Scientific Reviews
Product Guides
Blogs
Topics
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
11 Results for "
indole ring
" in MedChemExpress (MCE) Product Catalog:
Products (11)
11 Results for "indole ring" in MCE Product Catalog:
Synonyms: Multhiomycin; RP 9671
Category:
Infection Microorganisms Antibiotics Animal Husbandry Disease Research Antibacterial Disease Research Fields Other Antibiotics
Target:
Cat. No.: HY-W048688
CAS No.: 1334509-86-2
Target:
Research Areas:
Fmoc-Trp(Me)-OH is an amino acid derivative. Fmoc-Trp(Me)-OH is formed by introducing a methyl group onto the nitrogen atom (N-1 position) of the indole ring of tryptophan (Trp) and protecting the amino group with Fmoc (9-fluorenylmethyloxycarbonyl). Fmoc-Trp(Me)-OH can be used in the synthesis of proteins or peptides .
Cat. No.: HY-W012848
CAS No.: 618-36-0
Synonyms: DL-α-Methylbenzylamine
Target:
Research Areas:
1-Phenylethanamine is a potential central nervous system stimulant and a related compound of β-phenylethylamine. Due to the replacement of its benzene ring with an indole group, its brain glycogenolytic activity is significantly reduced. Therefore, 1-Phenylethanamine can be used to study the impact of the chemical structure of phenylethylamine derivatives on central nervous system activity. In addition, 1-Phenylethanamine can also be used to synthesize the tyrosine kinase (tyrosine kinase) inhibitor CLM3 (HY-164413) .
Cat. No.: HY-N10117
CAS No.: 138250-72-3
Category:
Alkaloids Hordeum vulgare var. coeleste Linnaeus Gramineae Other Diseases Plants Disease Research Fields Indole Alkaloids
Target:
Cat. No.: HY-107486R
CAS No.: 56377-79-8
Synonyms: Multhiomycin (Standard); RP 9671 (Standard)
Category:
Microorganisms Antibiotics Animal Husbandry Disease Research Antibacterial Other Antibiotics
Target:
Cat. No.: HY-W007509
CAS No.: 5192-03-0
Synonyms: 5-Aminoindole
Cat. No.: HY-115004
CAS No.: 1006604-91-6
Target:
Research Areas:
MM-433593 is a potent and selective inhibitor of fatty acid amide hydrolase-1 (FAAH-1) that is orally administered to inhibit pain, inflammation, and related disorders. Pharmacokinetic studies of MM-433593 in macaques revealed a biphasic elimination profile with a rapid distribution phase and a slower elimination phase, with a systemic clearance of 8-11 mL/min/kg. MM-433593 exhibits moderate oral bioavailability (14-21%) and its metabolism primarily involves oxidation of the methyl group on the indole ring, resulting in a variety of sulfate, glucuronide, or glutathione-conjugated metabolites .
Cat. No.: HY-N19716
CAS No.: 34427-31-1
Category:
Target:
Target:
Category:
Target:
Cat. No.: HY-W115741S
CAS No.: 474267-40-8
Synonyms: (±)-1-Phenylethylamine-d3; DL-alpha-Methylbenzylamine-d3
- 1
-
-
Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
