Isatin, also known as tribulin, is an organic compound derived from indole with formula C8H5NO2. The compound was first obtained by Otto Linné Erdman and Auguste Laurent in 1840 as a product from the oxidation of indigo dye by nitric acid and chromic acids.
Isatin is a well-known natural product which can be found in plants of the genus Isatis, in Couroupita guianensis, and also in humans, as a metabolic derivative of adrenaline.
It looks like a red-orange powder, and it is usually employed as building block for the synthesis of a wide variety of biologically active compounds including antitumorals, antivirals, anti-HIVs, and antituberculars.
The isatin core is also responsible for the color of “Maya blue” and “Maya yellow” dyes. |
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InChI=1S/C13H14N2/c14-12-5-1-10(2-6-12)9-11-3-7-13(15)8-4-11/h1-8H,9,14-15H2 |
YBRVSVVVWCFQMG-UHFFFAOYSA-N |
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Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
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carcinogenic agent
A role played by a chemical compound which is known to induce a process of carcinogenesis by corrupting normal cellular pathways, leading to the acquistion of tumoral capabilities.
allergen
A chemical compound, or part thereof, which causes the onset of an allergic reaction by interacting with any of the molecular pathways involved in an allergy.
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View more via ChEBI Ontology
4,4'-Diaminodiphenylmethane
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KEGG COMPOUND
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4,4'-Diaminodiphenylmethane
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ChemIDplus
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4,4'-Diphenylmethanediamine
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ChemIDplus
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4,4'-Methylenebis(benzeneamine)
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ChemIDplus
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4,4'-methylenedianiline
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ChEMBL
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4-(4-aminobenzyl)aniline
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ChEMBL
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α-(p-aminophenyl)-p-toluidine
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NIST Chemistry WebBook
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Bis(4-aminophenyl)methane
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ChemIDplus
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Bis(p-aminophenyl)methane
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ChemIDplus
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bis-p-aminophenylmethane
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ChEBI
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DADPM
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NIST Chemistry WebBook
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DAPM
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NIST Chemistry WebBook
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DDM
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NIST Chemistry WebBook
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di-(4-aminophenyl)methane
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ChEBI
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di-(p-aminophenyl)methane
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ChEBI
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Dianilinomethane
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ChemIDplus
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p,p'-Diaminodiphenylmethane
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ChemIDplus
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p,p'-Methylenedianiline
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ChemIDplus
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101-77-9
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CAS Registry Number
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NIST Chemistry WebBook
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101-77-9
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CAS Registry Number
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ChemIDplus
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474706
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Reaxys Registry Number
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Reaxys
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17061110
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PubMed citation
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Europe PMC
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17482318
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PubMed citation
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ChEMBL
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18844695
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PubMed citation
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Europe PMC
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22393703
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PubMed citation
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Europe PMC
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2607764
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PubMed citation
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Europe PMC
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7265110
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PubMed citation
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ChEMBL
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9022650
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PubMed citation
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Europe PMC
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