20
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T70030 | SPR-00305 | ||
SPR-00305 is a novel potent inhibitor of the mvfr pathway | |||
T70679 | Spr 210 | ||
Spr 210 is an aldose reductase (AR) inhibitor with potential uses as a therapeutic agent for preventing and improving some diabetic complications. | |||
T16924 | SPR inhibitor 3 | SPRi3 | Others |
SPR inhibitor 3 is an effective sepiapterin reductase inhibitor. SPR inhibitor 3 decreases neuropathic and inflammatory pain through a reduction of BH4 levels. SPR inhibitor 3 shows a high binding affinity to human SPR i... | |||
T12992 | SPR741 acetate | SPR741 acetate,NAB741 acetate,SPR741 acetate (1179330-52-9 free base) | Antibacterial |
SPR741 acetate is a cationic peptide derived from polymyxin B. It exhibits antimicrobial activity against gram-negative bacteria by inhibiting severe gram-negative bacterial sensory by increasing the permeability of the ... | |||
T4340 | SPI-112 | Phosphatase | |
SPI-112, the SPI-112 methyl ester analog, can inhibit cellular Shp2 PTP activity. SPI-112 bound to Shp2 by surface plasmon resonance (SPR) and displayed competitive inhibitor kinetics to Shp2. | |||
T12991 | SPR206 | Others | |
SPR206 is a polymyxin analogue and an important class of antibiotic for the treatment of bacterial infections due to multidrug resistant Gram-negative pathogen. | |||
TP1090 | SPR741 | NAB741 | |
SPR741, formerly NAB741 (12), is a cationic peptide derived from polymyxin B and is one such potentiator molecule that is under development for the treatment of serious Gram-negative bacterial infections. | |||
T39983 | SPR206 acetate | ||
SPR206 acetate is a polymyxin analog that exhibits antibiotic activity against Gram-negative pathogens, including multidrug-resistant (MDR) variants. By interacting with the outer membrane of the bacterium, SPR206 acetat... | |||
T13326 | SPR719 | VXc-486 | Others |
SPR719 is an inhibitor of gyrase B, has bactericidal activity. | |||
T70790 | Pateamine A | ||
Pateamine A is a marine macrolide that is isolated from the sponge Mycale hentscheli and exhibits anticancer and antiviral properties. It has a role as a marine metabolite, an antiviral agent, an antineoplastic agent, an... | |||
T38801 | Fobrepodacin | SPR720,pVXc-486 | |
Fobrepodacin (SPR720) is an orally active and potent phosphate prodrug of SPR719 (VXc-486). Fobrepodacin has potent bactericidal activities in vivo. | |||
T70029 | Ibrexafungerp citrate | ||
Ibrexafungerp citrate is a triterpenoid antifungal. Similarly to echinocandins, it inhibits the synthesis of 1,3-β-d-glucan. However, it binds to a different site on the enzyme than echinocandins, resulting in limited cr... | |||
T19532 | Fobrepodacin disodium | pVXc-486 disodium,SPR720 disodium | Others |
SPR720 disodium is an orally active and potent phosphate VXc-486 prodrug,has potent bactericidal activities in vivo. | |||
T70677 | PLS-123 | ||
PLS-123 is a novel covalent irreversible Btk inhibitor with potential anti-proliferative activity. PLS-123 exhibited more potent anti-proliferative effects than ibrutinib in multiple cellular and in vivo preclinical mode... | |||
TP1089 | SPR741 TFA (1179330-52-9 free base) | NAB741 TFA,SPR741 TFA | |
SPR741 TFA (NAB741 TFA) is a cationic peptide derived from polymyxin B and is a potentiator molecule. | |||
T27636 | Ispronicline | AZD-3480,RJR-1734,AZD 3480,TC 1734,AZD3480,TC-01734,TC-1734-112 | AChR |
Ispronicline (TC-1734) An orally active, selective, and potent α4β2 nAChR partial agonist with antidepressant, neuroprotective, and long-lasting cognitive effects.Ispronicline has a high affinity for the α4β2 nAChR with ... | |||
T4S1247 | 14-Hydroxy sprengerinin C | Others | |
14-Hydroxy sprengerinin C is a natural product from Ophiopogon japonicus. | |||
TN1195 | 17-Hydroxy sprengerinin C | BCL , Others , Caspase | |
17-Hydroxy sprengerinin C is a glycoside compound isolated from rhizomes of Polygonatum sibiricum with stronger anticancer activities. 17-Hydroxy sprengerinin C reduces the expression of Blc-2 and pro-caspase3 and increa... | |||
T63610 | SPR7 | ||
SPR7 is a potent and selective rhodesain inhibitor (Ki: 0.51 nM). SPR7 exhibited antiparasitic effects against T. b. brucei (EC50: 1.65 μM). | |||
T69595 | Ispronicline hemigalactarate | ||
Ispronicline, also known as AZD3480; TC 1734; TC-0173, and RJR 1734, is a alpha4beta2 nicotinic acetylcholine receptor-selective agonist with cognition-enhancing and neuroprotective properties. Ispronicline is potenti... |