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T8808LLYN-1604 dihydrochlorideanti-tumor,Unc-51 like kinase,negative,LYN-1604,LYN 1604,cancer,Autophagy,br
LYN-1604 is a novel ULK1 activator.It inducing cell death involved in ATF3, RAD21, and caspase3, accompanied by autophagy and apoptosis.
价 格：￥电议型 号：T8808L产 地：中国大陆
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T6961PX-478Inhibitor,Autophagy,HIFs,inhibit,PX-478,PX 478,HIF-PH,HIF/HIF Prolyl-Hydroxylase,PX478,Hypoxia
PX-478 2HCl is an orally active, and selective inhibitor of hypoxia-inducible factor-1α (HIF-1α).
价 格：￥电议型 号：T6961产 地：中国大陆
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T8825Capmatinib 2HCl.H2OS114,SNU-5,ATP competitive,Balb/c nu/nu mice,U-87MG,INCB-28060 dihydrochloride,or
Capmatinib 2HCl.H2O is an orally bioavailable inhibitor of the proto-oncogene c-Met (HGFR)with potential antineoplastic activity.
价 格：￥电议型 号：T8825产 地：中国大陆
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T35332THZ1 2HCl
THZ1 2HCl is a selective, covalent, and allosteric inhibitor of CDK7 with an IC50 of 3.2 nM. THZ1 2HCl has antiproliferative effects on a variety of cancer cell lines.
价 格：￥电议型 号：T35332产 地：中国大陆
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T6294NVP-BSK805 2HCl (1092499-93-8(free base))BSK 805
NVP-BSK805 2HCl(IC50=0.5 nM), a specific and effective ATP-competitive JAK2 inhibitor, is more than 20-fold specificity over JAK1, JAK3 and TYK2.
价 格：￥电议型 号：T6294产 地：中国大陆
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T6250H-89 dihydrochlorideH 89 2HCl；5-Isoquinolinesulfonamide；Protein kinase inhibitor H-89 dihydrochlorid
H 89 is a potent inhibitor of protein kinase A (PKA; IC50: 0.14 μM, Ki: 48 nM).
价 格：￥电议型 号：T6250产 地：中国大陆
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T6139LA-674563 2HCl(552325-73-2(fb-2hcl))
A-674563 is an Akt1 inhibitor with Ki of 11 nM, modest potent to PKA and >30-fold selective for Akt1 over PKC.
价 格：￥电议型 号：T6139L产 地：中国大陆
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T5398BMS 599626 2HCl (873837-23-1(HCl))AC480 dihydrochloride
BMS-599626 (AC480) is a selective inhibitor of HER1 and HER2 (IC50s: 20 nM and 30 nM), ~8-fold less potent to HER4, >100-fold to Lck, VEGFR2, c-Kit, MET, etc.
价 格：￥电议型 号：T5398产 地：中国大陆
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T4419UNC2025 2HCl (1429881-91-3(free base))
UNC2025 is a potent and orally bioavailable Mer/Flt3 dual inhibitor with IC50 of 0.8/0.74 nM for Mer/Flt3.
价 格：￥电议型 号：T4419产 地：中国大陆
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T4418GSK2879552 2HCl (1401966-69-5(free base))
GSK2879552 is an orally available, irreversible inhibitor of lysine specific demethylase 1 (LSD1), with potential antineoplastic activity.
价 格：￥电议型 号：T4418产 地：中国大陆
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T4260Capmatinib 2HClINCB28060盐酸盐；INCB28060 2HCl；INC-280 2HCl
INCB-28060(free base) is a novel, ATP-competitive inhibitor of c-MET kinase with an IC50 with 0.13 nM.INCB28060 exhibits picomolar enzymatic potency and is highly specific for c-MET with more than 10, 000-fold selectivity over a large panel of human kinas
价 格：￥电议型 号：T4260产 地：中国大陆
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T4023L-Argininamide dihydrochlorideL-精氨酰胺二盐酸盐；H-Arg-NH2.2HCl
L-Argininamide (L-Arm) is used as a model compound in studies of the physicochemical characteristic of ligand binding DNA aptamers and their potential development as fluorescent aptasensors.
价 格：￥电议型 号：T4023产 地：中国大陆
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T3664THZ1CDK7 inhibitor；THZ1 2HCl
THZ1 is a novel selective and potent covalent CDK7 inhibitor.
价 格：￥电议型 号：T3664产 地：中国大陆
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T3649BGP-15BGP15；BGP-15 2HCl；BGP 15
BGP-15 is a PARP inhibitor with protecting effect after ischemia-reperfusion injury.
价 格：￥电议型 号：T3649产 地：中国大陆
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T34911400W dihydrochloride1400W 2HCl；N-(3-(Aminomethyl)benzyl)acetamidine
1400 W is a highly effective and specific inhibitor of inducible NOS2 (iNOS).
价 格：￥电议型 号：T3491产 地：中国大陆
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T3360ZK 756326ZK756326 2HCl
ZK 756326 is a selective, non-peptide CCR8 chemokine receptor agonist (IC50: 1.8 μM, in human; 2.6 μM, in mouse). Displays no activity at CCR4/5 and CXCR3/4 and shows higher 28-fold selectivity over 26 other GPCRs (less selective at α2A and 5-HT receptors
价 格：￥电议型 号：T3360产 地：中国大陆
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T3034Eprazinone dihydrochlorideMucitux；Eprazinone 2HCl；NSC 317935；Resplen；Eftapan；盐酸依普拉酮；依普拉酮二盐酸
Eprazinone is a mucolytic with antitussive and mucolytic effect.
价 格：￥电议型 号：T3034产 地：中国大陆
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T2315GSK-LSD1 dihydrochlorideGSK-LSD1 2HCl
GSK-LSD1 2HCl is a specificity irreversible LSD1 inhibitor (IC50: 16 nM). The selectivity of GSK-LSD1 for LSD1 is >1000 fold over other closely related FAD utilizing enzymes (i.e. MAO-A, LSD2, MAO-B).
价 格：￥电议型 号：T2315产 地：中国大陆
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T2219Puromycin dihydrochloride嘌呤霉素二盐酸盐水合物；嘌呤霉素二盐酸盐；CL13900 dihydrochloride；Puromycin 2HCl
Puromycin hydrochloride is a cinnamamido ADENOSINE found in STREPTOMYCES alboniger. It inhibits protein synthesis by binding to RNA. It is an antineoplastic and antitrypanosomal agent and is used in research as an inhibitor of protein synthesis.
价 格：￥电议型 号：T2219产 地：中国大陆
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T2200Hydroxyzine dihydrochloride盐酸羟嗪；Hydroxyzine 2HCl
Hydroxyzine hydrochloride is a histamine H1 receptor antagonist that is effective in the treatment of chronic urticaria, dermatitis, and histamine-mediated pruritus. Unlike its major metabolite CETIRIZINE, it does cause drowsiness. It is also effective as
价 格：￥电议型 号：T2200产 地：中国大陆
