171 Results for "

Side effects

" in MedChemExpress (MCE) Product Catalog:
Products (171)

171 Results for "Side effects" in MCE Product Catalog:

Cat. No.: HY-106983
CAS No.: 192057-17-3
Research Areas:  

Inflammation/Immunology

GR 250495X is an inhaled glucocorticoid receptor agonist. GR 250495X is designed as a antedrug, which takes effect locally in the lungs but is rapidly metabolized and inactivated in the bloodstream after entering the systemic circulation, thereby minimizing systemic side effects. GR 250495X can be used in asthma research .
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Cat. No.: HY-19233
CAS No.: 155210-57-4
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

BAM-1110 is a dopamine receptor agonist. BAM-1110 exhibits dose-dependent antiparkinsonian activity in MPTP (HY-W114750)-treated monkey models of Parkinson's disease. BAM-1110 has minimal side effects and can be used for the research of Parkinson's disease and other neurological disorders .
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Cat. No.: HY-121841
CAS No.: 35482-50-9
Synonyms: O-1821; CBD-C1
Target:  

TRP Channel

Research Areas:  

Inflammation/Immunology Cancer

Cannabidiorcol (CBDO, CBD-C1, O-1821) is related to cannabidiol, with the pentyl side chain shortened to a methyl group. Cannabidiorcol has low affinity for cannabinoid receptors (CBs) and is an agonist of the transient receptor potential channel (TRP channel), through which it produces antiinflammatory effects, but can also promote tumorigenesis at high concentrations .
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Cat. No.: HY-109747
CAS No.: 261956-22-3
Target:  

MMP

Research Areas:  

Cancer

RO-28-2653 is an orally active matrix metalloproteinase (MMP) inhibitor. RO-28-2653 exhibits highly selective inhibitory effects on MMP2, MMP9 and membrane-type 1-MMP, and may reduce side effects (such as musculoskeletal pain) compared to broad-spectrum MMP inhibitors. RO-28-2653 shows significant tumor growth inhibition in a rat prostate model. RO-28-2653 can be used in studies of hormone-sensitive tumors .
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Cat. No.: HY-155313
Research Areas:  

Cancer

β-Glucuronide-NB-bis[N(Me)-methyl ester]-MMAE (compound 20) is auristatins-glucuronide conjugate. Antitumor agent-122 shows in vitro antiproliferative activities against β-glucuronidase pretreated and untreated cancer cells with an IC50 value of 5.7 nM - 9.7 nM. Antitumor agent-122 shows potent antitumor efficacy in HCT-116 xenograft mouse model without inducing side effects .
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Cat. No.: HY-118499
CAS No.: 81982-32-3
Synonyms: RIV-2093
Target:  

Drug Derivative

Research Areas:  

Endocrinology

Alpiropride (RIV-2093) is a metoclopramide (HY-17382) analog that is effective in reducing the gastrointestinal side effects of cancer chemotherapy drugs. In animal studies, alpiropride showed a stronger antiemetic effect than metoclopramide .
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Cat. No.: HY-123352A
Purity:  98.92%
(-)-ZK 216348 is the enantiomer of (+)-ZK 216348 (HY-123352). (+)-ZK 216348 is a nonsteroidal selective glucocorticoid receptor agonist with an IC50 of 20.3 nM. ZK 216348 also binds to Progesterone and mineralocorticoid receptors with IC50s of 20.4 nM and 79.9 nM, respectively. ZK 216348 has antiinflammatory activity similar to Prednisolone and induces less transactivation-mediated side effects .
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Cat. No.: HY-138110
CAS No.: 19804-27-4
Purity:  97.23%
Synonyms: 4-Methyldiphenhydramine
Toladryl is a derivative of Diphenhydramine (HY-B0303), capable of penetrating the blood-brain barrier and possessing oral activity, as well as antihistamine and anticholinergic activities. The anticholinergic activity of Toladryl is approximately one-tenth that of Diphenhydramine (HY-B0303), and its protective effect against lethal doses of histamine in guinea pigs is 2 to 4 times that of Diphenhydramine (HY-B0303). The side effects of Toladryl are fewer and milder than those of Diphenhydramine (HY-B0303), but at higher doses, it may cause central nervous system symptoms such as insomnia, agitation, and disorientation. Toladryl can be used for research in allergic diseases .
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Cat. No.: HY-138110R
CAS No.: 19804-27-4
Synonyms: 4-Methyldiphenhydramine (Standard)
Toladryl (Standard) is the analytical standard of Toladryl. This product is intended for research and analytical applications. Toladryl is a derivative of Diphenhydramine (HY-B0303), capable of penetrating the blood-brain barrier and possessing oral activity, as well as antihistamine and anticholinergic activities. The anticholinergic activity of Toladryl is approximately one-tenth that of Diphenhydramine (HY-B0303), and its protective effect against lethal doses of histamine in guinea pigs is 2 to 4 times that of Diphenhydramine (HY-B0303). The side effects of Toladryl are fewer and milder than those of Diphenhydramine (HY-B0303), but at higher doses, it may cause central nervous system symptoms such as insomnia, agitation, and disorientation. Toladryl can be used for research in allergic diseases .
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Cat. No.: HY-U00020
CAS No.: 287399-47-7
Target:  

Drug Derivative

Research Areas:  

Metabolic Disease

AU-224 is a benzamide derivative used as a promising gastrointestinal prokinetic agent without significant side effects.
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Cat. No.: HY-122461
CAS No.: 116-49-4
Target:  

Parasite

Research Areas:  

Infection

Glycobiarsol is an organic arsenical compound, which can be used as an amoebicidal agent. Glycobiarsol exhibits toxicity and side effects .
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Cat. No.: HY-139735
CAS No.: 2847856-44-2
Target:  

Drug Intermediate

Research Areas:  

Cancer

Antitumor agent-29 is a novel hepatocyte-targeting antitumor proagent, which exhibits good antitumor activity and low toxic side effects.
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Cat. No.: HY-W373206
CAS No.: 6503-95-3
Research Areas:  

Metabolic Disease

Triampizine is a potent gastric antisecretory agent without the side effects of anticholinergic drugs. Triampizine may react with the excipient magnesium stearate and is used in studies of hyperacidity .
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Cat. No.: HY-124406
CAS No.: 869802-44-8
Target:  

mGluR

Research Areas:  

Neurological Disease

A-794282 is a compound with analgesic activity and is a selective mGlu1 receptor antagonist that significantly reduces pain behaviors in a postoperative pain model, but motor side effects may occur at higher doses.
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Cat. No.: HY-144769
CAS No.: 2921601-78-5
Target:  

Topoisomerase

Research Areas:  

Cancer

SDOX is the Doxorubicin (DOX) proagent. The loaded DOX proagents (SDOX) which can release the parent agents DOX triggered by excessive GSH in tumor cells, minimize the unexpected side effects on normal tissues without compromising the potency .
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Cat. No.: HY-130587
CAS No.: 57775-27-6
Synonyms: Piperazine sultosylate; A-585
Target:  

LDLR Apolipoprotein

Research Areas:  

Metabolic Disease

Sultosilic acid piperazine salt (Piperazine sultosylate; A-585) is a lipid-lowering agent. Sultosilic acid piperazine salt modifies the blood lipids levels, reduces platelet adhesiveness without promoting peroxisomal activity of hepatocytes or producing other adverse side-effects .
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Cat. No.: HY-129451
CAS No.: 805326-00-5
Target:  

GABA Receptor

Research Areas:  

Others

HIE-124 is a potent ultra-short acting hypnotic that exhibits a rapid onset of action and a shorter duration of action with no acute tolerance or noticeable side effects. HIE-124 is promising for research of preanesthetic medication and anesthesia inducer .
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Cat. No.: HY-19846
CAS No.: 869493-26-5
Synonyms: PRX-03140 potassium salt
Target:  

5-HT Receptor

Research Areas:  

Others

VRX-03011 (PRX-03140 (potassium salt)) is a compound with the potential to enhance memory and regulate acetylcholine release. It is a 5-HT? agonist that can enhance memory, regulate hippocampal acetylcholine efflux, and regulate APP metabolism without gastrointestinal side effects.
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Cat. No.: HY-117091
CAS No.: 1538586-09-2
DDD-028 is a potent non-opioid, non-cannabinoid analgesic which attenuates neuropathic and inflammatory pain without the possible side effects or abuse potential associated with opioid or cannabinoid activities. DDD-028 can be utilized in analgesic research .
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Cat. No.: HY-162421
Target:  

Herbicide

Research Areas:  

Others

SL antagonist 1 (Compound D12) is strigolactones antagonists and can strongly interact with SL receptor proteins.SL antagonist 1 can combat root-parasitic weed infestations. SL antagonist 1 has no side effects on the germination or seedling growth .
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