Chemical structure
Cat.No.
Product Name
CAS no.
Target
YN251872 BAY-Y 3118 151213-16-0
BAY-Y 3118 is a new chlorofluoroquinolone with antimicrobial activity.
YN250162 Xinjiachalcone A 151410-32-1
Xinjiachalcone A is an active principle ofGlycyrrhiza inflataBatalin. Xinjiachalcone A shows both a low MIC and a strong bactericidal activity againstH. pylori, with MIC values ranged from 12.5 to 50 µM for seventeenH. pyl...
YN480785 7-O-Demethyl rapamycin 151519-50-5
7-O-Demethyl rapamycin, a derivative rapamycin (HY-10219), has antifungal activity and also immunosuppressant properties. 7-O-Demethyl rapamycin has useful tumor cell growth-inhibiting activity.
YN250697 Epothilone B 152044-54-7
Patupilone (EPO906, Epothilone B) is a paclitaxel-like microtubule-stabilizing agent with EC0.01 of 1.8 μM. Phase 2.
YN250012 Emtricitabine S-oxide 152128-77-3
Emtricitabine S-oxide (Emtricitabine sulfoxide) is a major degradation product of Emtricitabine. Emtricitabine is a potent nucleoside reverse transcriptase inhibitor used for the treatment of HIV infection.
YN251867 CAP18 (rabbit) 152742-15-9
CAP18 (rabbit) is a 37 amino acids antimicrobial peptide originally isolated from rabbit granulocytes. CAP18 (rabbit) has broad antimicrobial activity against bothGram-positive(IC50, 130-200nM) and Gram-negative(IC50, 20-100nM...
CEF20 is an HLA-A*0201-restricted epitope from cytomegalovirus pp65 (495-503).
YN250827 Pleconaril 153168-05-9
Pleconaril is a capsid inhibitor used previously to treat enterovirus infections. Pleconaril is effective in inhibiting replication with IC50 of < 0.050 μM.
AG-1478 (Tyrphostin AG-1478) is a selective EGFR inhibitor with IC50 of 3 nM in cell-free assays, almost no activity on HER2-Neu, PDGFR, Trk, Bcr-Abl and InsR.
YN481874 Thiamethoxam 153719-23-4
Thiamethoxam is a broad spectrum neonicotinoid insecticide.
YN250519 Ertapenem sodium 153773-82-1
Ertapenem Sodium is the sodium salt of ertapenem, a long-acting, broad-spectrum antibiotic of β-lactam subclass.
YN330672 IFN-α Receptor Recogniti... 153840-64-3
IFN-α Receptor Recognition Peptide 1 is a peptide of IFN-α associated with receptor interactions.
LY294002 is the first synthetic molecule known to inhibit PI3Kα/δ/β with IC50 of 0.5 μM/0.57 μM/0.97 μM in cell-free assays, respectively more stable in solution than Wortmannin, and also blocks autophagosome formation.
YN250120 Efavirenz 154598-52-4
Efavirenz is a synthetic non-nucleoside reverse transcriptase (RT) inhibitor with antiviral activity.
YN251785 Methyl brevifolincarboxylate 154702-76-8
Methyl brevifolincarboxylate (Brevifolincarboxylic acid methyl ester) is a potentinfluenza virus PB2 cap-bindinginhibitor. Methyl brevifolincarboxylate exhibits inhibitory activity against influenza virus A/Puerto Rico/8/34 (H1N1)...
YN251823 LL-37, Human 154947-66-7
LL37 (Human cathelicidin, Ropocamptide) is a cathelicidin-related antimicrobial peptide with potent chemotactic and immunomodulatory properties.
YN250056 Emodepside 155030-63-0
Emodepside (QHT06, BAY 44-4400, PF 1022-221), a semisynthetic derivative of PF1022A, is a cyclooctadepsipeptide with broad-spectrum anthelmintic activity. Emodepside activates Ca-dependent SLO-1-like K channels.
YN372698 Ritonavir 155213-67-5
Ritonavir is a Cytochrome P450 3A and Protease Inhibitor Also inhibits Cytochrome P450 2D6, P-Glycoprotein and induces Cytochrome P450 2C19, Cytochrome P450 1A2, Cytochrome P450 2C9, Cytochrome P450 2B6 and UDP G...
YN250907 Fluconazole hydrate 155347-36-7
Fluconazole (hydrate) is a triazole antifungal drug used in the treatment and prevention of superficial and systemic fungal infections. Fluconazole (hydrate) is the hydrate salt form of fluconazole, which is a triazole antifungal inte...
Alisol F is a triterpene isolated fromAlisma orientalis, has immunosuppressive and anti-virus functions. Alisol F exhibits inhibitory activity in vitro on hepatitis B virus (HBV) surface antigen (HBsAg) secretion of the HepG...
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