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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC8611 | Luliconazole Featured |
Luliconazole(NND 502) is an azole antifungal indicated for the topical treatment of interdigital tinea pedis.
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| DC20271 | LUT014 Featured |
LUT014 is a novel BRAF agonist.
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| DC26012 | LXS-196 Featured |
LXS196 is a potent, selective and orally active protein kinase C (PKC) inhibitor, with IC50 values of 1.9 nM, 0.4 nM and 3.1 μM for PKCα, PKCθ and GSK3β, respectively. It can be used for the treatment of uveal melanoma.
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| DC7944 | LY2090314 Featured |
LY2090314 is a potent inhibitor of glycogen synthase kinase-3 (GSK-3) with IC50s of 1.5 nM and 0.9 nM for GSK-3α and GSK-3β respectively.
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| DC23724 | SR1555 Featured |
SR1555 is a selective RORγ inverse agonist (IC50=1.5 uM) that suppresses T(H)17 cells and stimulates T regulatory cells.
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| DC23732 | KT-5823 Featured |
KT-5823 is a potent, highly specific PKG (cGMP-dependent protein kinase) inhibitor with Ki of 0.234 uM, displays little to no activity for MLCK, cAPK, and PKC.
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| DC23736 | Z62954982 Featured |
Z62954982 is a potent, specific Rac1 inhibitor, reduces the intracellular levels of Rac1-GTP in a concentration-dependent manner with IC50 of 12 uM, 4 times more effective than NSC23766 (IC50=50 uM).
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| DC23781 | YM-1 Featured |
YM-1 is a close derivative of MTK-077 that allosterically promotes Hsp70 binding to unfolded substrates, specificly binds to Hsp70 with Kd of 4.9 uM.
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| DC23834 | Rottlerin Featured |
Rottlerin (Mallotoxin.
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| DC23864 | AAL993 Featured |
AAL993 (ZK260253) is a potent, orally active VEGFR inhibitor with IC50 of 130, 23 and 18 nM for VEGFR-1, 2 and 3, respectively.
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| DC23934 | FTI-277 Featured |
A peptide mimetic of the C-terminal Cys-Val-Ile-Met of K-Ras4B that potently inhibits FTase (Farnesyltransferase) with IC50 of 0.5 nM.
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| DC23962 | Cilobradine Featured |
A hyperpolarization-activated cyclic nucleotide-gated (HCN) channel.
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| DC24118 | C75 Featured |
C75 is an inhibitor synthetic fatty-acid synthase (FASN) and inhibits prostate cancer cells PC3 (IC50: 35 μM).
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| DC25079 | Biperiden hydrochloride Featured |
Biperiden Hcl (NSC 170950, NSC 84989) is a centrally-acting antiparkinsonian agent that functions as a selective central M1 cholinoreceptors blocker..
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| DC28109 | Dilazep dihydrochloride Featured |
Dilazep dihydrochloride is an inhibitor of adenosine uptake. Dilazep dihydrochloride has cerebral and coronary vasodilating action through enhancement of effect of adenosine. Dilazep dihydrochloride also inhibits the ischemic damage, platelet aggregation, and membrane transport of nucleosides.
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| DC12478 | NSC 260594 Featured |
NSC260594 (NSC 260594) is a specific inhibitor of HIV-1 RNA packaging, which involves preventing the interaction of Gag with SL3 by stabilizing this small RNA stem-loop which then leads to stabilization of the global packaging signal region (psi or ψ).
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| DC28212 | Picrotin Featured |
Picrotin is an inhibitor of glycine receptors (GlyRs) which blocks α2 GlyR, α1 GlyR and α3 GlyR.
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| DCAPI1271 | Ubenimex (Bestatin) Featured |
Bestatin is a natural, broad-spectrum, and competitive aminopeptidase inhibitor.
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| DC9351 | Radezolid Featured |
Radezolid (RX-1741) is a novel oxazolidinone antibiotic agent.
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| DC26095 | QX 314 chloride Featured |
A membrane-impermeable sodium channel blocker, blocks sodium current in voltage-clamped nociceptive DRG neurons.
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| DC28267 | (Rac)-LM11A-31 dihydrochloride Featured |
(Rac)-LM11A-31 dihydrochloride is an isomer of LM11A-31 dihydrochloride. LM11A-31 dihydrochloride, a p75NTR (neurotrophin receptor p75) Ligand, is a potent proNGF (nerve growth factor) antagonist.
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| DC28517 | 2-Aminobenzanilide Featured |
2-Aminobenzamide is a neutral and stable compound used as fluorescent tag, numerously in Glycan analysis. 2-aminobenzamide acts as the starting material for several important reactions like Bargellini reaction as an competent ambident nucleophile. Specifically 2-aminobenzamide and its derivatives are used in the blood coagulation cascade.
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| DC28757 | 2-Di-1-ASP Featured |
2-Di-1-ASP (Compound 18a) is a mono-stryryl dye, and widely used as mitochondrial stain and groove-binding fluorescent probes for double-stranded DNA. 2-Di-1-ASP is selective for G-quadruplex (G4) and double-stranded DNA.
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| DC22312 | LY2940094 Featured |
LY2940094 is a potent and selective nociceptin receptor antagonist which inhibits excessive feeding behavior in rodents.
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| DC29050 | Fibrin Featured |
Fibrin, isolated from bovine blood, is an insoluble protein produced in response to bleeding. Fibrin is the major component of the blood clot and is used for coagulation.
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| DC29074 | (R)-(+)-Atenolol Featured |
(R)-(+)-Atenolol is the less active enantiomer of the (R,S)-atenolol. (R,S)-atenolol is a β-adrenergic receptor antagonist.
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| DC11290 | QC-3611 Featured |
QC-3611 is a selective inhibitor of JARID1A/1B, which is a target existing in various tumors (JARID1A IC50 = 13 nM ;JARID1B IC50 = 2 nM). QC-3611 is promisingly to be used as an antineoplastic drug.
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| DC29183 | Disodium succinate Featured |
Disodium succinate is the disodium salt of Succinic acid. Succinic acid is an intermediate product of the tricarboxylic acid cycle, as well as one of fermentation products of anaerobic metabolism.
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| DC29185 | 2-Acetamidophenol Featured |
Paracetamol (4-acetamidophenol). 2-Acetamidophenol is a promising analgesic and an anti-arthritic agent.
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| DC3159 | Gemifioxacin Featured |
Gemifloxacin mesylate (trade name Factive, Oscient Pharmaceuticals) is an oral broad-spectrum quinolone antibacterial agent used in the treatment of acute bacterial exacerbation of chronic bronchitis and mild-to-moderate pneumonia.
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