JMJD6 Human Pre-designed siRNA Set A contains three designed siRNAs for JMJD6 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

JMJD7 Human Pre-designed siRNA Set A contains three designed siRNAs for JMJD7 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

JMJD8 Human Pre-designed siRNA Set A contains three designed siRNAs for JMJD8 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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

JNJ-10181457 is a neutral, potent, brain-penetrant and selective non-imidazole H3 antagonist which increases NE and ACh concentrations in rat frontal cortex. JNJ-10181457 can be used for neurological research[1].

JNJ-26990990 is a broad-spectrum antiepileptic agent with oral activity. JNJ-26990990 can inhibit voltage-gated Na+ channels and N-type Ca2+ channels, but has a very weak inhibitory effect on human carbonic anhydrase-II (IC50 = 110 μM)[1].

JOSD1 Human Pre-designed siRNA Set A contains three designed siRNAs for JOSD1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

JOSD2 Human Pre-designed siRNA Set A contains three designed siRNAs for JOSD2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

JPH1 Human Pre-designed siRNA Set A contains three designed siRNAs for JPH1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

JPH2 Human Pre-designed siRNA Set A contains three designed siRNAs for JPH2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

JPH3 Human Pre-designed siRNA Set A contains three designed siRNAs for JPH3 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

JPH4 Human Pre-designed siRNA Set A contains three designed siRNAs for JPH4 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

JPL is a InhA-cofactor-ligand 3FNG inhibitor, and can be used for study of tuberculosis[1].

JPT1 Human Pre-designed siRNA Set A contains three designed siRNAs for JPT1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

JPT2 Human Pre-designed siRNA Set A contains three designed siRNAs for JPT2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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

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

JT21-25 (compound 9h) is a potent and selective inhibitor of apoptosis signal-regulating kinase 1 (ASK1), with IC50 of 5.1 nM[1].

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

JTT-654 is an orally active, potent and selective11β-Hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitor. The IC50 of JTT-654 for 11β-HSD1 is 4.65, 0.97, and 0.74 nM in human, rat, and mouse recombinant enzymes, respectively. JTT-654 showed competitive inhibition against human recombinant enzyme. The IC50 value for human 11β-HSD2 is > 30 μM (human 11β-HSD2 is responsible […]

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

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

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

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

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

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

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

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

JV-1-36 acetate is a growth hormone-releasing hormone (GHRH) antagonist. JV-1-36 acetate inhibits the production of reactive oxygen species in A549 lung cancer cells. JV-1-36 can be used to study the effect of GHRH antagonists in vitro [1].

JV-1-36 acetate is a growth hormone-releasing hormone (GHRH) antagonist. JV-1-36 acetate inhibits the production of reactive oxygen species in A549 lung cancer cells. JV-1-36 can be used to study the effect of GHRH antagonists in vitro [1].

JV-1-36 acetate is a growth hormone-releasing hormone (GHRH) antagonist. JV-1-36 acetate inhibits the production of reactive oxygen species in A549 lung cancer cells. JV-1-36 can be used to study the effect of GHRH antagonists in vitro [1].

JW 618 is a selective ABHD6 inhibitor, with IC50s of 38 and 13 nM for mouse and rat ABHD6[1].

JY-3-094 is a Myc inhibitor that inhibits Myc-Max heterodimer formation (IC50: 33 μM)[1].

K-8012, a sulindac (HY-B0008) analog, is a potent antagonist of RXRa. The IC50 value for K-8012 to inhibit 9-cis-RA-induced Gal4-RXRa-LBD trans-activation were about 9.2 μM. K-8012 exerts improved anticancer activity over sulindac in a RXRa-dependent manner. K-8012 exhibits activity in inhibiting the tRXRa-mediated PI3K/AKT signaling pathway. K-8012 induces apoptosis and inhibits AKT activation by preventing […]

K90-114TAT is an inhibitor for EAG2-Kvβ2 interaction, and exhibits antitumor efficacy against glioblastomas[1].

Kadsurenin C (compound 1) is a neolignan that can be isolated from the aerial part of Piper kadsura with anti-inflammation activity. Kadsurenin C exhibits significant PAF (Platelet Activating Factor) antagonistic activity with IC50 value of 5.1 μM[1].

Kaempferol 3-O-alpha-L-(2, 3-di-Z-p-coumaroyl) rhamnoside (compound 42) is a flavonol that can be isolated from Platanus Occidentalis. Kaempferol 3-O-alpha-L-(2, 3-di-Z-p-coumaroyl) rhamnoside is an inhibitor of alpha-amylase and DPP IV[1].

Kagimminols A is a cembrene-type diterpenoids and can be isolated from an Okeania sp. marine cyanobacterium. Kagimminols A shows selective growth-inhibitory activity against the causative agent of human African trypanosomiasis[1].

Kagimminol B, a cembrene-type diterpenoid, can be isolated from an Okeania sp. marine cyanobacterium. Kagimminol B shows selective growth-inhibitory activity against the causative agent of human African trypanosomiasis[1].

Kalata B7 is a cyclotide that can be isolated from Oldenlandia affinis DC (Rubiaceae) and possesses membrane-permeating capabilities. Kalata B7 is also a partial agonist of oxytocin- and vasopressin V1a- receptors[1][2].

Kalibor (Sodium tetraphenylborate; Tetraphenylboron sodium) is a precipitating agent, performing a precipitating function in the gravimetric determination of various monovalent cations such as basic organic nitrogen compounds and metal ions[1].

Kalibor (Sodium tetraphenylborate; Tetraphenylboron sodium) is a precipitating agent, performing a precipitating function in the gravimetric determination of various monovalent cations such as basic organic nitrogen compounds and metal ions[1].