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T61542VEGFR-2-IN-17；化合物 VEGFR-2-IN-17VEGFR-2-IN-17
VEGFR-2-IN-17 (Compound 15a) is a highly potent inhibitor of Vascular Endothelial Growth Factor Receptor 2 (VEGFR-2), with an IC50 value of 67.25 nM. This compound exhibits significant antitumor properties [1].
价 格：￥电议型 号：T61542产 地：中国大陆
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T61541sEH inhibitor-6；化合物 sEH inhibitor-6sEH inhibitor-6
sEH inhibitor-6 (Compound 3g) is a highly potent soluble epoxide hydrolase (sEH) inhibitor, exhibiting an IC 50 value of 0.5 nM [1].
价 格：￥电议型 号：T61541产 地：中国大陆
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T61540F15845；化合物 F15845F15845
F 15845 is a potent and persistent blocker of the sodium current. It possesses cardioprotective properties and exhibits both anti-ischemic activity and short- and long-term cardioprotection following myocardial infarction. Furthermore, F 15845 finds utility in the investigation of myocardial functional impairment [1].
价 格：￥电议型 号：T61540产 地：中国大陆
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T6154SU11274；化合物SU11274Met Kinase Inhibitor|||PKI-SU11274；Met Kinase Inhibitor|||PKI-SU11274
SU11274 (Met Kinase Inhibitor)(IC50=10 nM) is a specific Met inhibitor. It shows no significant effects on PGDFRβ, EGFR or Tie2.
价 格：￥电议型 号：T6154产 地：中国大陆
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T61154Colistin adjuvant-2；化合物 Colistin adjuvant-2Colistin adjuvant-2
Colistin adjuvant-2 is a compound that acts as a potentiation agent for colistin, effectively enhancing its activity against Gram-negative bacteria [1].
价 格：￥电议型 号：T61154产 地：中国大陆
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T6065Triciribine；曲西立滨VD-0002|||Tricyclic nucleoside|||NSC 154020|||API-2|||TCN；VD-0002|||Tricyclic nucleo
Triciribine (NSC-154020) is a DNA synthesis inhibitor, and it also inhibits Akt and HIV-1/2.
价 格：￥电议型 号：T6065产 地：中国大陆
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T60412BPN-15477；化合物 BPN-15477BPN-15477
BPN-15477 is a splicing modulator compound (SMC) that restores the correct splicing of ELP1 exon 20. It can be used for frontotemporal dementia research. BPN-15477 corrects the splicing of the ELP1 transcript which significantly increases the level of functional protein in vivo in all tissues, including the brain [1].
价 格：￥电议型 号：T60412产 地：中国大陆
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T60154CDK2-IN-13；化合物 CDK2-IN-13CDK2-IN-13
CDK2-IN-13 is a potent Cyclin-dependent kinase 2 (CDK2) inhibitor (IC50 value: 12 ?M).CDK2-IN-13 is involved in cell cycle regulation and can arrest the cell cycle. CDK2-IN-13 prevents cell division and proliferation, induces apoptosis, and can be used in cancer research.
价 格：￥电议型 号：T60154产 地：中国大陆
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T5842Bromocriptine mesylate甲磺酸溴隐亭甲磺酸溴隐亭|||CB-154
Bromocriptine mesylate (CB-154) is a potent dopamine receptor agonist that binds the D2 receptor with highest affinity (Ki = 2.5 nM)
价 格：￥电议型 号：T5842产 地：中国大陆
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T5154C-176；化合物C-176C176|||STING inhibitor 1；C176|||STING inhibitor 1
C-176 (STING inhibitor 1) is a strong, covalent mouse STING inhibitor
价 格：￥电议型 号：T5154产 地：中国大陆
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T4S1545Licarin B；(-)-利卡灵B(-)-Licarin B|||Licarine B；(-)-Licarin B|||Licarine B|||(-)-利卡灵B
1.(-)-Licarin B (Licarine B) has anti-mycobacterial activity.
价 格：￥电议型 号：T4S1545产 地：中国大陆
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T4S1540Myrislignan；肉豆蔻木脂素Myrislignan
Myrislignan has anti-inflammatory, and anti-cancer activities, it inhibited NF-κB signalling pathway activation, inhibited the proliferation of A549 cells in a dose- and time-dependent manner, it also significantly induced apoptosis and cell cycle arrest in A549 cells.
价 格：￥电议型 号：T4S1540产 地：中国大陆
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T4S0931Pseudolaric acid A；土荆皮甲酸NSC 615487；土槿皮甲酸|||NSC 615487|||土荆皮甲酸
Pseudolaric acid A (NSC 615487) and -B can inhibit the growth of particular cell type.
价 格：￥电议型 号：T4S0931产 地：中国大陆
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T4954SMILAGENIN ACETATE；乙酰知母皂苷元Nsc15488；Nsc15488|||乙酰知母皂苷元
Smilagenin acetate is a sapogenin derivative that has been shown to upregulate the expression of the acetylcholine M2 receptor in cell assays, making it a candidate for dementia research.
价 格：￥电议型 号：T4954产 地：中国大陆
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T4385PF-4840154；化合物PF4840154PF-4840154
PF-4840154 is a potent, selective agonist of the rat and human TrpA1 channel and elicited TrpA1-mediated nocifensive behaviour in mouse, with EC50 of 97 nM and 23 nM for rTrpA1 and hTrpA1, respectively.
价 格：￥电议型 号：T4385产 地：中国大陆
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T4376Nampt-IN-1；化合物Nampt-IN-1LSN3154567；LSN3154567
Nampt-IN-1 (LSN3154567) (LSN3154567) is a potent and selective NAMPT inhibitor. Nampt-IN-1 inhibits purified NAMPT with an IC50 of 3.1 nM.
价 格：￥电议型 号：T4376产 地：中国大陆
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T41157MS 154N；MS 154NMS 154N
MS 154N is a negative control for MS 154. The compound exhibits high binding-affinity for WT and L858R-mutant EGFR (Kdvalues are 3 and 4.3 nM, respectively), but does not significantly induce degradation of EGFR mutants.
价 格：￥电议型 号：T41157产 地：中国大陆
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T41155MS 154；MS 154MS 154
MS 154 is a potent and selective cereblon-recruiting Degrader (PROTAC?) of mutant epidermal growth factor receptor (EGFR), comprising a cereblon-binding moiety joined by a linker to gefitinib(Iressa). MS 154 decreases EGFR protein levels, inhibits downstream signaling in and inhibits proliferation of mutant EGFR-bearing lung cancer cells (DC50values are 11 and 25 nM in HCC-827 and H3255 cells, respectively; Dmax> 95% at 50 nM), but not in WT-EGFR-bearing ovarian and lung cancer cells lines. Bioa
价 格：￥电议型 号：T41155产 地：中国大陆
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T41152R-BC154；R-BC154R-BC154；R-BC154
R-BC154 is a high affinity fluorescent α4β1/α9β1 inhibitor (Kdvalues are 12.7 and 38 nM, respectively); fluorescent version of BOP. Rapidly and preferentially mobilizes HSCs and progenitorsin vivo. Excitation maximum, 561 nm; emissiosn maximum, 585 nm.
价 格：￥电议型 号：T41152产 地：中国大陆
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T40295Carindacillin sodiumCarindacillin sodiumCarindacillin sodium|||CP-15464-2|||Carbenicillin indanyl so
Carindacillin sodium, also known as Carbenicillin indanyl sodium, is an orally active, broad-spectrum antimicrobial agent. In vivo, it undergoes hydrolysis to Carbenicillin. Carindacillin sodium is specifically utilized in urinary tract infection research.
价 格：￥电议型 号：T40295产 地：中国大陆
