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T68565ANN33840；化合物 ANN33840ANN33840
ANN33840 is a novel selective 5-HT2C agonist with >300-fold functional selectivity over 5-HT2B and >70-fold functional selectivity over 5-HT2A, reducing food intake in an acute rat feeding model.
价 格：￥电议型 号：T68565产 地：中国大陆
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T654825-Amino-N1,N3-bis(2,3-dihydroxypropyl)-2,4,6-triiodoisophthalamide；化合物 5-Amino-N1,N3-bis(2,3-dihydro
5-Amino-N1,N3-bis(2,3-dihydroxypropyl)-2,4,6-triiodoisophthalamide is a useful organic compound for research related to life sciences. The catalog number is T65482 and the CAS number is 76801-93-9.
价 格：￥电议型 号：T65482产 地：中国大陆
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T64574N1,N3-Bis(4-fluorophenyl)malonamide；化合物 N1,N3-Bis(4-fluorophenyl)malonamideN1,N3-Bis(4-fluorophenyl)
N1,N3-Bis(4-fluorophenyl)malonamide is a useful organic compound for research related to life sciences. The catalog number is T64574 and the CAS number is 1677-29-8.
价 格：￥电议型 号：T64574产 地：中国大陆
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T6440CGP 57380；化合物CGP 57380MNK1 Inhibitor；N3-(4-氟苯基)-1H-吡唑并[3,4-D]嘧啶-3,4-二胺|||MNK1 Inhibitor
CGP 57380 (MNK1 Inhibitor) is a potent MNK1 inhibitor with IC50 of 2.2 μM, exhibiting no inhibitory activity on p38, JNK1, ERK1 and -2, PKC, or c-Src-like kinases.
价 格：￥电议型 号：T6440产 地：中国大陆
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T63166LSN3318839；化合物LSN3318839LSN-3318839|||LSN 3318839；LSN-3318839|||LSN 3318839
LSN3318839 is a potent and orally available glucagon-like peptide-1 receptor (GLP-1R) modulator.LSN3318839 enhances GLP-1R G-protein-coupled signaling and can be used to lower blood glucose.
价 格：￥电议型 号：T63166产 地：中国大陆
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T62660MLN3126；化合物 MLN3126MLN3126
MLN3126 is an orally active, potent CCR9 antagonist. MLN3126 inhibits CCL25-induced calcium mobilization and chemotaxis in mouse primary thymocytes with an IC50 value of 6.3 nM for calcium influx inhibition.
价 格：￥电议型 号：T62660产 地：中国大陆
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T61402PGN36；化合物 PGN36PGN36
PGN36 (Compound 18) is a potent and highly selective antagonist of the cannabinoid CB 2 receptor (CB 2 R). It exhibits exceptional affinity for CB 2 R, with a Ki value of 0.09 μM [1].
价 格：￥电议型 号：T61402产 地：中国大陆
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T61086HN37；化合物 HN37HN37
HN37 as a potent and chemically stable antiepileptic drug candidate, with an EC 50 of 37 nM for KCNQ2 [1].
价 格：￥电议型 号：T61086产 地：中国大陆
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T54533-Methyltoxoflavin；化合物3-methyl toxoflavin3-methyl toxoflavin；3-methyl toxoflavin
3-Methyltoxoflavin (3-methyl toxoflavin) is an effective inhibitor of protein disulfide isomerase (PDI) and its IC50 value is 170 nM.
价 格：￥电议型 号：T5453产 地：中国大陆
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T4611EN300-203561；化合物EN300-203561EN300-203561
EN300-203561 has a wide range of applications in life science related research.
价 格：￥电议型 号：T4611产 地：中国大陆
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T4376Nampt-IN-1；化合物Nampt-IN-1LSN3154567；LSN3154567
Nampt-IN-1 (LSN3154567) (LSN3154567) is a potent and selective NAMPT inhibitor. Nampt-IN-1 inhibits purified NAMPT with an IC50 of 3.1 nM.
价 格：￥电议型 号：T4376产 地：中国大陆
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T39908Rhodamine-N3 chloride；Rhodamine-N3 chlorideRhodamine-N3 chloride；Rhodamine-N3 chloride
Rhodamine-N3 chloride is an azide-rhodamine fluorescent dye utilized for labeling alkyne-containing biomolecules.
价 格：￥电议型 号：T39908产 地：中国大陆
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T39222Mc-VC-PAB-SN38；化合物Mc-VC-PAB-SN38Mc-VC-PAB-SN38；Mc-VC-PAB-SN38
Mc-VC-PAB-SN38 consists of a cleavable ADC linker (Mc-VC-PAB) and SN38, which is part of an antibody-coupled reactive molecule commonly used to synthesize antibody-coupled reactive molecules (ADCs) that target sites of action.
价 格：￥电议型 号：T39222产 地：中国大陆
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T39016β-D-tetraacetylgalactopyranoside-PEG1-N3；β-D-tetraacetylgalactopyranoside-PEG1-N3β-D-tetraacetylgala
β-D-tetraacetylgalactopyranoside-PEG1-N3 is a cleavable linker involving a one-unit polyethylene glycol (PEG) compound, employed during the synthesis of antibody-drug conjugates (ADCs). It serves as a crucial component in the formation of ADCs.
价 格：￥电议型 号：T39016产 地：中国大陆
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T38962MC-SN38；MC-SN38MC-SN38；MC-SN38
MC-SN38 is a drug-linker conjugate that pairs the potent microtubule-disrupting agent SN38 with a non-cleavable MC linker, designed for use in antibody drug conjugates (ADCs). SN38, the active metabolite of the Topoisomerase I inhibitor Irinotecan, works by inhibiting DNA synthesis and inducing DNA single-strand breaks.
价 格：￥电议型 号：T38962产 地：中国大陆
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T38538BGN3；BGN3BGN3
BGN3 is a good substrate for the SNAP- tag and H 5 enzymes. The activities of SNAP- tag and H 5 enzymes on BGN3 are reasonable (IC 50 = 15.6 and 23.5 μM, respectively).
价 格：￥电议型 号：T38538产 地：中国大陆
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T38474CL2-MMT-SN38；CL2-MMT-SN38CL2-MMT-SN38；CL2-MMT-SN38
CL2-MMT-SN38 is a derivative of SN-38, which is a potent anticancer agent and the active metabolite of Irinotecan (CPT-11), a Topoisomerase I inhibitor.
价 格：￥电议型 号：T38474产 地：中国大陆
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T38175MPro N3MPro N3MPro N3|||MPro N-3
Coronavirus main protease (Mpro) inhibitor (respective IC50 values are 2.7, 4 and 8.8 μM for MHV-A29, HCoV-229E and FOPV replication in vitro). Inhibits viral cell infection in an MHV plaque reduction assay. Also inhibits SARS-CoV-2 viral cell entry in a plaque reduction assay (IC50 = 16.8 μM).
价 格：￥电议型 号：T38175产 地：中国大陆
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T38174Mpro inhibitor N3 hemihydrate；Mpro inhibitor N3 hemihydrateMpro inhibitor N3 hemihydrate
Mpro inhibitor N3 hemihydrate is a potent antagonist of the SARS-CoV-2 main protease (Mpro), demonstrating an EC50 of 16.77 μM against SARS-CoV-2. It exhibits specific inhibition of Mpro in a range of coronaviruses, including SARS-CoV and MERS-CoV. Furthermore, it effectively inhibits HCoV-229E, FIPV, and MHV-A59, with IC50 values of 4.0 μM, 8.8 μM, and 2.7 μM, respectively[1][2].
价 格：￥电议型 号：T38174产 地：中国大陆
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T36649AN3661；AN3661AN3661
AN3661, a potent antimalarial lead compound, targets a Plasmodium falciparum cleavage and polyadenylation specificity factor homologue subunit 3 (PfCPSF3). AN3661 inhibits Plasmodium falciparum laboratory-adapted strains, Ugandan field isolates, and murine P. berghei and P. falciparum infections[1].
价 格：￥电议型 号：T36649产 地：中国大陆
