Cat. No. | Product Name | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
T12629L | MIK665
化合物MIK665
|
1799631-75-6 | 98% |
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MIK665 (S-64315) 对髓系细胞白血病具有抑制作用。 | ||||
T77332 | TV 3279
化合物TV 3279
|
209394-29-6 | 98% |
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TV 3279是一种新型ChE-MAI 抑制剂 ,神经保护特性取决于它们诱导抗凋亡蛋白PKC、Bcl-2、Bcl-x 和SOD 的能力,并阻止促凋亡酶甘油醛磷酸脱氢酶在PC-12和神经母细胞瘤细胞中的核易位。 | ||||
TN2180 | Sappanchalcone
化合物Sappanchalcone
|
94344-54-4 | 98% |
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Sappanchalcone shows xanthine oxidase inhibitory activity, is a xanthine oxidase inhibitor. | ||||
TN3404 | Altholactone
化合物 TN3404
|
65408-91-5 | 98% |
|
Altholactone may be a potential antimicrobial agent, particularly in ciprofloxacin-refractory S. aureus and E. faecalis infections. It can inhibit the growth of ... | ||||
TN2257 | Tanshinone IIB
化合物Tanshinone IIB
|
17397-93-2 | 98% |
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Co-treatment with Tanshinone IIB (TSB) significantly inhibits the DNA laddering, cytotoxicity and apoptosis of rat cortical neurons induced by staurosporine in a... | ||||
TN4394 | Kobophenol A
化合物 TN4394
|
124027-58-3 | 98% |
|
Kobophenol A has antimicrobial, and anti-inflammatory activities, it might be a candidate for treatment of inflammatory bone diseases relevant to osteoblast cell... | ||||
T10434 | AZD-5991
化合物 T10434
|
2143061-81-6 | 98% |
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AZD-5991 is a potent and selective Mcl-1 inhibitor (IC50: 0.7 nM in FRET assay; Kd: 0.17 nM in SPR assay). | ||||
T12824 | S55746 hydrochloride
化合物 T12824
|
1448525-91-4 | 98% |
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S55746 hydrochloride is a potent, orally active and selective inhibitor of BCL-2(Ki of 1.3 nM and a Kd of 3.9 nM),with antitumor activity with low toxicity. | ||||
TN1642 | Ferruginol
化合物Ferruginol
|
514-62-5 | 98% |
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Ferruginol has anti-plasmodial, leishmanicidal, anti-ulcerogenic, cardioprotective, anticancer, anti-oxidative and anti-inflammatory activities, it can induce ap... | ||||
T13454 | (S)-Purvalanol B
化合物 T13454
|
2310135-61-4 | 98% |
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(S)-Purvalanol B 是 Purvalanol B 的 S 对映体,Purvalanol B 是一种细胞周期蛋白依赖性激酶(CDK)抑制剂。 | ||||
TN3587 | Capillarisin
化合物 TN3587
|
56365-38-9 | 98% |
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Capillarisin is a novel blocker of STAT3 activation and thus may have a potential in negative regulation of growth, metastasis, and chemoresistance of tumor cell... | ||||
TN4877 | Quercetin 3,4'-dimethyl ether
化合物 TN4877
|
33429-83-3 | 98% |
|
Quercetin 3,4'-dimethyl ether shows anti-lipid peroxidation activity (IC 50 values of 0.3 uM), it also shows anti-inflammatory activity. Quercetin 3,4'-dimethyl ... | ||||
T13338 | WEHI-9625
化合物 T13338
|
2595314-46-6 | 98% |
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WEHI-9625 is a tricyclic sulfone small molecule apoptosis inhibitor (EC50: 69 nM). | ||||
TN3708 | Coronarin D
化合物 TN3708
|
119188-37-3 | 98% |
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Coronarin D shows promising antifungal activity against C. albicans in vitro, the minimum inhibitory concentration (MIC) and the minimum fungicidal concentration... | ||||
T11968 | MCL-1/BCL-2-IN-1
化合物 T11968
|
2493256-46-3 | 98% |
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MCL-1/BCL-2-IN-2 (Compound Nap-1) 是一种有效的选择性 Mcl-1和 Bcl-2双重抑制剂,IC50分别为 4.45 和 3.18 μM。 | ||||
T14846 | Bz 423
化合物 T14846
|
216691-95-1 | 98% |
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Bz 423 is a pro-apoptotic 1,4-benzodiazepine with selectivity for autoreactive lymphocytes and activates Bax and Bak. | ||||
T16089 | MK-0674
化合物 T16089
|
887781-62-6 | 98% |
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MK-0674 is an effective and selective cathepsin K inhibitor (IC50: 0.4 nM). It also displays 1156, 1465, 11857, and 243 fold selectivity over Cat B, Cat F, Cat L... | ||||
T10463 | Bax inhibitor peptide V5
化合物 T10463
|
579492-81-2 | 98% |
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Bax inhibitor peptide V5 (BIP-V5) is a Bax-mediated apoptosis inhibitor with anticancer activity. | ||||
TN4774 | Physalin A
化合物 TN4774
|
23027-91-0 | 98% |
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Physalin A exerts anti-tumor activity in non-small cell lung cancer cell lines by suppressing JAK/STAT3 signaling, it inhibits androgen-independent prostate canc... | ||||
T6650 | Sabutoclax
化合物Sabutoclax
|
1228108-65-3 | 98% |
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Sabutoclax 是一种泛 Bcl-2 抑制剂,包括 Bcl-xL、Bcl-2、Mcl-1 和 Bfl-1,IC50 分别为 0.31 μM、0.32 μM、0.20 μM 和 0.62 μM。 |