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T11155Eg5 Inhibitor V, trans-24Eg5 Inhibitor V, trans 24,Eg-5 Inhibitor V, trans-24,Eg5 Inhibitor V, trans
Eg5 Inhibitor V, trans-24 is a specific and potent Eg5 inhibitor that can be used in cancer research with an IC50 value of 0.65 uM.
价 格：￥电议型 号：T11155产 地：中国大陆
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T11158EGFR-IN-11EGFRIN11,EGFR IN 11
EGFR-IN-11 is a selective inhibitor of EGFR-tyrosine kinase and induces cell apoptosis. EGFR-IN-11 inhibits triple mutant EGFRL858R/T790M/C797S with an IC50 of 18 nM and arrests cell cycle at G0/G1.
价 格：￥电议型 号：T11158产 地：中国大陆
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TN1115Pseudolaric acid A-O-β-D-glucopyranosideinhibit,Inhibitor,Pseudolaric acid AOβDglucopyranoside,Pseud
Pseudolaric acid A-O-beta-D-glucopyranoside is a natural product with antibacterial, anticancer
价 格：￥电议型 号：TN1115产 地：中国大陆
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T11157LEGFR-IN-1 hydrochlorideEGFRIN1 hydrochloride,EGFR IN 1 hydrochloride
EGFR-IN-1 hydrochloride is an irreversible and specific inhibitor of L858R/T790M mutant EGFR with 100-fold selectivity over wild-type EGFR. EGFR-IN-1 hydrochloride exhibits potent antitumor and antiproliferative activity in H1975 cells and the mutant HCC827 cells with IC50s of 4 and 28 nM, respectively.
价 格：￥电议型 号：T11157L产 地：中国大陆
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TP1115L-AsparaginaseL-?ASNase,Apoptosis,DNA synthesis,L-Asparaginase,inhibit,L Asparaginase,DNA/RNA Synthe
L-Asparaginase (L-?ASNase), a hydrolase that catalyzes the conversion of L-asparagine, used in acute lymphoblastic leukemia treatment.Asparaginase is an enzyme that is used as a medication. As a medication, L-asparaginase is used to treat acute lymphoblastic leukemia (ALL), acute myeloid leukemia (AML), and non-Hodgkin´s lymphoma. It is given by injection into a vein, muscle, or under the skin.
价 格：￥电议型 号：TP1115产 地：中国大陆
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T11153EG00229EG00229,EG-00229
EG00229 selectively inhibits VEGF-A binding to NRP1 b1 domain with an IC50 of 3 μM, but has no effect on VEGFA binding to VEGFR-1 and VEGFR-2. EG00229 is a neuropilin 1 (NRP1) receptor antagonist.
价 格：￥电议型 号：T11153产 地：中国大陆
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T23201PSB 1115
PSB 1115 is an A2B receptor antagonist and can counteract the inhibitory effect of NECA.
价 格：￥电议型 号：T23201产 地：中国大陆
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T1115Doxylamine succinateDecapryn；琥珀酸多西拉敏
Doxylamine Succinate is a pyridine derivate histamine H1 antagonist with pronounced sedative properties. Doxylamine succinate competitively blocks the histamine H1 receptor and limits the typical allergic and anaphylactic responses, including bronchoconst
价 格：￥电议型 号：T1115产 地：中国大陆
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T10547BioE-1115
BioE-1115 is a highly selective PAS kinase (PASK) inhibitor (IC50: ~4 nM). It is also a potent inhibitor of casein kinase 2α (IC50: ~10 μM).
价 格：￥电议型 号：T10547产 地：中国大陆
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T1115Doxylamine succinateDoxylamine succinate,Decapryn,
Doxylamine Succinate is a pyridine derivate histamine H1 antagonist with pronounced sedative properties. Doxylamine succinate competitively blocks the histamine H1 receptor and limits the typical allergic and anaphylactic responses, including bronchoconst
价 格：￥电议型 号：T1115产 地：美洲
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T11150Ecteinascidin 770Ecteinascidin 770,Ecteinascidine 770,Et-770
Ecteinascidin 770 (ET-770) inhibits U373MG cells and is a 1,2,3, 4-tetrahydroisoquinoline alkaloid with strong anticancer activity.IC50 is 4.83 nM.
价 格：￥电议型 号：T11150产 地：美洲
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T11151Ecteinascidin-Analog-1Ecteinascidin-Analog-1
Ecteinascidins is a family of tetrahydroisoquinoline alkaloids with wide range of antitumor and antimicrobial activities. Ecteinascidin-Analog-1 is a useful intermediate for chemical sythesis of Ecteinascidin analogues.
价 格：￥电议型 号：T11151产 地：美洲
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T11153EG00229EG00229
EG00229 selectively inhibits VEGF-A binding to NRP1 b1 domain with an IC50 of 3 μM, but has no effect on VEGFA binding to VEGFR-1 and VEGFR-2. EG00229 is a neuropilin 1 (NRP1) receptor antagonist.
价 格：￥电议型 号：T11153产 地：美洲
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T11156Nazartinib S-enantiomerNazartinib S-enantiomer,EGF816 (S-enantiomer),
Nazartinib is an EGFR inhibitor. Nazartinib S-enantiomer is the less active S-enantiomer of Nazartinib.
价 格：￥电议型 号：T11156产 地：美洲
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T81115sPLA2-IIA Inhibitor；化合物 sPLA2-IIA InhibitorsPLA2-IIA Inhibitor
The sPLA2-IIA Inhibitor is a cyclic pentapeptide analog of FLSYK, specifically cyclic 2-Nal-Leu-Ser-2-Nal-Arg (c2), which interacts with human IIA phospholipase A2 (hGIIA) to impede its ester bond hydrolyzing function. As part of the esterase superfamily, sPLA2 enzymatically cleaves the sn-2 ester bond in glycerophospholipids, releasing arachidonic acid and lysophospholipids[1].
价 格：￥电议型 号：T81115产 地：中国大陆
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T71115Formoterol HCl；化合物 Formoterol HClFormoterol HCl
Formoterol HCl is a long-acting beta-2 adrenergic agonist (LABA).
价 格：￥电议型 号：T71115产 地：中国大陆
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T69483CGC 11150；化合物 CGC 11150CGC 11150
CGC 11150 is a polyamine analogue inhibit tumor growth in vitro and in vivo.
价 格：￥电议型 号：T69483产 地：中国大陆
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T61115HBV-IN-25；化合物 HBV-IN-25HBV-IN-25
HBV-IN-25 is a novel chemical compound that acts as a potent HBV cccDNA reducer when administered orally. It exhibits significant anti-HBeAg potency and anti-HBV activity, with IC50 values of 0.58 μM and 1.15 μM, respectively. Moreover, HBV-IN-25 demonstrates favorable aqueous solubility (LYSA＞452 μg/mL) and no cellular toxicity, making it a promising candidate for further investigation and development [1].
价 格：￥电议型 号：T61115产 地：中国大陆
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T41115N-Boc-C1-PEG5-C3-NH2；N-Boc-C1-PEG5-C3-NH2N-Boc-C1-PEG5-C3-NH2；N-Boc-C1-PEG5-C3-NH2
N-Boc-C1-PEG5-C3-NH2 is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T41115产 地：中国大陆
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T33706NNC 11-1585；化合物 T33706NNC-11-1585|||NNC 111585；NNC-11-1585|||NNC 111585
NNC 11-1585 is a bioactive chemical.
价 格：￥电议型 号：T33706产 地：中国大陆
