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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T25055 | Alpha-RA-F | α RA F,alphaRAF,α-RA-F,αRAF | |
alpha-RA-F can modulate collagen synthesis and matrix metalloproteinases (MMPs) expression levels by boosting collagen synthesis and reducing MMPs expression levels in human fibroblasts without cytotoxicity. | |||
T16989 | Tarafenacin D-tartrate | SVT-40776 D-tartrate | Others |
Tarafenacin D-tartrate is a highly selective M3 muscarinic receptor antagonist (Ki= 0.19 nM), ~200 fold selectivity over the M2 receptor. | |||
T63333 | Uplarafenib | B-Raf IN 10 | Raf |
Uplarafenib (B-Raf IN 10) is a potent BRAF inhibitor with an IC50 in the range of 50-100 nM.B-Raf IN 10 has antitumor activity that may affect cell proliferation and differentiation did not, and can be used to study soli... | |||
T20774 | Sarafloxacin | A-56620,A 56620,A56620 | Antibacterial , Antibiotic |
Sarafloxacin (A56620) has antibacterial activities against Gram-positive and Gram-negative bacteria. | |||
T1107 | Sarafloxacin hydrochloride | Sarafloxacin HCl,A-56620 (hydrochloride),A-56620 HCl | Antibacterial , Antibiotic |
Sarafloxacin hydrochloride (A-56620 (hydrochloride)), a quinolone antibiotic drug, is a hydrochloride salt form of sarafloxacin. | |||
T63644 | Exarafenib | RAF/KIN_2787 | Raf , p38 MAPK |
Exarafenib (RAF/KIN_2787) is a potent and orally available pan-RAF inhibitor.Exarafenib has antitumor activity and acts by inhibiting downstream MAPK pathway signaling.Exarafenib is used in cancer research. | |||
T5634 | Belvarafenib | Raf | |
Belvarafenib is a potent and pan RAF inhibitor with antineoplastic activity. The IC50 values of Belvarafenib are 56 nM, 7 nM and 5 nM for B-RAF, B-RAFv600E and C-RAF respectively. | |||
T64194 | Belvarafenib TFA | ||
Belvarafenib TFA (HM95573 TFA) is a potent and broadly available rapidly accelerating inhibitor of fibrosarcoma kinase (RAF) that acts on B-RAF (IC50: 56 nM), B-RAFv600E (IC50: 7 nM) and C-RAF (IC50: 5 nM). | |||
T25919 | Paraflutizide | LD3612,LD 3612,Paraflutizida,LD-3612 | |
Paraflutizide is a thiazide analog antihypertensive. | |||
T16990 | Tarafenacin | SVT-40776 | Others |
Tarafenacin is a highly selective M3 muscarinic receptor antagonist (Ki= 0.19 nM), ~200 fold selectivity over the M2 receptor. | |||
T75807 | Sarafotoxin S6a TFA | ||
Sarafotoxin S6a TFA, an analogue of sarafotoxin, functions as an endothelin receptor agonist with an ET_A/ET_B selectivity profile akin to Endothelin-3. It demonstrates an EC_50 of 7.5 nM in stimulating the pig coronary ... | |||
TP2120 | Sarafotoxin S6c | ||
Highly selective ETB endothelin receptor agonist (Ki values are 0.29 and 28000 nM at ETB and ETA receptors respectively). | |||
TP2290 | Sarafotoxin S6b | Others | |
non-selective endothelin receptor agonist | |||
T64746 | Paraffin liquid | ||
Paraffin liquid is a useful organic compound for research related to life sciences and the catalog number is T64746. | |||
T80240 | Ala-parafluoroPhe-Arg-Cha-Cit-Tyr-NH2 | ||
Ala-parafluoroPhe-Arg-Cha-Cit-Tyr-NH2 is a biologically active peptide functioning as a selective agonist for Protease Activated Receptor 1 (PAR-1), a subtype of G-protein coupled receptors involved in mediating thrombin... | |||
T81176 | Ser-parafluoroPhe-Aad-Leu-Arg-Asn-Pro-NH2 | ||
Ser-parafluoroPhe-Aad-Leu-Arg-Asn-Pro-NH2 is a biologically active peptide. Structure-activity studies of the thrombin receptor-tethered ligand SFLLRNP underscored the pivotal role of the Phe-2-phenyl group in receptor r... | |||
T76302 | [Lys4] Sarafotoxin S6c | ||
[Lys4] Sarafotoxin S6c, an analogue of sarafotoxin, serves as a potent, partial agonist of the endothelin receptor, inducing contraction in pig coronary artery with an effective concentration (EC 50) of 1.5 nM [1]. | |||
TP2119 | Sarafotoxin S6a | ||
Endothelin receptor agonist (EC50 values are 7.5 and > 150 nM for contraction of pig coronary artery and guinea pig aorta respectively). Nociceptive in vivo. | |||
T11898 | LXH254 | Raf | |
LXH254 is a potent C-Raf and B-Raf inhibitor. |