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T16583Propargyl-PEG1-acid；化合物 T16583Propargyl-PEG1-acid
Propargyl-PEG1-acid, a PEG-based PROTAC linker, enables the synthesis of BTK-CRBN PROTACs, specifically Ibrutinib-based PROTAC 4 and PROTAC 5. At a concentration of 10 μM, PROTAC 5 facilitates the degradation of BTK and induces the degradation of CSK, LYN, and LAT2[1].
价 格：￥电议型 号：T16583产 地：中国大陆
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T16582Propanil；敌稗Propanil
Propanil is a widely used contact herbicide. It is mainly used in rice production.
价 格：￥电议型 号：T16582产 地：中国大陆
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T16581Progabide；化合物ProgabideSL 76002|||Halogabide|||Gabren|||Gabrene；SL 76002|||Halogabide|||Gabren|||Gabr
Progabide (SL 76002) is an agonist of the gamma-aminobutyric acid receptor.
价 格：￥电议型 号：T16581产 地：中国大陆
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T16580Prodigiosin；灵菌红素Prodigiosine；Prodigiosine|||灵菌红素
Prodigiosin is a secondary metabolite of Symbiotic bacteria. It also has anti-fungal and anti-cancer activity.
价 格：￥电议型 号：T16580产 地：中国大陆
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T1658Selenomethionine硒代蛋氨酸DL-Selenomethionine|||DL-硒代蛋氨酸|||Seleno-DL-methionine|||硒代蛋氨酸
DL-Selenomethionine (Seleno-DL-methionine) is a selenium (Se) analogue of methionine in which sulfur is replaced with the trace element selenium. Selenomethionine (SeMet) can incorporate into proteins in place of methionine with no effects on protein structure and function, providing a mechanism for reversible Se storage in organs and tissues.
价 格：￥电议型 号：T1658产 地：中国大陆
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T16579Pro-xylane；玻色因Hydroxypropyl tetrahydropyrantriol；玻色因|||Hydroxypropyl tetrahydropyrantriol
Pro-Xylane is a biochemical which induces neo-synthesis of matrix proteins. It is a biologically active C-glycoside in aqueous media, acts as an activator of glycosaminoglycans (GAGs) biosynthesis. Pro-xylane (Hydroxypropyl tetrahydropyrantriol) is the first example of ´Green´ chemical used in cosmetic.
价 格：￥电议型 号：T16579产 地：中国大陆
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T16578PRN694；化合物 T16578PRN694
PRN694 shows extended target residence time on ITK and RLK, enabling durable attenuation of effector cells in vitro and in vivo. PRN694 is an irreversible, highly selective, and effective covalent interleukin-2-inducible T-cell kinase (ITK) and resting lymphocyte kinase (RLK) dual inhibitor (IC50s: 0.3 nM and 1.4 nM, respectively).
价 格：￥电议型 号：T16578产 地：中国大陆
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T16577PRMT5-IN-2；化合物 T16577PRMT5-IN-2
PRMT5-IN-2 is an inhibitor of protein arginine methyltransferase 5.
价 格：￥电议型 号：T16577产 地：中国大陆
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T16576Pritelivir mesylate化合物 T16576BAY 57-1293 mesylate|||AIC316 mesylate
Pritelivir mesylate is active against herpes simplex virus types 1 and 2 (IC50: 0.02 μM against HSV1-2). Pritelivir mesylate is an inhibitor of the viral helicase-primase complex. Pritelivir mesylate shows antiviral activity in vitro and in animal models of herpes simplex virus (HSV) infection.
价 格：￥电议型 号：T16576产 地：中国大陆
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T16575Pritelivir mesylate hydrate化合物 T16575BAY 57-1293 mesylate hydrate|||AIC316 mesylate hydrate
Pritelivir mesylate hydrate is active against herpes simplex virus types 1 and 2 (IC50: 0.02 μM against HSV1-2). Pritelivir mesylate hydrate is an inhibitor of the viral helicase-primase complex. Pritelivir mesylate hydrate shows antiviral activity in vitro and in animal models of herpes simplex virus (HSV) infection.
价 格：￥电议型 号：T16575产 地：中国大陆
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T16574Pregnenolone monosulfate sodium salt；化合物 T165743β-Hydroxy-5-pregnen-20-one monosulfate sodium salt；3
Pregnenolone monosulfate sodium salt is a powerful neurosteroid, the main precursor of various steroid hormones including steroid ketones. Pregnenolone monosulfate sodium salt can protect the brain from cannabis intoxication. Pregnenolone monosulfate sodium salt acts as a signaling-specific inhibitor of the cannabinoid CB1 receptor. Pregnenolone monosulfate sodium salt also inhibits the effects of tetrahydrocannabinol (THC) that are mediated by the CB1 receptors.
价 格：￥电议型 号：T16574产 地：中国大陆
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T16573Pratosartan；化合物 T16573KT 3671|||FW 7203|||KD 3-671；KT 3671|||FW 7203|||KD 3-671
Pratosartan is a selective antagonist of angiotensin II receptor.
价 格：￥电议型 号：T16573产 地：中国大陆
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T16572Prasugrel (Maleic acid)；马来酸普拉格雷PCR 4099 (Maleic acid)；马来酸普拉格雷|||PCR 4099 (Maleic acid)
Prasugrel Maleic acid is an orally active and potent P2Y12 receptor antagonist and inhibits ADP-induced platelet aggregation. Prasugrel Maleic acid is a thienopyridine and prodrug. Prasugrel Maleic acid also inhibits platelet function.
价 格：￥电议型 号：T16572产 地：中国大陆
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T16571Pranidipine；普拉地平OPC-13340；普拉地平|||OPC-13340
Pranidipine (OPC-13340) is a novel, long-acting 1,4-dihydropyridine calcium channel blocker. It prolongs acetylcholine-induced relaxation in presence of endothelium as well as nitroglycerin-induced relaxation in absence of endothelium. It also has antihypertensive activity.
价 格：￥电议型 号：T16571产 地：中国大陆
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T16570Pralnacasan；化合物 T16570VX-740|||HMR 3480；VX-740|||HMR 3480
Pralnacasan inhibits proinflammatory cytokines IL-18, IL-1β , and IFN-γ. Pralnacasan is an effective, non-peptide, and orally active interleukin-1β converting enzyme inhibitor (Ki: 1.4 nM). Pralnacasan has the potential for osteoarthritis and rheumatoid arthritis treatment.
价 格：￥电议型 号：T16570产 地：中国大陆
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T1657Varenicline Tartrate；酒石酸伐尼克兰Champix tartrate|||Chantix tartrate|||CP 526555-18；Champix tartrate|||酒石
Varenicline Tartrate (CP 526555-18) is a benzazepine derivative that functions as an ALPHA4/BETA2 NICOTINIC RECEPTOR partial agonist. It is used for SMOKING CESSATION.
价 格：￥电议型 号：T1657产 地：中国大陆
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T1656LVandetanib Fumarate；化合物 T1656LHSDB 8198|||Zactima|||Caprelsa|||ZD 6474|||Vandetanib；HSDB 8198|||Zact
Vandetanib Fumarate is an orally available tyrosine kinase inhibitor. Vandetanib Fumarate works by blocking RET (REarranged during Transfection), vascular endothelial growth factor receptor (VEGFR-2, VEGFR-3), and epidermal growth factor receptor and to a lesser extent VEGFR-1, which are important targets in thyroid cancer (TC).
价 格：￥电议型 号：T1656L产 地：中国大陆
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T16569Praliciguat；化合物PraliciguatIW-1973；IW-1973
Praliciguat (IW-1973) stimulates sGC in HEK-293 cells (EC50: 197 nM). Praliciguat is an effective and orally active soluble guanylate cyclase stimulator. It also enhances NO signaling and acts as a vasodilator.
价 格：￥电议型 号：T16569产 地：中国大陆
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T16568PR-924；化合物 T16568PR-924
PR-924 is a selective inhibitor of tripeptide epoxyketone immunoproteasome subunit LMP-7 (IC50: 22 nM). PR-924 inhibits growth and triggers apoptosis in multiple myeloma (MM) cells. PR-924 has antitumor activities. PR-924 covalently modifies proteasomal N-terminal threonine active sites.
价 格：￥电议型 号：T16568产 地：中国大陆
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T16567PQR530；化合物PQR-530PQR-530；PQR-530
PQR530 is a highly potent dual pan-PI3K/mTORC1/2 inhibitor. PQR530 inhibited protein kinase B (PKB, pSer473) and ribosomal protein S6 (pS6, pSer235/236) phosphorylation with IC50 values of 0.07 μM. It also showing antitumor activity.
价 格：￥电议型 号：T16567产 地：中国大陆
