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 (73781):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-102057
    Felcisetrag 916075-84-8 99.94%
    Felcisetrag (TD-8954) is an orally active, potent and selective 5-HT4 receptor agonist with gastrointestinal prokinetic properties. Felcisetrag has high affinity (pKi =9.4) for human 5-HT4(c) receptors.
    Felcisetrag
  • HY-103158
    BW B70C 134470-38-5 98%
    BW B70C is a potent, selective and orally activearachidonic acid 5-lipoxygenase inhibitor. BW B70C inhibits both acute and allergic bronchoconstriction and late-phase eosinophil accumulation subsequent to allergen inhalation in guinea-pigs. BW B70C prevents leukotriene C4 synthesis and reduces leucocyte migration to the airways lumen as well as albumin microvascular leakage. BW B70C has the potential for the research of anti-asthma agent.
    BW B70C
  • HY-103305
    cis-Ned19 1137264-00-6 99.25%
    cis-Ned19 is an irreversible nicotinic acid adenine dinucleotide phosphate (NAADP) antagonist. cis-Ned19 localizes to lysosomes and endolysosomal vesicles, stains two-pore calcium channels and fluorescently labels NAADP receptors (Ex/Em = 365/410 nm).
    cis-Ned19
  • HY-103455
    ZK164015 177583-70-9 99.94%
    ZK164015 is an estrogen-glucocorticoid receptor chimera that can be used as a compound screening tool to evaluate tissue-selective estrogen activity. ZK164015 was used to evaluate its effects on ER function in osteoblasts in studies based on green fluorescent protein (GFP)-receptor chimeras. In osteoblast-like (ROS and U2OS) and breast cancer (MCF7) cells, ZK164015 showed different effects in response to ER agonists, including modulation of ERE-luc activity and effects on nuclear mobility.
    ZK164015
  • HY-103613
    Thalidomide-O-amido-C4-NH2 TFA 1799711-25-3 99.92%
    Thalidomide-O-amido-C4-NH2 TFA (Cereblon Ligand-Linker Conjugates 6 TFA) is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology.
    Thalidomide-O-amido-C4-NH2 TFA
  • HY-104017
    DMT-2'-O-MOE-rA(Bz) phosphoramidite 251647-53-7 ≥98.0%
    DMT-2'-O-MOE-rA(Bz) phosphoramidite is an adenine nucleoside analog. DMT-2'-O-MOE-rA(Bz) phosphoramidite can be used in research on oligonucleotide synthesis.
    DMT-2'-O-MOE-rA(Bz) phosphoramidite
  • HY-104056
    Fura Red 149732-62-7 98%
    Fura Red is a Ca2+-sensitive fluorescent dye, which decreases in fluorescence with rising [Ca2+].
    Fura Red
  • HY-10569S
    Ponesimod-d4 98%
    Ponesimod-d4 (ACT-128800-d4) is the deuterium labeled Ponesimod (HY-10569). Ponesimod (ACT-128800) is a potent, selective and orally active agonist of S1P1, with an IC50 of 6 nM in a radioligand binding assay. Ponesimod activates S1P1-mediated signal transduction with high potency (EC50=5.7 nM). Ponesimod can protect against lymphocyte-mediated tissue inflammation.
    Ponesimod-d4
  • HY-106873
    Nepinalone 22443-11-4 98%
    Nepinalone, an alchilaminate derivative of β-tetralone and an orally active cough suppressant, possesses a non-opioid antitussive activity.
    Nepinalone
  • HY-107210
    Avenasterol 23290-26-8 98.90%
    Avenasterol is a natural sterol isolated from seed oils of Testouri and Jebali cultivars.
    Avenasterol
  • HY-107242
    Raddeanoside R8 124961-61-1 99.76%
    Raddeanoside R8 is a saponin that can be isolated from fresh rhizoma of Anemone raddeana Regel.
    Raddeanoside R8
  • HY-107330
    (6R,7S)-Cefminox sodium heptahydrate 92636-39-0 98.19%
    (6R,7S)-Cefminox sodium heptahydrate is an isomer of Cefminox sodium heptahydrate. Cefminox sodium heptahydrate is a β-lactam cephalosporin antibiotic, which exhibits a broad spectrum of antibacterial activity.
    (6R,7S)-Cefminox sodium heptahydrate
  • HY-107538
    YE120 383124-82-1 99.80%
    YE120 is a potent GPR35 agonist with an EC50 of 32.5 nM.
    YE120
  • HY-107570
    IWP-12 688353-45-9 ≥99.0%
    IWP-12 is a potent inhibitor of porcupine (PORCN) and inhibits cell-autonomous Wnt signaling with an IC50 of 15 nM.
    IWP-12
  • HY-107820
    Ethylvanillin acetate 72207-94-4 99.65%
    Ethyl vanillin acetate is acectate form of ethyl vanillin. Ethyl vanillin acetate is a flavorant used in chocolate or candy.
    Ethylvanillin acetate
  • HY-107832
    Ketoisophorone 1125-21-9 99.90%
    Ketoisophorone (4-Oxoisophorone) is the active small molecule that can be used as building block.
    Ketoisophorone
  • HY-107840
    RGW-611 6497-78-5 98.16%
    RGW 611 is a morpholine derivative that enhances radiation-induced cell death of hypoxic V79-379A cells. RGW 611 also stimulates fatty acid synthesis.
    RGW-611
  • HY-107870
    1,2,4-Triazole-3-carboxylic acid, 97% 4928-87-4 98%
    1,2,4-Triazole-3-carboxylic acid, 97% is a biochemical assay reagent.
    1,2,4-Triazole-3-carboxylic acid, 97%
  • HY-107950
    Invert sugar 8013-17-0 99.1%
    Invert sugar is a mixture of dextrose and levulose. Invert sugar is formed when sucrose is split in two by an enzyme or acid. Invert sugar can be used as a sweetener.
    Invert sugar
  • HY-108299
    Perfluamine 338-83-0 98.0%
    Perfluamine (Perfluorotripropylamine), a hydrophobic carrier fluid, is used in the surface modification of droplet polymeric microfluidic devices. Perfluamine has a role as a blood substitute.
    Perfluamine