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Catalog	name	Description	price
R-R-4666	4-Azide-TFP-Amide-SS-Sulfo-NHS	Ruixi provides you with high-purity 4-Azide-TFP-Amide-SS-Sulfo-NHS which is a linker composed of aryl azide, cleavable disulfide bond and NHS ester, and the disulfide bond can be reduced agent cleavage, NHS esters react with amines, and fluorine helps stabilize the free-radical intermediate.	price>
R-C-2997	Fenoldopam CAS：67227-56-9	Fenoldopam is used as an antihypertensive agent postoperatively,and also intravenously(IV)to treat a hypertensive crisis.Only for scientific research, not for human body.	price>
R-R-4667	Cyamemazine sulfoxide CAS No:13384-45-7	Cyamemazine sulfoxide/10-[3-(Dimethylamino)-2-methylpropyl]-10H-phenothiazine-2-carbonitrile 5-oxide/CAS No:13384-45-7 is a histamine H1 receptor antagonist. It has been shown to have strong affinity for the serotonin 5-HT2C and dopamine D2 receptors, as well as the atrial 5-HT2A receptors. Cyamemazine sulfoxide has a low oral bioavailability of about 10% and is metabolized in the liver to cyamemazine and its active form, cyamemazine sulfoxide. Cyamemazine sulfoxide binds to serotonin 5-HT2C receptors with a high affinity, which leads to inhibition of serotonin release from nerve endings in the brain. This drug also inhibits dopamine release from nerve endings in the brain and has been shown to have cardiac effects on heart rate and contractility.	price>
R-C-2998	Adrenorphin CAS:88377-68-8	Adrendorphin is an opioid octapeptide μ- Opioid receptor agonist with Ki value of 12 nm.Only for scientific research, not for human body.	price>
R-C-4668	Gallium arsenide-PEG750-DSPE	1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[(polyethylene glycol)-methoxy] (sodium salt)It is a long circulating liposome membrane,formation of micelles in water dispersion,so the drug stability is better,even by hemodilution,can maintain the integrity of the micelle particle,has certain targeting,easy accumulation in solid tumors. Suitable for the development of long circulating liposomes.	price>
R-R-4668	2,4-Dideoxy-2,4-difluoro-D-glucose CAS No:38711-44-3	2,4-Dideoxy-2,4-difluoro-D-glucose/CAS No:38711-44-3 is a fluorinated glucose analog that has been synthesized to be used as an imaging agent for positron emission tomography (PET) and single photon emission computed tomography (SPECT). It is labeled with fluorine-18 and can be metabolically incorporated into the cellular glycolytic pathway. 2,4-Dideoxy-2,4-difluoro-D-glucose emits positrons that are detected by PET or SPECT cameras. The incorporation of 2,4-dideoxy-2,4-difluoro--D--glucose into the glycolytic pathway allows it to be used as a marker for positron emission tomography.	price>
R-C-2999	Trimidox cas:95933-74-7	Trimidox (3.4.5-tri-hydroxybenzohydroxamidoxime) is a specific and patented ribonucleotide reductase (RNR) inhibitor.Only for scientific research, not for human body.	price>
R-R-4669	2,4,5-Trimethoxyamphetamine CAS No;1083-09-6	2,4,5-Trimethoxyamphetamine (TMA)/CAS No;1083-09-6 is a psychoactive drug and psychedelic that belongs to the class of substituted amphetamines. It has high affinity for serotonergic 5-HT 1A receptors and moderate affinity for dopaminergic D 2 receptors. TMA also interacts with 5-HT 1A and 5-HT 2C serotonin receptors. TMA is used in humans as an adjunct to psychotherapy. It has a low potential for abuse, but can produce adverse reactions such as skin irritation or neurotoxicity.	price>
R-C-3000	Didox (NSC-324360) CAS:69839-83-4	Didox(nsc-324360)is a synthetic ribonucleotide reductase (RR) inhibitor.Only for scientific research, not for human body.	price>
R-R-4670	JWH 019 5-hydroxyindole metabolite CAS No:1379604-70-2	JWH 019/JWH 019 5-hydroxyindole metabolite/CAS No:1379604-70-2 is a synthetic cannabinoid that has been shown to be an analog of Δ9-tetrahydrocannabinol (THC). In animal models, JWH 019 has been shown to have similar effects on the central nervous system to THC. It is metabolized in human urine and remains detectable for longer periods of time than THC. The detection of this drug in urine samples can be accomplished using analytical methods such as xlr-11, fluorine, and monohydroxylation.	price>
R-C-3001	Rutaecarpine CAS:84-26-4	Rutaecarpine, also known as NSC 258317, is a quinazolinone alkaloid originally isolated from E. rutaecarpa that has diverse biological activities. Only for scientific research,not for human body.	price>
R-R-4671	1-Trityl-4-vinyl-1H-imidazole CAS No:86803-29-4	1-Trityl-4-vinyl-1H-imidazole/CAS No:86803-29-4 is a heterocycle that has been shown to be reactive with boronic acid, oxidant, and hydrogen fluoride. It has been shown to react with fluorine containing compounds from the fluoroalkyl group. This molecule is also capable of undergoing pericyclic reactions and catalysis. 1-Trityl-4-vinyl-1H-imidazole has been shown to be functionalized with various substituents and can form complex molecules. This molecule has also been used as a precursor for synthesizing imidazole derivatives.	price>
R-C-3002	Luotonin A cas:205989-12-4	Luotonin A binds to and stabilizes the topoisomerase I-DNA binary complex.Topoisomerase DNA complexes have been reported as the primary target of several important antitumor agents. Only for scientific research, not for human body.	price>
R-R-4672	JPH203 CAS No:1037592-40-7	JPH203/O-[(5-Amino-2-phenyl-7-benzoxazolyl)methyl]-3,5-dichloro-L-tyrosine/CAS No:1037592-40-7 is a compound that has been shown to inhibit the growth of hypoxic tumor cells. It was found to induce apoptosis in tubule cells through a number of mechanisms, including the inhibition of cyclin D2 protein synthesis and the disruption of cellular signaling pathways. JPH203 is structurally similar to organic anion transporters (OATs), which are drug transporters in the body. This property may help it to cross the blood-brain barrier and reach tumors in the brain. JPH203 has also been shown to inhibit cancer cell proliferation and induce apoptosis in colorectal adenocarcinoma cells, as well as inhibiting tumor growth in animal models.	price>
R-C-3003	EIDD-1931 CAS:3258-02-4	EIDD-1931 is a novel nucleoside analog and behaves as a potent anti-virus agent.Only for scientific research, not for human body.	price>
R-R-4673	9-Mesityl-10-phenylacridinium tetrafluoroborate CAS No:1621019-96-2	9-Mesityl-10-phenylacridinium tetrafluoroborate/CAS No:1621019-96-2 is a synthetic, hydrophobic molecule. It has been shown to be an advance in the field of disulfide chemistry. 9-Mesityl-10-phenylacridinium tetrafluoroborate has been used as a catalyst for radical reactions and is known to undergo exergonic reactions with carbonyls and nucleophiles. This compound activity is based on its ability to adsorb onto hydrophobic surfaces, such as carbon black or sulfuric acid particles. The equilibrium constants are determined by both thermodynamic and kinetic factors.	price>
R-C-3004	PF-07321332 CAS:2628280-40-8	PF-07321332 is an orally bioavailable 3C-like protease (3CLPRO) inhibitor.Only for scientific research, not for human body.	price>
R-R-4674	Tris(1,10-phenanthroline)ruthenium(II) Bis(hexafluorophosphate) CAS No:60804-75-3	Tris(1,10-phenanthroline)ruthenium(II) Bis(hexafluorophosphate)/CAS No:60804-75-3 is a coordination complex that contains a ruthenium(II) ion surrounded by three 1,10-phenanthroline ligands. These ligands coordinate to the ruthenium ion, forming a stable and distinctive molecular structure. Additionally, the complex includes two hexafluorophosphate anions to balance the charge of the ruthenium center.This complex is known for its interesting photophysical and electrochemical properties. It is often used in the fields of coordination chemistry, catalysis, and photophysics due to its ability to absorb light and transfer electrons efficiently. The ruthenium ion, in combination with the phenanthroline ligands, imparts unique optical and redox properties to the complex, making it valuable for various applications such as sensors, light-emitting diodes, and photovoltaic devices.	price>
R-C-3005	Remimazolam CAS：308242-62-8	This product has ceased production.	price>
R-R-4675	BMVC CAS No.627810-06-4	BMVC/CAS No.627810-06-4 is a potent G-quadruplex (G4) stabilizer and a selective telomerase inhibitor with an IC50 of ~0.2 μM. BMVC inhibits Taq DNA polymerase with an IC50 of ~2.5 μM. BMVC increases the melting temperature of G4 structure of telomere and accelerates telomere length shortening. Anticancer activities.	price>

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