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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 |
