   23                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   15                                                  
CONECT    7    6    8   16                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14    6    9                                                  
CONECT   16    7   17   23                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   22                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   18                                                       
CONECT   23   16    4                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₁₆N₄O₃

Average Mass

312.3290 Da

Monoisotopic Mass

312.12224 Da

IUPAC Name

(1S,3S)-6-hydroxy-1-[(1H-imidazol-5-yl)methyl]-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-3-carboxylic acid

Traditional Name

(1S,3S)-6-hydroxy-1-(3H-imidazol-4-ylmethyl)-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-3-carboxylic acid

CAS Registry Number

Not Available

SMILES

OC(=O)[C@@H]1CC2=C(NC3=CC=C(O)C=C23)[C@H](CC2=CN=CN2)N1

InChI Identifier

InChI=1S/C16H16N4O3/c21-9-1-2-12-10(4-9)11-5-14(16(22)23)19-13(15(11)20-12)3-8-6-17-7-18-8/h1-2,4,6-7,13-14,19-21H,3,5H2,(H,17,18)(H,22,23)/t13-,14-/m0/s1

InChI Key

VXURZHPEJYLPGK-KBPBESRZSA-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
Hyrtios reticulatus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as harmala alkaloids. Harmala alkaloids are compounds with a structure based on harmaline, harmine, harmalol, harman or a derivative of those parents. These parents are beta-carbolines, consisting of a pyrimidine fused to the pyrrole moiety of an indole to form a pyrido[3,4-b]indole.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Harmala alkaloids

Sub Class

Not Available

Direct Parent

Harmala alkaloids

Alternative Parents

Substituents

Harman
Pyridoindole
Beta-carboline
Alpha-amino acid
Alpha-amino acid or derivatives
Hydroxyindole
L-alpha-amino acid
3-alkylindole
Indole or derivatives
Indole
Imidazolyl carboxylic acid derivative
1-hydroxy-2-unsubstituted benzenoid
Phenol
Aralkylamine
Benzenoid
Imidazole
Pyrrole
Azole
Heteroaromatic compound
Amino acid or derivatives
Amino acid
Azacycle
Carboxylic acid derivative
Carboxylic acid
Secondary aliphatic amine
Organoheterocyclic compound
Secondary amine
Monocarboxylic acid or derivatives
Organic oxygen compound
Carbonyl group
Amine
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
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	-1.7	ChemAxon
pKa (Strongest Acidic)	1.52	ChemAxon
pKa (Strongest Basic)	8.94	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	114.03 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	83.37 m³·mol⁻¹	ChemAxon
Polarizability	32.51 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

28505724

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

70684035

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3s)-6-hydroxy-1-(3h-imidazol-4-ylmethyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indole-3-carboxylic acid (NP0252459)

MOL for NP0252459 ((1s,3s)-6-hydroxy-1-(3h-imidazol-4-ylmethyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indole-3-carboxylic acid)

3D MOL for NP0252459 ((1s,3s)-6-hydroxy-1-(3h-imidazol-4-ylmethyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indole-3-carboxylic acid)

3D SDF for NP0252459 ((1s,3s)-6-hydroxy-1-(3h-imidazol-4-ylmethyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indole-3-carboxylic acid)

3D-SDF for NP0252459 ((1s,3s)-6-hydroxy-1-(3h-imidazol-4-ylmethyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indole-3-carboxylic acid)

PDB for NP0252459 ((1s,3s)-6-hydroxy-1-(3h-imidazol-4-ylmethyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indole-3-carboxylic acid)

3D PDB for NP0252459 ((1s,3s)-6-hydroxy-1-(3h-imidazol-4-ylmethyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indole-3-carboxylic acid)

SMILES for NP0252459 ((1s,3s)-6-hydroxy-1-(3h-imidazol-4-ylmethyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indole-3-carboxylic acid)

INCHI for NP0252459 ((1s,3s)-6-hydroxy-1-(3h-imidazol-4-ylmethyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indole-3-carboxylic acid)

Structure for NP0252459 ((1s,3s)-6-hydroxy-1-(3h-imidazol-4-ylmethyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indole-3-carboxylic acid)

3D Structure for NP0252459 ((1s,3s)-6-hydroxy-1-(3h-imidazol-4-ylmethyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indole-3-carboxylic acid)