j 115814j-115814,

J-115814 is a potent feeding stimulant.

J-147 is an experimental drug with reported effects against both Alzheimer's disease and ageing in mouse models of accelerated aging. It is a curcumin derivative and a potent neurogenic and neuroprotective drug candidate initially developed for the treatment of neurodegenerative conditions associated with aging that impacts many pathways implicated in the pathogenesis of diabetic neuropathy.

J-104871 (UNII-6137X5QNJF) is a novel farnesyltransferase (FTase) inhibitor that competitively blocks Ras farnesylation in vivo, inhibits Ras processing in activated H-ras-transformed NIH3T3 cells, and suppresses tumor growth in nude mice transplanted with activated H-ras-transformed NIH3T3 cells.

ZX-J-19J (N-(2,3-Diphenyl-6-quinoxalinyl)octanamide), an inhibitor of Cyclophilin J (CyPJ), demonstrates remarkable inhibition of tumor cell growth, comparable to cyclosporine A but much stronger than 5-fluorouracil.

Ginkgolide J (BN 52024) has neuroprotective activity, it can prevent A beta(1-42) induced inhibition of long-term potentiation in the CA1 region of mouse hippocampal slices.

Gomisin J is a natural product and have vasodilatory activity. Gomisin J suppresses lipid accumulation by regulating the expression of lipogenic and lipolytic enzymes and inflammatory molecules through activation of AMPK, LKB1 and Ca2+ calmodulin-dependent protein kinase II and inhibition of fetuin-A in HepG2 cells.

Picrasidine J is a useful organic compound for research related to life sciences and the catalog number is T126552.

Gnetin J is a useful organic compound for research related to life sciences and the catalog number is T125758.

J 2644 is a bioactive chemical.

Taxinine J possesses inhibitory activity on heptoma cell in vitro.

Dodoviscin J can promote adipocyte differentiation as characterized by increased triglyceride levels in 3T3L1 cells.

7-Deacetoxytaxinine J is a natural product for research related to life sciences. The catalog number is TN3222 and the CAS number is 18457-45-9.

Dysolenticin J shows significant vasodilative effects on intact rat aortic rings with a diastolic degree of 87.4% at 10 ug/mL.

2,7-Dideacetoxytaxinine J is a natural product for research related to life sciences. The catalog number is TN2742 and the CAS number is 115810-14-5.

Derrisisoflavone J is a natural product for research related to life sciences. The catalog number is TN5469 and the CAS number is 2172624-67-6.

2-Deacetoxytaxinine J shows significant in vitro activity against breast cancer cell line at a concentration of 20 microM and 10 microM in MCF-7 and MDA-MB-231 respectively.

Decinnamoyltaxinine J is a natural product from Taxus brevifolia Nutt.

Sofosbuvir impurity J is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.

Celosin H, celosin I, celosin J could be used as chemical markers for the quality control of C. argentea seeds.

Cyclocarioside J is a useful organic compound for research related to life sciences. The catalog number is T125649 and the CAS number is 1644624-86-1.

Glycoside St-J (Compound 2), a triterpenoid saponin isolated from Anemone flaccida, exhibits antitumor activity by inhibiting HeLa cell proliferation and shows potential for use in the development of novel anticancer agents [1].

J 2931 is an inhibitor of mosquito larvae growth.

Trans-J-113863 serves as a potent antagonist of chemokine receptors CCR1 and CCR3, effectively inhibiting MIP-1α-induced chemotaxis in CCR1 transfectants and eotaxin-induced chemotaxis in CCR3 transfectants, with respective half-maximal inhibitory concentrations (IC50) of 9.57 nM and 93.8 nM [1] [2].

(±)-J-113397 is a potent and selective non-peptidyl ORL1 receptor antagonist (K(i): cloned human ORL1=1.8 nM). J-113397 inhibited nociceptin orphanin FQ-stimulated GTPγS binding to CHO cells expressing ORL1 with an IC50 value of 5.3 nM. J-113397 can be used for researching the physiological roles of nociceptin orphanin FQ [1].

J-113863 is also a potent antagonist of the human CCR3 (IC50 of 0.58 nM) , but a weak antagonist of the mouse CCR3 (IC50 of 460 nM). J-113863 is inactive against CCR2, CCR4 and CCR5, as well as the LTB4 or TNF-α receptors. Anti-inflammatory effect. J-113863 is a potent and selective CCR1 (CD18) antagonist with IC50 values of 0.9 nM and 5.8 nM for human and mouse CCR1 receptors, respectively.

Nikkomycin pseudo-J is a nikkomycin isolated from Streptomyces tendae.

Bruceine J, a quassinoid naturally derived from the fruits of Br. javanica, exhibits anti-Babesial activity [1].

Senkyunolide J, a phthalide isolated from the rhizome of Ligusticum Chuanxiong [1], exhibits medicinal properties.

Gleditsioside J is a useful organic compound for research related to life sciences. The catalog number is T125199 and the CAS number is 253123-52-3.

Macrocarpal J has anti-bacterial activity, it also has anti-glucosyltransferase activity.

Longipedlactone J is a natural product of Kadsura, Schisandraceae. The catalog number is TN4448 and the CAS number is 1011762-93-8. Longipedlactone J can be used as a reference standard.

Cis-J-113863 is a competitive antagonist for the chemokine receptor 1 (CCR1), demonstrating inhibitory concentration 50 (IC50) values of 0.9 nM for human CCR1 receptors and 5.8 nM for mouse CCR1 receptors, respectively [1].

Verrucarin J (Muconomycin B), derived from the Myrothecium fungus family, effectively generates reactive oxygen species (ROS) to induce apoptosis in various cancer cell lines, including A549, HCT 116, and SW-620. Besides its anticancer properties, it exhibits antifungal activity against Candida albicans and Mucor miehei. Furthermore, it notably inhibits the arenavirus Junin (JUNV) yield with an IC 50 of 1.2 ng/mL.

Monacolin J (Antibiotic MB 530A) is a cholesterol biosynthesis inhibitor.

Cynanoside J, a C21 steroidal glycoside derived from Cynanchum taihangense, exhibits IC50 values of 6.38, 5.82, and 6.76 μM against HL-60, THP1, and Caco2 cell lines, respectively. This compound can be utilized in cancer research [1].

J-104129 fumarate is a potent M3 muscarinic receptor antagonist.

Forskolin J is a natural product for research related to life sciences. The catalog number is TN4074 and the CAS number is 81873-08-7.

Diosbulbin J is a natural product for research related to life sciences. The catalog number is TN3873 and the CAS number is 1187951-06-9.

Tenuifoliose J is a natural product from Polygala tenuifolia Willd

Gancaonin J is a natural product for research related to life sciences. The catalog number is TN5635 and the CAS number is 129280-37-1.

Mudanpioside J is a natural product for research related to life sciences. The catalog number is TN5856 and the CAS number is 262350-52-7.

J-31 is an inactive conformation inhibitor of ITK.

J-30 is a bioactive chemical.

J-1924 is a bioactive chemical.

J-1048, an activin receptor-like kinase 5 (ALK5) inhibitor, effectively suppresses TAA-induced liver fibrosis in mice through specific inhibition of the TGF-β/Smad signaling pathway [1].

Kadsuphilin J, a lignan isolated from Kadsura longipedunculata roots, exhibits significant cytotoxicity against several human tumor cell lines, demonstrating its potential as an anticancer agent.

The ED50 of J-2156 in rats for the relief of mechanical allodynia and mechanical hyperalgesia in the ipsilateral hindpaws was 3.7 and 8.0 mg/kg, respectively. J-2156 is a high potent, selective somatostatin receptor type 4 (SST4 receptor) agonist with IC5