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| 货号 | 产品名 | CAS号 | 信息 |
|---|---|---|---|
| CSN18158 | CH 5450 | 252557-97-4 | Z-Ile-Glu-Pro-Phe-Ome is a peptide inhibitor of human heart chymase. |
| CSN17692 | YS-49 | 132836-42-1 | YS 49 inhibits Ang II-stimulated proliferation of VSMCs via induction of HO-1. |
| CSN18108 | Upf-648 | 213400-34-1 | UPF-648 is a potent kynurenine 3-monooxygenase (KMO) inhibitor, exhibits highly active at 1 μM(81 ± 10% KMO inhibition), and is ineffective at blocking KAT activity. |
| CSN18119 | Olesoxime | 22033-87-0 | TRO19622, a small cholesterol-like molecule, is a neuroregenerative and neuroprotective compound. |
| CSN18064 | Tenacissoside H | 191729-45-0 | Tenacissoside H is a Chinese medicine monomer extracted, isolated from Caulis Marsdeniae Tenacissimae. |
| CSN17920 | Stauprimide | 154589-96-5 | Stauprimide is a small molecule that increases the efficiency of the directed differentiation of mouse and human ESCs and interacts with NME2 and inhibits its nuclear localization. |
| CSN18306 | Sortin1 | 503837-98-7 | Sortin1 is a chemical genetic-hit molecule that causes specific mislocalization of plant and yeast-soluble and membrane vacuolar markers. |
| CSN17442 | SMND-309 | 1065559-56-9 | SMND-309 is a derivative of salvianolic acid B, and has shown protective effects against rat cortical neuron damage in vitro and in vivo. |
| CSN18237 | SIBA | 35899-54-8 | SIBA selectively inhibits spermine synthase, IC50=8 μM. |
| CSN17895 | Seco Rapamycin sodium salt | 148554-65-8 | Seco-rapamycin is the first in vivo open-ring metabolite of rapamycin that does not affect mTOR, inhibit the ChT-L (D) (IC50> 20 μM)and PGPH(E) (IC50=6.45 ± 0.78 μM) peptidases, and activate the T-L (F) peptidase. |
| CSN18298 | SBC-115076 | 489415-96-5 | SBC-115076 is an anti-proprotein convertase subtilisin kexin type 9 (anti-PCSK9) compounds, for the treatment and/or prevention of cardiovascular diseases. |
| CSN17672 | pGlu-Pro-Arg-MNA | 130835-45-9 | pGlu-Pro-Arg-MNA is a peptide. |
| CSN18238 | Octahydrocurcumin | 36062-07-4 | Octahydrocurcumin is a hydrogenated derivatives of curcumin and a metabolite of curcumin. |
| CSN18077 | Sodium (OC-6-11)-tetrachlorobis(1H-indazole-κN2)ruthenate(1-) (1:1) | 197723-00-5 | NKP-1339 is a ruthenium (iii) coordination anticancer compound based on target to transferrin. |
| CSN17858 | Mebeverine alcohol | 14367-47-6 | Mebeverine alcohol is a metabolite of Mebeverine, which is a musculotropic antispasmodic drug. |
| CSN18249 | Madrasin | 374913-63-0 | Madrasin is a potent and cell penetrant splicing inhibitor that interferes with the early stages of spliceosome assembly. |
| CSN18202 | Ldn-27219 | 312946-37-5 | LDN-27219 is a potent inhibitor of hTGase (Tissue transglutaminase) with an IC50 of 0.6 μM. |
| CSN17564 | (R,R)-BD-AcAc 2 | 1208313-97-6 | Ketone ester, added in diet, could elevated mean blood ketone bodies of 3.5 mm and lowered plasma glucose, insulin, and leptin in animals and ketone ester given orally would delay CNS-OT seizures in rats breathing hyperbaric oxygen. |
| CSN17494 | Ikarisoside F | 113558-14-8 | Ikarisoside F is a flavonol glycoside from Vancouveria hexandra and can bind to AdoHcy hydrolase. |
| CSN18207 | Hydroxyhexamide | 3168-01-2 | Hydroxyhexamide is a pharmacologically active metabolite of Acetohexamide, used as a hypoglycemic agents. |
| CSN17718 | Linerixibat | 1345982-69-5 | GSK2330672 is a highly potent, nonabsorbable ASBT (apical sodium-dependent bile acid transporter) inhibitor (hASBT IC50=42 ± 3 nM) which lowers glucose in an animal model of type 2 diabetes and shows excellent developability properties for evaluating the potential therapeutic utility of a nonabsorbable ASBT inhibitor for treatment of patients with type 2 diabetes. |
| CSN17498 | GSK2256294A | 1142090-23-0 | GSK2256294A is a potent, reversible, tight binding inhibitor of isolated recombinant human sEH (soluble epoxide hydrolase) (IC50 = 27 pM; t1/2 = 121 min) and displays potent inhibition against the rat (IC50 = 61 pM) and murine (IC50 = 189 pM) orthologs of sEH. |
| CSN17698 | GSK2194069 | 1332331-08-4 | GSK2194069 is a potent and specific inhibitor of the β-ketoacyl reductase (KR) activity of hFAS with an IC50 of 7.7 ± 4.1 nM in an assay detecting released CoA. |
| CSN17870 | Voxelotor | 1446321-46-5 | GBT 440 is a modulator of sickle hemoglobin (HbS), which can be used in treating disorders mediated by hemoglobin and disorders that would benefit from tissue and/or cellular oxygenation. |
| CSN18239 | F16 | 36098-33-6 | F16 is a small molecule that selectively inhibits proliferation of mammary epithelial, neu-overexpressing cells, as well as a variety of mouse mammary tumor and human breast cancer cell lines. |
| CSN18142 | ADH-1 | 229971-81-7 | Exherin is a small, cyclic pentapeptide vascular-targeting agent with potential antineoplastic and antiangiogenic activities and selectively and competitively binds to and blocks N-cadherin. |
| CSN18375 | Etimizol | 64-99-3 | Etimizol is shown to relieve amnesia effectively in the origin of which there is the hypoxic component (hypobaric hypoxia, actinomycin D, mechanical injury of the brain). |
| CSN18299 | EN460 | 496807-64-8 | EN460 is a small molecule inhibitor of endoplasmic reticulum oxidation 1 (ERO1) and interacts selectively (IC50=1.9 μM) with the reduced, active form of ERO1α and prevents its reoxidation. |
| CSN18140 | EBE-A22 | 229476-53-3 | EBE-A22 is a derivative of PD 153035 which can inhibit ErbB-1-phosphorylation, whereas EBE-A22 is inactive. |
| CSN18221 | Dz2002 | 33231-14-0 | DZ2002 is a potent and reversible S-adenosyl-L-homocysteine hydrolase (SAHH; AdoHcy Hydrolase) inhibitor with Ki of 17.9 nM. |
| CSN17704 | DiZPK | 1337883-32-5 | DiZPK is a genetically encoded, highly efficient photocrosslinking amino acid valuable in unveiling the physiological interaction partners of given proteins and their functions. |
| CSN17896 | (S)-4,4'-(Propane-1,2-diyl)bis(piperazine-2,6-dione) hydrochloride | 1263283-43-7 | Dexrazoxane HCl is a cardioprotective agent. |
| CSN18132 | Collagen proline hydroxylase inhibitor-1 | 223663-32-9 | Collagen proline hydroxylase inhibitor-1 is an antifibroproliferative agents. |
| CSN18133 | Collagen proline hydroxylase inhibitor | 223666-07-7 | Collagen proline hydroxylase inhibitor is a collagen proline hydroxylase inhibitor and is useful for antifibroproliferative agents. |
| CSN17859 | Chromafenozide | 143807-66-3 | Chromafenozide is a lepidopteran insecticide and it is highly effective in controlling various lepidopteran pests. |
| CSN17935 | Chitinase-IN-2 | 1579991-63-1 | Chitinase-IN-2 is an insect chitinase and N- acetyl hexosaminidase inhibitor and pesticide and 50 μM/20 μM compound concentration's inhibitory percentage are 98%/92% for chitinase/N- acetyl-hexosaminidase respectively. |
| CSN17934 | Chitinase-IN-1 | 1579991-61-9 | Chitinase-IN-1 is an insect chitinase and N- acetyl hexosaminidase inhibitor and pesticide and 50 μM/20 μM compound concentration's inhibitory percentage are 75%/67% for chitinase/N- acetyl-hexosaminidase respectively. |
| CSN18345 | BFCAs-1 | 585531-74-4 | BFCAs-1 is a polyamino polycarboxylic bifunctional chelating agent (BFCAs) with a broad range of applications in chemistry, biology and medicine and diagnostic imaging (MRI, SPECT, PET). |
| CSN18367 | Benzoylmesaconine | 63238-67-5 | Benzoylmesaconine is the most abundant component of Wutou decoction, which is widely used in China because of its therapeutic effect on rheumatoid arthritis. |
| CSN17996 | Benoxafos | 16759-59-4 | Benoxafos is an insecticide. |
| CSN18178 | Bavachalcone | 28448-85-3 | Bavachalcone, a major bioactive compounds isolated from Psoralea corylifolia L., has been widely used as traditional Chinese medicine and is an antibiotic or anticancer agent. |
| CSN17477 | 2-(Chloromethyl)-4-(4-nitrophenyl)thiazole | 89250-26-0 | Astragalus polysaccharide, as one kind of biological macromolecule extracted from Astragalus, has antiviral activities. |
| CSN18266 | Antitumor agent-3 | 420126-30-3 | Antitumor compound 1 is a potent compound which comprises an imidazopyridine having excellent antitumor activity as an active ingredient. |
| CSN18320 | Ajugol | 52949-83-4 | Ajugol is an iridiod glucoside. |
| CSN17631 | AI-10-49 | 1256094-72-0 | AI-10-49 is a protein-protein interaction inhibitor that selectively binds to CBFβ-SMMHC and disrupts its binding to RUNX1 with a FRET IC50 of 0.26 μM. |
| CSN17861 | Aglafoline | 143901-35-3 | Aglafoline inhibits in a selective and concentration-dependent manner the aggregation and ATP release reaction induced in washed rabbit platelets by PAF (platelet-activating factor). |
| CSN18011 | Fabomotizole HCl | 173352-39-1 | Afobazole HCl is an anxiolytic drug and produces anxiolytic and neuroprotective effects without any sedative or muscle relaxant actions. |
| CSN18310 | 6''-O-Malonylgenistin | 51011-05-3 | 6''-O-Malonylgenistin is an isoflavone derivative. |
| CSN17933 | (Z)-2-Decenoic acid | 15790-91-7 | (Z)-2-decenoic acid is an unsaturated short chain fatty acid that is secreted by P. aeruginosa and induces a dispersion response in biofilms formed by Gram-negative and Gram-positive bacteria, as well as by the yeast C. albicans. |
