2. Signaling Pathways
  3. Others
  4. Others

Others

 
Cat. No. Product Name Effect Purity Chemical Structure
  • HY-167273
    4-Methyldecane
    4-Methyldecane is a branched saturated hydrocarbon found in the Dufour gland of Formica lemani workers.
    4-Methyldecane
  • HY-N10637
    N-Acetyldopamine dimer-1
    N-Acetyldopamine dimer-1 is a 2-(3',4'-dihydroxyphenyl)-1,4-benzodioxane derivative. N-Acetyldopamine dimer-1 is optically active, can be isolated from crude agent "Zentai," a cast-off shell of the cicada of Cryptotympana sp. (Cicadidae).
    N-Acetyldopamine dimer-1
  • HY-N19883
    Drim-9(11)-en-8α-ol
    Drim-9(11)-en-8α-ol is a pimarane-type sesquiterpenol. Drim-9(11)-en-8α-ol can be generated via saponification of drim-9(11)-en-8α-yl acetate.
    Drim-9(11)-en-8α-ol
  • HY-151121
    Anticancer agent 80
    Anticancer agent 80 (Compound 3c) is an anticancer agent. Anticancer agent 80 exhibits the dark cytotoxicity against T47-D with IC50 of 10.14 µM.
    Anticancer agent 80
  • HY-148969
    FPPS-IN-1
    FPPS-IN-1 is a potent non-bisphosphonate Farnesyl pyrophosphate synthase (FPPS) inhibitor with an IC50 0.2 μM. FPPS-IN-1 can be used for the research of cancers.
    FPPS-IN-1
  • HY-116220
    Mcl1-IN-14
    Mcl1-IN-14 (compound 5) is a reversible covalent inhibitor of Mcl-1 with the activity of inhibiting Mcl-1. Mcl1-IN-14 covalently targets the non-catalytic lysine side chain of Mcl-1 and has higher potency than non-covalent counterparts, which can be used to develop Mcl-1 inhibitory compounds and study related biological phenomena.
    Mcl1-IN-14
  • HY-119681
    YM 11124
    YM 11124 is an orally active selective immunosuppressive agent. YM 11124 can inhibit cell-mediated immune responses (type IV allergic reactions, such as delayed-type hypersensitivity and allogenic skin graft rejection) and type III allergic reactions (such as passive Arthus reaction). YM 11124 has no effect on type I, type II allergic reactions or acute inflammation. YM 11124 can be used in research related to organ transplantation and immune hypersensitivity.
    YM 11124
  • HY-N9304
    Fern-7-en-19α-ol
    Fern-7-en-19α-ol (9a-Hydroxyferna-7,9(11)-diene) is a triterpenoid compound isolated from Adiantum caudatum.
    Fern-7-en-19α-ol
  • HY-109036A
    (S)-Landipirdine
    (S)-Landipirdine ((S)-RO5025181), a selective and potent 5-HT6R antagonist, significantly impacts the hERG pharmacophore and serves as a valuable tool for investigating neurological disorders, particularly within the context of Alzheimer's disease.
    (S)-Landipirdine
  • HY-149077
    2′-Deoxy-5-methoxyuridine
    2′-Deoxy-5-methoxyuridine is a uridine analogue. Uridine has potential antiepileptic effects, and its analogs can be used to study anticonvulsant and anxiolytic activities, as well as to develop new antihypertensive agents.
    2′-Deoxy-5-methoxyuridine
  • HY-165469
    Methetoin
    Methetoin is an anticonvulsant.
    Methetoin
  • HY-159820
    Veonetinib
    		Inhibitor
    Veonetinib (example 3) is a potent inhibitor of tyrosine kinase, with the IC50 of 0.1 μM and 0.4 μM in A549 cells and LOVO cells, respectively.
    Veonetinib
  • HY-147053
    2-(Diethylamino)ethyl (3-(octyloxy)phenyl)carbamate hydrochloride
    2-(Diethylamino)ethyl (3-(octyloxy)phenyl)carbamate hydrochloride is a small molecule compound.
    2-(Diethylamino)ethyl (3-(octyloxy)phenyl)carbamate hydrochloride
  • HY-155726
    Cy-FBP/SBPase-IN-1
    Cy-FBP/SBPase-IN-1 (compound S5) is a Cy-FBP/SBPase inhibitor, which is an important regulatory enzyme in cyanobacterial photosynthesis. Thus Cy-FBP/SBPase-IN-1 inhibits Calvin cycle and photosystem, and decreases photosynthetic efficiency in cyanobacterial photosynthesis. Cy-FBP/SBPase-IN-1 potently inhibits the growth of cyanobacteria, as well as Synechocystis sp.PCC6803. Cy-FBP/SBPase-IN-1 shows safety profile in human-derived cells and zebrafish models.
    Cy-FBP/SBPase-IN-1
  • HY-W353225
    Pyricarbate
    Pyricarbate (Pyridinol carbamate) is an orally active 2,6-pyridine dimethanol biscarbamate with cholesterol-lowering and antiatherosclerotic effects.
    Pyricarbate
  • HY-183624
    Trimer44NMe
    Trimer44NMe is a polyamine transport inhibitor (PTI). Trimer44NMe inhibits the polyamine transport of putrescine (Put), spermidine (Spd), and spermine (Spm). Trimer44NMe can be used for research of Pancreatic ductal adenocarcinoma (PDAC).
    Trimer44NMe
  • HY-N1676
    2′,3,5,6′,7-Pentahydroxyflavanone
    2′,3,5,6′,7-Pentahydroxyflavanone (compound 4) is a flavonoid compound isolated from Scutellaria baicalensis roots.
    2′,3,5,6′,7-Pentahydroxyflavanone
  • HY-119775
    U92016A
    U92016A is a potent and selective agonist of the 5-HT1A receptor, with activities such as high affinity binding to the 5-HT1A receptor in vitro, causing a decrease in body temperature in vivo, and high potency and high intrinsic activity as an agonist in single-cell firing studies.
    U92016A
  • HY-159837
    Nispomeben
    		Inhibitor
    Nispomeben is a potent non-opioid pain relief drug.
    Nispomeben
  • HY-183806
    ANTXR1-IN-1
    ANTXR1-IN-1 is a ANTXR1 inhibitor with a Ka of 2.88 μM for hANTXR1, and exhibits anti-tumor cell activity. ANTXR1-IN-1 undergoes acylation with Ser229 of ANTXR1, thereby inhibiting tumor cell proliferation. ANTXR1-IN-1 induces G2/M phase arrest and apoptosis in tumor cells. ANTXR1-IN-1 can be used for research on melanoma, non-small cell lung cancer, hepatocellular carcinoma, and colorectal cancer.
    ANTXR1-IN-1
Cat. No. Product Name / Synonyms Application Reactivity