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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC21405 | Chetomin Featured |
Chetomin (NSC 289491) is a natural product isolated from Chaetomium species which shows antibacterial and antifungal properties, disrupts the interaction of HIF-1α/p300 at low nanomolar concentrations, strongly increases retinal pigment epithelial cells d
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| DC57042 | DEOXYNIVALENOL Featured |
Deoxynivalenol, a mycotoxin of the trichothecenes family, crosses the intestinal mucosa by a paracellular pathway through the tight junctions. The Deoxynivalenol transport is not affected by P-glycoprotein (PgP) or multidrug resistance-associated proteins (MRPs) inhibitors[1].
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| DC50028 | Laninamivir Octanoate Featured |
Laninamivir (L174000) prodrug; a novel long-acting neuraminidase inhibitor.
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| DC70441 | GR-127935 Featured |
GR-127935 is a potent and selective 5-HT1B/1D receptor antagonist with pKi of 8.5 for both guinea pig 5-HT1D and rat 5-HT1B receptor; displays >100-fold selectivity over 5HT1A, 5-HT2A, 5-HT2C receptors and other receptor types; blocks porcine carotid vascular response to sumatriptan in vivo; orally bioavailable and centrally active.
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| DC7766 | Ravoxertinib Featured |
GDC-0994 is a potent, orally available ERK1/2 inhibitor with IC50 of 1.1 nM and 0.3 nM, respectively. Phase 1.
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| DC5190 | 3-Deazaneplanocin A (DZNep) Featured |
3-deazaneplanocin A (DZNeP), an analog of adenosine, is a competitive inhibitor of S-adenosylhomocysteine hydrolase with Ki of 50 pM.
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| DC9011 | Mizoribine Featured |
Mizoribine(NSC 289637; HE 69; β-Bredinin) is an immunosuppressive agents (IC50=100 uM) that inhibit the proliferation of lymphocytes selectively, via inhibition of IMPDH.
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| DC10446 | (3R,4S,5S)-tert-butyl 3-Methoxy-5-Methyl-4-(MethylaMino)heptanoate hydroc hloride Featured |
Diltiazem hydrochloride is a calcium ion influx inhibitor (slow channel blocker or calcium antagonist).
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| DC23093 | 双甜 Featured |
Steviolbioside is a natural sweetener, it presents notable inhibition on human hepatocarcinoma cell Hep3B, human breast cancer cell MDA-MB-231 and human pancreatic cancer cell BxPC-3
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| DC42267 | Eleutheroside D Featured |
Eleutheroside D is an active lignan isolated from the root of Eleutherococcus senticosus, has anti-inflammatory and hypoglycemic activities. Eleutheroside D is an optical isomer of Eleutheroside E.
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| DC65698 | 4-Methylumbelliferyl a-D-Glucopyranoside Featured |
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| DC43943 | Gadobutrol Featured |
Gadobutrol (Gadovist, Gadavist) is a non-ionic macrocyclic gadolinium-based contrast agent (GBCA) that is usedfor tissue contrast enhancement in magnetic resonance imaging (MRI).
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| DC7114 | Dinaciclib (SCH727965) Featured |
Dinaciclib (SCH727965) is a novel and potent CDK inhibitor for CDK2, CDK5, CDK1 and CDK9 with IC50 of 1 nM, 1 nM, 3 nM and 4 nM, respectively.
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| DCAPI1410 | Eldecalcitol Featured |
Eldecalcitol (ED-71; 2.beta.-(3-Hydroxypropoxy)-1.alpha.,25-dihydroxyvitamin D3) is an analog of 1,25-dihydroxyvitamin D3 that improves bone mineral density. Eldecalcitol (ED-71; 2.beta.-(3-Hydroxypropoxy)-1.alpha.,25-dihydroxyvitamin D3) is more efficaci
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| DC7320 | Ganetespib(STA-9090) Featured |
Ganetespib(STA-9090) is a unique triazolone-containing Hsp90 inhibitor with an IC50 of 4 nM in OSA 8 cells.
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| DC72747 | Elenestinib Featured |
Elenestinib (BLU-263) is a potent and orally active tyrosine kinase inhibitor. Elenestinib has the potential for the research of systemic mastocytosis (SM).
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| DC46693 | DAMGO Featured |
DAMGO (DAGO) is a potent and selective μ opioid receptor agonist with ki of 17 nM.
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| DC7228 | PF-04691502 Featured |
PF-04691502 is an ATP-competitive PI3K(α/β/δ/γ)/mTOR dual inhibitor with Ki of 1.8 nM/2.1 nM/1.6 nM/1.9 nM and 16 nM, little activity against either Vps34, AKT, PDK1, p70S6K, MEK, ERK, p38, or JNK.
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| DC60020 | Nω-Hydroxy-nor-L-Arginine Dihydrochloride Featured |
nor-NOHA, also known as N-Hydroxy-nor-L-Arginine, is an Arginase inhibitor. nor-NOHA induces apoptosis in leukemic cells specifically under hypoxic conditions but CRISPR/Cas9 excludes arginase 2 (ARG2) as the functional target. Nor-NOHA can induce cell apoptosis and inhibit the ability of invasion and migration of HepG2 cells by inhibiting Arg1, which is related with the increase of iNOS expression and the high concentration of NO.
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| DC65199 | 1-(4-nitrophenyl)-3-(1-(6-(trifluoromethyl)pyridin-2-yl)piperidin-4-yl)thiourea Featured |
DUN51106, also known as USP8-IN-3, is a deubiquitinase USP8 inhibitor (IC50 = 4.0 μM) for treatment of malignant tumors.
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| DC9963 | Kribb11 Featured |
KRIBB11 is a Heat shock factor (HSF) inhibitor (IC50 = 1.2 μM).
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| DC8905 | Lercanidipine Featured |
Lercanidipine is a calcium channel blocker of the dihydropyridine class.
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| DC7486 | PX-478 2HCL Featured |
PX-478 is an inhibitor of HIF-1a with an IC50 of 20-30μM enhances radiosensitivity of prostate carcinoma cells.
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| DC7991 | 8-Chloro-11-(4-methyl-1-piperazinyl)-5H-dibenzo[b,e](1,4)diazepine N-oxide Featured |
Clozapine N-oxide is a major metabolite of Clozapine noted to decrease SR-2A (5-HT2 serotonin receptor) density in vitro.
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| DC23823 | Benzenesulfonamide, n-b-d-glucopyranosyl-4-(hydroxyamino)-n-[2-(2-naphthalenyloxy)ethyl]- Featured |
SCH 54292 is a potent Ras-GEF interaction inhibitor with IC50 of 0.7 uM..
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| DC45591 | 2′-Deoxyadenosine 5′-monophosphate disodium Featured |
2′-Deoxyadenosine 5′-monophosphate disodium, a nucleic acid AMP derivative, is a deoxyribonucleotide found in DNA. 2′-Deoxyadenosine 5′-monophosphate disodium can be used to study adenosine-based interactions during DNA synthesis and DNA damage.
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| DC60293 | Potassium osmate(VI) dihydrate Featured |
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| DC60177 | Heparan N-sulfate Featured |
Heparan Sulfate is a complex and linear polysaccharide, exists as part of glycoproteins named heparan sulfate proteoglycans, which are expressed abundantly on the cell surface and in the extracellular matrix.
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| DC9687 | WST-8 Featured |
WST-8 is a next generation tetrazolium reagent that serves as a sensitive chromogenic indicator for NADH.
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| DC4207 | Fondaparinux sodium Featured |
Fondaparinux sodium is a synthetic and specific inhibitor of activated Factor X (Xa).
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