TRAF7 Human Pre-designed siRNA Set A contains three designed siRNAs for TRAF7 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

TRAFD1 Human Pre-designed siRNA Set A contains three designed siRNAs for TRAFD1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

TRAIP Human Pre-designed siRNA Set A contains three designed siRNAs for TRAIP gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

TRAK1 Human Pre-designed siRNA Set A contains three designed siRNAs for TRAK1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

TRAK2 Human Pre-designed siRNA Set A contains three designed siRNAs for TRAK2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

Tralkoxydim is a cyclohexanedione herbicide that inhibits Acetyl-CoA Carboxylase in corn[1].

TRAM1 Human Pre-designed siRNA Set A contains three designed siRNAs for TRAM1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

TRAM2 Human Pre-designed siRNA Set A contains three designed siRNAs for TRAM2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

Tranexamic acid (Standard) is the analytical standard of Tranexamic acid. This product is intended for research and analytical applications. Tranexamic acid (cyclocapron), a cyclic analog of lysine, is an orally active antifibrinolytic agent. Tranexamic acid attenuates the effects of severe trauma, inhibits urokinase plasminogen activator and ameliorates dry wrinkles. Tranexamic acid can used for the […]

Tranexamic acid-13C2,15N (Cyclocapron-13C2,15N) is the 13C2 and 15N labeled Tranexamic acid. Tranexamic acid is an antifibrinolytic agent that alleviates liver damage and fibrosis in mouse models of chronic bile duct injury[1][2].

TRANK1 Human Pre-designed siRNA Set A contains three designed siRNAs for TRANK1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

trans-11-Methyl-2-dodecenic acid is a isomer of cis-11-Methyl-2-dodecenoic acid (HY-134215). cis-11-Methyl-2-dodecenoic acid is a quorum sensing (QS) signal that acts as a diffusion signaling factor (DSF) in extracellular microbial and fungal communication systems[1].

trans-2-Decenal-d2 is deuterated labeled Coumarin (HY-N0709). Coumarin is a potent and orally active anti-inflammatory agent. Coumarin shows an antinociceptive effect. Coumarin shows antibacterial, antifungal and anticancer activity[1][2].

trans-2-Nonenal-d2 is deuterated labeled Acetylpyrazine (HY-W007692). Acetylpyrazine (2-Acetylpyrazine) is used to form many polycyclic compounds, as useful structures in pharmaceuticals and perfumes. Acetylpyrazine is a component of the folates (vitamin B compounds)[1].

trans-2-Undecenal-d5 is deuterated labeled 4-Vinylphenol (HY-W005288). 4-Vinylphenol is found in the medicinal herb Hedyotis diffusa Willd, wild rice and is also the metabolite of p-coumaric and ferulic acid by lactic acid bacteria in wine. 4-Vinylphenol induces apoptosis and inhibits blood vessels formation and suppresses invasive breast tumor growth in vivo[1].

trans-2,cis-6-Nonadienal-13C2 is 13C labeled 4-Ethylphenol (HY-W012836). 4-Ethylphenol is a volatile phenolic compound associated with off-odour in wine.

trans-3,4-Difluorocinnamic acid ((E)-3-(3,4-Difluorophenyl)acrylic acid) is a biochemical reagent that can be used as a biological material or organic compound for life science related research[1].

3,4,5-Trimethoxycinnamyl alcohol is a natural phenolic compound that can be obtained from the bark of the cinnamon tree[1].

trans-3’-Hydroxycotinine-O-β-glucuronide-d3 is deuterated labeled trans-3’-Hydroxycotinine-O-β-glucuronide.

Trans-Anethole-d3 is deuterated labeled α-Terpineol (HY-N5142). α-Terpineol is isolated from Eucalyptus globulus Labill, exhibits strong antimicrobial activity against periodontopathic and cariogenic bacteria[1]. α-Terpineol possesses antifungal activity against T. mentagrophytes, and the activity might lead to irreversible cellular disruption[2].

trans-Latanoprost acid is an isomer of Latanoprost acid. trans-Latanoprost acid may have the activity of reducing intraocular pressure. trans-Latanoprost acid is mainly prepared as an analytical standard for impurity detection and quantification[1].

trans-Resveratrol-3-O-β-D-Glucuronide is an active metabolite of trans-resveratrol. trans-Resveratrol-3-O-β-D-Glucuronide reduces the proliferation of several intestinal cancer cell line. trans-Resveratrol-3-O-β-D-Glucuronide increases pyruvate production in livers[1][2][3].

trans-Resveratrol-3-O-β-D-Glucuronide is an active metabolite of trans-resveratrol. trans-Resveratrol-3-O-β-D-Glucuronide reduces the proliferation of several intestinal cancer cell line. trans-Resveratrol-3-O-β-D-Glucuronide increases pyruvate production in livers[1][2][3].

Trans-Resveratrol-4′-O-D-Glucuronide (R-4G) is a metabolite of resveratrol with anti-fat accumulation property, and can be used for metabolic research[1].

trans-VUF25471 (Compound trans-3e) is a photoswitchable ACKR3 agonist. trans-VUF25471 binds and activates ACKR3 at 10-fold lower concentrations compared to its cis-isomer[1].

trans,trans-2,4-Decadienal-d4 is deuterated labeled Elemicin (HY-N6807). Elemicin is an orally active alkenylbenzene widely distributed in many herbs and spices. Elemicin inhibits Stearoyl-CoA Desaturase 1 (SCD1) by metabolic activation. Elemicin has anti-influenza activities, antimicrobial, antioxidant, and antiviral activities. Elemicin and its reactive metabolite of 1′-Hydroxyelemicin can induce hepatotoxicity[1][2][3][4].

Transketolase-IN-5 (compound 6ba) is a transketolase inhibitor. Transketolase-IN-5 shows herbicidal activity for Amaranthus retroflexus, Setariaviridis, Digitaria sanguinalis[1].

Transketolase-IN-6 (Compound 6bj) is a herbicide lead compound. Transketolase-IN-6 displays a highly inhibitory effect with the root inhibition of about 80% against Amaranthus retroflexus and Setaria viridis. Transketolase-IN-6 is a potent transketolase (TK) inhibitor[1].