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Catalog	name	Description	price
R-C-3224	AR-C117977 CAS:216685-07-3	AR-C117977 is a potent MCT1 inhibitor,which can reduce vimmune responses both in vitro and in vivo,maintains long-term graft survival,and induces operational tolerance.Our products are only suitable for scientific research experiments, not for clinical experiments and human body.	price>
R-R-4894	4-C-Azidouridine CAS No.139442-01-6	4-C-azidouridine (4-Azidouridine)/CAS No.139442-01-6 is a uridine analogue. Uridine has potential antiepileptic effects, and its analogs can be used to study anticonvulsant and anxiolytic activities, as well as to develop new antihypertensive agents. 4-C-Azidouridine is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.	price>
R-C-3225	UK 5099 CAS:56396-35-1	UK 5099 is a potent inhibitor of plasma membrane monocarboxylate transporters(MCTs) and the mitochondrial pyruvate carrier(MPC);inhibits pyruvate-dependent O2 consumption with an IC50 of 50nM.Our products are only suitable for scientific research experiments, not for clinical experiments and human body.	price>
R-R-4895	a-Cytidine CAS No.13913-16-1	α-Cytidine/CAS No.13913-16-1 is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc.	price>
R-C-3226	Tezampanel CAS :154652-83-2	Tezampanel is an antagonist at the AMPA and kainate families of ionotropic glutamate receptors, with selectivity for the GluR5 subtype of the kainate receptor.Our products are only suitable for scientific research experiments, not for clinical experiments and human body.	price>
R-R-4896	7-TFA-ap-7-Deaza-dG CAS No.666847-77-4	5-O-TBDMS-dG/CAS No.666847-77-4 is a modified nucleoside. 5-O-DMT-2-O-TBDMS-rI can be used in the synthesis of deoxyribonucleic acid or nucleic acid. 7-TFA-ap-7-Deaza-dG is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.	price>
R-C-3227	JNJ-61432059 CAS:2035814-50-5	JNJ-61432059 is an oral active and selective negative modulator of AMPAR associated with trans-membrane AMPAR regulatory protein(TARP)γ-8,with a pIC50 of 9.7 for GluA1/γ-8.Our products are only suitable for scientific research experiments, not for clinical experiments and human body.	price>
R-R-4897	Formycin A CAS No.6742-12-7	Formycin A (NSC 102811)/CAS No.6742-12-7, a purine nucleoside antibiotic, is a potent human immunodeficiency virus type 1 (HIV-1) inhibitor with an EC50 of 10 μM. Formycin A shows antitumor and antiviral activities.	price>
R-C-3228	Fanapanel(ZK200775) CAS:161605-73-8	Fanapanel(ZK200775)is a highly selective AMPA/kainate antagonist with little activity against NMDA;have Ki values of 3.2nM,100nM,and 8.5μM against quisqualate,kainate, and NMDA,respectively.Our products are only suitable for scientific research experiments, not for clinical experiments and human body.Our products are only suitable for scientific research experiments, not for clinical experiments and human body.	price>
R-R-4898	N1-Methyl-2-deoxyadenosine CAS No.60192-55-4	N1-Methyl-2-deoxyadenosine/CAS No.60192-55-4, DNA adduct is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc.	price>
R-C-3229	Mibampator CAS:375345-95-2	Mibampator (LY451395) is a potent and highly selective potentiator of the AMPA receptors.Our products are only suitable for scientific research experiments, not for clinical experiments and human body.	price>
R-R-4899	5-Hydroxyuridine CAS No.957-77-7	5-Hydroxyuridine (OHUrd)/CAS No.957-77-7 is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc.	price>
R-C-3230	CMPDA CAS:380607-77-2	CMPDA is a positive allosteric modulator of AMPA receptors with EC50s of 45.4 ± 4.2 nM/63.4 ± 5.6 nM for GluA2i/GluA2o receptor.Our products are only suitable for scientific research experiments, not for clinical experiments and human body.	price>
R-R-4900	Alpha-Guanosine CAS No.15398-66-0	Alpha-Guanosine/CAS No.15398-66-0 is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc.	price>
R-C-3231	Naspm CAS:122306-11-0	Naspm (1-Naphthyl acetyl spermine), a synthetic analogue of Joro spider toxin, is a calcium permeable AMPA (CP-AMPA) receptors antagonist.Our products are only suitable for scientific research experiments, not for clinical experiments and human body.	price>
R-R-4901	Pseudothymidine CAS No.65358-15-8	Pseudothymidine/CAS No.65358-15-8 is a C-nucleoside analog of thymidine.	price>
R-C-3232	LY404187 CAS:211311-95-4	LY404187 is a selective, potent and centrally active positive allosteric modulator of AMPA receptors.	price>
R-R-4902	1-(a-D-ribofuranosyl)uracil CAS No.3258-07-9	1-(a-D-ribofuranosyl)uracil/CAS No.3258-07-9 is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc.	price>
R-C-3233	LY450108 CAS:376594-67-1	LY450108 is a potent AMPA receptor potentiator.LY450108 has the potential for depression and Parkinson is disease research.	price>
R-R-4903	2-Deoxy-2-fluoro-b-D-arabinocytidine CAS No.56632-83-8	2-Deoxy-2-fluoro-b-D-arabinocytidine/CAS No.56632-83-8 is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc.	price>

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