NP-MRD: Showing NP-Card for 2'-hydroxy-1'h-[2,3'-biindol]-3-one (NP0283711)

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Record Information

Version

2.0

Created at

2022-09-09 11:05:15 UTC

Updated at

2022-09-09 11:05:15 UTC

NP-MRD ID

NP0283711

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2'-hydroxy-1'h-[2,3'-biindol]-3-one

Description

Indirubin, also known as indigo red, belongs to the class of organic compounds known as hydroxyindoles. These are organic compounds containing an indole moiety that carries a hydroxyl group. 2'-hydroxy-1'h-[2,3'-biindol]-3-one is found in Calanthe discolor, Couroupita guianensis and Isatis tinctoria. 2'-hydroxy-1'h-[2,3'-biindol]-3-one was first documented in 2022 (PMID: 36060126). Based on a literature review a significant number of articles have been published on Indirubin (PMID: 36104717) (PMID: 36098267) (PMID: 35956988) (PMID: 35890405) (PMID: 35876239) (PMID: 35845683).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 30 33  0  0  0  0  0  0  0  0999 V2000
    0.7492   -2.1505   -0.3457 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1365   -1.0209   -0.0433 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4500    0.1988    0.2270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9868    0.5481    0.2414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4503    1.8382    0.5406 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6623    2.9376    0.8558 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7612    1.8727    0.4827 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1966    0.6511    0.1549 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4751    0.1459   -0.0365 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6672   -1.1784   -0.3777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5813   -2.0124   -0.5312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2995   -1.5172   -0.3421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1022   -0.1945   -0.0011 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3636    1.1070    0.5007 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6637    0.5835    0.4358 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8919    1.2134    0.6558 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0514    0.4846    0.5324 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9577   -0.8498    0.1937 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7392   -1.4691   -0.0232 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6009   -0.7399    0.1014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3342    3.6142    0.1991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4349    2.6758    0.6494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3167    0.8081    0.0864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6735   -1.5377   -0.5187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6997   -3.0548   -0.7980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4737   -2.1757   -0.4650 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9520    2.2519    0.9188 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0271    0.9155    0.6898 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8613   -1.4327    0.0938 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6705   -2.5127   -0.2879 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0
  5  4  2  0
  4 13  1  0
 13 12  2  0
 12 11  1  0
 11 10  2  0
 10  9  1  0
  9  8  2  0
  8  7  1  0
  4  3  1  0
  3 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20  2  1  0
  2  1  2  0
  7  5  1  0
  2  3  1  0
  8 13  1  0
 20 15  1  0
  6 21  1  0
 12 26  1  0
 11 25  1  0
 10 24  1  0
  9 23  1  0
  7 22  1  0
 16 27  1  0
 17 28  1  0
 18 29  1  0
 19 30  1  0
M  END


  Mrv1652309092213052D          

 20 23  0  0  0  0            999 V2000
    3.0637   -1.6867    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3186   -0.9020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8337   -0.2346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0087   -0.2346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5237   -0.9020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7787   -1.6867    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7391   -0.6471    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7391    0.1779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1260    0.7299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2976    1.5369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0822    1.7918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6953    1.2398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5237    0.4328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3186    0.4328    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1032    0.1779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8177    0.5904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5322    0.1779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5322   -0.6471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8177   -1.0596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1032   -0.6471    0.0000 C   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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  4 13  1  0  0  0  0
  8 13  1  0  0  0  0
  3 14  2  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
  2 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0283711

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=C(C2=CC=CC=C2N1)C1=NC2=CC=CC=C2C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H10N2O2/c19-15-10-6-2-4-8-12(10)17-14(15)13-9-5-1-3-7-11(9)18-16(13)20/h1-8,18,20H

> <INCHI_KEY>
JNLNPCNGMHKCKO-UHFFFAOYSA-N

> <FORMULA>
C16H10N2O2

> <MOLECULAR_WEIGHT>
262.268

> <EXACT_MASS>
262.07422757

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
30

> <JCHEM_AVERAGE_POLARIZABILITY>
27.600905335089596

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2'-hydroxy-1'H,3H-[2,3'-biindole]-3-one

> <JCHEM_LOGP>
3.3177269606666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.10374943114448

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.532729990371651

> <JCHEM_PKA_STRONGEST_BASIC>
-2.6887818971370523

> <JCHEM_POLAR_SURFACE_AREA>
65.44999999999999

> <JCHEM_REFRACTIVITY>
77.0811

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2'-hydroxy-1'H-[2,3'-biindole]-3-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  O   UNK     0       5.719  -3.148   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       6.195  -1.684   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.290  -0.438   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.750  -0.438   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.844  -1.684   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       3.320  -3.148   0.000  0.00  0.00           O+0
HETATM    7  N   UNK     0       1.380  -1.208   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       1.380   0.332   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.235   1.363   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.555   2.869   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.020   3.345   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.165   2.314   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.844   0.808   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       6.195   0.808   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       7.659   0.332   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.993   1.102   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.327   0.332   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.327  -1.208   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.993  -1.978   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.659  -1.208   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   20                                                  
CONECT    3    2    4   14                                                  
CONECT    4    3    5   13                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    4    8                                                  
CONECT   14    3   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    2                                                  
MASTER        0    0    0    0    0    0    0    0   20    0   46    0
END

View in JSmol

Synonyms

Value	Source
Indigo red	MeSH

Chemical Formula

C₁₆H₁₀N₂O₂

Average Mass

262.2680 Da

Monoisotopic Mass

262.07423 Da

IUPAC Name

2'-hydroxy-1'H,3H-[2,3'-biindole]-3-one

Traditional Name

2'-hydroxy-1'H-[2,3'-biindole]-3-one

CAS Registry Number

Not Available

SMILES

OC1=C(C2=CC=CC=C2N1)C1=NC2=CC=CC=C2C1=O

InChI Identifier

InChI=1S/C16H10N2O2/c19-15-10-6-2-4-8-12(10)17-14(15)13-9-5-1-3-7-11(9)18-16(13)20/h1-8,18,20H

InChI Key

JNLNPCNGMHKCKO-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
Calanthe discolor	LOTUS Database	35616633
Couroupita guianensis	LOTUS Database	35616633
Isatis tinctoria	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxyindoles. These are organic compounds containing an indole moiety that carries a hydroxyl group.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Hydroxyindoles

Direct Parent

Hydroxyindoles

Alternative Parents

Substituents

Hydroxyindole
Indole
Aryl ketone
Benzenoid
Substituted pyrrole
Pyrrole
Heteroaromatic compound
Ketimine
Ketone
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Imine
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic oxide
Organic oxygen 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	3.32	ChemAxon
pKa (Strongest Acidic)	7.53	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	65.45 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	77.08 m³·mol⁻¹	ChemAxon
Polarizability	27.6 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

C00026982

Chemspider ID

21395695

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Indirubin

METLIN ID

Not Available

PubChem Compound

10177

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Lu Q, Li J, Ding P, Mao T, Shi L, Sun Z, Tan X, Jiang H, Dong J, Li Y, Yang X, Shi R: Qingchang Wenzhong Decoction Alleviates DSS-Induced Inflammatory Bowel Disease by Inhibiting M1 Macrophage Polarization In Vitro and In Vivo. Biomed Res Int. 2022 Aug 25;2022:9427076. doi: 10.1155/2022/9427076. eCollection 2022. [PubMed:36060126 ]
Qin R, You FM, Zhao Q, Xie X, Peng C, Zhan G, Han B: Naturally derived indole alkaloids targeting regulated cell death (RCD) for cancer therapy: from molecular mechanisms to potential therapeutic targets. J Hematol Oncol. 2022 Sep 14;15(1):133. doi: 10.1186/s13045-022-01350-z. [PubMed:36104717 ]
Soundarya P, Sekar G: Cu-Catalyzed and iodine mediated synthesis of thioaurones via in situ C-S bond generation using xanthate as a sulfur surrogate. Org Biomol Chem. 2022 Sep 28;20(37):7405-7409. doi: 10.1039/d2ob01211a. [PubMed:36098267 ]
Baas J, Bieringer S, Frias C, Frias J, Soehnchen C, Urmann C, Ritter S, Riepl H, Prokop A: Dihydroxyquingdainone Induces Apoptosis in Leukaemia and Lymphoma Cells via the Mitochondrial Pathway in a Bcl-2- and Caspase-3-Dependent Manner and Overcomes Resistance to Cytostatic Drugs In Vitro. Molecules. 2022 Aug 8;27(15):5038. doi: 10.3390/molecules27155038. [PubMed:35956988 ]
Bajracharya R, Song JG, Lee SH, Jeong SH, Han HK: Enhanced Oral Bioavailability of MT-102, a New Anti-inflammatory Agent, via a Ternary Solid Dispersion Formulation. Pharmaceutics. 2022 Jul 21;14(7):1510. doi: 10.3390/pharmaceutics14071510. [PubMed:35890405 ]
Lee J, Kim J, Kim H, Park H, Kim JY, Kim EJ, Yang YH, Choi KY, Kim BG: Constructing multi-enzymatic cascade reactions for selective production of 6-bromoindirubin from tryptophan in Escherichia coli. Biotechnol Bioeng. 2022 Oct;119(10):2938-2949. doi: 10.1002/bit.28188. Epub 2022 Aug 4. [PubMed:35876239 ]
Zeng M, Zhong Y, Guo Z, Yang H, Zhu H, Zheng L, Diao Y: Expression and Functional Study of BcWRKY1 in Baphicacanthus cusia (Nees) Bremek. Front Plant Sci. 2022 Jul 1;13:919071. doi: 10.3389/fpls.2022.919071. eCollection 2022. [PubMed:35845683 ]
Ahmad SS, Khan H, Khalid M, Almalki AS: Emetine and Indirubin- 3- monoxime interaction with human brain acetylcholinesterase: A computational and statistical analysis. Cell Mol Biol (Noisy-le-grand). 2022 Jan 2;67(4):106-114. doi: 10.14715/cmb/2021.67.4.12. [PubMed:35809297 ]
Luo F, Li J, Liu J, Liu K: Stabilizing and upregulating Axin with tankyrase inhibitor reverses 5-fluorouracil chemoresistance and proliferation by targeting the WNT/caveolin-1 axis in colorectal cancer cells. Cancer Gene Ther. 2022 Nov;29(11):1707-1719. doi: 10.1038/s41417-022-00493-y. Epub 2022 Jun 24. [PubMed:35750753 ]
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LOTUS database [Link]

Showing NP-Card for 2'-hydroxy-1'h-[2,3'-biindol]-3-one (NP0283711)

MOL for NP0283711 (2'-hydroxy-1'h-[2,3'-biindol]-3-one)

3D MOL for NP0283711 (2'-hydroxy-1'h-[2,3'-biindol]-3-one)

3D SDF for NP0283711 (2'-hydroxy-1'h-[2,3'-biindol]-3-one)

3D-SDF for NP0283711 (2'-hydroxy-1'h-[2,3'-biindol]-3-one)

PDB for NP0283711 (2'-hydroxy-1'h-[2,3'-biindol]-3-one)

3D PDB for NP0283711 (2'-hydroxy-1'h-[2,3'-biindol]-3-one)

SMILES for NP0283711 (2'-hydroxy-1'h-[2,3'-biindol]-3-one)

INCHI for NP0283711 (2'-hydroxy-1'h-[2,3'-biindol]-3-one)

Structure for NP0283711 (2'-hydroxy-1'h-[2,3'-biindol]-3-one)

3D Structure for NP0283711 (2'-hydroxy-1'h-[2,3'-biindol]-3-one)