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T6280Enzastaurin；恩扎妥林LY317615；LY317615|||恩扎妥林
Enzastaurin (LY317615) (LY317615) is an effective PKCβ selective inhibitor (IC50: 6 nM), 6- to 20-fold selectivity against PKCα/γ/ε.
价 格：￥电议型 号：T6280产 地：中国大陆
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T62176POLA1 inhibitor 1；化合物 POLA1 inhibitor 1POLA1 inhibitor 1
POLA1 inhibitor 1 (Compound 12) is an orally active inhibitor of POLA1. POLA1 inhibitor 1 exhibits antitumour effects on several tumour tissue types and Adaroten-resistant cell lines.
价 格：￥电议型 号：T62176产 地：中国大陆
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T62074MYF-03-176；化合物 MYF-03-176MYF-03-176
MYF-03-176 is an orally active anticancer agent. MYF-03-176 exhibits strong antitumour effects in the MPM mouse xenograft tumour model following oral administration.
价 格：￥电议型 号：T62074产 地：中国大陆
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T61769hCAXII-IN-5；化合物 hCAXII-IN-5hCAXII-IN-5
hCAXII-IN-5 (compound 6o) is a highly effective and specific inhibitor of hCAXII. The compound exhibits impressive binding affinities, with Ki values of >10000, >10000, 286.1, and 1.0 nM for hCAI, hCAII, hCAIX, and hCAXII, respectively [1].
价 格：￥电议型 号：T61769产 地：中国大陆
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T61768FY-56；化合物 FY-56FY-56
FY-56, a highly potent and selective inhibitor of LSD1/KDM1A with an IC50 value of 42 nM, demonstrates significant selectivity over MAO-A/B. This compound effectively induces differentiation in MOLM-13 and MV4-11 cells, showing promise for acute myeloid leukemia (AML) research [1].
价 格：￥电议型 号：T61768产 地：中国大陆
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T61767IRAK4-IN-17；化合物 IRAK4-IN-17IRAK4-IN-17
IRAK4-IN-17 (Compound 5) is a highly potent inhibitor of IRAK4, exhibiting an impressive IC50 value of 1.3 nM [1]. This compound is particularly valuable for research focused on large B-cell lymphoma (DLBCL) [1].
价 格：￥电议型 号：T61767产 地：中国大陆
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T61766RSK4-IN-1；化合物 RSK4-IN-1RSK4-IN-1
RSK4-IN-1 is a compound exhibiting potent inhibition of RSK4, demonstrated by an IC50 value of 9.5 nM.
价 格：￥电议型 号：T61766产 地：中国大陆
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T61765Microtubule inhibitor 5；化合物 Microtubule inhibitor 5Microtubule inhibitor 5
Microtubule inhibitor 5 (compound 17f) is a highly potent cytotoxic agent that inhibits microtubule function. It exhibits a substantial cytotoxic effect on NCI-H460 cells, with an IC50 value of 154.5 nM. Moreover, this compound demonstrates excellent cell permeability [1].
价 格：￥电议型 号：T61765产 地：中国大陆
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T61764Zoledronic acid disodium tetrahydrate；化合物 Zoledronic acid disodium tetrahydrateZoledronic acid disod
Zoledronic Acid (Zoledronate) disodium tetrahydrate is a potent third-generation bisphosphonate (BP), exhibiting strong anti-resorptive activity. It effectively inhibits osteoclast differentiation and apoptosis, while also demonstrating anti-cancer properties [1].
价 格：￥电议型 号：T61764产 地：中国大陆
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T61763GRP-60367 hydrochloride；化合物 GRP-60367 hydrochlorideGRP-60367 hydrochloride
GRP-60367 hydrochloride is a novel small-molecule entry inhibitor of rabies virus (RABV), exhibiting nanomolar potency against select RABV strains. This first-in-class compound effectively targets the RABV G protein [1].
价 格：￥电议型 号：T61763产 地：中国大陆
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T61762Zika virus-IN-3；化合物 Zika virus-IN-3Zika virus-IN-3
Zika virus-IN-3 (Compd 7) is a Zika virus inhibitor, with an EC 50 of 3.4 μM [1].
价 格：￥电议型 号：T61762产 地：中国大陆
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T61761α-Glucosidase-IN-21；化合物 α-Glucosidase-IN-21α-Glucosidase-IN-21
α-Glucosidase-IN-21 (Compound 2B) is a highly potent and orally bioavailable inhibitor of α-glucosidase. With an impressive IC50 value of 2.62 μM, this compound exhibits remarkable anti-diabetic properties [1].
价 格：￥电议型 号：T61761产 地：中国大陆
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T61760COX-2-IN-18；化合物 COX-2-IN-18COX-2-IN-18
COX-2-IN-18 (Compound 3) is a highly effective COX-2 inhibitor with strong inhibitory activity against COX-2 (IC 50 = 0.775 μM). Its potency is comparable to the reference drug Celecoxib (IC 50 = 0.153 μM). This compound, COX-2-IN-18, shows promise in the field of cancer research [1].
价 格：￥电议型 号：T61760产 地：中国大陆
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T6176IKK 16；化合物IKK16IKK Inhibitor VII|||IKK-16|||IKK16；IKK Inhibitor VII|||IKK-16|||IKK16
IKK 16 (IKK Inhibitor VII) is a selective IκB kinase (IKK) inhibitor for IKK-2, IKK complex and IKK-1 with IC50 of 40 nM, 70 nM and 200 nM, respectively.
价 格：￥电议型 号：T6176产 地：中国大陆
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T61176MRK-623；化合物 MRK-623MRK-623
MRK-623 (Compound 14k) is a potent, orally active agonist of the GABA A receptor, exhibiting high affinity for subunits α1, α2, α3, and α5 with Ki values of 0.85 nM, 3.7 nM, 4.0 nM, and 0.53 nM, respectively. Notably, MRK-623 demonstrates anxiolytic effects [1].
价 格：￥电议型 号：T61176产 地：中国大陆
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T6006Romidepsin；罗米地辛FR 901228|||FK 228|||Depsipeptide|||NSC 630176；FR 901228|||FK 228|||Depsipeptide|||罗米
Romidepsin (FR 901228) is an HDAC inhibitor that inhibits HDAC1/2/4/6 (IC50=36/47/510/1400 nM). Romidepsin has antitumor activity and can be used for the treatment of peripheral T-cell lymphoma and cutaneous T-cell lymphoma.
价 格：￥电议型 号：T6006产 地：中国大陆
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T60016VV116；化合物 VV116GS-621763-d1|||JT001；GS-621763-d1|||JT001
VV116 (JT001) is a selective and orally active nucleoside antiviral agent against respiratory syncytial virus (RSV) and SARS-CoV-2 infection.
价 格：￥电议型 号：T60016产 地：中国大陆
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T5160SR3335；化合物SR3335ML 176；ML 176
SR3335 (ML 176) is a selective inverse agonist of RORα, competitively inhibiting the binding of 25-hydroxycholesterol to the ligand binding domain (Ki: 220 nM).
价 格：￥电议型 号：T5160产 地：中国大陆
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T5154C-176；化合物C-176C176|||STING inhibitor 1；C176|||STING inhibitor 1
C-176 (STING inhibitor 1) is a strong, covalent mouse STING inhibitor
价 格：￥电议型 号：T5154产 地：中国大陆
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T4S0176Alnustone；桤木酮(4E,6E)-1,7-Diphenyl-4,6-heptadien-3-one；(4E,6E)-1,7-Diphenyl-4,6-heptadien-3-one|||桤木酮
Alnustone ((4E,6E)-1,7-Diphenyl-4,6-heptadien-3-one) exerts significant anti-inflammatory activity in the assay of carrageenin-induced hind paw edema in rats.
价 格：￥电议型 号：T4S0176产 地：中国大陆
