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货号 产品名称 CAS号 简介
CSN26140 TRULI  1424635-83-5 TRULI is an ATP-competitive inhibitor of Lats kinases. It is a potent, non-toxic, and reversible inhibitor of Hippo signaling which causes Yap-depende
CSN26180 PU-02  313984-77-9 PU-02 is an antagonist of serotonin (5-HT) receptor subtype 5-HT3.
CSN27185 Col003  328565-16-8 Col003 is a cell penetrant, selective and potent inhibitor of the interaction of Hsp47 with collagen. Col003 is the cleavage product of AK778.It compe
CSN27205 ILK-IN-3  6975-75-3 ILK-IN-3 is an integrin linked kinase inhibitor.
CSN27206 CIL62  117593-36-9 CIL56 is a inducer of regulated, non-apoptotic cell death. It is a lead compound of FIN56,
CSN27211 JX06  729-46-4 JX06 is a selective covalent PDK1 inhibitor with IC50 values of 49, 101 and 313nM for PDK-1, PDK-2 and PDK-3, respectively.
CSN27236 AC-YVAD-CMK  178603-78-6 Ac-YVAD-CMK is a tetrapeptide ICE inhibitor.
CSN27229 RBN-2397  2381037-82-5 RBN-2397 is a potent, accross species and orally active NAD+ competitive inhibitor of PARP7 (IC50<3 nM). RBN-2397 selectively binds to PARP7 (Kd=0.001
CSN27231 GS143  916232-21-8 GS143 is a selective IκBα ubiquitination inhibitor with an IC50 of 5.2 μM for SCFβTrCP1-mediated IκBα ubiquitylation. GS143 sup­presses NF-κB activati
CSN27238 Nafenopin  3771-19-5 Nafenopin is a peroxisome proliferator that is used to promote liver tumors. It has been used as an antihyperlipoproteinemic agent.
CSN27244 2′,5′-Dideoxyadenosine  6698-26-6 2',5'-Dideoxyadenosine is a potent and non-competitive adenylyl cyclase inhibitor via binding the P-site with an IC50 of 3 µM . 2',5'-Dideoxyadenosine
CSN27247 PIK-75  372196-67-3 PIK-75 is a selective p110α inhibitor with IC50 of 5.8 nM with 200-fold more potently than p110β, and also potently inhibits DNA-PK with IC50 of 2 nM.
CSN27252 KM91104  304481-60-5 KM91104 is a specific v-ATPase inhibitor. It specifically targets the interaction between v-ATPase subunit a3 and subunit B2.
CSN27270 SR-717  2375421-09-1 SR-717 is a non-nucleotide STING agonist with EC50s of 2.1 μM and 2.2 μM in ISG-THP1 (WT) and ISG-THP1 cGAS KO (cGAS KO) cell lines, respectively. Ant
CSN27278 ACY-775  1375466-18-4 ACY-775 is a potent and selective inhibitor of the of histone deacetylase 6 (HDAC6) with an IC50 of 7.5 nM.
CSN27285 TH 1020  1841460-82-9 TH1020 is Toll-like receptor (TLR) 5/Flagellin complex antagonist with IC50 of 0.85 μM. TH1020 competes with flagellin for TLR5 binding to inhibit the
CSN27303 Org-12962  132834-56-1 Org-12962 is a potent, selective and orally active 5-HT2C receptor agonist with a pEC50 value of 7.01. Org-12962 also exhibits high effacy for the 5-H
CSN27306 Fmoc-8-amino-3,6-dioxaoctanoic acid  166108-71-0 Fmoc-8-amino-3,6-dioxaoctanoic acid (Fmoc-NH-PEG2-CH2COOH) is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
CSN27302 Dehydroaripiprazole  129722-25-4 Dehydroaripiprazole (OPC-14857) is an active metabolite of Aripiprazole. Aripiprazole is an antipsychotic agent and is metabolized by CYP3A4 and CYP2D
CSN27575 Isoastilbin  54081-48-0 Isoastilbin is a dihydroflavonol glycoside compound in Rhizoma Smilacis glabrae and Astragalus membranaceus. Isoastilbin inhibits glucosyltransferase
CSN27383 Levamlodipine  103129-82-4 Levamlodipine ((S)-Amlodipine) is a powerful dihydropyridine calcium channel blocker, possessing vasodilation properties and used in the treatment of
CSN27585 FG-7142  78538-74-6 FG 7142 (ZK 39106; LSU-65), a non-selectively benzodiazepine inverse agonist, has high affinity for the α1 subunit-containing GABAA receptor (Ki=91 nM
CSN27586 VU0119498  79183-37-2 VU0119498 is a M1 muscarinic receptor agonist with EC50 of 3.1 μM, and pan mAChR M3, M5 positive allosteric modulator (PAM),and is a neuroprotective a
CSN27595 VU0238441  85511-68-8 VU0238441 is a potent agonist of muscarinic acetylcholine receptor M5 with EC50 of 2.1 μM.
CSN27598 GOT1 inhibitor 2c  732973-87-4 GOT1 inhibitor 2c is a GOT1 inhibitor with IC50 value of 8.2μM.
CSN27656 GABAA receptor agent 1  1571-87-5
CSN27669 GRP60367  1309241-34-6
CSN27673 Ceapins-A7  2323027-38-7
CSN27658 DHODH-IN-11  1263303-95-2
CSN27661 Myoseverin  267402-71-1
CSN27671 ASTX029  2095719-92-7
CSN27659 MSAB  173436-66-3
CSN27706 NVP-ACC789  300842-64-2
CSN27710 SKF-34288 HCl  320386-54-7 SKF-34288 HCl is a PEPCK inhibitor which could inhibit glucose synthesis through inhibition of PEPCK in the gluconeogenesis pathway.
CSN27722 AZ9482  1825345-33-2
CSN27724 MitoBloCK-10  394694-98-5
CSN27725 COH-SR4  73439-19-7
CSN-BF1001 NP-40 Cell Lysis Buffer  N/A
CSN27723 MID-1  312608-54-1
CSN27735 MALAT1-IN-1  827327-28-6
CSN27766 Lavendustinb  125697-91-8
CSN27767 ICCB280  2041072-41-5
CSN27773 mTOR inhibitor-1  468747-17-3
CSN27768 AT-56  162640-98-4
CSN27841 PFM01  1558598-41-6
CSN27837 Rhodamine 123  62669-70-9
CSN27843 Sulforhodamine 101  60311-02-6
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