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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T4316 | ML365 | Potassium Channel | |
ML365 is a novel selective small molecule inhibitor of TASK1(KCNK3). | |||
T1781 | GW9508 | GW 9508 | GPR , Potassium Channel |
GW9508(GW 9508) is a potent and selective agonist for FFA1 (GPR40), stimulates insulin secretion in a glucose-sensitive manner. | |||
T20881 | 2-Iodobenzoic acid | o-Iodobenzoic acid,Kyselina o-jodbenzoova,2Iodobenzoic acid | Others |
2-Iodobenzoic acid (o-Iodobenzoic acid) is the impact-sensitive intermediate in the synthesis of the Dess-Martin periodinane. | |||
T0613 | 3-Hydroxyisovaleric acid | Beta-Hydroxyisovaleric acid | Others , Endogenous Metabolite |
3-Hydroxyisovaleric acid (Beta-Hydroxyisovaleric acid) is an endogenous metabolite excreted in the urine and can serve as an early and sensitive indicator of biotin deficiency. | |||
T11579 | HSL-IN-3 | HSL inhibitor 3,Ethyl 2-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)benzoate | Others |
HSL-IN-3 (HSL inhibitor 3) is a boronic acid derivative that is an inhibitor of hormone-sensitive lipase(HSL). | |||
T3929 | Kaurenoic acid | Kauren-19-Oic Acid,kaurenoate,kaur-16-en-18-oic acid | Others |
Kaurenoic acid (kaurenoate) has anti-inflammatory potential in acetic acid-induced colitis, decreases in MDA level. Kaurenoic acid exerts a uterine relaxant effect acting principally through calcium blockade and in part,... | |||
T4845 | L-Lactic acid | 2-HYDROXYPROPIONIC ACID,L-(+)-Lactic acid,(S)-2-Hydroxypropanoic acid | Endogenous Metabolite , Antibacterial , Antibiotic |
L-Lactic acid ((S)-2-Hydroxypropanoic acid) is a natural product produced by the anaerobic glycolysis of pyruvic acid. L-Lactic acid is a sensitive indicator of tissue hypoxia and can be used as a hemodynamic indicator i... | |||
T3S0870 | Paederosidic acid methyl ester | ATPase , Potassium Channel , NO Synthase | |
Paederosidic acid methyl ester has antinociception, is possibly related to the pathway of NO-cGMP-ATP sensitive K(+) channels. | |||
T7774 | A2793 | Potassium Channel | |
A2793 is a dual inhibitor of TWIK-associated acid-sensitive K+ channel 1 (TASK-1)/TRESK, with an IC50 for mTRESK of 6.8 μM. It is more selective for TRESK, and relatively weaker for TREK-1 and TALK-1. | |||
T29067L | Upacicalcet HCl | Upacicalcet HCl(1333218-50-0 Free base) | CaSR |
Upacicalcet HCl is an intravesical calcium mimetic that inhibits excessive parathyroid hormone (PTH) secretion by directly acting on calcium-sensitive receptors in parathyroid cell membranes, thereby lowering PTH levels ... | |||
T6301 | Tosedostat | CHR-2797 | Aminopeptidase , AChR |
Tosedostat (CHR-2797) is an orally bioavailable inhibitor of the M1 family of aminopeptidases with potential antineoplastic activity. Tosedostat is converted intracellularly into a poorly membrane-permeable active metabo... | |||
T5219 | L-Alloisoleucine | L-allo-Isoleucine,(3R)-LS-Isoleucine,L(+)-Alloisoleucine | Others , Endogenous Metabolite |
L-Alloisoleucine (L-allo-Isoleucine) is a branched chain amino acid and is a stereoisomer of L-isoleucine. It is a common constituent of human plasma (albeit at low levels). L-alloisoleucine is produced as a byproduct of... | |||
T6474 | Divalproex Sodium | Valproate semisodium,Epival | HDAC |
Divalproex Sodium (Valproate semisodium) binds to and inhibits gamma-aminobutyric acid (GABA) transaminase and its anticonvulsant activity may be exerted by increasing brain concentration of GABA and by inhibiting enzyme... | |||
TCS0102 | Pulegone | (+)-Pulegone | Calcium Channel , Endogenous Metabolite , TRP/TRPV Channel |
1. Pulegone ((+)-Pulegone) has cytotoxicity followed by regenerative cell proliferation is the MOA for Pulegone-induced urothelial tumors in female rats. 2. Pulegone induces a verapamil-sensitive psychostimulant effect t... | |||
T7057 | Methylstat | Histone Demethylase , Others | |
Methylstat is a methyl ester prodrug of a Jumonji C domain-containing histone demethylase (JMJD) inhibitor that has favorable cell permeability. The free acid of methylstat inhibits JMJD2A, JMJD2C, JMJD2E, PHF8, and JMJD... | |||
T21831 | UCM05 | G28UCM | Fatty Acid Synthase |
UCM05 (G28UCM) is a potent inhibitor of fatty acid synthase (FASN) with efficacy against HER2+ breast cancer xenografts, including in cell lines resistant to anti-HER2 drugs [1]. Additionally, it functions as an inhibito... | |||
T22640 | CCMQ | Others | |
inhibits [3H]-homoquinolinic acid binding to non-NMDA sensitive sites | |||
T38735 | (2-Hydroxyethoxy)acetic acid | β-hydroxyethoxyacetic acid,HEAA | |
(2-Hydroxyethoxy)acetic acid (β-hydroxyethoxyacetic acid) is the primary urinary metabolite of 1,4-Dioxane. It serves as a dependable and sensitive short-term biomarker in urine. | |||
T19020 | L-ANAP | Others | |
L-ANAP is a polarity-sensitive and genetically encodable fluorescent unnatural amino acid. | |||
T19021 | L-ANAP hydrochloride (1313516-26-5 free base) | L-ANAP hydrochloride | Others |
L-ANAP hydrochloride is a polarity-sensitive and genetically encodable fluorescent unnatural amino acid. |