Chemical structure
Cat.No.
Product Name
CAS no.
Target
YN250125 Gatifloxacin sesquihydrate 180200-66-2
Gatifloxacin sesquihydrate (AM-1155; BMS-206584; PD135432) is a potent fluoroquinoloneantibioticwith broad-spectrum antibacterial activity. Gatifloxacin sesquihydrate inhibits bacterialtype II topoisomerases(IC50=13.8 μg/ml fo...
YN372357 FTI-277 hydrochloride 180977-34-8
FTI 277 HCl is the methyl ester of FTI 277, which is a potent and selective farnesyltransferase (FTase) inhibitor with IC50 of 500 pM, about 100-fold selectivity over the closely related GGTase I.
YN251724 InteriotherinA 181701-06-4
Interiotherin A is a lignan with a dibenzocyclooctadiene skeleton isolated fromKadsura interior. Interiotherin A inhibitsHIVreplication to exhibit anti-HIV activity, it has a role as a metabolite and an anti-HIV agent.
YN250584 Ravuconazole 182760-06-1
Ravuconazole (BMS-207147;ER-30346) is an orally available triazoleantifungle agent that potently inhibits a wide range of fungi.
YN320547 Kendomycin 183202-73-5
Kendomycin ((−)-TAN 2162) is a polyketideantibioticwith remarkable antibacterial and cancer cells cytotoxic activities. Kendomycin tends to be bacteriostatic rather than bactericidal and inhibits the growth of the methicillin-resi...
YN483288 Nuezhenidic acid 183238-67-7
Nuezhenidic acid, isolated from the fruits ofLigustrum lucidum, posseses inhibitory activities against influenza A virus.
Apicidin (OSI 2040) is a fungal metabolite, acts as ahistone deacetylase (HDAC)inhibitor, with antiparasitic activity and a broad spectrum antiproliferative activity.
YN483703 L-Pentaguluronic acid 183668-72-6
L-Pentaguluronic acid is a linear polysaccharide copolymer composed of four L-guluronic acid (G).
YN483704 L-Hexaguluronic acid 183668-74-8
L-Hexaguluronic acid is a linear polysaccharide copolymer composed of six L-guluronic acid (G).
YN371603 PfDHODH-IN-1 183945-55-3
PfDHODH-IN-1 is an analogue of the active metabolite of Leflunomide. PfDHODH-IN-1 is aPlasmodium falciparumdihydroorotate dehydrogenase (PfDHODH)inhibitor. PfDHODH-IN-1 has antimalarial activity.
YN380263 Picfeltarraenin IV 184288-35-5
Picfeltarraenin IV, a triterpenoid obtained fromPicriafel-terraeLour (P.fel-terrae), is an acetylcholinesterase (AChE) inhibitor. Picfeltarraenin IV can be used for the treatment of herpes infections, cancer and inflammation.
YN484133 NS2 (114-121), Influenza 184763-32-4
NS2 (114-121), Influenza, the 114-121 fragment of influenza nonstructural protein 2 (NS2), is a influenza-derived epitope. NS2 (114-121), Influenza can be used for the research of CD8+cytotoxic T lymphocyte (CTL) in antiviral ...
YN250800 Ferroquine 185055-67-8
Ferroquine (Ferrochloroquine), a ferrocenyl analogue of Chloroquine, is an antimalarial agent. Ferroquine shows parasiticidal effect onPlasmodiumby inducing oxidative stress and the subsequent destruction of the membrane.
YN1590005 Bis-propargyl-PEG5 185378-83-0
Bis-propargyl-PEG5 is aPEG-based PROTAC linkerused in the synthesis of PROTACs. Bis-propargyl-PEG5 is used for the synthesis of carbohydrate receptors (SCRs) with anti-Zika activity.
YN321050 AMD 3465 hexahydrobromide 185991-07-5
AMD 3465 hexahydrobromide (GENZ-644494 hexahydrobromide) is a potent antagonist ofCXCR4, inhibits binding of 12G5 mAb and CXCL12AF647toCXCR4, with IC50s of 0.75nM and 18nM in SupT1 cells; AMD 3465 also po...
AMD 3465 (GENZ-644494) is a potent antagonist ofCXCR4, inhibits binding of 12G5 mAb and CXCL12AF647toCXCR4, with IC50s of 0.75nM and 18nM in SupT1 cells; AMD 3465 also potently inhibits the replication of...
YN483993 Influenza HA (518-526) 186302-15-8
Influenza HA (518-526) is an H-2Kd-restricted epitope of the influenza virus hemagglutinin comprised amino acids 533 to 541.
GPI-1046 is a immunophilin lig and without antibiotic action and attenuates ethanol intake in part through the upregulation ofglutamate transporter 1 (GLT1)in PFC and NAc-core. GPI-1046 is an analog of FK506, which is a...
YN250837 Moxifloxacin Hydrochloride 186826-86-8
Moxifloxacin is a fourth-generation synthetic fluoroquinolone antibacterial agent.
YN250614 Pafuramidine 186953-56-0
Pafuramidine (DB289) is an orally bioavailable prodrug of furamidine, which has activity against Pneumocystis pneumonia. DB289 (pafuramidine maleate; 2,5-bis[4-(N-methoxyamidino)phenyl]furan monomaleate) is a prodrug of DB75 (furam...
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