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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T38961 | DP-1 | ||
DP-1, a Ganetespib degradation product, represents a fragment derived from SDC-TRAP-0063. Ganetespib itself functions as an inhibitor of heat shock protein 90 (HSP90), exhibiting notable anti-tumor properties. | |||
T38961L | DP-1 hydrochloride | DP-1 hydrochloride(1472616-61-7 Free base) | Drug Metabolite |
DP-1 hydrochloride is a degradation product of SDC-TRAP-0063, a fragment of Ganetespib, a heat shock protein 90 (HSP90) inhibitor with antitumor activity. | |||
T4297 | Flibanserin | BIMT-17BS,Girosa,BIMT-17 | Dopamine Receptor , 5-HT Receptor |
Flibanserin (Girosa) is a serotonergic antidepressant used to treat hypoactive sexual desire disorder. Flibanserin has been associated with a low rate of minor serum aminotransferase elevations during treatment but has n... | |||
T78033 | SDP116 | ||
SDP116, a synthetic peptide derivative of the GPR116 Stachel sequence, exhibits ADGRF5 agonistic activity [1]. | |||
TN2358 | Fructo-oligosaccharide DP10/GF9 | Fructo-oligosaccharide DP10/GF9 | Others |
Fructo-oligosaccharide DP10/GF9 is a compound classified as a fructooligosaccharide (FOS) with a degree of polymerization (DP) of 10. FOS consists of a chain of 9 fructose units connected by (2→1)-β-glycosidic bonds, wit... | |||
T76219 | MDP1 | ||
MDP1, derived from Melittin, disrupts the membrane integrity of both Gram-positive and Gram-negative bacteria, leading to bacterial death through membrane damage. This compound exhibits potent antibacterial activity agai... | |||
T19328 | Fructo-oligosaccharide DP11/GF10 | Others | |
Fructo-oligosaccharide DP11/GF10 is a fructooligosaccharide (FOS) compound with a degree of polymerization (DP) equal to 11. FOS consists of 10 fructose units connected by (2→1)-β-glycosidic bonds, with a single D-glucos... | |||
T76219L | MDP1 acetate | ||
MDP1 acetate, a derivative of Melittin, compromises the membrane integrity of both Gram-positive and Gram-negative bacteria leading to bacterial death through membrane damage. It exhibits potent antibacterial activity ag... | |||
T82369 | Fructo-oligosaccharide DP14 | ||
Fructo-oligosaccharide DP14, an oligosaccharide derived from Atractylodes lancea [1], represents a specific polysaccharide subclass with a degree of polymerization of 14. | |||
T82370 | Fructo-oligosaccharide DP13 | ||
Fructo-oligosaccharide DP13 is an inulin-type fructan that can be isolated from Morinda officinalis [1]. | |||
T19329 | Fructo-oligosaccharide DP12/GF11 | Others | |
Fructo-oligosaccharide DP12/GF11 is a member of fructooligosaccharides (FOS) characterized by a degree of polymerization (DP) of 12. FOS compounds consist of 11 fructose units connected by (2→1)-β-glycosidic bonds, with ... | |||
T13109 | TDP1 Inhibitor-1 | Others | |
TDP1 Inhibitor-1 is a potent inhibitor of Tyrosyl-DNA Phosphodiesterase 1 (TDP1) (IC50 of 7 μM). | |||
T62965 | TDP1 Inhibitor-2 | ||
TDP1 Inhibitor-2 is a potent inhibitor of TDP1 (tyrosyl-DNA phosphodiesterase 1) (IC50: 99 nM) and inhibits SCAN1 (spinal cerebellar ataxia syndrome with axonal neuropathy) (IC50: 3.5 μM). | |||
T5386 | Asapiprant | Prostaglandin Receptor | |
Asapiprant (S-555739) is a potent and selective DP1 receptor antagonist (Ki: 0.44 nM). It exhibited high affinity and selectivity for the DP1 receptor. | |||
T5150 | Treprostinil | LRX-15,Orenitram,Remodulin | Prostaglandin Receptor |
Treprostinil (Orenitram) is a potent DP1, IP and EP2 agonist (EC50: 0.6/1.9/6.2 nM). | |||
T14842 | BW 245C | BW245C | Prostaglandin Receptor |
BW 245C is a selective prostaglandin-like DP receptor (DP1) agonist, a prostaglandin analogue with inhibitory effects on the aggregation response of collagen, which can be used to study diseases such as stroke. | |||
T15712 | Laropiprant | MK-0524 | Prostaglandin Receptor |
Laropiprant (MK-0524) is a potent and selective antagonist of prostaglandin D2 (PGD2) receptor (DP) such as and DP/DP1 receptor(Ki = 0.57 nM) and TP Receptor(Ki = 2.95 nM). | |||
T4635 | Ralinepag | APD811 | Others , Prostaglandin Receptor |
Ralinepag (APD811) is a potent, orally bioavailable agonist of non-prostanoid prostacyclin (IP) receptor, with EC50s of 8.5 nM, 530 nM and 850 nM for human and rat IP receptor and human DP1 receptor, respectively. | |||
T5171 | Treprostinil Sodium | UT-15 | VEGFR , c-RET , Prostaglandin Receptor |
Treprostinil Sodium (UT-15) is a potent DP1, IP and EP2 agonist (EC50: 0.6/1.9/6.2 nM). | |||
T63349 | Treprostinil diethanolamine | UT-15C | Prostaglandin Receptor |
Treprostinil diethanolamine (UT-15C) is a potent agonist of EP2, DP1 and IP, with values of 3.6, 4.4, 32.1, 212, 826, 2505 and 4680 nM for EP2, DP1, IP, EP1, EP4, EP3 and FPKi, respectively. Treprostinil diethanolamine i... |