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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T8450 | TCN 213 | TCN213 | NMDAR |
TCN 213 is an antagonist of NMDA receptor that has a selective for NR1/NR2A over NR1/NR2B | |||
T5104 | BTSA1 | Apoptosis , BCL | |
BTSA1 is a BAX activator that binds with high affinity and specificity to the N-terminal activation site and induces conformational changes to BAX leading to BAX-mediated apoptosis. | |||
T2131 | Articaine hydrochloride | Ultracaine,Articaine HCl,Hoe-045 | Sodium Channel |
Articaine hydrochloride (Hoe-045) is a thiophene-containing local anesthetic pharmacologically similar to MEPIVACAINE. | |||
T1447 | Fenclonine | Fenchlonine,PCPA,CP-10188,4-Chloro-DL-phenylalanine,DL-4-Chlorophenylalanine | Hydroxylase |
Fenclonine (CP-10188) is a selective and irreversible inhibitor of tryptophan hydroxylase, a rate-limiting enzyme in the biosynthesis of serotonin (5-HYDROXYTRYPTAMINE). Fenclonine(CP-10188) acts pharmacologically to dep... | |||
T0150 | Hydroxyhexamide | (±)-Hydroxyhexamid | Potassium Channel , Drug Metabolite |
Hydroxyhexamide ((±)-Hydroxyhexamid) is a pharmacologically active metabolite of Acetohexamide, used as a hypoglycemic agent. | |||
T12145L | N-Desethylsunitinib hydrochloride | VEGFR , PDGFR , c-Kit | |
N-Desethylsunitinib hydrochloride is a major and pharmacologically active metabolite of sunitinib, which is potent, ATP-competitive VEGFR, PDGFRβ, and KIT inhibitor. | |||
T7806 | Licarbazepine | 10,11-hydroxy-10,11 Dihydrocarbamezer | Others |
Licarbazepine (10,11-hydroxy-10,11 Dihydrocarbamezer) is the pharmacologically active metabolite of oxcarbazepine, a drug indicated for the treatment of partial seizures and bipolar disorders. | |||
T0785 | Dexchlorpheniramine Maleate | S-(+)-Chlorpheniramine maleate salt | Dopamine Receptor , 5-HT Receptor , Norepinephrine , Histamine Receptor |
Dexchlorpheniramine Maleate (S-(+)-Chlorpheniramine maleate salt) is an antihistamine with anticholinergic properties used to treat allergic conditions such as hay fever or urticaria. It is the pharmacologically active d... | |||
T22431 | SU5204 | 3-[(2-Ethoxyphenyl)methylidene]-1H-indol-2-one | EGFR , VEGFR , HER |
SU5204 (3-[(2-Ethoxyphenyl)methylidene]-1H-indol-2-one), an analogue of SU5025, pharmacologically inhibits VEGFR2(IC50s of 4 and 51.5 μM for FLK-1 (VEGFR-2) and HER2) | |||
T0182L2 | (±) Clopidogrel hydrogen sulfate | Plavix,Clopidogrel hydrogen sulfate,Iscover | P2Y Receptor |
(±) Clopidogrel hydrogen sulfate (Iscover) , an antiplatelet agent pharmacologically and structurally analogous to ticlopidine, is used to inhibit blood clots in various conditions such as cerebrovascular disease, periph... | |||
TP1277 | Bradykinin | Endogenous Metabolite , Bradykinin Receptor | |
Bradykinin is an inflammatory mediator. It is a peptide that causes blood vessels to dilate (enlarge) via the release of prostacyclin, nitric oxide, and Endothelium-Derived Hyperpolarizing Factor. Bradykinin is a physiol... | |||
T13177 | Taquidil | ||
Tocainide hydrochloride is a sodium channel blocker, it blocks the sodium channels in the pain-producing foci in the nerve membranes. Tocainide hydrochloride is an orally effective antiarrhythmic agent, structurally and ... | |||
T20714 | Levolansoprazole | (S)-Lansoprazole,(-)-Lansoprazole | Proton pump |
Levolansoprazole ((S)-Lansoprazole), a proton pump inhibitor, irreversibly inhibits H+/K+-stimulated ATPase pumps in parietal cells (IC50: 5.2 μM). It also inhibits acid formation in isolated canine parietal cells (IC50:... | |||
T1545 | Levamlodipine | (S)-Amlodipine,S-amlodipine | Calcium Channel |
Levamlodipine (S-amlodipine) belongs to the dihydropyridine group of calcium channel blockers. Levamlodipine, also known as S-amlodipine, is a pharmacologically active enantiomer of amlodipine, an antihypertensive and an... | |||
TN2080 | Pinoresinol | (+)-Pinoresinol | Apoptosis , NF-κB , CDK , p53 |
Pinoresinol ((+)-Pinoresinol) has antiinflammatory, hepatoprotective, and fungicidal activities, it can protect pial microcirculation from I-reperfusion injury, to increase nitric oxide release and to reduce oxidative st... | |||
T4284 | Levamlodipine besylate | (S)-Amlodipine Besylate (103129-82-4(free base)) | Calcium Channel |
Levamlodipine besylate ((S)-Amlodipine Besylate (103129-82-4(free base))) , also known as S-amlodipine, is a pharmacologically active enantiomer of amlodipine, an antihypertensive and anti-anginal medication. Levamlodipi... | |||
T32886 | Lorzafone | Lorzafonum,45-0088S | |
Lorzafone is used in the detection & analysis of pharmacologically active benzodiazepines. | |||
T16272 | Naproxen etemesil | LT-NS 001,MX 1094 | PDE |
Naproxen is a COX-1 and COX-2 inhibitor (IC50s: 8.72 and 5.15 μM, respectively in cell assay). Naproxen etemesil is a lipophilic and non-acidic prodrug of naproxen. It is hydrolyzed to pharmacologically active Naproxen o... | |||
T32704 | Levoleucovorin | levo-Folinic,LFP-754,Levofolinic acid,Levofolene,LFP 754 | |
Levoleucovorin, as a folate analog, consists of the pharmacologically active isomer of leucovorin. | |||
T21155 | Metoprolol acid | Atenolol acid,H117-04,H 117/04,SL 77-010 | |
Metoprolol acid is a urinary metoprolol metabolite and doesn't work pharmacologically. |