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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T1687 | Doxycycline | Vibramycin,Doxiciclina,Doxytetracycline,Doxycyclinum | MMP , ribosome , Antibacterial , Antibiotic , Parasite |
Doxycycline (Doxiciclina) belongs to the tetracycline class of antibiotics and is a broad-spectrum metalloproteinase (MMP) inhibitor with oral activity. Doxycycline has antibacterial activity and antitumor activity. | |||
T1687L | Doxycycline (hyclate) | Doxycycline hydrochloride hemiethanolate hemihydrate,WC2031,Doxycycline hyclate | MMP , ribosome , Antibacterial , Antibiotic |
Doxycycline hyclate (WC2031) belongs to the tetracycline class of antibiotics and is a broad-spectrum metalloproteinase (MMP) inhibitor with oral activity. Doxycycline hyclate has antibacterial activity and antitumor act... | |||
T1140 | Doxycycline hydrochloride | Doxylin,Vibramycin,Hyclate | MMP , Antibacterial , Antibiotic |
Doxycycline hydrochloride (Hyclate) is a synthetic tetracycline derivative with similar antimicrobial activity. | |||
T3918 | Ginsenoside Rb3 | Gypenoside IV | NF-κB , COX , NO Synthase |
Ginsenoside Rb3 (Gypenoside IV) is a natural triterpenoid saponin, exhibiting inhibition effect on TNFα-induced NF-κB transcriptional activity. It also inhibits the induction of COX-2 and iNOS mRNA. | |||
T5318 | 666-15 | CREB inhibitor | Epigenetic Reader Domain |
666-15 (CREB inhibitor) is a potent and selective CREB inhibitor (IC50: 81 nM). | |||
T10200 | 9-Hydroxyellipticine hydrochloride | Others | |
9-Hydroxyellipticine hydrochloride is a inhibitor of Topo II and RyR. It exhibits antitumor, antioxidant and catecholamine-releasing activities. 9-Hydroxyellipticine hydrochloride inihibits Hela S-3 and 293T cells (IC50s... | |||
T83857 | Soluble Epoxide Hydrolase PROTAC 1a | sEH Proteolysis-targeting Chimera 1a,Soluble Epoxide Hydrolase Proteolysis-targeting Chimera 1a,sEH PROTAC 1a | |
Soluble epoxide hydrolase (sEH) PROTAC 1a is a proteolysis-targeting chimera (PROTAC) comprising a cereblon ligand linked to the sEH inhibitor t-TUCB via a linker, promoting selective sEH degradation and inhibiting its h... | |||
T78758 | IHMT-IDH1-053 | Isocitrate Dehydrogenase (IDH) | |
IHMT-IDH1-053 (compound 16) is an irreversible inhibitor exhibiting high selectivity for the IDH1 R132H mutant, achieving an IC50 of 4.7 nM. It preferentially targets IDH1 mutants over wild-type IDH1 and IDH2, both wild-... | |||
T36684 | Ipivivint | ||
Ipivivint, a first-in-class, orally active and potent CDC-like kinase (CLK) inhibitor, inhibits CLK1 (IC50=1.4 μM), CLK2 (IC50=0.002 μM) and CLK3 (IC50=0.022 μM). Ipivivint reduces Wnt pathway signaling gene expression t... |