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UAA crosslinker 1
Catalog No. A19947 UAA crosslinker 1 hydrochloride is an amber codon used for non-canonical amino acids (ncAAs) incorporation. The ncAAs can be incorporated into proteins in vivo by making use of the promiscuous activity of certain wildtype and engineered aminoacyl-tRNA synthetases. 了解更多 -
3',4'-Dihydroxyflavonol
Catalog No. A19946 3',4'-Dihydroxyflavonol (DiOHF) is an effective antioxidant, which reduces superoxide and improves nitric oxide (NO) function in diabetic rat mesenteric arteries. 了解更多 -
Oleoylethanolamide
Catalog No. A19944 PPAR-α agonistOleoylethanolamide is a high affinity endogenous PPAR-α agonist, which plays an important role in the treatment of obesity and arteriosclerosis. 了解更多 -
1,4-Chrysenequinone
Catalog No. A19937 aryl hydrocarbon receptor activator1,4-Chrysenequinone, a polycyclic aromatic quinone, acts as an activator of aryl hydrocarbon receptor (AhR). 了解更多 -
3,7,4'-Trihydroxyflavone
Catalog No. A19936 3,7,4'-Trihydroxyflavone, isolated from Rhus javanica var. roxburghiana, is a flavonoid with DNA strand-scission activity. 了解更多 -
Kanosamine hydrochloride
Catalog No. A19932 Kanosamine hydrochloride is an antibiotic which inhibits the growth of plant-pathogenic oomycetes, certain fungi and a few bacterial species. Kanosamine inhibits Phytophthora medicaginis M2913 and Aphanomyces euteiches WI-98 with MICs of 25 and 60 ?g/mL, respectively. 了解更多 -
Ro 22-3581
Catalog No. A19929 Tx synthetase inhibitorRo 22-3581 (4'-(Imidazol-1-yl) acetophenone) is a selective thromboxane (Tx) synthetase inhibitor. 了解更多 -
SNAP 94847
Catalog No. A19925 MCHR1 antagonistSNAP 94847 is a novel, high affinity selective melanin-concentrating hormonereceptor1 (MCHR1) antagonist with (Ki= 2.2 nM, Kd=530 pM), it displays >80-fold and >500-fold selectivity over MCHα1A and MCHD2 receptors respectively. 了解更多 -
N6-Ethyladenosine
Catalog No. A19918 Adenosine receptor agonistN6-Ethyladenosine is an adenosine derivative, acts as a Adenosine receptor agonist, with Kis of 4.9 and 4.7 nM for hA1AR and hA3AR, respectively. 了解更多 -
Leelamine hydrochloride
Catalog No. A19910 CB1 agonistLeelamine hydrochloride is a tricyclic diterpene molecule that is extracted from the bark of pine trees. Leelamine hydrochloride is a cannabinoid receptor type 1 (CB1) agonist and a inhibitor of SREBP1-regulated fatty acid/lipid synthesis in prostate cancer cells that is not affected by androgen receptor status. 了解更多 -
Homomangiferin
Catalog No. A19899 Homomangiferin, isolated from the leaves of M. indica L., is mangiferin monomethyl ether. Homomangiferin has important medicinal properties and is widely used to relieve many symptoms, for example coughing and asthma. 了解更多 -
Deriglidole
Catalog No. A19898 peripheral adrenoceptor antagonistDeriglidole is a peripheral adrenoceptor antagonist with a high affinity for α2-adrenoceptors. 了解更多 -
Fmoc-1,6-diaminohexane
Catalog No. A19892 Fmoc-1,6-diaminohexane is an analog of Osw-1 which can be used to treat Alzheimer's disease and cancer, extracted from patent US 20140135279 A1. 了解更多 -
Nitroxazepine
Catalog No. A19888 serotonin-norepinephrine reuptake inhibitorNitroxazepine is a tricyclic antidepressant (TCA) for the treatment of depression. Nitroxazepine acts as a serotonin-norepinephrine reuptake inhibitor. 了解更多 -
INF39
Catalog No. A19887 -
GSK3186899
Catalog No. A19884 CRK12 inhibitorGSK3186899 (DDD-853651) is an inhibitor of cdc-2-related kinase 12 (CRK12), with an EC50 of 1.4 μM for L. donovani in an intra-macrophage assay. 了解更多 -
STING agonist-3
Catalog No. A19882 STING agonistSTING agonist-3, compound 3, is a selective and non-nucleotide small-molecule STING agonist, which has durable anti-tumor effect and tremendous potential to improve treatment of cancer. 了解更多 -
Nosantine racemate
Catalog No. A19864 IL-2 inducerNosantine racemate is the racemate of Nosantine. Nosantine is an inducer of IL-2 or enhancer of IL-2 induction by phytohemagglutinin (PHA). 了解更多 -
GR 159897
Catalog No. A19862 NK2 antagonistGR 159897 is a highly potent, selective, competitive, brain-penetrated non-peptide antagonist at tachykinin NK2 receptors, inhibits binding of [3H]GR100679 to hNK2-CHO cells and rat colon membranes with pKis of 9.51 and 10, respectively. Antagonizes bronchoconstriction, with anxiolytic-like activity. 了解更多 -
VH032-thiol-C6-NH2
Catalog No. A19847 VH032-thiol-C6-NH2 (VHL Ligand-Linker Conjugates 14) is a synthesized E3 ligase ligand-linker conjugate that incorporates the VH032 based VHL ligand and a linker used in PROTAC technology. 了解更多 -
CGP71683 hydrochloride
Catalog No. A19844 neuropeptide Y5 receptor antagonistCGP71683 hydrochloride is a competitive neuropeptide Y5 receptor antagonist with a Ki of 1.3 nM, and shows no obvious activity at Y1 receptor (Ki, >4000 nM) and Y2 receptor (Ki, 200 nM) in cell membranes. 了解更多 -
L-368,899 hydrochloride
Catalog No. A19843 oxytocin receptor antagonistL-368,899 hydrochloride is a potent, selective, orally bioavailable, non-peptide oxytocin receptor antagonist, with IC50s of 8.9 nM and 26 nM for rat uterus and human uterus oxytocin receptor, respectively, used as a tocolytic agent. 了解更多 -
AMPD2 inhibitor 1
Catalog No. A19839 AMPD2 inhibitorAMPD2 inhibitor 1 is an adenosine monophosphate deaminase 2 (AMPD2) inhibitor, used in the research of sugar craving, salt craving, umami craving, and addictions including drug, tobacco, nicotine and alcohol addictions. 了解更多 -
Aristeromycin
Catalog No. A19832 AHCY inhibitorAristeromycin, an adenosine analog, is an antibiotic and a potent S-adenosylhomocysteine hydrolase (AHCY) inhibitor. 了解更多 -
S-1-Propenyl-L-cysteine
Catalog No. A19819 S-1-Propenyl-L-cysteine is a stereoisomer of S-allyl-l-cysteine, extracted from garlic, with immunomodulatory effects and reduces blood pressure in a hypertensive animal model. 了解更多 -
EP1-antanoist-1
Catalog No. A19810 EP1 antagonistEP1-antanoist-1 is a EP1 antagonist with a pKi of 7.54 and an pIC50 of 8.5. 了解更多
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