Cat. No. | Product Name | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
T17039 | Terbogrel
特波格雷
|
149979-74-8 | 98% |
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Terbogrel 是一种可口服的 、具有选择性 thromboxane A2 受体拮抗剂(IC50 约为 10 nM),是一种 thromboxane A2 synthase 抑制剂(IC50 约为 10 nM)。Terbogrel 是一种抗血小板化合物,可抑制血小板聚集,是预防血栓的潜在化合物。 | ||||
T68155 | Tebufelone
特丁非隆
|
112018-00-5 | 98% |
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Tebufelone 是一种体外高效的CO 抑制剂 ,是一种新型的非甾体抗炎药(NSAID),属于二叔丁基苯酚(DTBP)类,在各种动物模型中显示出强大的抗炎、镇痛和抗网膜炎特性。Tebufelone 能有效地抑制前列腺素(PGE2)的形成,阻止大鼠巨噬细胞(IC50 = 20 microM)和人类全血(IC50 = 2... | ||||
T24567 | Octimibate
辛米贝特
|
89838-96-0 | 98% |
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Octimibate 是一种非前列腺素类血小板聚集抑制剂和环前列腺素激动剂。Octimibate 可用于治疗心血管疾病,可用于研究动脉粥样硬化和血栓形成。 | ||||
T27630 | Isbogrel
伊波格雷
|
89667-40-3 | 98% |
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Isbogrel是一种小分子血栓素A2合成酶(TXA2 synthase)抑制剂,可用来研究心律失常、短暂性脑缺血发作和血栓形成。 | ||||
T13563 | AZ-1355
化合物AZ-1355
|
75451-07-9 | 98% |
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AZ-1355是一种新型二苯并恶西平衍生物,具有降脂效果。 | ||||
T3P2855 | Chamigrenal
恰米醛
|
19912-84-6 | 98% |
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β-Chamigrenal has anti-inflammatory activity, it has inhibitory effects on lipopolysaccharide-induced nitric oxide and prostaglandin E2 production in RAW 264.7 m... | ||||
TN1109 | 3-O-Acetyl-16α-hydroxydehydrotrametenolic acid
3-O-乙酰基-16Α-羟基松苓新酸
|
168293-14-9 | 98% |
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3-O-Acetyl-16α-hydroxydehydrotrametenolic acid 是三萜类化合物。它能够作用于 LPS 刺激的 Raw264.7 细胞,减少NO 产生和 iNOS 表达,具有消炎作用。 | ||||
TN4592 | Murrangatin
化合物 TN4592
|
37126-91-3 | 98% |
|
Murrangatin may be a valuable anti-tumor-promoting agent, it can significantly inhibit Epstein-Barr virus early antigen (EBV-EA) activation, and preserve the hig... | ||||
TN5248 | Voleneol
化合物 TN5248
|
70389-88-7 | 98% |
|
1β,6α-Dihydroxyeudesm-4(15)-ene (Voleneol,DE) can attenuate the lipopolysaccharide (LPS)-induced inflammation in BV2 microglial cells, it also can dose-dependent... | ||||
TN3366 | Ailanthoidol
化合物 TN3366
|
156398-61-7 | 98% |
|
Ailanthoidol has anti-inflammatory activity, it inhibits inflammatory reactions by macrophages and protects mice from endotoxin shock. It also possesses potentia... | ||||
T13488 | 2-(E-2-decenoylamino)ethyl 2-(cyclohexylethyl) sulfide
化合物 T13488
|
137089-36-2 | 98% |
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2-(E-2-decenoylamino)ethyl 2-(cyclohexylethyl) sulfide is a compound that inhibits stress-induced ulcer. It can maintain the content of phospholipase A2 and pros... | ||||
T4484 | 1,7-Dihydroxy-2,3-methylenedioxyxanthone
1,7-二羟基-2,3-亚甲二氧基呫吨酮
|
183210-63-1 | 98% |
|
1,7-Dihydroxy-2,3-methylenedioxyxanthone has antiulcerogenic, anti-oxidation, and antihyperalgesic activities, it can inhibit the carrageenan-induced hyperalgesi... | ||||
T14500 | BAY-1316957
化合物 T14500
|
1613264-40-6 | 98% |
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BAY-1316957 is a highly potent and selective EP4 receptor antagonist. With an IC50 of 15.3 nM. Good oral bioavailability[1]. | ||||
TN4465 | Luvangetin
化合物 TN4465
|
483-92-1 | 98% |
|
Luvangetin may have anti-inflammatory activity, it can inhibit NO and PGE2 production in LPS-stimulated BV2 cells. Luvangetin shows significant protection agains... | ||||
TN4038 | Eupatolide
泽兰内酯
|
6750-25-0 | 98% |
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Eupatolide 是从 Inula japonica 的花中分离出来的,具有抗炎活性。 Eupatolide 可用于研究乳腺癌细胞对 TRAIL 的耐药性。 | ||||
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... | ||||
T16388 | Omidenepag isopropyl
化合物 T16388
|
1187451-19-9 | 98% |
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Omidenepag isopropyl is converted to the active product Omidenepag during corneal penetration. Omidenepag isopropyl is a selective EP2 receptor agonist. Omidenep... | ||||
TN5033 | Skullcapflavone I
化合物 TN5033
|
41060-16-6 | 98% |
|
Skullcapflavone I has anti-inflammatory and anti-allergic potential, it can significantly inhibit LPS stimulated NO and PGE(2) release in J774A.1 macrophages and... | ||||
TN1485 | Chicanine
襄五脂素
|
78919-28-5 | 98% |
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Chicanine has anti-inflammatory activity in macrophages by down-regulating LPS-induced inflammatory cytokines in IκBα±/MAPK/ERK signaling pathways. | ||||
T16011 | Manumycin A
手霉素A
|
52665-74-4 | 98% |
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Manumycin A is an antibiotic. Manumycin A induces apoptosis and exerts antitumor activity. Manumycin A inhibits exosome biogenesis and secretion via targeted inh... |