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T30531BMS-561392
BMS-561392 is a tumor necrosis factor-α ( TNF-α) Invertase inhibitor.
价 格：￥电议型 号：T30531产 地：中国大陆
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T5390BMS-599626 HydrochlorideBMS 599626 Hydrochloride,BMS599626 Hydrochloride
BMS-599626 Hydrochloride (AC480 Hydrochloride) is a selective and orally bioavailable inhibitor of HER1 and HER2, with IC 50 s of 20 and 30 nM, respectively. BMS-599626 Hydrochloride shows ~8-fold less potent to HER4 (IC 50 =190 nM), >100-fold to VEGFR2, c-Kit, Lck, MEK. BMS-599626 Hydrochloride inhibits tumor cell proliferation, and has potential to increase tumor response to radiotherapy [1] [2].
价 格：￥电议型 号：T5390产 地：中国大陆
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T6420BMS-707035BMS 707035,HIV-1 integrase strand transfer,HIV,Human immunodeficiency virus,antiviral,BMS7
BMS-707035 is a specific HIV-I integrase (IN) inhibitor with IC50 of 15 nM. Phase 2.
价 格：￥电议型 号：T6420产 地：中国大陆
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T6418BMS-378806BMS 378806,BMS 806,Human immunodeficiency virus,inhibit,HIV,BMS-378806,BMS806,Inhibitor
BMS-378806 selectively inhibits the binding of HIV-1 gp120 to the CD4 receptor with EC50 of 0.85-26.5 nM in virus.
价 格：￥电议型 号：T6418产 地：中国大陆
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T14688BMS CCR2 22BMS CCR2 22,BMS CCR-2 22
BMS CCR2 22 is a potent and selective antagonist of CCR2 with calcium flux IC50 of 18 nM, chemotaxis IC50 of 1 nM, and binding IC50 of 5.1 nM.
价 格：￥电议型 号：T14688产 地：中国大陆
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T7787BMS817378BMS817378,BMS-817378
BMS817378 is a potent and selective inhibitor of MET(IC50 : 1.7 nM).
价 格：￥电议型 号：T7787产 地：中国大陆
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T22049BMS 753BMS 753
BMS 753 is an agonist of isotype-selective retinoic acid receptor α (RARα, Ki= 2 nM).
价 格：￥电议型 号：T22049产 地：中国大陆
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T8991BMS986187leu-enkephalin,inhibit,PAM,BMS 986187,δ-opioid,Opioid Receptor,CHO-OPRD1 cell,BMS986187,BMS
BMS986187 is a novel Potent and Selective Positive Allosteric Modulators of the delta-Opioid Receptor.
价 格：￥电议型 号：T8991产 地：中国大陆
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T8992BMS986188BMS986188,Opioid Receptor,inhibit,BMS-986188,Inhibitor,BMS 986188
BMS986188 is a novel Potent and Selective Positive Allosteric Modulator of the delta-Opioid Receptor.
价 格：￥电议型 号：T8992产 地：中国大陆
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T7512BMS-191011Potassium Channel,rodent models of stroke,Panc-1,neuroprotective activity,inhibit,IGR39,BM
BMS-191011 is an activator of large-conductance calcium-activated potassium (BKCa) channels ,effective in stroke models
价 格：￥电议型 号：T7512产 地：中国大陆
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T22192BMS 195614
BMS 195614 is a selective RARα antagonist. BMS 195614 can bind to the RARα subunit.
价 格：￥电议型 号：T22192产 地：中国大陆
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T8342BRD9876Kinesin,microtubule,Inhibitor,BRD9876,BMSC,multiple,myeloma,α4-α6,CD34,tyrosine,ATP,MM1S,G2/M
BRD9876 is a selective inhibitor of MM1S growth.
价 格：￥电议型 号：T8342产 地：中国大陆
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T8542BMS-345541 hydrochlorideI kappa B kinase,BMS345541 hydrochloride,Inhibitor,BMS345541,BMS-345541,BMS
BMS-345541 hydrochloride is a selective IKK inhibitor (IKK2 and IKK1 with IC50 of 0.3 μM and 4 μM,respectively).
价 格：￥电议型 号：T8542产 地：中国大陆
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T30544BMS-919373
BMS-919373 is a potassium channel Kv1.5 (KCNA5) inhibitor for atrial fibrillation and acute coronary syndrome.
价 格：￥电议型 号：T30544产 地：中国大陆
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T6419BMS-536924inhibit,Insulin Receptor,Inhibitor,Apoptosis,insulin-like,BMS536924,BMS-536924,IGF-1R,canc
BMS-536924 is an ATP-competitive IGF-1R/IR inhibitor with IC50 of 100 nM/73 nM, modest activity for Mek, Fak, and Lck with very little activity for Akt1, MAPK1/2.
价 格：￥电议型 号：T6419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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T6326BMS-345541BMS345541；IKK Inhibitor III；BMS 345541；BMS-345541 free base
BMS-345541 is a highly selective inhibitor of the catalytic subunits of IKK-2 and IKK-1 with IC50 of 0.3 μM and 4 μM, respectively.
价 格：￥电议型 号：T6326产 地：中国大陆
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T6297Alvespimycin hydrochlorideAlvespimycin (17-DMAG) HCl；NSC 707545；17-DMAG hydrochloride；KOS-1022；BMS 8
17-DMAG is a potent HSP90 inhibitor with IC50 of 62 nM. Phase 2.
价 格：￥电议型 号：T6297产 地：中国大陆
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T6267Lomitapide洛美他派；AEGR-733；BMS-201038
Lomitapide is a small molecule inhibitor of microsomal triglyceride transfer protein (MTP), an enzyme located in the lumen of the endoplasmic reticulum responsible for absorbing dietary lipids and transferring triglycerides onto apolipoprotein B (apo-B) i
价 格：￥电议型 号：T6267产 地：中国大陆
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T6249AvagacestatBMS-708163
Avagacestat (BMS-708163) is a potent, selective, orally bioavailable γ-secretase inhibitor of Aβ40 and Aβ42 with IC50 of 0.3 nM and 0.27 nM, demonstrating a 193-fold selectivity against Notch. Phase 2.
价 格：￥电议型 号：T6249产 地：中国大陆
