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T833916α-HydroxyprednisoloneInhibitor,16α-Hydroxyprednisolone,16α Hydroxyprednisolone,inhibit,Drug Metabo
16alpha-Hydroxyprednisolone is a stereoselective metabolite of the 22(R) epimer of the glucocorticoid budesonide
价 格：￥电议型 号：T8339产 地：中国大陆
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T7767FMoc-Val-Cit-PAB-PNPFMocValCitPABPNP,ADC Linkers,inhibit,Antibody-drug conjugates linkers,Inhibitor,
Fmoc-Val-Cit-PAB-PNP is a linker for Antibody-Drug-Conjugation (ADC).
价 格：￥电议型 号：T7767产 地：中国大陆
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T19676Tributyrinantiproliferative,fatty acid triglyceride,Inhibitor,proapoptotic,prodrug,inhibit,21920,Tri
Tributyrin (Glyceryl tributyrate), a neutral short-chain fatty acid triglyceride, is a stable and rapidly absorbed prodrug of Butyric Acid. Tributyrin diffuses through biological membranes and is metabolized by intracellular lipases, releasing effective butyrate directly into the cell in vivo. Tributyrin has potent proapoptotic, antiproliferative, and differentiation-inducing effects.
价 格：￥电议型 号：T19676产 地：中国大陆
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TN1740HomoeriodictyolEriocitrin,flavonoid,inhibit,metabolite,Inhibitor,Drug Metabolite,Homoeriodictyol
Homoeriodictyol, a naturally occurring, bitter-masking flavanone, as a promising agent to increase appetite and food intake. The flavanone homoeriodictyol can increase SGLT-1-mediated glucose uptake but decrease serotonin release in differentiated Caco-2 cells.
价 格：￥电议型 号：TN1740产 地：中国大陆
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T9116SMCCSMCC,ADC Linkers,inhibit,Antibody-drug conjugates linkers,Inhibitor
N-Succinimidyl 4-(N-maleimidomethyl)cycl(SMCC), also known as succinimidyl-4-[N-maleimidomethyl]cyclohexane-1-carboxylate, is a heterobifunctional protein crosslinker.
价 格：￥电议型 号：T9116产 地：中国大陆
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T60014SHEN26RNA,SHEN26,viral load,ATV 006,ATV006,antiviral,SARS coronavirus,Vero E6 cells,podrugs,Inhibito
SHEN26 has antiviral activity and can be used in research on the treatment of viral infections.
价 格：￥电议型 号：T60014产 地：中国大陆
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T9282DBCO-C3-AcidDBCO C3 Acid,inhibit,Inhibitor,DBCO-C-3-Acid,Antibody-drug conjugates linkers,DBCOC3Acid
DBCO acid 2 is a Click Chemistry intermidate used for antibody-drug conjugates.
价 格：￥电议型 号：T9282产 地：中国大陆
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T7744Piperaquine tetraphosphate tetrahydrateartemisinin,Parasite,inhibit,antimalarial,drug-based,Inhibito
Piperaquine tetraphosphate tetrahydrate is a potent anti-parasites agent.
价 格：￥电议型 号：T7744产 地：中国大陆
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T9783Boc-C16-COOHAntibody-drug conjugates linkers,Boc-C-16-COOH,ADC Linkers,Inhibitor,Boc C16 COOH,BocC16
Boc-C16-COOH is a alkyl-chain-based PROTAC linker. Boc-C16-COOH is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T9783产 地：中国大陆
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T7174Urolithin AAutophagy,Urolithin A,Inhibitor,DNA/RNA Synthesis,Reactive Oxygen Species,Drug Metabolite
Urolithin A is a secondary metabolite of ellagic acid, a polyphenolic antioxidant, that has antiproliferative, anti-inflammatory, and anti-oxidant properties.
价 格：￥电议型 号：T7174产 地：中国大陆
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T8547DCBADEET,DCBA,Drug Metabolite,Insect,inhibit,urine,Inhibitor,repellent
DCBA is a endogenous metabolite of insect repellent N-N-diethyl-meta-toluamide (DEET). The concentration of DCBA in urine can assess exposure to DEET.
价 格：￥电议型 号：T8547产 地：中国大陆
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T8149Dobutamine hydrochloridedrug,Adrenergic Receptor,Dobutamine hydrochloride,Dobutamine,heart failure,I
Dobutamine (hydrochloride) is a catecholamine that acts as a β-adrenergic receptor agonist with potent positive inotropic effects.
价 格：￥电议型 号：T8149产 地：中国大陆
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T4661PKG drug G1
PKG drug G1 targets C42 of PKG Iα. PKG drug G1 can couple to vasodilation and blood pressure lowering by a C42 PKG Iα-independent mechanism.
价 格：￥电议型 号：T4661产 地：中国大陆
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T4661PKG drug G1PKG drug G1
PKG drug G1 targets C42 of PKG Iα. PKG drug G1 can couple to vasodilation and blood pressure lowering by a C42 PKG Iα-independent mechanism.
价 格：￥电议型 号：T4661产 地：美洲
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T7767FMoc-Val-Cit-PAB-PNP；化合物FMoc-Val-Cit-PAB-PNPFMocValCitPABPNP|||ADC Linkers|||inhibit|||Antibody-drug
Fmoc-Val-Cit-PAB-PNP is a linker for Antibody-Drug-Conjugation (ADC).
价 格：￥电议型 号：T7767产 地：中国大陆
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T72406Tofacitinib Prodrug-1；化合物 Tofacitinib Prodrug-1Tofacitinib Prodrug-1
Tofacitinib Prodrug-1 is an effective and oral active prodrug to mitigate the systemic adverse effects of Tofacitinib. Tofacitinib Prodrug-1 can effectively attenuate the oxazolone-induced colitis in mice model with low toxicity. Tofacitinib Prodrug-1 is a potential drug candidate for the treatment of ulcerative colitis [1] .
价 格：￥电议型 号：T72406产 地：中国大陆
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T64414PRI-724；化合物PRI-724C-82 prodrug|||Foscenvivint；C-82 prodrug|||Foscenvivint
PRI-724 (C-82 prodrug) is a selective small-molecule inhibitor of β-catenin/CBP interaction.
价 格：￥电议型 号：T64414产 地：中国大陆
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T64076Spermine Prodrug-1；化合物 Spermine Prodrug-1Spermine Prodrug-1
Spermine Prodrug-1 is a redox-sensitive spermine prodrug. Spermine Prodrug-1 inhibits wild-type (CMS-24949) and spermine synthase gene (SMS) mutant (CMS-26559, and CMS-6233) fibroblasts with IC50 values of 326.7. 198.5, and 244.1 μM, respectively. Spermine Prodrug-1 can be used in the treatment of Snyder Robinson syndrome.
价 格：￥电议型 号：T64076产 地：中国大陆
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T4661PKG drug G1；化合物PKG drug G1PKG drug G1
PKG drug G1 targets PKG Iα C42. PKG drug G1 can couple to vasodilation and blood pressure lowering by a C42 PKG Iα-independent mechanism.
价 格：￥电议型 号：T4661产 地：中国大陆
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T33281Melflufen；化合物 T33281Prodrug J-1, Melflufen, Melphalan flufenamide|||Melphalan flufenamide|||J 1|||J1
Melphalen fluoroaniline, also known as melphalen, J-1, or prodrug J-1, is a prodrug of melphalen, in which the alkylating agent melphalen is combined with fluoroaniline and has potential antitumor and antiangiogenic activities.
价 格：￥电议型 号：T33281产 地：中国大陆
