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T6756AMG 925；化合物AMG 925AMG 925
AMG 925 is a potent and orally bioavailable dual FLT3/CDK4 inhibitor with IC50 of 1 nM and 3 nM, respectively.
价 格：￥电议型 号：T6756产 地：中国大陆
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T669254-Hydroxy-1-indanone；化合物 4-Hydroxy-1-indanone4-Hydroxy-1-indanone
4-Hydroxy-1-indanone is a useful organic compound for research related to life sciences. The catalog number is T66925 and the CAS number is 40731-98-4.
价 格：￥电议型 号：T66925产 地：中国大陆
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T6595Moexipril hydrochloride；莫昔普利盐酸盐Moexipril HCl|||RS-10085|||SPM 925|||CI-925；莫昔普利盐酸盐|||Moexipril HCl||
Moexipril hydrochloride (Moexipril HCl) is a potent orally active nonsulfhydrylangiotensin converting enzyme (ACE)inhibitor, used for the treatment of hypertension and congestive heart failure.
价 格：￥电议型 号：T6595产 地：中国大陆
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T65925H-Asp(ome)-OMe HCl；化合物 H-Asp(ome)-OMe HClH-Asp(ome)-OMe HCl
H-Asp(ome)-OMe HCl is a useful organic compound for research related to life sciences. The catalog number is T65925 and the CAS number is 32213-95-9.
价 格：￥电议型 号：T65925产 地：中国大陆
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T64925(S)-2,5-Dioxopyrrolidin-1-yl 2-(((benzyloxy)carbonyl)amino)-3-methylbutanoate；化合物 (S)-2,5-Dioxopyrro
(S)-2,5-Dioxopyrrolidin-1-yl 2-(((benzyloxy)carbonyl)amino)-3-methylbutanoate is a useful organic compound for research related to life sciences. The catalog number is T64925 and the CAS number is 3496-11-5.
价 格：￥电议型 号：T64925产 地：中国大陆
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T63925FHT-1015；化合物 FHT-1015FHT-1015
FHT-1205 is a potent inhibitor (IC50 ≤ 10 nM) of SMARCA4/SMARCA2 ATPase (BRG1 and BRM).
价 格：￥电议型 号：T63925产 地：中国大陆
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T63487AMG 925 HCl；化合物 AMG 925 HClAMG 925 HCl
AMG 925 HCl is a selective and potent dual inhibitor of FLT3 (IC50: 2±1 nM) and CDK4 (IC50: 3±1 nM).
价 格：￥电议型 号：T63487产 地：中国大陆
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T62925FASN-IN-5；化合物 FASN-IN-5FASN-IN-5
FASN-IN-5 (example 11) is a FASN inhibitor that can be used in studies of TH17 or CSF1-mediated diseases or disorders (e.g. cancer, immune disorders, obesity).
价 格：￥电议型 号：T62925产 地：中国大陆
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T61925AKR1C3-IN-7；化合物 AKR1C3-IN-7AKR1C3-IN-7
AKR1C3-IN-7 (Compound 13) is an effective and selective AKR1C3 inhibitor (IC50=0.19 μM). AKR1C3-IN-7 has antitumor activity.
价 格：￥电议型 号：T61925产 地：中国大陆
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T60925TRβ agonist 3；化合物 TRβ agonist 3TRβ agonist 3
TRβ agonist 3 (Compound 3) is a potent TRβ agonist that is a new potential TRβ-selective thyromimetics. In vitro investigation, TRβ agonist 3 reduces lipid accumulation in HepG2 and promote lipolysis [1].
价 格：￥电议型 号：T60925产 地：中国大陆
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T5124SRT 1720 dihydrochloride[925434-55-5(free base)]；化合物SRT 1720 dihydrochloride[SRT 1720 dihydrochlorid
SRT 1720 is a selective activator of SIRT1 (EC1.5: 0.16 μM) and shows less potent activities on SIRT2 (EC1.5: 37 μM) and SIRT3 (EC1.5: 300 μM).
价 格：￥电议型 号：T5124产 地：中国大陆
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T4925Thiamine monophosphate chloride (dihydrate)胺氯化亚磷酸酯Thiamine monophosphate chloride dihydrat|||胺氯化亚磷酸酯
Thiamine monophosphate chloride dihydrate (Aneurine monophosphate chloride) is a compound used in the screening of ligands that promote protein stability
价 格：￥电议型 号：T4925产 地：中国大陆
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T40925Peripheral Myelin Protein P2 (53-78), bovine；Peripheral Myelin Protein P2 (53-78), bovinePeripheral
Bovine Peripheral Myelin Protein P2 (53-78) is a derivative composed of amino acid residues 53 to 78 from the peripheral myelin P2 protein of bovine origin. It acts as a T cell epitope and is used to induce experimental autoimmune neuritis (EAN) in Lewis rats.
价 格：￥电议型 号：T40925产 地：中国大陆
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T3S1925Schisantherin E；化合物 T3S1925Schisantherin E
Schisantherin E is an organic compound obtained from the active fraction of Schisandra sphenanthera Rehd. et Wils. fruit.
价 格：￥电议型 号：T3S1925产 地：中国大陆
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T39925Thalidomide-NH-PEG3-COOH；Thalidomide-NH-PEG3-COOHThalidomide-NH-PEG3-COOH；Thalidomide-NH-PEG3-COOH
Thalidomide-NH-PEG3-COOH is a conjugate of the E3 ligase ligand-linker synthesized compound, which integrates a cereblon ligand based on Thalidomide and a linker employed in PROTAC technology.
价 格：￥电议型 号：T39925产 地：中国大陆
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T39259ArzoxifeneArzoxifeneLY353381|||Arzoxifene|||SERMIII
Arzoxifene (LY353381) is an orally active selective estrogen receptor modulator (SERM) exhibiting a fixed ring structure analogous to raloxifene. This compound demonstrates potent antiestrogenic effects on breast cancer and endometrium while displaying minimal side effects. Additionally, Arzoxifene elicits favorable estrogenic effects on bone health and lipid profile.
价 格：￥电议型 号：T39259产 地：中国大陆
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T39258PulrodemstatPulrodemstatLSD1-IN-7|||CC-90011
Pulrodemstat (CC-90011) is a highly potent and selective inhibitor of lysine specific demethylase-1 (LSD1). It exhibits a reversible mode of action and can be administered orally. With an impressive IC50 of 0.25 nM, Pulrodemstat effectively suppresses the enzymatic activity of LSD1. Notably, it demonstrates minimal inhibition against LSD2, MOA-A, and MAO-B enzymes. Moreover, Pulrodemstat possesses remarkable anticancer properties, promoting differentiation in acute myeloid leukemia (AML) and sma
价 格：￥电议型 号：T39258产 地：中国大陆
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T39257Ugodotin；UgodotinUgodotin
Ugodotin is an antibody-drug conjugate. Ugodotin can binds IGF-1R with antitumor activity.
价 格：￥电议型 号：T39257产 地：中国大陆
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T39256MMV674850；MMV674850MMV674850；MMV674850
MMV674850 exhibits potency against asexual stage parasites, with IC50 values of 2.7 and 4.5 nM. Furthermore, it demonstrates a preferential affinity for early-stage gametocytes, displaying an IC50 value of 4.5 ± 3.6 nM, compared to late-stage gametocytes with an IC50 value of 28.7 ± 0.2 nM.
价 格：￥电议型 号：T39256产 地：中国大陆
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T39255β-Cyfluthrin；β-Cyfluthrinbeta-Cyfluthrin|||β-Cyfluthrin；beta-Cyfluthrin|||β-Cyfluthrin
β-Cyfluthrin is a type II synthetic pyrethroid compound commonly utilized as an active ingredient in agricultural insecticide products. It exerts its insecticidal properties by acting as a neurotoxicant, primarily impacting the calcium concentration within nervous tissue. This effect is achieved through the inhibition of Ca 2+ ATPase, a crucial component involved in calcium transport.
价 格：￥电议型 号：T39255产 地：中国大陆
