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T60010BTT-266；化合物 BTT-266BTT-266
BTT-266 is a blocker of voltage-gated calcium channel for pain management.
价 格：￥电议型 号：T60010产 地：中国大陆
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T60008BCL6-IN-6；化合物BCL6-IN-6BCL6-IN-6
BCL6-IN-6 is an inhibitor of Bcl-6 and can be used in studies about diffuse large B-cell lymphoma. BCL6-IN-6 blocks the interaction of Bcl-6 with its corepressors and dose-dependently reactivates Bcl-6 target genes.
价 格：￥电议型 号：T60008产 地：中国大陆
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T5697BMS-1166；化合物BMS1166BMS-1166
BMS-1166 is a potent PD-1/PD-L1 interaction inhibitor.
价 格：￥电议型 号：T5697产 地：中国大陆
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T41153BOP-JF646；BOP-JF646BOP-JF646；BOP-JF646
BOP-JF646 is a fluorescent dual α9β1/α4β1 integrin inhibitor. Comprises BOP conjugated to Janelia Fluor?646. Fluorogenic: fluoresces only once bound to integrins, enabling hassle-free no-wash experiments. Bright and photostable, enabling live cell tracking of integrin receptors over long time-course experiments. Excitation maximum = 655 nm; emission maximum = 672 nm.
价 格：￥电议型 号：T41153产 地：中国大陆
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T40944Bis-acrylate-PEG6；Bis-acrylate-PEG6Bis-acrylate-PEG6；Bis-acrylate-PEG6
Bis-acrylate-PEG6 is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T40944产 地：中国大陆
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T40903ACG416B；ACG416BACG416B
ACG416B (compound 18) exhibits formidable inhibitory effects on choline kinase (ChoK), with an IC 50 measurement of 0.4 μM. Notably, ACG416B demonstrates superior inhibitory activities against HT-29 human colon cancer cells, resulting in pronounced antiproliferative effects.
价 格：￥电议型 号：T40903产 地：中国大陆
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T40153BAMEA-O16B；BAMEA-O16BBAMEA-O16B；BAMEA-O16B
BAMEAO16B is a lipid nanoparticle that incorporates disulfide bonds for efficient delivery of Cas9 mRNA and sgRNA into cells. In the intracellular environment, BAMEAO16B responds to reduction by releasing RNA, facilitating genome editing. This compound is valuable for gene editing research purposes.
价 格：￥电议型 号：T40153产 地：中国大陆
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T39779BMT-297376；BMT-297376BMT-297376
BMT-297376, the optimized Linrodostat, is a potent IDO1 inhibitor.
价 格：￥电议型 号：T39779产 地：中国大陆
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T39593SPOP-IN-6b hydrochloride；SPOP-IN-6b hydrochlorideSPOP-IN-6b hydrochloride
SPOP-IN-6b hydrochloride is a highly effective inhibitor of speckle-type POZ protein (SPOP), exhibiting an IC50 value of 3.58 μM.
价 格：￥电议型 号：T39593产 地：中国大陆
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T39484BACE1-IN-6BACE1-IN-6BACE1-IN-6
BACE1-IN-6 is a BACE1 inhibitor with an IC 50 value of 1.5 nM.
价 格：￥电议型 号：T39484产 地：中国大陆
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T38930BAY-826；化合物 BAY-826BAY-826
BAY-826 is a novel, potent and selective TIE-2 inhibitor that inhibits TIE-2 phosphorylation and can be used to study tumors.
价 格：￥电议型 号：T38930产 地：中国大陆
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T38397BMS-753426；BMS-753426BMS-753426
BMS-753426 is a potent and orally bioavailable antagonist of CCR2 .
价 格：￥电议型 号：T38397产 地：中国大陆
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T38322A-54556B；A-54556BA-54556B
A-54556B is a natural acyldepsipeptide (ADEP) antibiotic isolated from the fermentation broth of S. hawaiiensis. Like the closely related ADEP, A-54556A , A-54556B is effective against Gram-positive bacteria, including penicillin-resistant S. aureus. A-54556B is also effective against many strains of anaerobic bacteria.
价 格：￥电议型 号：T38322产 地：中国大陆
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T38167BE-24566B；BE-24566BBE-24566B
BE-24566B is a polyketide fungal metabolite originally isolated fromS. violaceusniger.1It is active againstB. subtilis,B. cereus,S. aureus,M. luteus,E. faecalis, andS. thermophilus(MICs = 1.56, 1.56, 1.56, 1.56, 3.13, and 3.13 μg/ml, respectively). BE-24566B is an endothelin (ET) receptor antagonist (IC50s = 11 and 3.9 μM for ETAand ETBreceptors, respectively).2
价 格：￥电议型 号：T38167产 地：中国大陆
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T378116-Chloro-3-indolyl-β-D-Glucuronide CHA；6-Chloro-3-indolyl-β-D-Glucuronide 环已胺盐16beta-Methyl-16alpha,
6-Chloro-3-indolyl-β-D-Glucuronide (cyclohexylammonium salt) is a chromogenic substrate for β-glucuronidase. 6-Chloro-3-indolyl-β-D-Glucuronide (cyclohexylammonium salt) can be used in the histochemical analysis of β-glucuronidase activity.
价 格：￥电议型 号：T37811产 地：中国大陆
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T3713BAY-876；化合物BAY-876BAY-876
BAY-876 is an orally active and selective inhibitor of glucose transporter 1 (GLUT1, IC50= 2 nM). BAY-876 exhibits >130-fold more selective for GLUT1 than GLUT2, GLUT3, and GLUT4. BAY-876 also inhibits glycolytic metabolism and ovarian cancer growth.
价 格：￥电议型 号：T3713产 地：中国大陆
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T35856BMS-986176；化合物BMS-986176BMS-986176
AAK1-IN-1 is a highly selective and potent inhibitor of adaptor associated kinase 1 (AAK1, IC50 = 2 nM).
价 格：￥电议型 号：T35856产 地：中国大陆
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T35216Xysmalogenin；化合物 T35216BRN0051836,|||BRN-0051836|||BRN 0051836；BRN0051836,|||BRN-0051836|||BRN 00518
Xysmalogenin is a biochemical.
价 格：￥电议型 号：T35216产 地：中国大陆
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T34717Stevastelin B3；化合物 T34717NK374186B3|||NK 374186B3|||Antibiotic NK 374186B3|||NK-374186B3；NK374186B3|
Stevastelin B3 is a depsipeptide isolated from Penicillium.
价 格：￥电议型 号：T34717产 地：中国大陆
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T34696Spirapril HCl；化合物 T34696BRN4277924|||BRN-4277924|||BRN 4277924|||Spiraprilum|||Spirapril|||Espirapri
Spiropril is an ACE inhibitor antihypertensive drug, which belongs to the bicarboxyl group of ACE inhibitors and is used in the treatment of hypertension.
价 格：￥电议型 号：T34696产 地：中国大陆
