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TargetMol产品目录中 "

bms-2

"的结果
  • 抑制剂&激动剂
    88
    TargetMol | Inhibitors_Agonists
  • 抗体抑制剂
    5
    TargetMol | Inhibitory_Antibodies
  • 天然产物
    1
    TargetMol | Natural_Products
  • 同位素
    1
    TargetMol | Isotope_Products
  • BMS-2
    1-(4-氟苯基)-N-[3-氟-4-(1H-吡咯并[2,3-B]吡啶-4-基氧基)苯基]-1,2-二氢-2-氧代-3-吡啶甲酰胺
    T8326888719-03-7
    BMS-2 是 Met Flt-3 VEGFR2 酪氨酸激酶抑制剂。
    • ¥ 655
    In stock
    规格
    数量
  • BMS-202
    PD1-PDL1 inhibitor 2, PD-1 PD-L1 inhibitor 2
    T31461675203-84-5
    BMS-202 (PD1-PDL1 inhibitor 2) 是一种非肽类 PD-1 PD-L 复合物抑制剂,其 IC50为 18 nM,KD 为 8 μM。它与 PD-L1 直接结合并阻断人类 PD-1 PD-L 的相互作用,具有抗肿瘤活性。
    • ¥ 311
    In stock
    规格
    数量
    TargetMol | Inhibitor Hot
  • BMS-214662
    BMS214662
    T10567195987-41-8In house
    BMS-214662是一种选择性的 farnesyl transferase 抑制剂,具有抗肿瘤活性,可用于研究胰腺癌、头颈癌和肺癌。
    • ¥ 2570
    In stock
    规格
    数量
  • BMS-212122
    UNII-0Z473OO6GB, BMS212122, BMS 212122
    T30506194213-64-4In house
    BMS-212122 (UNII-0Z473OO6GB) 是一种有效的微粒体甘油三酯转移蛋白(MTP )抑制剂,在动物实验中显示出降血脂作用。BMS-212122 显著减少动脉粥样硬化斑块中的脂质含量和单核细胞衍生(CD68+)细胞。
    • ¥ 2350
    In stock
    规格
    数量
  • BMS-265246
    BMS265246
    T2679582315-72-8
    BMS-265246 是一种有效的选择性 CDK1 2 抑制剂,对 CDK1 cyclin B 和 CDK2 cyclin E 的 IC50分别为6 nM 和9 nM。
    • ¥ 296
    In stock
    规格
    数量
    TargetMol | Inhibitor Sale
  • BMS-279700
    T30511240814-54-4
    BMS-279700 is a potent oral activity inhibitor that is part of a new family of aniline 5-azimidazolaquoxaline analogs and has excellent anti-inflammatory activity in vivo, as well as in vitro activity against p56LCK and T cell proliferation, blocking the
    • ¥ 10600
    6-8周
    规格
    数量
  • N-deacetylated BMS-202
    T121432310135-18-1
    N-deacetylated BMS-202 是 PD-1 PD-L1 相互作用的抑制剂,具有潜在的抗癌活性,可用于研究癌症。
    • ¥ 553
    In stock
    规格
    数量
  • BMS-248360
    T14672254737-87-6
    BMS-248360 is a potent and orally active dual antagonist of both angiotensin II receptor (AT1) and endothelin A (ETA) receptor. With Kis of 10 nM and 1.9 nM for hAT1 and hETA receptor, respectively. BMS-248360 shows hypertensive effects[1].
    • 待询
    3-6月
    规格
    数量
  • BMS-214662 mesylate
    T204276474010-58-7
    BMS-214662 mesylate 是一种高效且选择性的farnesyl transferase抑制剂,IC50值为1.35 nM,并且展现出抗肿瘤活性,适用于癌症研究。
    • 待询
    10-14周
    规格
    数量
  • BMS-242
    BMS242
    T238051675204-51-9
    BMS-242 is an effective inhibitor of PD-1/PD-L1 interaction.
    • ¥ 10600
    6-8周
    规格
    数量
  • BMS-250749
    BMS 250749,BMS250749
    T26845406913-72-2
    BMS-250749 is a fluoroglycosylated fluoroindolocarbazole, it has antitumor activity.
    • ¥ 13900
    8-10周
    规格
    数量
  • BMS-281384
    T26847261769-44-2
    BMS-281384 is a highly potent, phosphodiesterase 5 (PDE 5)-selective inhibitor.
    • ¥ 10600
    6-8周
    规格
    数量
  • BMS-210285
    CHEMBL60116,UNII-WS7S13Q9RH,WS7S13Q9RH,BMS210285
    T30505344607-69-8
    BMS-210285 is a bio-active chemical.
    • ¥ 10600
    待询
    规格
    数量
  • BMS-229724
    LS-46643,42AD6D8ECA,BMS229724,SCHEMBL3304414,BMS 229724
    T30507221914-85-8
    BMS-229724 is a tightly bound inhibitor of cytoplasmic phospholipase A2 with anti-inflammatory activity.
    • ¥ 10600
    6-8周
    规格
    数量
  • BMS-243117
    UNII-MBE6KWV0QI, MBE6KWV0QI, CHEMBL67237
    T30508225521-80-2
    BMS-243117 is an effective selective LCK inhibitor with good cell activity (IC(50)=1.1 microM) and inhibition of T cell proliferation, which has great potential for therapeutic immunosuppression and the treatment of diseases such as rheumatoid arthritis a
    • ¥ 10600
    6-8周
    规格
    数量
  • BMS-247243
    BMS247243,UNII-KG8365V22L
    T30509307316-55-8
    BMS-247243 is a novel cephalosporin inhibitor that is mainly active against Gram-positive bacteria and also against methicillin-resistant Staphylococcus.
    • ¥ 10600
    待询
    规格
    数量
  • BMS-262084
    BMS 262084,I0IR71971G,UNII-I0IR71971G,CHEMBL71037
    T30510253174-92-4
    BMS-262084 is a potent selective β-lactam trypsin inhibitor with therapeutic potential in the treatment of asthma.
    • ¥ 15000
    8-10周
    规格
    数量
  • BMS-284640
    UNII-XP87V064PV,CHEMBL51879,XP87V064PV
    T30512230640-88-7
    BMS-284640 is a Na(+) H(+) exchange agent (NHE) inhibitor that has provided substantial protection in various animal models of myocardial ischemia (MI) and reperfusion in preclinical studies.
    • ¥ 10600
    6-8周
    规格
    数量
  • BMS-214662 HCl
    T68227195981-08-9
    BMS-214662 is a Farnesyltransferase inhibitor , is also a nonsedating benzodiazepine derivative with potential antineoplastic activity. BMS-214662 inhibits the enzyme farnesyltransferase and the post-translational farnesylation of number of proteins involved in signal transduction, which may result in the inhibition of Ras function and apoptosis in susceptible tumor cells. This agent may reverse the malignant phenotype of H-Ras-transformed cells and has been shown to be active against tumor cells with and without Ras mutations.
    • ¥ 11700
    6-8周
    规格
    数量
  • BMS-200
    T702851675203-82-3
    BMS-200 is a potent PD-1 PD-L1 interaction inhibitor with IC50 of 80 nM.
    • ¥ 10600
    6-8周
    规格
    数量
  • Ixabepilone
    伊沙匹隆, Ixempra, BMS 247550-1, BMS 247550, Azaepothilone B
    T6864219989-84-1
    Ixabepilone (Azaepothilone B) 是一种可口服的微管抑制剂,能够与微管蛋白结合,促进微管蛋白的聚合和微管的稳定,使细胞停滞在 G2-M 期,诱导细胞凋亡。
    • ¥ 528
    In stock
    规格
    数量
    TargetMol | Inhibitor Hot
  • muraglitazar
    莫格列地, Pargluva, BMS-298585
    T21587331741-94-7In house
    Muraglitazar (BMS-298585) 是一种 PPAR α γ的双激动剂,用于治疗2型糖尿病及相关血脂异常。Muraglitazar 对人 PPARα (EC50 = 320 nM)和 PPARγ(EC50 = 110 nM)具有较强的体外活性。
    • ¥ 1960
    In stock
    规格
    数量
  • edonentan
    艾多南坦, BMS-207940, BMS207940, BMS 207940
    T31605210891-04-6In house
    Edonentan 是一种有效的内皮素A(ETA)受体拮抗剂,可用于研究心脏衰竭。
    • ¥ 6970
    In stock
    规格
    数量
  • Entecavir monohydrate
    恩替卡韦一水合物, 恩替卡韦 (1水合物), SQ 34676, Entecavir hydrate, BMS-200475
    T0085209216-23-9
    Entecavir monohydrate (BMS-200475) 是一种选择性HBV 抑制剂,在HepG2细胞中的EC50值为3.75 nM。
    • ¥ 215
    In stock
    规格
    数量