New Products
  1. Cat.No. Product Name Information
  2. GC28246 2-(Methylthio)-7,8-dihydroquinazolin-5(6H)-one

    2-(Methylthio)-7,8-dihydroquinazolin-5(6H)-one is a compound featuring a saturated ring fused to an aromatic (hetero)cyclic ring.

    2-(Methylthio)-7,8-dihydroquinazolin-5(6H)-one
  3. GK10050 JC-1 Mitochondrial Membrane Potential Assay Kit JC-1 Mitochondrial Membrane Potential Assay Kit
  4. GC28245 JNJ-26489112

    JNJ-26489112 is a CNS-active agent and inhibitor of voltage-gated Na+ channels and N-type Ca2+ channels with broad-spectrum anticonvulsant activity in rodents and can be used to study neurological disorders.

    JNJ-26489112
  5. GC28244 HALOFUGINONE LACTATE

    HALOFUGINONE LACTATE is a halogenated derivative of febrifugine, a natural quinazolinone-containing compound found in the Chinese herb D. febrifuga.

    HALOFUGINONE LACTATE
  6. GC28243 Sulcardine 2HCl

    Sulcardine 2HCl is a multi-ion channel blocker with antiarrhythmic effects that blocks the properties of hERG and hNav1.5 channels and can be used to study atrial fibrillation and ventricular arrhythmias.

    Sulcardine 2HCl
  7. GC28242 Anisodine

    Anisodine is an inhibitor of muscarinic acetylcholine receptors (mAChR) with neuroprotective activity, used in research on multiple myeloma and metastatic breast cancer.

    Anisodine
  8. GC28241 Selinexor HCl

    Selinexor HCl (1393477-72-9 free base) is an oral selective XPO1 (XPO1/CRM1) inhibitor that induces cell cycle arrest and apoptosis in tumor cells by blocking the transport of tumor suppressor proteins from the nucleus to the cytoplasm, thereby promoting their accumulation within the nucleus.

    Selinexor HCl
  9. GC28239 VRT-325

    VRT-325 is a CFTR modulator with the ability to promote ΔF508-CFTR folding and endoplasmic reticulum trafficking.

    VRT-325
  10. GC28240 Ivacaftor-D9

    Ivacaftor-D9 is transmembrane conductance regulator (CFTR) channel activator, is used potentially for the treatment of cystic fibrosis.

    Ivacaftor-D9
  11. GC28238 P7-2302

    P7-2302 inhibits PDE7 and PDE4B with IC50 values of 0.18 nM and 77.3 nM, respectively. It also inhibits the efflux of P-gp and BCRP (breast cancer resistance protein) and shows low uptake in rat brains.

    P7-2302

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  1. Cat.No. Product Name Information
  2. GC19064 Dihydrotestosterone Dihydrotestosterone(DHT) is an endogenous androgenic steroid and hormone that acts as an agonist for androgen receptors. Dihydrotestosterone
  3. GC49153 Didemnin B Didemnin B is a cyclic depsipeptide produced by marine tunicates that specifically binds the GTP-bound conformation of EEF1A. Didemnin B
  4. GC40103 Herboxidiene Herboxidiene, as a potent antitumor agent, can target the SF3B subunit of the spliceosome. Herboxidiene also induces both G1 and G2/M cell cycle arrest in a human normal fibroblast cell line WI-38. Herboxidiene
  5. GC10398 Heparin sodium Heparin sodium, as as anti-coagulants, belongs to a class of glucans, which can interact with a variety of proteins to produce a variety of biological activities. Heparin sodium
  6. GC10074 H 89 2HCl H-89 2HCl is A potent and selective camp-dependent protein kinase A inhibitor with IC50 value of 48 nM, showing weak inhibition of PKG,PKC,Casein kinase and other kinases. H 89 2HCl
  7. GC41630 H2S Donor 5a H2S (Hydrogen sulfide) Donor 5a, as a stable, cysteine activated hydrogen sulfide donor, can react with reducing agents containing sulfhydryl groups such as cysteine and reduced glutathione to release H2S. H2S Donor 5a
  8. GC32804 HUHS015 A PCA-1 inhibitor HUHS015
  9. GC91632 Verrucarin H

    Verrucarin H is a macrocyclic trichothecene mycotoxin that has been found in M. verrucaria.

    Verrucarin H
  10. GC79707 ST1072

    ST1072 is an inhibitor of CerS4 and CerS6.

    ST1072
  11. GC62861 BAY-298 BAY-298 is an orally active and selective luteinizing hormone receptor (LH-R) antagonist with IC50s of 96 nM, 23 nM and 78 nM for hLH (human LH) and rLH (rat LH) and cLH (cynomolgus monkey LH), respectively. BAY-298

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