19 Results for "

Oxcarbazepine

" in MedChemExpress (MCE) Product Catalog:
Products (19)

19 Results for "Oxcarbazepine" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-B0114
CAS No.: 28721-07-5
Synonyms: GP 47680
Research Areas:  

Neurological Disease Cancer

Oxcarbazepine is a sodium channel blocker . Oxcarbazepine significantly inhibits glioblastoma cell growth and induces apoptosis or G2/M arrest in glioblastoma cell lines . Anti-cancer and anticonvulsant effects .
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Cat. No.: HY-P1726
CAS No.: 1416983-77-1
MSG606 is a selective melanocortin 1 receptor (MC1R) antagonist. MSG606 can abolish the neuroprotective effects of BMS-470539 (HY-15616) (MC1R agonist). MSG606 can inhibit cancer cell proliferation and transition from the G1 to the S phase. MSG606 can delay pain hypersensitivity and reduce cholesterol levels. MSG606 can be used for the researches of cancer, inflammation, neurological and metabolic disease, such as breast cancer and subarachnoid hemorrhage (SAH) .
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Cat. No.: HY-B0114R
CAS No.: 28721-07-5
Synonyms: GP 47680 (Standard)
Oxcarbazepine (Standard) is the analytical standard of Oxcarbazepine. This product is intended for research and analytical applications. Oxcarbazepine is a sodium channel blocker . Oxcarbazepine significantly inhibits glioblastoma cell growth and induces apoptosis or G2/M arrest in glioblastoma cell lines . Anti-cancer and anticonvulsant effects .
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Cat. No.: HY-B0114S
CAS No.: 1020719-71-4
Synonyms: GP 47680-d4
Oxcarbazepine-d4 (GP 47680-D4) is the deuterium labeled Oxcarbazepine. Oxcarbazepine is a sodium channel blocker . Oxcarbazepine significantly inhibits glioblastoma cell growth and induces apoptosis or G2/M arrest in glioblastoma cell lines . Anti-cancer and anticonvulsant effects .
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Cat. No.: HY-B2124
CAS No.: 3564-73-6
Target:  

Drug Metabolite

Research Areas:  

Neurological Disease

10,11-Dihydrocarbamazepine is the active metabolite of Oxcarbazepine. 10,11-Dihydrocarbamazepine also is an intermediate. Oxcarbazepine is rapidly and almost completely converted to 10,11-Dihydrocarbamazepine with probable Anticonvulsant efficacy .
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Cat. No.: HY-B0114S2
CAS No.: 1261396-65-9
Synonyms: GP 47680-d8
Oxcarbazepine-d8-1 is a deuterium of Oxcarbazepine. Oxcarbazepine is a sodium channel blocker . Oxcarbazepine significantly inhibits glioblastoma cell growth and induces apoptosis or G2/M arrest in glioblastoma cell lines . Oxcarbazepine-d8-1 has anti-cancer and anticonvulsant effects .
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Cat. No.: HY-B0114S3
CAS No.: 2749432-28-6
Synonyms: GP 47680-d10
Oxcarbazepine-d10 (GP 47680-d10) is deuterium labeled Oxcarbazepine. Oxcarbazepine is a sodium channel blocker . Oxcarbazepine significantly inhibits glioblastoma cell growth and induces apoptosis or G2/M arrest in glioblastoma cell lines . Anti-cancer and anticonvulsant effects .
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Cat. No.: HY-B0114S1
CAS No.: 1134188-71-8
Synonyms: GP 47680-d4-1
Oxcarbazepine-d4-1 is deuterium labeled Oxcarbazepine. Oxcarbazepine is a sodium channel blocker . Oxcarbazepine significantly inhibits glioblastoma cell growth and induces apoptosis or G2/M arrest in glioblastoma cell lines . Anti-cancer and anticonvulsant effects .
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Cat. No.: HY-P0077
CAS No.: 1190083-57-8
Target:  

Oxytocin Receptor

Research Areas:  

Endocrinology

Merotocin is a selective, short-acting peptidic oxytocin receptor agonist. Merotocin can be used to support lactation .
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Cat. No.: HY-P1726A
MSG606 TFA is a selective melanocortin 1 receptor (MC1R) antagonist. MSG606 TFA can abolish the neuroprotective effects of BMS-470539 (HY-15616) (MC1R agonist). MSG606 TFA can inhibit cancer cell proliferation and transition from the G1 to the S phase. MSG606 TFA can delay pain hypersensitivity and reduce cholesterol levels. MSG606 TFA can be used for the researches of cancer, inflammation, neurological and metabolic disease, such as breast cancer and subarachnoid hemorrhage (SAH) .
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Cat. No.: HY-P0041A
Target:  

Vasopressin Receptor

Research Areas:  

Neurological Disease

F992 TFA is an antidiuretic peptide and vasopressin (antidiuretic hormone) analogue .
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Cat. No.: HY-B2124R
CAS No.: 3564-73-6
Research Areas:  

Neurological Disease

10,11-Dihydrocarbamazepine (Standard) is the analytical standard of 10,11-Dihydrocarbamazepine. This product is intended for research and analytical applications. 10,11-Dihydrocarbamazepine is the active metabolite of Oxcarbazepine. 10,11-Dihydrocarbamazepine also is an intermediate. Oxcarbazepine is rapidly and almost completely converted to 10,11-Dihydrocarbamazepine with probable Anticonvulsant efficacy .
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Cat. No.: HY-W424831
CAS No.: 537693-29-1
Synonyms: 11-Keto Oxcarbazepine
Target:  

Drug Intermediate

Research Areas:  

Others

Oxcarbazepine impurity 3 (11-Keto Oxcarbazepine) is an impurity of Oxcarbazepine.
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Cat. No.: HY-W012373
CAS No.: 4698-11-7
Target:  

Drug Intermediate

Research Areas:  

Others

Oxcarbazepine impurity 1 is an impurity of Oxcarbazepine.
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Cat. No.: HY-W103288
CAS No.: 21737-58-6
Target:  

Drug Intermediate

Research Areas:  

Others

Oxcarbazepine impurity 2 is an impurity of Oxcarbazepine.
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Cat. No.: HY-P2331
CAS No.: 59165-34-3
Synonyms: Antibiotic A 3802-IV-3; Gardimycin
Target:  

Antibiotic

Research Areas:  

Infection

Actagardin is a tetracyclic lantibiotic produced by several species of Actinoplanes. It is composed of macrocyclic rings formed by thioether bridges. Actagardin preferably targets Gram-positive bacteria, inhibiting the synthesis of peptidoglycan.
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Cat. No.: HY-P10014
CAS No.: 153507-46-1
Target:  

Inhibitory Antibodies

Research Areas:  

Cardiovascular Disease

Bibapcitide, a 26 amino acid, inhibits thrombosis .
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Cat. No.: HY-P0041
CAS No.: 162277-99-8
Target:  

Vasopressin Receptor

Research Areas:  

Neurological Disease

F992 is an antidiuretic peptide and vasopressin (antidiuretic hormone) analogue .
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Cat. No.: HY-P11823
Target:  

Fluorescent Dye

Research Areas:  

Inflammation/Immunology Cancer

FAPα/DPP4 fluorogenic substrate-1 is a fluorogenic macrocyclic peptide substrate that can be cleaved by FAPα and DPP4. FAPα/DPP4 fluorogenic substrate-1 can be used in the research of cancer and type 2 diabetes .
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