2. Others

Others

Others

Related Products

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There are a number of inhibitors, agonists, and antagonists which we cannot make precise classification because the research area is still unknown.

Others Related Products (73764):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-Z9976
    Aripiprazole impurity 5 1424857-63-5 98%
    Aripiprazole impurity 5 is an impurity of Aripiprazole.
    Aripiprazole impurity 5
  • HY-Z9999
    Amikacin impurity 2 1793053-92-5 98%
    Amikacin impurity 2 (compound Impurity VI) is an impurity of Amikacin (HY-B0509A) identified in Amikacin sulfate (HY-107813).
    Amikacin impurity 2
  • HY-100042
    Ketoprofen impurity 9 21288-34-6 98%
    Ketoprofen impurity 9 is an impurity of Ketoprofen.
    Ketoprofen impurity 9
  • HY-100067
    Quetiapine impurity 1 1076199-40-0 98%
    Quetiapine impurity 1 is an impurity of Quetiapine (HY-14544).
    Quetiapine impurity 1
  • HY-100082
    Irbesartan impurity 3 748812-53-5 98%
    Irbesartan impurity 3 is an impurity of Irbesartan.
    Irbesartan impurity 3
  • HY-100175
    Guanidinoethyldisulfide bicarbonate 348079-19-6 98%
    Guanidinoethyldisulfide bicarbonate is a peroxynitrite scavenger.
    Guanidinoethyldisulfide bicarbonate
  • HY-10021R
    Varenicline Tartrate (Standard) 375815-87-5 98%
    Varenicline (Tartrate) (Standard) is the analytical standard of Varenicline (Tartrate). This product is intended for research and analytical applications. Varenicline (CP 526555) is an orally active partial agonist of α4β2 nicotinic acetylcholine receptor (α4β2 nAChR, IC50 = 250 nM), which is the principal mediator of nicotine dependence. Varenicline is also a partial agonist of α6β2 nAChR and a full agonist of α6β2 nAChR. Varenicline blocks the direct agonist effects of nicotine on nAChR while stimulates nAChR in a more moderate way, being widely used as an aid of smoking cessation.
    Varenicline Tartrate (Standard)
  • HY-100230
    ML-133 185669-79-8 98%
    ML133 is a selective Kir2 family channels inhibitor, with an IC50 of 1.8 μM at pH 7.4 and 290 nM at pH 8.5.
    ML-133
  • HY-100926
    MDL 72832 hydrochloride 113777-40-5 98%
    MDL 72832 (hydrochloride) is a 2,3-dihydro-1,4-benzodioxane derivative and a 5-HT1a receptor ligand with high affinity for the 5-HT1a receptor.
    MDL 72832 hydrochloride
  • HY-101434
    Cetamolol 34919-98-7 98%
    Cetamolol is an active compound.
    Cetamolol
  • HY-101875
    Bumetanide impurity 7 153012-65-8 98%
    Bumetanide impurity 7 is an impurity of Bumetanide.
    Bumetanide impurity 7
  • HY-101904
    2-Chloro-2'-deoxycytidine 10212-19-8 98%
    2-Chloro-2'-deoxycytidine is a cytidine nucleoside analog. Cytidine analogs have a mechanism of inhibiting DNA methyltransferases (such as Zebularine, HY-13420), and have potential anti-metabolic and anti-tumor activities.
    2-Chloro-2'-deoxycytidine
  • HY-10201B
    Sorafenib impurity 3 1431697-81-2 99.93%
    Sorafenib impurity 3 is an impurity of Sorafenib (HY-10201).
    Sorafenib impurity 3
  • HY-10280S
    YM-60828-d3 1794812-00-2 98%
    YM-60828-d3 is the deuterium labeled YM-60828 (HY-10280). YM-60828 is an orally active, selective and competitive factor Xa inhibitor with a Ki of 1.3 nM and an IC50 of 2.3 nM. YM-60828 inhibits thrombus formation and platelet aggregation. YM-60828 can be used for the research of venous thrombosis, arterial thrombosis, and thromboembolic disorders.
    YM-60828-d3
  • HY-103008
    Annulatin 1486-67-5 98%
    Annulatin (3-O-Methylmyricetin) is an α-helical peptide. Annulatin shows histamine releasing activity from mast cells and low hemolytic activity.
    Annulatin
  • HY-10360S
    (Rac)-Letermovir-d6 1961287-47-7
    (Rac)-Letermovir-d6 is the deuterium labeled (Rac)-Letermovir.
    (Rac)-Letermovir-d6
  • HY-104046
    Octaaminocryptand 1 135469-17-9 98%
    Octaaminocryptand 1 is a macrobicyclic azacryptand is reasonably well preorganized for complexation.
    Octaaminocryptand 1
  • HY-10448S
    (E/Z)-Capsaicin-d3 1185237-43-7 98%
    (E/Z)-Capsaicin-d3 is the deuterium labeled (E/Z)-Capsaicin[1].
    (E/Z)-Capsaicin-d3
  • HY-105120
    Vapiprost 85505-64-2 98%
    Vapiprost (GR 32191) is a thromboxane A2 receptor (TXA2 Receptor) antagonist. Vapiprost hydrochloride (GR 32191 hydrochloride) inhibits the aggregation and ATP release stimulated with U-46619, collagen or arachidonic acid (AA) at an IC50 of less than 2.1×10-8 M.
    Vapiprost
  • HY-105186
    Mapinastine 140945-32-0 98%
    Mapinastine is a biochemical assay reagent.
    Mapinastine