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T61083DN-F01；化合物 DN-F01DN-F01
DN-F01 exhibits a potent calcium-dependent inhibitory effect on cardiac myofibrillar ATPase activity, with an IC50 of 11 ± 4 nmol/L.
价 格：￥电议型 号：T61083产 地：中国大陆
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T61082CYP1B1-IN-2；化合物 CYP1B1-IN-2CYP1B1-IN-2
CYP1B1-IN-2 (compound 9j) is a highly potent and selective inhibitor of CYP1B1, a cytochrome P450 enzyme. It exhibits an IC50 value of 0.52 nM [1].
价 格：￥电议型 号：T61082产 地：中国大陆
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T61081DFPM；化合物 DFPMDFPM
DFPM, a chemical compound, acts as an activator of the plant resistance protein signaling in roots, thereby causing inhibition of root growth. It also reduces the viability of root cells specifically in the Col-0 accession. Notably, DFPM displays sensitivity to light when dissolved in aqueous solutions. It acquires bioactivity through light-induced and oxygen-dependent modification [1].
价 格：￥电议型 号：T61081产 地：中国大陆
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T61080L-I-OddU；化合物 L-I-OddUL-I-OddU
L-I-OddU, a potent and selective anti-Epstein-Barr virus (EBV) agent, is a L-5´-halo-dioxolane nucleoside analogue. It demonstrates antiviral activity by effectively suppressing replicative EBV DNA and viral protein synthesis [1] [2]. With an EC 50 value of 0.03 μM, L-I-OddU exhibits high potency against EBV while maintaining low cytotoxicity, as indicated by its CC 50 value of 1000 nM.
价 格：￥电议型 号：T61080产 地：中国大陆
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T6108Ki16425；化合物Ki16425Debio 0719；Debio 0719
Ki16425 (Debio 0719) is a competitive, potent and reversible antagonist to LPA1, LPA2 and LPA3 with Ki of 0.34 μM, 6.5 μM and 0.93 μM, respectively.
价 格：￥电议型 号：T6108产 地：中国大陆
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T6068MK-5108；化合物MK-5108VX-689|||MK5108；VX-689|||MK5108
MK-5108 (VX-689) is a highly potent and specific Aurora-A kinase inhibitor with an IC50 value of 0.064 nM.
价 格：￥电议型 号：T6068产 地：中国大陆
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T60300BPH-1086；化合物 BPH-1086BPH-1086
BPH-1086 (compound 10) is an inhibitor of IspH. IspH domain fused with ribosomal protein S1 (RPS1) can bind to mRNA or form part of the bacterial ribosome [1] [2].
价 格：￥电议型 号：T60300产 地：中国大陆
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T60108PDGFR Tyrosine Kinase Inhibitor III；PDGFR酪氨酸激酶抑制剂IIIPDGF Receptor Tyrosine Kinase Inhibitor III；PDGF
PDGFR Tyrosine Kinase Inhibitor III (PDGF Receptor Tyrosine Kinase Inhibitor III) (PDGF Receptor Tyrosine Kinase Inhibitor III) is a multikinase inhibitor that inhibits PDGFR, EGFR, FGFR, PKA, and PKC, respectively. PDGFR Tyrosine Kinase Inhibitor III can be used for the research of amyotrophic lateral sclerosis [1].
价 格：￥电议型 号：T60108产 地：中国大陆
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T60034TH1085；化合物TH1085TH1085
TH1085 is an enhancer of OGG1. TH1085 stimulates DNA repair and protects cells from the environmental hazard paraquat (PQ).
价 格：￥电议型 号：T60034产 地：中国大陆
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T5108ML311；化合物ML311ML311
ML311 is a selective inhibitor of the Mcl-1/Bim interaction.
价 格：￥电议型 号：T5108产 地：中国大陆
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T4198T.cruzi-IN-1；T.cruzi InhibitorMDK1088|||T.cruzi Inhibitor；MDK1088|||T.cruzi Inhibitor
T.cruzi-IN-1 (MDK1088) is a Trypanosoma cruzi inhibitor.
价 格：￥电议型 号：T4198产 地：中国大陆
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T41108Nor-Acetildenafil；Nor-AcetildenafilNor-Acetildenafil
Nor-Acetildenafil is a derivative of Acetildenafil, a synthetic phosphodiesterase inhibitor.
价 格：￥电议型 号：T41108产 地：中国大陆
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T41089L-Homopropargylglycine hydrochloride；L-Homopropargylglycine hydrochlorideL-Homopropargylglycine hydr
L-Homopropargylglycine hydrochloride is an alkyl-based PROTAC linker used in PROTAC synthesis. It is an amino acid analog of methionine with an alkyne group, enabling a click chemical reaction with azide-containing Alexa Fluor.
价 格：￥电议型 号：T41089产 地：中国大陆
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T41088Diadenosine pentaphosphate pentalithium；Diadenosine pentaphosphate pentalithiumDiadenosine pentaphos
Diadenosine pentaphosphate pentalithium is an endogenous vasoactive purine dinucleotide, isolated from thrombocytes. It is a member of the diadenosine polyphosphates (ApnA, n=2–7) and is found in secretory vesicles of platelets, chromaffin cells, Torpedo synaptic terminals, and brain synaptosomes.
价 格：￥电议型 号：T41088产 地：中国大陆
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T41087Penetratin；PenetratinPenetratin
Penetratin is a peptide derived from the amphiphilic Drosophila Antennapedia homeodomain.
价 格：￥电议型 号：T41087产 地：中国大陆
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T41086IDR-1；IDR-1IDR-1
IDR-1 is an antimicrobial peptide with activity against both Gram-positive and Gram-negative bacteria. This compound modulates innate immunity to counter infections while avoiding evident toxicities. Additionally, IDR-1 exhibits anti-inflammatory and anti-infective properties, increases the levels of monocyte chemokines, and reduces the release of pro-inflammatory cytokines.
价 格：￥电议型 号：T41086产 地：中国大陆
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T41085UK122UK122UK122
UK122 is a highly effective and specific inhibitor of urokinase-type plasminogen activator (uPA) with an IC50 value of 0.2 μM. It displays negligible to minimal inhibition towards tissue-type plasminogen activator (tPA), plasmin, thrombin, and trypsin (all IC50 >100 μM). Functioning as a 4-oxazolidinone analogue, UK122 is an anticancer agent that effectively inhibits cancer cell migration and invasion.
价 格：￥电议型 号：T41085产 地：中国大陆
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T41084MDM2-IN-21MDM2-IN-21MDM2-IN-21
MDM2-IN-21 is a potent MDM2 inhibitor. MDM2-IN-21 can be used for the research of cancer.
价 格：￥电议型 号：T41084产 地：中国大陆
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T41083pNP-ADPr；pNP-ADPrpNP-ADPr|||ADP-ribose-pNP；pNP-ADPr|||ADP-ribose-pNP
pNP-ADPr is a colorimetric substrate employed in the first continuous activity assays for Poly(ADP-ribose) glycohydrolase (PARG) and ADP-ribosyl hydrolase 3 (ARH3). Its utilization facilitates research on poly(ADP-ribose) polymerase (PARP) enzymes.
价 格：￥电议型 号：T41083产 地：中国大陆
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T41081Pyrazosulfuron-ethyl；Pyrazosulfuron-ethylPyrazosulfuron-ethyl
Pyrazosulfuron-ethyl, a sulphonylurea herbicide belonging to the acetolactate synthase inhibiting category, has gained extensive application in the suppression of weed proliferation within commercial cereal, soybean, and vegetable fields.
价 格：￥电议型 号：T41081产 地：中国大陆
