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TP1737LUrotensin II (114-124), human acetateUrotensin II (114 124), human acetate,Urotensin II (114124), hu
Urotensin II (114-124), human acetate is an 11-amino acid residue peptide, is a potent vasoconstrictor and agonist for the orphan receptor GPR14.
价 格：￥电议型 号：TP1737L产 地：中国大陆
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TN1736HibifolinAdenosine Deaminase,Hibifolin,adenosine,anti-proliferative,anti-inflammatory,neurotoxicity,
Hibifolin is a flavonol glycoside natural product,is a potential inhibitor of adenosine deaminase (Ki of 49.92 μM). Hibifolin protects neurons against beta-amyloid-induced neurotoxicity.
价 格：￥电议型 号：TN1736产 地：中国大陆
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T7354H-Val-Pro-Pro-OHinhibit,Angiotensin Receptor,Inhibitor,H Val Pro Pro OH,HValProProOH
H-Val-Pro-Pro-OH is an inhibitor of Angiotensin I converting enzyme (ACE)( IC50 : 9 μM).
价 格：￥电议型 号：T7354产 地：中国大陆
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T7359CAY10471 RacemateCAY 10471,CAY10471,TM30089,Inhibitor,CAY-10471,TM 30089,TM-30089,CAY10471 Racemate,
CAY 10471 is a potent, highly selective CRTH2/DP 2 receptor antagonist. CAY10471 binds to the human CRTH2/DP2, DP1, and TP receptors( Ki values of 0.6, 1200, and >10,000 nM,respectively)
价 格：￥电议型 号：T7359产 地：中国大陆
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TN6739Angolinephosphorylation,proliferation,STAT3,anticancer,inhibit,Angoline,Inhibitor,STAT,IL-6
Angoline hydrochloride is a potent and selective IL6/STAT3 signaling pathway inhibitor(IC50 : 11.56 μM). It inhibits STAT3 phosphorylation and its target gene expression, and inhibits cancer cell proliferation.
价 格：￥电议型 号：TN6739产 地：中国大陆
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T21738PF-9184PF9184,PF 9184
PF-9184 is a potent and selective inhibitor of human microsomal prostaglandin E synthase-1 (mPGES-1), IC50 =16.5 nM. PF-9184 inhibits IL-1β-induced PGE2 synthesis in vitro.
价 格：￥电议型 号：T21738产 地：中国大陆
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T2545Lomitapide MesylateInhibitor,Lomitapide,Lomitapide Mesylate,AEGR-733,inhibit,AEGR 733,BMS-201038,AEG
Lomitapide Mesylate is a methanesulfonic acid form of lomitapide, a small molecule inhibitor of microsomal triglyceride transfer protein.
价 格：￥电议型 号：T2545产 地：中国大陆
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TP1973LOXA (17-33) acetateOXA (1733) acetate,OXA (17 33) acetate
OXA (17-33) acetate is a more potent agonist of orexin-1 receptor (OX1, EC50 = 8.29 nM)) over OX2 (EC50 = 187 nM).
价 格：￥电议型 号：TP1973L产 地：中国大陆
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T6619Desmethyl Erlotinib hydrochlorideDesmethyl Erlotinib hydrochloride,CP 373420,inhibit,CP-373420,Inhib
OSI-420 (Desmethyl Erlotinib, CP-473420) is an active metabolite of erlotinib which is an orally active EGFR tyrosin kinase inhibitor with IC50 of 2 and 20 nM for human EGFR and EGFR autophosphorylation in tumor cells.
价 格：￥电议型 号：T6619产 地：中国大陆
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T16448PD173212PD173212,PD-173212
PD 173212 is a blocker that blocks N-type voltage sensitive calcium channel (Cav2.2). PD173212 (0.0017-1.7 μmol/kg, Intraperitoneal Injection.) dose-dependently reduced DNBS-induced visceral hypersensitivity in mice.
价 格：￥电议型 号：T16448产 地：中国大陆
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T27319FIIN-4FIIN 4
FIIN-4 is a covalent inhibitor of FGFR and can be used in studies about metastatic breast cancer.
价 格：￥电议型 号：T27319产 地：中国大陆
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TQ0273Neopterininhibit,Endogenous Metabolite,Inhibitor,Neopterin
D-(+)-Neopterin is produced by human monocytes/macrophages upon stimulation with the cytokine interferon-γ. In humans, neopterin is involved in purine biosynthesis.
价 格：￥电议型 号：TQ0273产 地：中国大陆
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TP1672LN-Formyl-Met-Ala-Ser TFA(17351-32-5 free base)N Formyl Met Ala Ser TFA(17351 32 5 free base),NFormyl
N-Formyl-Met-Ala-Ser TFA is a peptide, binds to formyl peptide receptors on neutrophils.N-Formyl-Met-Ala-Ser Peptide (fMet-Ala-Ser) binds to formyl peptide receptors on neutrophils. N-Formylmethionine-containing peptides including the most potent and known member, N-formyl-Met-Leu-Phe (FMLP or fMet-Leu-Phe) stimulate human neutrophils by a receptor-dependent mechanism.
价 格：￥电议型 号：TP1672L产 地：中国大陆
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T8673FMOC-L-1,2,3,4-TETRAHYDRONORHARMAN-3-CARFMOCL1,2,3,4TETRAHYDRONORHARMAN3CAR,FMOC L 1,2,3,4 TETRAHYDR
FMOC-L-1,2,3,4-TETRAHYDRONORHARMAN-3-CAR is a chemical compound.
价 格：￥电议型 号：T8673产 地：中国大陆
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T7081CCCPCCCP,MPYS,IFNAR,TMEM173,Interferon-alpha/beta receptor,Stimulator of Interferon Genes,Bacterial,
CCCP inhibits activation of STING and its downstream signalling molecules, TBK1 and IRF3. CCCP inhibits STING-mediated IFN-β production via disrupting mitochondrial membrane potential (MMP).
价 格：￥电议型 号：T7081产 地：中国大陆
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TN6734Quercetin-3-O-D-glucosyl]-(1-2)-L-rhamnosideinhibit,Quercetin3ODglucosyl](12)Lrhamnoside,Quercetin 3
Quercetin-3-O-D-glucosyl]-(1-2)-L-rhamnoside is main antioxidant of Shuxuening, an herbal medicines injection.
价 格：￥电议型 号：TN6734产 地：中国大陆
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T6352(-)-Dizocilpine maleate(-)-MK 801 (Maleate)；C13737；(-)-MK 801 Maleate；(-)-MK 801马来酸
MK-801 is a potent, selective and non-competitive NMDA receptor antagonist with Kd of 37.2 nM in rat brain membranes.
价 格：￥电议型 号：T6352产 地：中国大陆
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T6328Desmethyl ErlotinibO-Desmethyl Erlotinib；OSI-420；CP-473420
OSI-420 is the active metabolite of Erlotinib (EGFR inhibitor with IC50 of 2 nM).
价 格：￥电议型 号：T6328产 地：中国大陆
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T6305SNX2112SNX 2112；PF 04928473；SNX-2112
SNX-2112 is an orally active Hsp90 inhibitor, with a Kd of 16 nM.
价 格：￥电议型 号：T6305产 地：中国大陆
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T6290TanespimycinKOS 953；17-AAG；CP 127374；NSC 330507；坦螺旋霉素
Tanespimycin (17-AAG) is an inhibitor of Hsp90 that selectively inhibits BT474 tumor cell Hsp90 (IC50: 5 nM).
价 格：￥电议型 号：T6290产 地：中国大陆
