Cat. No. | Product Name | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
T12539L | Prinomastat
普啉司他
|
192329-42-3 | 98% |
|
Prinomastat inhibits MMP-2, MMP-3 and MMP-9 (Kis: 0.05 nM, 0.3 nM and 0.26 nM, respectively). Prinomastat crosses the blood-brain barrier. It also has antitumor ... | ||||
T17201 | UK 356618
化合物 T17201
|
230961-08-7 | 98% |
|
UK 356618 is a potent and selective inhibitor of matrix metalloprotease-3 (IC50: 5.9 nM). | ||||
TN4978 | Scutellarein-7-O-glucoside
化合物 TN4978
|
26046-94-6 | 98% |
|
Scutellarein-7-O-glucoside inhibites MMP-2 activity. | ||||
TN1998 | Notoginsenoside T5
三七皂苷T5
|
769932-34-5 | 98% |
|
Total panax notoginsenosides (TPNS) are the main active ingredients in San-Chi, the root of(Burk) F.H. Chen, which belongs to the Araliaceae family and has been ... | ||||
T16137 | MRS1177
化合物 T16137
|
183721-13-3 | 98% |
|
MRS1177 is an effective and selective antagonist of the human Adenosine A3 receptor (hA3AR) (Ki: 0.3 nM). | ||||
T13249 | UK-370106
化合物 T13249
|
230961-21-4 | 98% |
|
UK-370106 is a potent and highly selective inhibitor of MMP-3 with IC50 of 23 nM and MMP-12 with IC50 of 42 nM, and potently inhibits cleavage of [3H]-fibronecti... | ||||
T28985 | TMI-1
化合物TMI-1
|
287403-39-8 | 98% |
|
TMI-1 (WAY-171318) 是一种有效的抑制剂,用于抑制去整合素金属酶17 (ADAM17) 和其他基质金属蛋白酶MMPs。TMI-1 能够有效地抑制LPS 诱导的人原代单核细胞和人全血中TNF-α的分泌。TMI-1 在三阴性 (TN) 和过度表达ERBB2的乳腺肿瘤细胞系中选择性地诱导Caspase 依赖的细... | ||||
T10461 | Batimastat sodium salt
化合物 T10461
|
130464-84-5 | 98% |
|
Batimastat (BB-94) sodium salt is a broad-spectrum MMP inhibitor (IC50s: 3, 4, 4, 6, and 20 nM for MMP-1, MMP-2, MMP-9, MMP-7, and MMP-3). | ||||
TN4046 | Excisanin A
化合物 TN4046
|
78536-37-5 | 98% |
|
ExcisaninA may be a potent inhibitor of AKT signaling pathway in tumor cells, it can inhibit invasion by suppressing MMP-2 and MMP-9 expression, it may be a pote... | ||||
T14312 | Apratastat
化合物 T14312
|
287405-51-0 | 98% |
|
Apratastat is an orally active, potent, and reversible dual inhibitor of tumor necrosis factor-α converting enzyme (TACE) and matrix metalloproteinases (MMPs) an... | ||||
T16986 | Tanomastat
化合物 T16986
|
179545-77-8 | 98% |
|
Tanomastat is an orally bioavailable and non-peptidic biphenyl matrix metalloproteinases inhibitor. For MMP-2, MMP-3, MMP-9, MMP-13 the Ki values are 11, 143, 30... | ||||
TN5153 | Torilin
窃衣素
|
13018-10-5 | 98% |
|
Torilin 是一种睾酮5α还原酶抑制剂,它(IC50=31.7+/-4.23μM)对5α还原酶的抑制作用强于α-亚麻酸(IC50=160.3+/-24.62μM),但弱于非那雄胺(IC50=0.38+/-0.06μM)。Torilin 具有免疫调节、肝脏保护和抗炎特性,它通过限制 TAK1介导的 MAP 激酶和 NF... | ||||
T1402 | Fenofibric acid
非诺贝特酸
|
42017-89-0 | 99.94% |
|
Fenofibric acid (FNF acid) 是 fenofibrate 的活性代谢物,是PPAR 激动剂,对 PPARα、PPARγ 和 PPARδ 的EC50值分别为 22.4、1.47 和 1.06 µM。它抑制COX-2的活性,IC50值为 48 nM。 | ||||
T1592 | Acetohydroxamic acid
乙酰氧肟酸
|
546-88-3 | 99.91% |
|
Acetohydroxamic acid (N-Hydroxyacetamide) 是一种不可逆的细菌和植物尿素酶抑制剂,可研究慢性尿路感染。 | ||||
T4082 | Astragaloside
黄芪甲苷
|
17429-69-5 | 99.9% |
|
Astragaloside 是黄芪中的主要活性成分之一。 | ||||
T1687 | Doxycycline
多西环素
|
564-25-0 | 99.88% |
|
Doxycycline (Doxiciclina) 属于四环素类抗生素,是一种广谱的金属蛋白酶 (MMP) 抑制剂,具有口服活性。Doxycycline 具有抗菌活性和抗肿瘤活性。 | ||||
T7044 | Norepinephrine
去甲肾上腺素
|
51-41-2 | 99.84% |
|
Norepinephrine (Levophed) 是β1选择性的肾上腺素能受体激动剂,EC50值为 5.37 μM。它可上调鼻咽癌肿瘤细胞中血管内皮生长因子、基质金属蛋白酶MMP-2和MMP-9的表达。 | ||||
T3414 | Morroniside
莫诺苷
|
25406-64-8 | 99.84% |
|
Morroniside 通过抑制神经元凋亡和 MMP9/2 的表达从而发挥神经保护作用,可作为 db/db 小鼠肝脏炎症反应和脂质代谢的调节剂。它通过抑制高血糖和氧化应激表现出对糖尿病肾损伤和人脐静脉内皮细胞的保护作用。 | ||||
T2993 | Cordycepin
虫草素
|
73-03-0 | 99.78% |
|
Cordycepin (3'-Deoxyadenosine) 是一种核苷衍生物,在类风湿性关节炎滑膜成纤维细胞中,剂量依赖性抑制 IL-1β 诱导的 MMP-1和 MMP-3表达。它也抑制细菌的腺苷激酶从而抗结核分枝杆菌。 | ||||
T77617 | MMP-9-IN-6
化合物MMP-9-IN-6
|
2241964-36-1 | 99.75% |
|
MMP-9-IN-6 是一种 MMP-9 抑制剂,其 IC50 值为50 μM, 具有较好的抗溃疡功效。MMP-9-IN-6 具有潜在的抗肿瘤活性,可用于研究组织重塑、伤口修复和动脉粥样硬化。 |