12 Results for "

N-dealkylation

" in MedChemExpress (MCE) Product Catalog:
Products (12)

12 Results for "N-dealkylation" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-B2023
CAS No.: 15545-48-9
Synonyms: Chlortoluron
Research Areas:  

Others

Chlorotoluron (Chlortoluron) is a urea herbicide. Chlorotoluron serves as a degradation substrate that undergoes dissipation in soil and produces demethylated chlorotoluron metabolites via N-dealkylation. Chlorotoluron is used for pre-emergence and post-emergence weed control in cereals and various other crops .
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Cat. No.: HY-77910
CAS No.: 57988-58-6
Synonyms: BPHP
Target:  

Drug Metabolite

Research Areas:  

Neurological Disease

4-(4-Bromophenyl)-4-hydroxypiperidine (BPHP) is a metabolite of Bromperidol (BRO) (HY-B0901) and is produced by N-dealkylation of BRO .
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Cat. No.: HY-B1547A
CAS No.: 5633-14-7
Synonyms: R4929; Dioxatrine
Target:  

mAChR

Research Areas:  

Neurological Disease

Benzetimide hydrochloride (R4929) is a blood-brain barrier-permeable muscarinic acetylcholine receptor antagonist. Benzetimide hydrochloride blocks cholinergic receptor sites. Benzetimide hydrochloride induces mydriasis, prevents acetylcholine-induced muscle contraction, inhibits pilocarpine (HY-B0726A)-induced parasympathomimetic effects, and exhibits antisecretory activity. Benzetimide hydrochloride can be used in research related to Parkinson's disease .
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Cat. No.: HY-15899
CAS No.: 1192224-24-0
Research Areas:  

Infection

Des(benzylpyridyl) Atazanavir (compound M1) is a N-dealkylation product of Atazanavir (HY-17367) metabolite. Atazanavir is a highly selective HIV-1 protease inhibitor. Des(benzylpyridyl) Atazanavir may contribute to the effectiveness Atazanavir but also to the toxicity and interactions. Des(benzylpyridyl) Atazanavir can be used for further research of Atazanavir effects .
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Cat. No.: HY-105894
CAS No.: 102251-91-2
Research Areas:  

Metabolic Disease

SC-42867 is a PGE2 antagonist. SC-42867 can be metabolized in the liver through oxidative N-dealkylation, aromatic hydroxylation, and binding reactions. SC-42867 can be used for research on metabolic conditions .
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Cat. No.: HY-B1547AR
CAS No.: 5633-14-7
Synonyms: R4929 (Standard); Dioxatrine (Standard)
Research Areas:  

Neurological Disease

Benzetimide hydrochloride (Standard) (R4929 (Standard); Dioxatrine (Standard)) is the analytical standard of Benzetimide hydrochloride (HY-B1547A). This product is intended for research and analytical applications. Benzetimide hydrochloride (R4929) is a blood-brain barrier-permeable muscarinic acetylcholine receptor antagonist. Benzetimide hydrochloride blocks cholinergic receptor sites. Benzetimide hydrochloride induces mydriasis, prevents acetylcholine-induced muscle contraction, inhibits pilocarpine (HY-B0726A)-induced parasympathomimetic effects, and exhibits antisecretory activity. Benzetimide hydrochloride can be used in research related to Parkinson's disease .
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Cat. No.: HY-184428
Target:  

PROTACs Ser/Thr Kinase

Research Areas:  

Endocrinology

PROTAC TSSK1 Degrader-1 is a TSSK1 PROTAC degrader with a DC50 of 10.8 nM and an IC50 of 56.8 nM. PROTAC TSSK1 Degrader-1 reduces sperm motility and impairs in vitro fertilization capacity. PROTAC TSSK1 Degrader-1 undergoes metabolic N-dealkylation and exhibits high efflux properties. PROTAC TSSK1 Degrader-1 is applicable to studies related to male fertility .
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Cat. No.: HY-184464
Target:  

PROTACs Ser/Thr Kinase

Research Areas:  

Endocrinology

PROTAC TSSK1 Degrader-2 is a cereblon-recruiting PROTAC degrader targeting TSSK1, with a DC50 of 10.8 nM and an IC50 of 56.8 nM against TSSK1. PROTAC TSSK1 Degrader-2 recruits the cereblon E3 ubiquitin ligase to induce proteasomal degradation of TSSK1. PROTAC TSSK1 Degrader-2 reduces the motility and in vitro fertilization capacity of mouse sperm. PROTAC TSSK1 Degrader-2 undergoes metabolic N-dealkylation and exhibits high efflux. PROTAC TSSK1 Degrader-2 can be used in studies related to male fertility .
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Cat. No.: HY-187120
CAS No.: 1422528-30-0
Target:  

Cytochrome P450

Research Areas:  

Cancer

PAIB-SOs-12 is a CYP1A1-activated antimitotic prodrug with affinity for human CYP1A1, with a Ki value of 1.2 μM. PAIB-SOs-12 exhibits nanomolar antiproliferative activity in cancer cells expressing CYP1A1, with a selectivity ratio of over 100 against cancer cells that do not express CYP1A1. PAIB-SOs-12 undergoes CYP1A1-mediated N-dealkylation to form the active metabolite PIB-SO, which induces G2/M cell cycle arrest and microtubule disruption, and shows significantly improved stability in rodent liver microsomes compared to its n-butyl analog. PAIB-SOs-12 can be used in breast cancer-related research .
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Cat. No.: HY-180471
CAS No.: 1361197-33-2
Target:  

Drug Metabolite

Research Areas:  

Others

Desisopropyl-fesoterodine (compound 1), an oxidative Ndealkylation of the tertiary amine function of Fesoterodine (HY-70053), is a degradation product (compound PP-6) of Fesoterodine .
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Cat. No.: HY-77833
CAS No.: 143782-20-1
Research Areas:  

Endocrinology Cancer

RU 56279 is an androgen receptor (AR) antagonist with strong and systemic anti-androgenic activity. RU 56279 is also a common, potent and long-lasting anti-androgen metabolite of RU 56187 (HY-117486) and RU 58841 (HY-10561) in vivo. RU 56279 can be used as an AR ligand to construct an AR-targeted prodrug system for the study of AR-positive tumor cells .
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Cat. No.: HY-W714180
CAS No.: 27218-04-8
Research Areas:  

Others

Desmethyl-formamido-pirimicarb is an intermediate metabolite of Pirimicarb (HY-119419). Desmethyl-formamido-pirimicarb is detected in both Pirimicarb-exposed soil environments and advanced oxidation water treatment processes .
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