午夜插插,噜噜噜影院,啪啪伊人网,欧美熟夫,景甜吻戏视频,男人强操性感蕾丝美女视频在线网站,日本美女跳舞视频

Welcome to chemicalbook!
+1 (818) 612-2111
RFQ
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

RFQ
skype
MY Account
Top
Postion:Product Catalog >Biochemical Engineering>Inhibitors>Neuronal Signaling>Histamine Receptor agonists>Histamine dihydrochloride
Histamine dihydrochloride
  • Histamine dihydrochloride

Histamine dihydrochloride NEW

Price $38
Package 500mg
Min. Order:
Supply Ability: 10g
Update Time: 2025-07-22

Product Details

Product Name: Histamine dihydrochloride CAS No.: 56-92-8
Purity: 100.00% Supply Ability: 10g
Release date: 2025/07/22

Product Introduction

Bioactivity

NameHistamine dihydrochloride
DescriptionHistamine dihydrochloride (Ceplene) is dihydrochloride form of Histamine. Histamine is an organic nitrogen compound which is a powerful stimulant of gastric secretion, a constrictor of bronchial smooth muscle, a vasodilator, and also a centrally acting neurotransmitter.
In vitroHistamine suppresses the generation of ROS through the Histaminetype-2 receptor (H2 receptor).[1] Histamine inhibits the generation and release of reactive oxygen species (ROS) by monocytes/macrophages (MO) during respiratory burst. Histamine and interleukin-2 (IL-2) act synergistically to activate NK cell cytotoxicity (NKCC). Histamine combined with IL-2 might improve response rates and disease-free survival by protecting the cells of the immune system from oxidative stress and inducing natural endogenous immune cytotoxicity. [2]
In vivoHistamine treatment (0.5 mg/kg or 5.0 mg/kg, twice daily) protects against liver injury as evident by normal serum transaminase levels and significantly reduced liver pathology scores in a rat model with early alcohol-induced liver injury. The protective effect of histamine is blocked by Ranitidine (10 mg/kg), an H2 receptor antagonist, indicating that the histamine effect is predominantly mediated through the H2 receptor. [1] Histamine (30 pg/rat, icv) increases both 3,4-dihydroxyphenylalanine accumulation and 3,4-dihydroxyphenylalanine acid concentrations in the nucleus accumbens in male rats, and this effect is not affect by H2 antagonist zolantidine, indicating that histamine stimulates mesolimbic DA neurons through an action at the H1 receptor. [3] Histamine (0.5 mg/kg s.c.) reduces the liver tumour weight by 46% and subcutaneous tumour weight by 41% versus rats receiving subcutaneous saline injections. The anti-tumour effect observed by subcutaneous histamine injections is inhibited by Ranitidine (50 mg/kg s.c.) in rats sarcoma. [4] Histamine (1000 mg/kg s.c.) displays acute tissue damage after 24 hours and indications of pathological inflammation at the injection sites at 5 days and 28 days in Sprague-Dawley rats. Histamine (1000 mg/kg s.c.) results in Cmax of 167 mM, tmax of 0.5 hour, t1/2 of 0.95 and AUC of 186 mmol-h/L in male Sprague-Dawley rats. [5]
StoragePure form: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility InformationH2O : 18.4 mg/mL (99.96 mM), Sonication is recommended.
DMSO : 70 mg/mL (380.29 mM), Sonication is recommended.
KeywordsInhibitor | inhibit | HistamineReceptor | Histamine Receptor | Histamine dihydrochloride | Histamine Dihydrochloride | Histamine | H2 receptor | H1 receptor | EndogenousMetabolite | Endogenous Metabolite
Inhibitors RelatedSucrose | Cysteamine hydrochloride | D(+)-Raffinose pentahydrate | Daidzein | Guanidine hydrochloride | Ferulic Acid | Glycerol | Thymidine | Naringin | Alginic acid | 3-Indoleacetic acid | Oxalic acid
Related Compound LibrariesPain-Related Compound Library | Bioactive Compound Library | Membrane Protein-targeted Compound Library | EMA Approved Drug Library | Anti-Viral Compound Library | Natural Product Library | FDA-Approved Drug Library | Natural Product Library for HTS | Bioactive Compounds Library Max | GPCR Compound Library | Anti-Cancer Drug Library | Anti-Cancer Active Compound Library

Company Profile Introduction

Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers. TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.

You may like

Recommended supplier

Product name Price   Suppliers Update time
$/
VIP5Y
RongNa Biotechnology Co.,Ltd
2025-04-29
$1.00/1KG
VIP7Y
Hebei Chuanghai Biotechnology Co., Ltd
2024-10-24
$60.00/1kg
Hebei Zhuanglai Chemical Trading Co.,Ltd
2024-06-04
$339.00/1kg
VIP5Y
Shanghai UCHEM Inc.
2023-11-16
$260.00/1ton
VIP4Y
Hebei Dangtong Import and export Co LTD
2023-09-14
$0.00/1g
VIP3Y
shandong perfect biotechnology co.ltd
2023-08-22
$0.00/1kg
VIP3Y
Henan Aochuang Chemical Co.,Ltd.
2022-09-30
$0.00/1KG
Honest Joy Holdings Limited
2022-02-18
$100.00/25Kg/Bag
VIP6Y
Hebei Mujin Biotechnology Co.,Ltd
2021-10-14
$0.00/1Kg/Bag
VIP5Y
WUHAN FORTUNA CHEMICAL CO., LTD
2021-08-23
  • Since: 2011-01-07
  • Address: 36 Washington Street, Wellesley Hill, USA
INQUIRY