2. Signaling Pathways
  3. Others
  4. Others

Others

 
Cat. No. Product Name Effect Purity Chemical Structure
  • HY-16147
    Combretastatin A1 phosphate
    		98.00%
    Combretastatin A1 phosphate (Oxi4503; CA1P; Combretastatin A1 diphosphate) is a potent vascular disruptive agent. Combretastatin A1 phosphate exerts anti-angiogenic effects on tumors. Combretastatin A1 phosphate has the potential for the research of pancreatic neuroendocrine tumors.
    Combretastatin A1 phosphate
  • HY-108322
    NBTGR
    		Inhibitor 99.13%
    NBTGR (p-Nitrobenzylthioguanosine) is a potent inhibitor of nucleoside transport; inhibits adenosine uptake with a Ki of 70 nM.
    NBTGR
  • HY-P991631
    Human IgG1 (L234F/L235E/P331S) kappa, Isotype Control
    Human IgG1 (L234F/L235E/P331S) kappa, Isotype Control, a human-derived antibody, is an isotype control for human IgG1 (L234F/L235E/P331S)κ antibody.
    Human IgG1 (L234F/L235E/P331S) kappa, Isotype Control
  • HY-Y1876
    Guaiacol Carbonate
    		99.89%
    Guaiacol Carbonate acts as an expectorant by virtue of a reflex from the stomach by way of the afferent gastric nerves to the medullary centres and thenperipherally again to the respiratory tract.
    Guaiacol Carbonate
  • HY-W193844
    MLS001006105
    MLS001006105 is used for biological test against the protein target: lamin isoform A-delta10.
    MLS001006105
  • HY-B1179
    Dipyrocetyl
    		98.69%
    Dipyrocetyl is an anti-inflammatory and analgesic agent extracted from patent WO 2011132171 A1.
    Dipyrocetyl
  • HY-157269
    J10-1
    J10-1 is a hapten. J10-1 promotes peptide exchange of all DR alleles (DR1, DR2, DR4 (DRB1*0401)) and promotes peptide binding to MHC II, which can be used in the study of immune regulation.
    J10-1
  • HY-16403
    Polythiazide
    		98.22%
    Polythiazide is a potent and orally active thiazide diuretic agent that has antihypertensive effect. Polythiazide can decrease edema and decrease blood pressure. Polythiazide also has phototoxicity.
    Polythiazide
  • HY-132888
    NCATS-SM4487
    NCATS-SM4487 is a highly selective unique dihydropyrimidine inhibitor against GALK1, with an IC50 value of 0.05 μM.
    NCATS-SM4487
  • HY-147064
    DL-4-Hydroxy-2-ketoglutarate lithium
    DL-4-Hydroxy-2-ketoglutarate lithium is the substrate of 4-hydroxy-2-oxoglutarate aldolase (HOGA). DL-4-Hydroxy-2-ketoglutarate lithium can be cleaved by HOGA to produce pyruvate and glyoxylate.
    DL-4-Hydroxy-2-ketoglutarate lithium
  • HY-116780A
    Prothipendyl hydrochloride
    		Inhibitor 99.9%
    Prothipendyl hydrochloride is a tricyclic azaphenothiazine neuroleptic agent. Prothipendyl hydrochloride is a substrate of the CYP isozymes CYP1A2, CYP2D6, CYP2C19 and CYP3A4. Prothipendyl hydrochloride has sedating and psychomotorically damping effects. Prothipendyl hydrochloride can be used for psychomotoric agitation, sleep disorder and anxiety research .
    Prothipendyl hydrochloride
  • HY-162735
    BRD5080
    BRD5080 is a potent GPR65 positive allosteric modulator. BRD5080 induces GPR65-dependent cAMP production. BRD5080 exhibits a robust induction of cAMP activity and recruits G protein for the WT and variant hGPR65 as well as for the mouse ortholog. BRD5080 has the potential for autoimmune and inflammatory diseases research.
    BRD5080
  • HY-P3040A
    PHI-27 (rat) TFA
    PHI-27 (rat) TFA is a 27 amino acid peptide.PHI-27 (rat) TFA is used to find peptide hormones and other active peptides.
    PHI-27 (rat) TFA
  • HY-U00383
    Rafigrelide
    Rafigrelide is a platelet-lowering agent, and also has antithrombotic properties.
    Rafigrelide
  • HY-N2570
    Corytuberine
    Corytuberine is an aporphine alkaloid found in Dicranostigma leptopodum. Corytuberine displays cytotoxicity against SMMC-7721 tumor cells.
    Corytuberine
  • HY-160438A
    PBX-7011 mesylate
    		Inhibitor
    PBX-7011 mesylate is an active Camptothecin (HY-16560) derivative. PBX-7011 can bind to the DDX5 protein in cells, thereby inducing cell death through DDX5 protein degradation.
    PBX-7011 mesylate
  • HY-P11051
    GE11, Cys Conjugated
    GE11, Cys Conjugated is a peptide conjugate. GE11, Cys Conjugated consists of a GE11 (HY-P10128) conjugated with a GGGGC sequence. GE11, Cys Conjugated can be used for synthesis of stimuli-responsive peptide nanomaterials (SRPNs) for photoacoustic imaging and cancer therapy, such as triple-negative breast cancer (TNBC)
    GE11, Cys Conjugated
  • HY-150252
    ATIC-IN-1
    		99.69%
    ATIC-IN-1(compound 14) is an inhibitor targeting to Aminoimidazole carboxamide ribonucleotide transformylase/inosine monophosphate cyclohydrolase (ATIC) dimerization with a Ki value of 685 nM. ATIC dimerization is crucial for its aminoimidazole carboxamide ribonucleotide (AICAR) transformylase activity. ATIC-IN-1 exhibits anti-tumor activity via reduction in cell numbers and cell division rates.
    ATIC-IN-1
  • HY-W005637
    Orthocaine
    		99.81%
    Orthocaine is a local agent that can suppress or relieve pain (extracted from patent WO2002089849A1).
    Orthocaine
  • HY-N1131A
    Triacetonamine hydrochloride
    		≥98.0%
    Triacetonamine (2,2,6,6-Tetramethyl-4-piperidone) hydrochloride is used as an intermediate for the synthesis of pharmaceutical products, pesticides and photostabilizers for polymers. Triacetonamine hydrochloride has oral activity and can induce acute liver failure (ALF) in rats.
    Triacetonamine hydrochloride
Cat. No. Product Name / Synonyms Application Reactivity