Cat. No. | Product Name | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
T2573 | Misoprostol
米索前列醇
|
59122-46-2 |
|
|
Misoprostol 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T2573,CAS号为 59122-46-2。 | ||||
T3P2855 | Chamigrenal
恰米醛
|
19912-84-6 |
|
|
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 |
|
|
3-O-Acetyl-16α-hydroxydehydrotrametenolic acid (3-O-Acetyl-16 alpha-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% |
|
2-(E-2-decenoylamino)ethyl 2-(cyclohexylethyl) sulfide is a compound known to inhibit stress-induced ulcers, effectively maintaining the levels of phospholipase ... | ||||
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% |
|
BAY-1316957 is a highly potent and selective EP4 receptor antagonist. With an IC50 of 15.3 nM. Good oral bioavailability[1]. | ||||
T78582 | 15-keto-Prostaglandin E2
化合物 15-keto-Prostaglandin E2
|
26441-05-4 | 98% |
|
15-keto-Prostaglandin E2为内源性代谢产物,通过与STAT3Cys259残基结合,抑制STAT3激活作用。该化合物能够结合并稳定EP2与EP4受体,进而抑制乳腺癌细胞生长与进展,并通过激活PPAR-γ促进真菌生长。 | ||||
T78584 | Prostaglandin D3
化合物 Prostaglandin D3
|
71902-47-1 | 98% |
|
Prostaglandin D3 (PGD3) 是具有抑制人类血小板聚集和调节自主神经传递功能的前列腺素类化合物。 | ||||
T78710 | AMX12006
化合物 AMX12006
|
2639775-01-0 | 98% |
|
AMX12006为一种口服活性EP4拮抗剂,显示出高度的选择性与有效性,IC50为4.3 nM,并具备细胞毒性和抗肿瘤活性。 | ||||
T79432 | NXT-10796
化合物 NXT-10796
|
98% |
|
|
NXT-10796为具口服活性且肠道限制性EP4受体激动剂。 | ||||
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% |
|
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% |
|
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% |
|
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% |
|
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% |
|
Manumycin A is an antibiotic. Manumycin A induces apoptosis and exerts antitumor activity. Manumycin A inhibits exosome biogenesis and secretion via targeted inh... |