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Cat. No. Product Name Field of Application Chemical Structure
DC10672 DNQX Featured DNQX is a elective non-NMDA antagonist
DC11464 DO-264 Featured DO264 is an inhibitor of α/β-hydrolase domain-containing protein 12 (ABHD12; IC50 = 11 nM).It inhibits ABHD12-dependent hydrolysis of lysophosphatidylserine (lyso-PS) in mouse brain membrane lysates (IC50 = 2.8 nM) and human THP-1 cells.
DC4187 Docetaxel Featured Docetaxel, an analog of taxol, is an inhibitor of depolymerisation of microtubules through binding to stabilized microtubules.
DC9648 Dodecanoic acid ingenol ester Featured Dodecanoic acid ingenol ester is a natural compound.
DC12216 Dodecanoylcarnitine Featured Dodecanoylcarnitine is present in fatty acid oxidation disorders such as long-chain acyl CoA dehydrogenase deficiency, carnitine palmitoyltransferase I/II deficiency, and is also associated with celiac disease.
DCAPI1022 Dofetilide (Tikosyn) Featured Dofetilide (Tikosyn)
DC7273 Dolutegravir Featured Dolutegravir (DTG, GSK1349572) is an integrase inhibitor(IC50= 2.7 nM), modest activity against raltegravir-resistant signature mutants Y143R, Q148K, N155H, and G140S/Q148H.
DC10250 Dolutegravir Sodium Featured Dolutegravir is a HIV integrase inhibitor with IC50 of 2.7 nM.
DC3155 Donepezil hydrochloride Featured Donepezil is a specific and potent AChE inhibitor for bAChE and hAChE with IC50 of 8.12 nM and 11.6 nM , respectively.
DC11103 Tavapadon Featured Tavapadon is a potent, orally-bioavailable, selective partial agonist of the dopamine D1 and D5 receptors.
DC9308 Doravirine (MK-1439) Featured Doravirine (MK-1439) is a non-nucleoside reverse transcriptase inhibitor.
DC7115 Dorsomorphin dihydrochloride Featured Dorsomorphin 2Hcl (Compound C; BML-275) has been shown to act as a potent and selective inhibitor of AMPK (AMP-activated protein kinase; Ki = 109 nM), induced by AICAR and metformin; also inhibits ALK2, ALK3, and ALK 6 .
DC3142 Dovitinib Dilacticacid Featured Dovitinib (TKI258, CHIR-258) is a multitargeted tyrosine kinase inhibitor of FLT3 and c-KIT with IC50 of 1 nM and 2 nM, respectively.
DC4157 Dovitinib (TKI258, CHIR258) Featured Dovitinib (TKI258, CHIR258) is a novel multi-target inhibitor for Flt3, c-Kit, FGFR1/3, VEGFR1/2/3, PDGFRα/β with IC50 of 1 nM, 2 nM, 8 nM/9 nM and 10 nM/13 nM/8 nM, 210 nM/27 nM respectively.
DC3141 Dovitinib (TKI258) Lactate Featured Dovitinib (TKI258, CHIR258) is a novel multi-target inhibitor for Flt3, c-Kit, FGFR1/3, VEGFR1/2/3, PDGFRα/β with IC50 of 1 nM, 2 nM, 8 nM/9 nM and 10 nM/13 nM/8 nM, 210 nM/27 nM respectively.
DC9664 Doxapram Featured Doxapram inhibits TASK-1, TASK-3, TASK-1/TASK-3 heterodimeric channel function with EC50 of 410 nM, 37 μM, 9 μM, respectively.
DCAPI1241 Doxercalciferol (Hectorol) Featured Doxercalciferol is a synthetic vitamin D2 analog, suppressing parathyroid synthesis and secretion, used to treat secondary hyperparathyroidism and metabolic bone disease.
DC4188 Doxorubicin hydrochloride Featured Doxorubicin (Adriamycin) is an antibiotic agent that inhibits DNA topoisomerase II and induces DNA damage and apoptosis.
DC8383 Dp44mT Featured Dp44mT is a potent iron chelator, which shows selective antitumor activity.
DC20966 DPM-1001 Featured DPM-1001 is a potent, selective, orally bioavailable inhibitor of the protein-tyrosine phosphatase PTP1B with IC50 of 100 nM, also chelates copper, which enhanced its potency as a PTP1B inhibitor.
DC9949 DprE1-IN-2 Featured DprE1-IN-2 is a potent DprE1 inhibitor.
DC11173 DRAinh-A250 Featured DRAinh-A250 is a specific inhibitor of Cl-/anion exchanger SLC26A3 (DRA), fully and reversibly inhibits SLC26A3-mediated Cl- exchange with HCO3-, I-, and thiocyanate (SCN-) with IC50 of ~0.2 uM.
DC10039 DREADD Agonist 21 Featured DREADD agonist 21 is a potent muscarinic hM3Dq DREADD agonist (EC50 = 1.7 nM). Highly selective for hM3Dq DREADDs over endogenous hM3 receptors.
DC20103 D-Ribose(mixture of isomers) Featured D-Ribose(mixture of isomers) is an energy enhancer, and acts as a sugar moiety of ATP, and widely used as a metabolic therapy supplement for chronic fatigue syndrome or cardiac energy metabolism. D-Ribose(mixture of isomers) is active in protein glycation
DCAPI1562 Drospirenone Featured Drospirenone is a synthetic progestogen exhibiting antiandrogenic and antimineralocorticoid activity.
DC2056 Droxidopa (L-DOPS,SM-5688) Featured Droxidopa (L-DOPS) is a psychoactive drug and acts as a prodrug to the neurotransmitters norepinephrine (noradrenaline) and epinephrine (adrenaline).
DC8350 Droxinostat Featured Droxinostat is a selective HDAC3, HDAC6 and HDAC8 inhibitor.
DC20975 DS-2330 Featured DS-2330 is a phosphorous lowering agent for treating hyperphosphatemia in chronic kidney disease..
DC11726 Milademetan Featured Milademetan (DS-3032) is a specific and orally active MDM2 inhibitor for the research of acute myeloid leukemia (AML) or solid tumors. Milademetan (DS-3032) induces G1 cell cycle arrest, senescence and apoptosis.
DC12410 8-{1-[(1R,4R)-4-aminocyclohexyl]ethenyl}-5,5-dimethyl-5,6-dihydrobenzo[h]quinazolin-4-amine Featured DS42450411 (DS 42450411, DS-42450411) is a potent, orally active hepcidin production inhibitor with IC50 of 32 nM.

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