1. Signaling Pathways
  2. Others
  3. Others

Others

 
Cat. No. Product Name Effect Purity Chemical Structure
  • HY-76222
    Isatoic anhydride
    98.23%
    Isatoic anhydride is a molecule with a structure similar to trans-bis-isatoic anhydride (TBIA), but has only one reactive group. Isatoic anhydride forms monoadducts.
    Isatoic anhydride
  • HY-156777
    Antiproliferative agent-36
    ≥98.0%
    Antiproliferative agent-36 (compound 8i) is a benzothiazolyl hydrazones derived compound with antiproliferative activity. Antiproliferative agent-36 has a broad-spectrum anticancer activity.
    Antiproliferative agent-36
  • HY-136433
    N,N'-Dinitrosopiperazine
    99.94%
    N,N'-Dinitrosopiperazine (1,4-Dinitrosopiperazine; DNP) is a carcinogen with specificity for nasopharyngeal epithelium and facilitates NPC metastasis. N,N'-Dinitrosopiperazine regulates multiple signaling pathways through protein phosphorylation, including LYRIC at serine 568.
    N,N'-Dinitrosopiperazine
  • HY-109151
    Milategrast
    99.94%
    Milategrast is useful as cell adhesion inhibitor or cell infiltration inhibitor. Milategrast in vitro inhibites the adhesion of Jurkat cells to human fibronectin with an IC50 of <5 μM.
    Milategrast
  • HY-153366
    TNG-0746132
    99.66%
    TNG-0746132 can be used for synthesis of the compound with anticancer activity.
    TNG-0746132
  • HY-161303
    ZNF207-IN-1
    98.03%
    ZNF207-IN-1 (compound C16) is a potent inhibitor of Zinc Finger Protein 207 (ZNF207), with IC50 values ranging from 0.5–2.5 μM for inhibiting sphere formation and 0.5–15 μM for cytotoxicity. ZNF207-IN-1 exhibites efficient permeability across the blood–brain barrier.
    ZNF207-IN-1
  • HY-P10629
    PSMα2
    98.81%
    PSMα2 is a potent PSM (phenol-soluble modulin) peptide toward mouse neutrophils, led to strong influx of leukocytes.
    PSMα2
  • HY-162448
    SerBut
    99.92%
    SerBut is a serine conjugated butyrate prodrug with oral activity. SerBut has anti-inflammatory activity.
    SerBut
  • HY-155181
    hCES2-IN-1
    98.18%
    hCES2-IN-1 (Compound 24) is a reversible and selective hCES2 inhibitor (IC50: 6.72 μM). hCES2-IN-1 reduces the level of hCES2 in living cells. hCES2-IN-1 is effective against Irinotecan (HY-16562)-induced delayed diarrhea and DSS-induced ulcerative colitis.
    hCES2-IN-1
  • HY-150013
    H-Met-Met-OH
    98.11%
    H-Met-Met-OH (L-Methionyl-L-methionine) is a dipeptide composed of two methionine residues.
    H-Met-Met-OH
  • HY-112722
    Neurotoxin Inhibitor
    99.02%
    Neurotoxin Inhibitor is a neurotoxin inhibitor.
    Neurotoxin Inhibitor
  • HY-108751
    Aripiprazole Lauroxil
    99.70%
    Aripiprazole lauroxil, an N-acyloxymethyl proagent of Aripiprazole (HY-14546), is a Long-acting injectable (LAI) typical antipsychotic for schizophrenia and a ligand of dopamine receptor D2R/D4R. Aripiprazole lauroxil is cleaved by body’s enzyme esterase to N-hydroxymethyl aripiprazole (plus lauric acid) and then to aripiprazole (plus formaldehyde), no toxicity.
    Aripiprazole Lauroxil
  • HY-119694
    Rotenolone
    Rotenolone is an antiproliferative agent. Rotenolone shows antiproliferative activity against the ovarian cancer A2780, breast cancer BT-549, prostate cancer DU 145, NSCLC NCI-H460, and colon cancer HCC-2998 cell lines, with IC50s of 0.95, 1.6, 2.7, 2.0, and 2.9 μM, respectively.
    Rotenolone
  • HY-158424
    LSN3353871
    99.62%
    LSN3353871 is a potent inhibitor of lipoprotein(a) (Lp(a)) that can binds to Kringle IV (KIV) 8, KIV7–8 and KIV5–8, with Kd of 756 nM, 605 nM and 423 nM, respectively. LSN3353871 disrupts the formation of Lp(a) with the IC50 of 1.69 µM. LSN3353871 has oral bioactivity.
    LSN3353871
  • HY-W104477
    3-Fluoro-L-tyrosine
    99.73%
    3-Fluoro-L-tyrosine is a tyrosine analogue, inhibits transamination by tyrosine aminotransferase (TAT). And 3-FluoroL-tyrosine has been shown to be biologically incorporated into proteins in place of tyrosine. 3-Fluoro-L-tyrosine pretends to be the substrate of rat liver tyrosine aminotransferase, markedly disturbs the Tyr-TAT association.
    3-Fluoro-L-tyrosine
  • HY-B0544
    Sodium Picosulfate
    ≥98.0%
    Sodium Picosulfate (Sodium Picosulphate) is a contact irritant laxative with oral activity. Sodium Picosulfate inhibits the absorption of water and electrolytes, increasing their production. Sodium Picosulfate can be used in colonoscopy applications.
    Sodium Picosulfate
  • HY-154992
    2,4-Difluorophenylethynylcobalamin
    99.73%
    2,4-Difluorophenylethynylcobalamin is a potential B12 antivitamin via binding to human B12 -processing enzyme CblC with high affinity (KD=130 nm). 2,4-Difluorophenylethynylcobalamin withstood tailoring by CblC, and stabilizes the ternary complex with the cosubstrate glutathione (GSH). 2,4-Difluorophenylethynylcobalamin is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    2,4-Difluorophenylethynylcobalamin
  • HY-B0950A
    Mefexamide hydrochloride
    99.45%
    Mefexamide hydrochloride is a particular psychostimulant that is capable of reversing the psychodepressant effects induced by diazepam and benzodiazepine sedatives.
    Mefexamide hydrochloride
  • HY-17482
    Difenpiramide
    99.05%
    Difenpiramide (Z-876) is a bisphenylalcanoic derivative with marked anti-inflammatory, analgesic, antipyretic and uricosuric properties. Difenpiramide has platelet anti-aggregation activity.
    Difenpiramide
  • HY-108017
    Ferric maltol
    99.93%
    Ferric maltol is an orally active monovalent iron (Fe3+) complex. Ferric maltol is used in the study of iron deficiency anemia in inflammatory bowel disease.
    Ferric maltol
Cat. No. Product Name / Synonyms Application Reactivity