Cat. No. | Product Name | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
TN4446 | Longiferone B
化合物 TN4446
|
1639810-67-5 | 98% |
|
Longiferone B shows anti-inflammatory activity against NO release with IC50 values of 21.0 uM, it also suppresses the iNOS and COX-2 mRNA expression. | ||||
T10152L | 4-Methylamino antipyrine hydrochloride
化合物 T10152L
|
856307-27-2 | 98% |
|
4-Methylamino antipyrine hydrochloride is an active metabolite of Metamizole. Metamizole is a pyrazolone non-steroidal anti-inflammatory drug (NSAID) and inhibit... | ||||
TN4420 | Latifolin
化合物 TN4420
|
10154-42-4 | 98% |
|
Latifolin is a strong DPPH-scavenger, it attenuates inflammatory responses by inhibiting NF-κB activation via Nrf2-mediated heme oxygenase-1 expression. Latifol... | ||||
TN3922 | Effusanin E
化合物 TN3922
|
76470-15-0 | 98% |
|
Effusanin E shows antibacterial and anti-cancer activities, it significantly inhibits cell proliferation and induces apoptosis in NPC cells by suppressing p50/p6... | ||||
TN4586 | Mulberrofuran A
化合物 TN4586
|
68978-04-1 | 98% |
|
Mulberrofuran A can inhibit the formations of 12-hydroxy-, 8, 10-heptadecatrienoic acid (HHT) and thromboxane B2, but it can increase the formation of 12-hydroxy... | ||||
TN4584 | Morolic acid
化合物 TN4584
|
559-68-2 | 98% |
|
Morolic acid and moronic acid have shown sustained antidiabetic and antihyperglycemic action possibly mediated by an insulin sensitization with consequent change... | ||||
TN5019 | Siegeskaurolic acid
化合物Siegeskaurolic acid
|
52645-97-3 | 98% |
|
Siegeskaurolic acid 是一种具有抗炎活性的天然产物。 | ||||
T13263 | COX/5-LO-IN-1
化合物 T13263
|
154355-75-6 | 98% |
|
COX/5-LO-IN-1 is a cyclooxygenase and 5-lipoxygenase (5-LO) inhibitor, and used for inflammatory and allergic disease states. | ||||
TN4879 | Questinol
化合物 TN4879
|
35688-09-6 | 98% |
|
Questinol exhibits significant anti-obesity activity. It shows anti-inflammatory effect in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells, it can inhibit th... | ||||
TN3070 | 4beta-Hydroxywithanolide E
化合物 TN3070
|
54334-04-2 | 98% |
|
4beta-Hydroxywithanolide E(4bHWE) can inhibit the growth of colon cancer monolayer and spheroid cultures, it assert its anti-tumor activity in carcinogenic progr... | ||||
T15630 | Tilmacoxib
替马考昔
|
180200-68-4 | 98% |
|
Tilmacoxib is a highly selective, time-dependent, and irreversible inhibitor of human COX-2 ( IC50: 85 nM in an enzyme assay). | ||||
T15449 | GW-406381
化合物 T15449
|
221148-46-5 | 98% |
|
GW406381 is a highly selective inhibitor of cyclooxygenase-2 (COX-2). GW406381 also attenuates spontaneous ectopic discharge in the sural nerves of rats followin... | ||||
TN4162 | Goshonoside F5
化合物 TN4162
|
90851-28-8 | 98% |
|
Goshonoside F5 has anti-inflammatory activity, it significantly inhibits the pro-inflammatory response induced by LPS, both in vitro and in vivo. | ||||
TN3810 | Dehydroperilloxin
化合物 TN3810
|
263241-09-4 | 98% |
|
Dehydroperilloxin possesses inhibitory activity against cyclooxygenase-1, with the IC(50) value of 30.4 microM. | ||||
T12419 | PF-04634817 succinate
化合物 T12419
|
2140301-98-8 | 98% |
|
PF-0463481 succinate is a potent and orally active dual antagonist of CCR2/CCR5 with comparable human and rodent CCR2 potency with IC50 of 20.8 nM. | ||||
TN4581 | Moracin D
化合物 TN4581
|
69120-07-6 | 98% |
|
Moracin C and moracin D, new phytoalexins from diseased mulberry, are antifungal compounds. Moracin may be protective influence in tumor promotion, utilization o... | ||||
TN1562 | Dehydromiltirone
去氢丹参新酮
|
116064-77-8 | 98% |
|
Dehydromiltirone has antioxidant activity, it shows significant anti-neuroinflammatory effects through inhibiting PI3K/Akt phosphorylation and then inhibiting NF... | ||||
TMA0291 | Dehydroglyasperin D
化合物 TMA0291
|
517885-72-2 | 98% |
|
Dehydroglyasperin D exhibits anticancer, anti-inflammatory, anti-obesity, antioxidant and anti-aldose reductase effects, it inhibits the proliferation of HT-29 h... | ||||
T11605 | (-)-Ibuprofenamide
化合物 T11605
|
121839-78-9 | 98% |
|
(-)-Ibuprofenamide is an amide prodrug of Ibuprofen with anti-inflammatory activity. | ||||
T13160 | Timegadine
替美加定
|
71079-19-1 | 98% |
|
Timegadine is a competitive inhibitor of COX and lipo-oxygenase, with IC50s ranging from 5 nM (washed rabbit platelets) to 20 μM (rat brain) for COX and 100 μM f... |