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 (73784):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-D0043
    5(6)-ROX 198978-94-8 98.50%
    5(6)-ROX (5(6)-Carboxy-X-rhodamine) is a nucleic acid fluorescent label which can be used as a reference dye for real-time polymerase chain reaction (Em/Ex = 605/585 nm).
    5(6)-ROX
  • HY-D0833
    Tricalcium phosphate 7758-87-4 98.00%
    Tricalcium phosphate is a kind of biological materials or organic compounds that are widely used in life science research.
    Tricalcium phosphate
  • HY-D2250
    Disulfo-ICG carboxylic acid 2757507-18-7
    Disulfo-ICG carboxylic acid is a derivative of ICG dye. ICG (Indocyanine Green) is a NIR fluorescent dye.
    Disulfo-ICG carboxylic acid
  • HY-I0167
    1-(2-(4-(Chloromethyl)phenoxy)ethyl)azepane hydrochloride 223251-25-0 99.77%
    1-(2-(4-(Chloromethyl)phenoxy)ethyl)azepane hydrochloride is a drug intermediate for synthesis of various active compounds.
    1-(2-(4-(Chloromethyl)phenoxy)ethyl)azepane hydrochloride
  • HY-I0459
    Apixaban impurity 41 503614-92-4 99.88%
    Apixaban impurity 41 is an impurity of Apixaban (HY-50667).
    Apixaban impurity 41
  • HY-N3666
    Cycloeucalenol 469-39-6
    Cycloeucalenol is a triterpenoid compound derived from Eucalyptus microcorys.
    Cycloeucalenol
  • HY-N8433
    Dhurrin 499-20-7 98.67%
    Dhurrin is a cyanogenic glucoside isolated from Sorghum.
    Dhurrin
  • HY-Y0793
    Mesalazine impurity 2 3970-35-2 99.60%
    Mesalazine impurity 2 is an impurity of Mesalazine.
    Mesalazine impurity 2
  • HY-Y0880
    Rivaroxaban impurity 48 109-11-5 98%
    Rivaroxaban impurity 48 is an impurity of Rivaroxaban.
    Rivaroxaban impurity 48
  • HY-Z0022
    Nintedanib impurity 4 380427-39-4 99.73%
    Nintedanib impurity 4 is an impurity of Nintedanib (HY-50904).
    Nintedanib impurity 4
  • HY-Z0465
    Methyl 2-tert-Butyloxycarbonylaminoacrylate 55477-80-0
    Methyl 2-tert-Butyloxycarbonylaminoacrylate is a drug impurity.
    Methyl 2-tert-Butyloxycarbonylaminoacrylate
  • HY-Z0533
    3-ethoxy-4-hydroxybenzonitrile 60758-79-4 98%
    3-ethoxy-4-hydroxybenzonitrile is a drug impurity.
    3-ethoxy-4-hydroxybenzonitrile
  • HY-Z0840
    1-(4-(Benzyloxy)phenyl)-2-bromopropan-1-one 35081-45-9 99.83%
    1-(4-(Benzyloxy)phenyl)-2-bromopropan-1-one (4'-Benzyloxy-2-bromopropiophenone) is a drug intermediate for synthesis of various active compounds.
    1-(4-(Benzyloxy)phenyl)-2-bromopropan-1-one
  • HY-103015
    WZ4141 1222776-76-2
    WZ4141 is an intermediate in the synthesis of compounds.
    WZ4141
  • HY-118292
    Hydroquinone diacetate 1205-91-0 98.30%
    Hydroquinone diacetate (1,4-Diacetoxybenzene) is a diester product and also a commonly used synthetic intermediate for agrochemicals and fine chemicals. Hydroquinone diacetate can be produced via the acetylation of hydroquinone (HY-B0951) with acetic anhydride.
    Hydroquinone diacetate
  • HY-118622
    Isogentisin 491-64-5
    Isogentisin is a cell protector. Isogentisin can shield human umbilical vein endothelial cells (HUVEC) from cell death caused by H202 and UV exposure. Isogentisin can also prevent endothelial damage triggered by smoking by activating cell repair functions to promote cell survival.
    Isogentisin
  • HY-120354
    YU142670 133847-06-0 99.50%
    YU142670 is an inhibitor of OCRL/INPP5B with IC50 values of 0.71 μM and 1.78 μM respectively.
    YU142670
  • HY-121337
    Flurochloridone 61213-25-0 99.61%
    Flurochloridone (R-40244) is a selective preemergence and persistent herbicide. Flurochloridone induces endoplasmic reticulum (ER) stress and activated unfolded protein response (UPR) signaling pathways. Flurochloridone impairs cell viability and induces cytotoxicity and apoptosis mediated by ER stress via activating eIF2α-ATF4/ATF6-CHOP-Bim/Bax signaling pathways in TM4 cells.
    Flurochloridone
  • HY-124795
    FPMINT 924866-33-1 99.0%
    FPMINT is a potent, irreversible and non-competitive inhibitor of Equilibrative nucleoside transporters (ENTs), which is more selective to ENT2 than to ENT1. FPMINT plays an important role in uridine uptake.
    FPMINT
  • HY-127061
    Palmitoleoyl ethanolamide 94421-67-7 99.77%
    Palmitoleoyl ethanolamide (POEA) is an endogenous fatty amide with biological activity.
    Palmitoleoyl ethanolamide