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T16432Pan-RAS-IN-1
Pan-RAS-IN-1 is an inhibitor of pan-Ras. It disrupts the interaction of Ras proteins and their effectors.
价 格：￥电议型 号：T16432产 地：中国大陆
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T1643Penciclovir喷昔洛韦；VSA 671；BRL 39123
Penciclovir is a Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor. In HSV infected cells, penciclovir is phosphorylated by viral thymidine kinase and subsequently converted by cellular kinases into the active metabolite, penciclovir triphosphate, wh
价 格：￥电议型 号：T1643产 地：中国大陆
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T16343NRC-2694
NRC-2694 is an antagonist of the epidermal growth factor receptor (EGFR). It has anti-cancer and anti-proliferative properties.
价 格：￥电议型 号：T16343产 地：中国大陆
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T1615Irbesartan厄贝沙坦；SR-47436；BMS-186295
Irbesartan is an Angiotensin 2 Receptor Blocker. The mechanism of action of irbesartan is as an Angiotensin 2 Receptor Antagonist.
价 格：￥电议型 号：T1615产 地：中国大陆
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T16144MRX-2843UNC2371
MRX-2843 is a potent and orally active inhibitor of MERTK and FLT3(IC50s of 1.3 nM and 0.64 nM, respectively).
价 格：￥电议型 号：T16144产 地：中国大陆
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T16143MRTX-1257
MRTX-1257 is a selective, irreversible, and covalent inhibitor of KRAS G12C. It has an IC50 of 900 pM for KRAS dependent ERK phosphorylation in H358 cells. MRTX1257 demonstrated 31% bioavailability in the mouse, with free fraction exposures well above the
价 格：￥电议型 号：T16143产 地：中国大陆
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T1610MetaxaloneMethaxalonum；Zorane；AHR438；Skelaxin；NSC170959；美他沙酮
Metaxalone (marketed by King Pharmaceuticals under the brand name Skelaxin ) is a muscle relaxant used to relax muscles and relieve pain caused by strains, sprains, and other musculoskeletal conditions.
价 格：￥电议型 号：T1610产 地：中国大陆
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T16068MF-438
MF-438 is an effective and orally bioavailable stearoyl-CoA desaturase 1 (SCD1) inhibitor (EC50: 2.3 nM for rSCD1).
价 格：￥电议型 号：T16068产 地：中国大陆
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T1587Exemestane依西美坦；FCE 24304；EXE；PNU155971
Exemestane is an Aromatase Inhibitor. The mechanism of action of exemestane is as an Aromatase Inhibitor.
价 格：￥电议型 号：T1587产 地：中国大陆
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T15635JZP-430
JZP-430 is an effective, highly selective, irreversible inhibitor of α/β-hydrolase domain 6 (ABHD6) (IC50: 44 nM). It also shows ~230-fold selectivity over fatty acid amide hydrolase (FAAH) and lysosomal acid lipase (LAL).
价 格：￥电议型 号：T15635产 地：中国大陆
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T15623JNJ-61432059
JNJ-61432059 is an oral active and selective negative modulator of TARP γ?8 Selective AMPAR(pIC50: 9.7).
价 格：￥电议型 号：T15623产 地：中国大陆
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T15568Imirestat咪瑞司他；Alcon 1576；AL 1576；HOE 843
Imirestat is an aldose reductase inhibitor that can be used in diabetes research.
价 格：￥电议型 号：T15568产 地：中国大陆
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T15545ICA-27243
ICA-27243 is less effective at activating KCNQ4 and KCNQ3/Q5. ICA-27243 is a potent and orally active KCNQ2/Q3 potassium channel opener (EC50: 0.38 μM). ICA-27243 also has antiepileptic and anticonvulsant effects.
价 格：￥电议型 号：T15545产 地：中国大陆
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T15543IA-AlkyneN-Hex-5-ynyl-2-iodo-acetamide；Iodoacetamide-alkyne
IA-Alkyne is a TRP channel (TRPC) agonist. IA-Alkyne can be used to develop an isotopically tagged probe for quantitative cysteine-reactivity profiling. It also has the potential for the study of respiratory infection.
价 格：￥电议型 号：T15543产 地：中国大陆
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T15454GW843682XGW843682
GW843682X is a selective and ATP-competitive inhibitor of PLK1 and PLK3 (IC50s: 2.2 nM and 9.1 nM, respectively). It is also >100-fold selective against ～30 other kinases.
价 格：￥电议型 号：T15454产 地：中国大陆
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T15437GSK3145095
GSK3145095 is an orally active inhibitor of RIPK1 with IC50 of 5 nM, with potential immunomodulatory activities and antineoplastic.
价 格：￥电议型 号：T15437产 地：中国大陆
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T15436GSK2838232
GSK2838232 inhibit HIV reverse transcriptase activity across a broad panel of HIV-1 isolates,GSK2838232 is novel human immune virus (HIV) maturation inhibitor.
价 格：￥电议型 号：T15436产 地：中国大陆
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T15435GSK2837808A
GSK2837808A is a potent and selective inhibitor of lactate dehydrogenase A (LDHA) (IC50s: 1.9 and 14 nM for LDHA and LDHB, respectively).
价 格：￥电议型 号：T15435产 地：中国大陆
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T15433GSK2795039
GSK2795039 inhibits reactive oxygen species (ROS) production and NADPH consumption. GSK2795039 decreases apoptosis. GSK2795039 is an inhibitor of NADPH oxidase 2 (NOX2) (pIC50: 6 in different cell-free assays).
价 格：￥电议型 号：T15433产 地：中国大陆
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T15432GSK256073
GSK256073 is an orally active GPR109A agonist. GSK256073 also is a long-lasting and non-flushing HCA2 (hydroxy-carboxylic acid receptor 2) full agonist (pEC50: 7.5). GSK256073 acutely improves glucose homeostasis via inhibition of lipolysis.
价 格：￥电议型 号：T15432产 地：中国大陆
