DC23229 |
Eltoprazine hydrochloride |
An antiaggressive agent that acts as an agonist at the 5-HT1A and 5-HT1B receptors and as an antagonist at the 5-HT2C receptor.. |
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DC22604 |
Anisomycin
Featured
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An antibiotic that inhibits eukaryotic protein synthesis by inhibiting peptidyl transferase or the 80S ribosome system. |
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DC24146 |
Vancomycin |
An antibiotic used to treat a number of bacterial infections that acts by inhibiting proper cell wall synthesis.. |
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DC24004 |
Norvancomycin hydrochloride |
An antibiotic used to treat a number of bacterial infections that acts by inhibiting proper cell wall synthesis.. |
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DC24148 |
Penicillin G potassium |
An antibiotic used to treat a number of bacterial infections.. |
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DC22927 |
Thymoquinone |
An anticancer phytochemical commonly found in black cumin. |
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DC24149 |
Dichlorophen |
An anticestodal agent, fungicide, germicide, and antimicrobial agent. |
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DC24147 |
Clotrimazole |
An antifungal agent that works by altering the permeability of the fungal cell wall. |
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DC22836 |
Cerulenin |
An antifungal antibiotic that inhibits fatty acid synthase (FASN), also blocks cellular proliferation of KRAS-associated lung cancer cells. |
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DC22350 |
Hexachlorophene |
An anti-infective, anti-bacterial agent. |
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DC20373 |
Epeleuton |
An anti-inflammation agent.. |
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DC24172 |
Oxaceprol |
An anti-inflammatory agent used in the treatment of osteoarthritis. |
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DC23252 |
GNF-Pf-5660 |
An antimalarial candidate that demonstrates potent blood-stage and transmission-blocking activity, shows potent ABS activity (IC50 <25 nM) against drug-sensitive 3D7 and multidrug-resistant Dd2 parasites. |
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DC25077 |
Naphthoquine phosphate
Featured
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Naphthoquine phosphate is a potent and orally active antimalarial agent. Naphthoquine phosphate has thorough killing function for various schizonts of plasmodia, including resistance of P. falciparum to Chloroquine. |
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DC10594 |
Tolcide 2230
Featured
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An antimicrobial agent used as a substitute for chlorophenols |
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DC22497 |
MMAF-OMe
Featured
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MMAF-Ome belongs to ADC, and inhibits several tumor cell lines with IC50s of 0.056 nM, 0.166 nM, 0.183 nM, and 0.449 nM for MDAMB435/5T4, MDAMB361DYT2, MDAMB468, and Raji (5T4-) cell lines, respectively. |
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DC22483 |
Quinacrine dihydrochloride |
An antiprotozoal, antirheumatic and intrapleural sclerosing agent. |
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DC22614 |
Risperidone hydrochloride |
An antipsychotic agent with serotonin-S2 and dopamine-D2 antagonistic properties. |
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DC22613 |
Risperidone mesylate |
An antipsychotic agent with serotonin-S2 and dopamine-D2 antagonistic properties. |
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DC24155 |
Suramin |
An antitrypansomal drug that also possesses antitumor activity. |
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DC22844 |
WIN 52084 |
An antiviral compound that inhibits attachment to cells, inhibits human rhinovirus type 14 (HRV14) replication.. |
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DC22869 |
E3 Ligand-Linker Conjugate 3(E3 Ligase Ligand-Linker Conjugates 19)
Featured
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An E3 ligase ligand-linker conjugate for PROTAC. |
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DC26084 |
LE-135
Featured
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LE135 is a retinoid acid receptor antagonist, produces pain through direct activation of TRP channels. |
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DC22495 |
Lenampicillin hydrochloride |
An efficient prodrug of ampicillin with enhanced absorption and decreased side effects.. |
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DC24168 |
(R)-(-)-Ibuprofen
Featured
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An enantiomer of Ibuprofen that is generally not considered a COX inhibitor and is instead thought to be involved in pathways of lipid metabolism as it is incorporated into triglycerides along with fatty acids. |
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DC22361 |
(S)-(+)-Ibuprofen |
An enantiomer of Ibuprofen that more potently inhibits COX activity, thromboxane formation, and platelet aggregation than the (R)-form. |
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DC24138 |
Synaptamide |
An endogenous DHA metabolite that promotes neurite growth, synaptogenesis, and synaptic function both in vitro and in vivo. |
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DC23324 |
C-1311 dihydrochloride |
An imidazoacridinone analogue with potent in vivo antitumour activity, inhibits the catalytic activity of Topoisomerase II. |
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DC25076 |
Imazamox |
An imidazolinone herbicide that effectively controls a broad spectrum of weed species.. |
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DC23914 |
Thymalfasin
Featured
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An immunoactive peptide that has been shown to inhibit cell proliferation and induce apoptosis in human leukemia, non-small cell lung cancer, melanoma, and other human cancers. |
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