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Home > Indoles and Oxindole > 2380-94-1
2380-94-1 | 4-Hydroxyindole
CAS No: 2380-94-1 Catalog No: AG0037R9 MDL No:MFCD00005667
Product Description
Catalog Number:
AG0037R9
Chemical Name:
4-Hydroxyindole
CAS Number:
2380-94-1
Molecular Formula:
C8H7NO
Molecular Weight:
133.1473
MDL Number:
MFCD00005667
IUPAC Name:
1H-indol-4-ol
InChI:
InChI=1S/C8H7NO/c10-8-3-1-2-7-6(8)4-5-9-7/h1-5,9-10H
InChI Key:
NLMQHXUGJIAKTH-UHFFFAOYSA-N
SMILES:
Oc1cccc2c1cc[nH]2
EC Number:
219-177-2
UNII:
1W4VD9085V
Properties
Complexity:
126
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
133.053g/mol
Formal Charge:
0
Heavy Atom Count:
10
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
2
Isotope Atom Count:
0
Molecular Weight:
133.15g/mol
Monoisotopic Mass:
133.053g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
36A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.4
Literature
| Title | Journal |
|---|---|
| Exploration of natural compounds as sources of new bifunctional scaffolds targeting cholinesterases and beta amyloid aggregation: the case of chelerythrine. | Bioorganic & medicinal chemistry 20121115 |
| Prospective acetylcholinesterase inhibitory activity of indole and its analogs. | Bioorganic & medicinal chemistry letters 20120415 |
| Fluorescence-based high-throughput screening assay for drug interactions with UGT1A6. | Assay and drug development technologies 20111001 |
| Glucuronidation of psilocin and 4-hydroxyindole by the human UDP-glucuronosyltransferases. | Drug metabolism and disposition: the biological fate of chemicals 20100301 |
| Bicyclic compounds repress membrane vesicle production and Pseudomonas quinolone signal synthesis in Pseudomonas aeruginosa. | FEMS microbiology letters 20100301 |
| Inhibitory effect of hydroxyindoles and their analogues on human melanoma tyrosinase. | Zeitschrift fur Naturforschung. C, Journal of biosciences 20100101 |
| Halogenated indole alkaloids from marine invertebrates. | Marine drugs 20100101 |
| Synthesis of indoleamine 2,3-dioxygenase inhibitory analogues of the sponge alkaloid exiguamine A. | Journal of medicinal chemistry 20080508 |
| Synthesis and biological evaluation of novel angular fused Pyrrolocoumarins. | Journal of enzyme inhibition and medicinal chemistry 20080201 |
| Indoloxypropanolamine analogues as 5-HT(1A) receptor antagonists. | Bioorganic & medicinal chemistry letters 20071015 |
| Inhibition of amyloid fibril formation and cytotoxicity by hydroxyindole derivatives. | Biochemistry 20060418 |
| Protein engineering of toluene ortho-monooxygenase of Burkholderia cepacia G4 for regiospecific hydroxylation of indole to form various indigoid compounds. | Applied microbiology and biotechnology 20050101 |
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