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T9554SN-008STING,Stimulator of Interferon Genes,SN-011,TMEM173,MITA,inhibit,ERIS,SN008,Inhibitor,SN 008,M
SN-008 is a less active analog SN-011 which is a STING antagonist. SN-008 can be used as a negative control.
价 格：￥电议型 号：T9554产 地：中国大陆
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T9575MRTX9768SDMA,toxicity,glioblastoma,orally,MRTX9768,low,Inhibitor,hematological,MRTX-9768,MTAP,CDKN2A
MRTX-9768 is a synthetic lethal-based inhibitor designed to bind the PRMT5-MTA complex and selectively target MTAP/CDKN2A-deleted tumors.
价 格：￥电议型 号：T9575产 地：中国大陆
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T6660SB-705498SB 705498,SB705498,inhibit,Inhibitor,SB-705498,TRP Channel,Transient receptor potential cha
SB705498 is a TRPV1 antagonist for hTRPV1. SB-705498 has been investigated for the treatment of Rhinitis, Chronic Cough, and Non-allergic Rhinitis.
价 格：￥电议型 号：T6660产 地：中国大陆
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T4594SR1078SR 1078
SR1078 is an agonist of retinoic acid receptor-related orphan receptor (ROR)α/γ.
价 格：￥电议型 号：T4594产 地：中国大陆
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T22565AMD-070 hydrochlorideN-(1H-苯并咪唑-2-基甲基)-N-[(8S)-5,6,7,8-四氢-8-喹啉基]-1,4-丁二胺单盐酸盐
AMD-070 hydrochloride is a CXCR4 antagonist, is useful for Anti HIV.
价 格：￥电议型 号：T22565产 地：中国大陆
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T22115SM-7368SM 7368
The NF-κB Activation Inhibitor III, controls the biological activity of NF-κB. It is primarily used for Inflammation/Immunology applications.
价 格：￥电议型 号：T22115产 地：中国大陆
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T2109SD-208SD208；SD 208；ALK5 Inhibitor V
SD-208, a selective TGF-βRI (ALK5) inhibitor (IC50: 48 nM), is >100-fold selectivity over TGF-βRII.
价 格：￥电议型 号：T2109产 地：中国大陆
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T12895SHA 68SHA 68
SHA 68 is a potent and selective non-peptide antagonist of neuropeptide S receptor (NPSR)(NPSR Asn107 and NPSR Ile107 with IC50s of 22.0 and 23.8 nM, respectively).
价 格：￥电议型 号：T12895产 地：美洲
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T12907SIAIS178SIAIS178
SIAIS178 is a potent and selective degrader of BCR-ABL based on PROTAC technology (IC50 of 24 nM).
价 格：￥电议型 号：T12907产 地：美洲
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T16848SB-218078SB-218078
SB-218078 is less potently inhibits Cdc2 (IC50: 250 nM) and PKC (IC50: 1000 nM). SB-218078 is a potent, ATP-competitive, and cell-permeable checkpoint kinase 1 inhibitor that inhibits Chk1 phosphorylation of cdc25C (IC50: 15 nM).
价 格：￥电议型 号：T16848产 地：美洲
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T2109SD-208SD-208,SD208,SD 208
SD-208, a selective TGF-βRI (ALK5) inhibitor (IC50: 48 nM), is >100-fold selectivity over TGF-βRII.
价 格：￥电议型 号：T2109产 地：美洲
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T4594SR 1078SR 1078
SR1078 is an agonist of retinoic acid receptor-related orphan receptor (ROR)α/γ.
价 格：￥电议型 号：T4594产 地：美洲
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T83893SLB1122168；化合物 SLB1122168SLB1122168
SLB1122168, an inhibitor targeting the sphingosine-1-phosphate (S1P) transporter Spns2 (with an IC50 of 94 nM for the mouse transporter), selectively reduces circulating lymphocyte counts without altering plasma S1P concentrations in mice at a dosage of 10 mg/kg.
价 格：￥电议型 号：T83893产 地：中国大陆
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T81203SARS-CoV-2-IN-68；化合物 SARS-CoV-2-IN-68SARS-CoV-2-IN-68
SARS-CoV-2-IN-68 (compound 6C) is a covalent inhibitor of both SARS-CoV-2 PLpro and Mpro, exhibiting potent antiviral properties by targeting the Zn-finger domain of PLpro [1].
价 格：￥电议型 号：T81203产 地：中国大陆
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T81164SHP2-IN-18；化合物 SHP2-IN-18SHP2-IN-18
SHP2-IN-18 (compound 183) is a potent SHP2 inhibitor, exhibiting an IC50 of 3 nM and applicable to glioblastoma research [1].
价 格：￥电议型 号：T81164产 地：中国大陆
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T81084STING agonist-18；化合物 STING agonist-18STING agonist-18
STING Agonist-18 (Compound 1a) is a precursor for the synthesis of antibody-drug conjugates (ADCs), including Trastuzumab conjugates [1].
价 格：￥电议型 号：T81084产 地：中国大陆
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T80306A8SGLP-1 TFA；化合物 A8SGLP-1 TFAA8SGLP-1 TFA
A8SGLP-1 TFA, an orally active GLP-1 analogue, features a serine substitution for alanine at position 8. This compound effectively lowers blood glucose in db/db mice, maintaining its function [1].
价 格：￥电议型 号：T80306产 地：中国大陆
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T80305A8SGLP-1；化合物 A8SGLP-1A8SGLP-1
A8SGLP-1, an orally active GLP-1 analogue, features serine substituted for alanine at position 8. It effectively reduces blood glucose in db/db mice, maintaining its function [1].
价 格：￥电议型 号：T80305产 地：中国大陆
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T80262SMAP-18；化合物 SMAP-18SMAP-18
SMAP-18, an 18-amino acid residue peptide amide, is a biologically active truncated variant of Sheep myeloid antimicrobial peptide-29 (SMAP-29). It retains potent antimicrobial activity against Pseudomonas strains, other Gram-negative bacteria, and multidrug-resistant pathogens. Notably, SMAP-18 exhibits increased cell selectivity relative to the parent peptide SMAP-29 due to its reduced hemolytic activity while maintaining its antimicrobial efficacy.
价 格：￥电议型 号：T80262产 地：中国大陆
