1. Others

Others

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 (73919):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-126054
    A1062 1821-13-2 98%
    A1062 is an inhibitor for Tn3 encoded resolvase with IC50 in micromolar level. A1062 suppresses the binding of resolvase proteins to res sites, and blocks resolvase-induced site-specific recombination.
    A1062
  • HY-126056
    3-Ethoxyphenol 621-34-1 98%
    3-Ethoxyphenol (Resorcinol monoethyl ether) is a phosphine ligand that can be used to evaluate the hydrogen bond acceptor ability of solutes.
    3-Ethoxyphenol
  • HY-126057AS
    (S)-Praziquantel-d11 2699607-88-8 98.23%
    (S)-Praziquantel-d11 is the deuterium labeled (S)-Praziquantel. (S)-Praziquantel, a toxic enantiomerof Praziquantel, is ineffective against worms.
    (S)-Praziquantel-d11
  • HY-126069
    15(R)-Iloprost 85026-51-3 98%
    15(R)-Iloprost is the unnatural or inverted C-15 epimer of lloprost (HY-A0096).
    15(R)-Iloprost
  • HY-126083
    17β-Hydroxywortmannin 58053-83-1 98%
    17β-Hydroxywortmannin (Wortmannin-17β-ol) is an orally active inhibitor for phosphatidylinositol-3-kinase (PI-3-kinase) with an IC50 of 0.5 nM, suppresses the osteoclast resorption with an IC50 of 10 nM. 17β-Hydroxywortmannin exhibits antitumor activity.
    17β-Hydroxywortmannin
  • HY-126115
    15(S)-Latanoprost 145773-22-4 98%
    15(S)-Latanoprost is an analog of latanoprost in which the hydroxyl at carbon 15 is inverted relative to latanoprost. The IC50 values for the free acid forms of latanoprost and 15(S)-latanoprost were determined to be 3.6 nM and 24 nM, respectively, in a FP receptor binding assay using the cat iris sphincter muscle. A 3 μg dose of 15(S)-latanoprost caused a 1 mmHg reduction of IOP in normotensive cynomolgus monkeys.
    15(S)-Latanoprost
  • HY-12613
    2-C-methylene-myo-inositol oxide 4068-87-5 98%
    2-C-methylene-myo-inositol oxide (NSC 45109), an inositol derivative, induces pseudohyphae formation in Saccharomyces spp.
    2-C-methylene-myo-inositol oxide
  • HY-126150
    Flucetosulfuron 412928-75-7 98%
    LGC-42153 is a new sulfonylurea herbicide.
    Flucetosulfuron
  • HY-126182S3
    Deacetyldiltiazem-d6 hydrochloride 1309283-22-4 98%
    Deacetyldiltiazem-d6 (hydrochloride) is the deuterium labeled Deacetyldiltiazem hydrochloride.
    Deacetyldiltiazem-d6 hydrochloride
  • HY-126182S4
    Desacetyl Diltiazem-d4 hydrochloride 98%
    Desacetyl Diltiazem-d4 (hydrochloride) is the deuterium labeled Desacetyl Diltiazem hydrochloride.
    Desacetyl Diltiazem-d4 hydrochloride
  • HY-126199R
    Tetrachlorvinphos (Standard) 22248-79-9
    Tetrachlorvinphos (Standard) is the analytical standard of Tetrachlorvinphos. This product is intended for research and analytical applications. Tetrachlorvinphos is an organophosphorus pesticide that has the activity of inhibiting cholinesterase. Tetrachlorvinphos is used as a pesticide, mainly for the control of pests. Tetrachlorvinphos has low toxicity to mammals.
    Tetrachlorvinphos (Standard)
  • HY-126199S
    (Z)-Tetrachlorvinphos-d6 2734300-40-2 98%
    (Z)-Tetrachlorvinphos-d6 is the deuterium labeled Tetrachlorvinphos (HY-126199). Tetrachlorvinphos is an organophosphorus pesticide that has the activity of inhibiting cholinesterase. Tetrachlorvinphos is used as a pesticide, mainly for the control of pests. Tetrachlorvinphos has low toxicity to mammals.
    (Z)-Tetrachlorvinphos-d6
  • HY-126209
    Isomaltol 3420-59-5 98%
    Isomaltol is a furan compound. Isomaltol can be produced by the Maillard reaction.
    Isomaltol
  • HY-126230
    PAT-494 1781233-84-8 98%
    PAT-494 is an ATX inhibitor with significant activity in biochemical and plasma assays. PAT-494 can reduce LPA levels in rat plasma through oral administration. The structure-activity relationship study of PAT-494 shows that its binding mode with ATX is novel and it can effectively occupy the hydrophobic pockets and channels of ATX.
    PAT-494
  • HY-12625
    MIV-6 1560968-27-5 98%
    MIV-6 is a small molecule inhibitor that inhibits menin-mixed lineage leukemia (MLL) interaction and exhibits strong selective activity in MLL leukemia cells with IC50 = 56 nM.
    MIV-6
  • HY-12629
    PF470 1539296-45-1 98%
    PF470 (PF-06297470) is a negative allosteric modulator of metabotropic glutamate receptor 5 (mGluR5) with significant efficacy in Parkinson's disease models, but clinical development was halted due to potential issues found in toxicology studies.
    PF470
  • HY-126369
    Exametazime 105613-48-7 98%
    Exametazime (HM-PAO) is a lipophilic agent used for the preparation of brain imaging radiopharmaceuticals. 99Tcm-Exametazime is an effective in vitro leukocyte labeling agent.
    Exametazime
  • HY-126376
    Iso-​H7 dihydrochloride 140663-38-3 99.06%
    Iso-​H7 dihydrochloride is an inhibitor of protein kinase with IC50 values of 22 and 34 μM to PKC and PKA respectively. Iso-H7 dihydrochloride has negative control of PKA on satellite cell myogenesis.
    Iso-​H7 dihydrochloride
  • HY-126386A
    Pectinase, aspergillus acne 9032-75-1 98%
    Pectinase, aspergillus aculeatus is a pectin-degrading enzyme with the activity of catalyzing the decomposition of pectin into galacturonic acid. Pectinase, aspergillus aculeatus can be applied in a variety of industrial fields, including juice extraction and clarification, vegetable oil extraction, wine clarification, cocoa and coffee fermentation, paper bleaching, plant fiber degumming, cotton bioscouring, bioenergy production, wastewater treatment, and use as a poultry feed additive to reduce feed viscosity.
    Pectinase, aspergillus acne
  • HY-126418
    Methyl 3-O-feruloylquinate 154418-15-2 98%
    Methyl 3-O-feruloylquinate is a natural product that can be isolated from the roots of Murraya exotica.
    Methyl 3-O-feruloylquinate