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
48 Results for "
hypothalamus
" in MedChemExpress (MCE) Product Catalog:
Products (48)
48 Results for "hypothalamus" in MCE Product Catalog:
29
29
Category:
12
12 Cited Publications
Synonyms: BMS-927711; BHV-3000
Target:
Research Areas:
Rimegepant (BMS-927711; BHV-3000) is an orally bioavailable and blood-brain barrier permeable antagonist of CGRP and AMY1 receptors, with a pIC50 of 8.01 and a Ki of 0.027 nM for human CGRP receptors. Rimegepant antagonizes cAMP production induced by αCGRP, βCGRP and amylin at CGRP and AMY1 receptors in humans, rats and mice, as well as at rat AMY3 receptors. Rimegepant can be used in research related to migraine .
7
7 Cited Publications
Cat. No.: HY-B1811
CAS No.: 11000-17-2
Synonyms: Arginine vasopressin; Antidiuretic hormone
Target:
4
4 Cited Publications
Cat. No.: HY-P2161B
Target:
Research Areas:
1
1 Cited Publications
Cat. No.: HY-P1502
CAS No.: 61214-51-5
Target:
Research Areas:
1
1 Cited Publications
Target:
Research Areas:
JNJ-31020028 is a selective and brain penetrant antagonist of neuropeptide Y Y2 receptor with pIC50 values of 8.07 and 8.22 for human and rat Y2 receptor, respectively. JNJ-31020028 can be used for the research of nervous disease .
Category:
Target:
Cat. No.: HY-B0451AR
CAS No.: 62-31-7
Synonyms: ASL279 (Standard)
Cat. No.: HY-P3561A
Target:
Research Areas:
Cat. No.: HY-P0243
CAS No.: 86073-88-3
Synonyms: Salmon GnRH; Salmon gonadotropin-releasing hormone; sGnRH
Target:
Research Areas:
Cat. No.: HY-B0451AS7
CAS No.: 2193106-55-5
Synonyms: ASL279-d5 hydrochloride
Cat. No.: HY-N0046
CAS No.: 88105-29-7
Synonyms: Notoginseng triterpenes; Ginsenoside Mb
Cat. No.: HY-B1811AS1
Synonyms: Arginine vasopressin-d5 TFA; Antidiuretic hormone-d5 TFA
Cat. No.: HY-W1015419
CAS No.: 73804-75-8
Synonyms: α-Fluoromethylhistidine
Target:
Research Areas:
α-FMH (α-Fluoromethylhistidine) is an orally active histidine decarboxylase inhibitor. α-FMH depletes histamine in enterochromaffin-like (ECL) cells, reduces the number and volume density of secretory vesicles in ECL cells, and does not affect histamine storage in mast cells. α-FMH abolishes Omeprazole (HY-B0113)-induced vacuolization of ECL cells and decreases gastrin-induced histamine efflux from ECL cells. α-FMH does not alter the granular characteristics of ECL cells, omeprazole-induced hypertrophy of ECL cells, gastrin-induced pancreastatin-like immunoreactivity efflux, nor does it affect gastric acid secretion induced by histamine or vagal stimulation. α-FMH inhibits basal and gastrin-stimulated gastric acid secretion, reduces acid output induced by gastrin+IBMX (HY-12318), but does not directly affect acid generation in isolated parietal cells .
Cat. No.: HY-P1025A
Target:
Research Areas:
Cat. No.: HY-W747297
CAS No.: 17066-67-0
Cat. No.: HY-P3561
Target:
Research Areas:
Cat. No.: HY-P3675
CAS No.: 51776-33-1
Target:
Research Areas:
Cat. No.: HY-P3674
CAS No.: 38482-71-2
Target:
Research Areas:
-
-
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
