| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
V26447 | NH-bis(PEG3-Boc) | 2055024-51-4 | NH-bis(PEG3-C2-NH-Boc) is a PROTAC (PROteolysis TArgeting Chimera) linker of the PEG category, may be utilized to prepare PROTAC protein degraders. |
|
V26448 | NH-bis(PEG3-OH) | 63721-14-2 | NH-bis-PEG4 is a PROTAC (PROteolysis TArgeting Chimera) linker of the PEG category, may be utilized to prepare PROTAC protein degraders. |
|
V26449 | NH-bis(PEG3-t-butyl ester) | 1814901-03-5 | NH-bis(PEG3-Boc) is a PROTAC (PROteolysis TArgeting Chimera) linker of the PEG category, may be utilized to prepare PROTAC protein degraders. |
|
V26450 | NH-bis(PEG4-Boc) | 2182601-75-6 | NH-bis(PEG4-C2-NH-Boc) is a PROTAC (PROteolysis TArgeting Chimera) linker of the PEG category, may be utilized to prepare PROTAC protein degraders. |
|
V26451 | NH-bis(PEG4-OH) | 63721-06-2 | NH-bis-PEG5 is a PROTAC (PROteolysis TArgeting Chimera) linker of the PEG category, may be utilized to prepare PROTAC protein degraders. |
|
V26452 | NH-bis(PEG4-t-butyl ester) | 2055041-41-1 | NH-bis(PEG4-Boc) is a PROTAC (PROteolysis TArgeting Chimera) linker of the PEG category, may be utilized to prepare PROTAC protein degraders. |
|
V29839 | NHE3-IN-1 | 632355-68-1 | NHE3-IN-1 is a sodium/proton exchanger type 3 (NHE-3) inhibitor from patent WO 2011019784 A1. |
|
V26453 | NHNB | 106359-61-9 | NHNB is a novel and potent inhibitor of histone deacetylases-8 (HDAC8) |
|
V26455 | NHS-LC-Biotin | 72040-63-2 | Biotin-C5-NHS Ester is a PROTAC (PROteolysis TArgeting Chimera) linker, belonging to the alkyl/ether class, may be utilized to prepare PROTAC protein degraders. |
|
V26456 | NHS-PEG4-(m-PEG4)3-ester | 1333154-70-3 | NHS-PEG4-(m-PEG4)3-ester is a PROTAC (PROteolysis TArgeting Chimera) linker of the Polyethylene glycol (PEG) category, may be utilized to prepare PROTAC protein degraders. |
|
V26457 | NHS-SS-Biotin | 142439-92-7 | Biotin-bis-amido-SS-NHS is a PROTAC (PROteolysis TArgeting Chimera) linker based on Alkyl/ether structure, which can be used for the synthesis of PROTAC. |
|
V26459 | NI-42 | 1884640-99-6 | NI-42 (compound 13-d), a chemical probe of the orthogonal structure of BRPFS, is a biased bromodomain (BRD) inhibitor of BRPFs (IC50= BRPF1/2/3=7.9/48/260 nM; Kd: BRPF1/2/3=40/210/940 nM), has good selectivity compared with non-classification IV BRD proteins. |
|
V26463 | NIBR-0213 | 1233332-14-3 | NIBR-0213 is a potent, orally bioactive, selective S1P1 antagonist effective in experimental autoimmune encephalomyelitis. |
|
V26465 | NIBR3049 | 1260181-14-3 | TCS 21311 (NIBR3049) is a potent and selective JAK3 inhibitor (antagonist) with IC50 of 8 nM. |
|
V26467 | NIC | 114773-20-5 | NIC is a novel and potent inhibitor of host invasion |
|
V26483 | Nicotinamide, N-(5-(p-aminophenoxy)pentyl)- | 101578-28-3 | Nicotinamide, N-(5-(p-aminophenoxy)pentyl)- is a novel and potent bioactive compound |
|
V26482 | Nicotinamide, N-(m-difluoromethoxyphenyl)-, hydrochloride | 64038-00-2 | Nicotinamide, N-(m-difluoromethoxyphenyl)-, hydrochloride is a novel and potent bioactive compound |
|
V26485 | NIDA-41020 | 502486-89-7 | NIDA-41020 is a potent and specific cannabinoid receptor 1 (CB1) antagonist (inhibitor) with Ki of 4.1 nM. |
|
V26487 | Nidurufin | 28458-23-3 | Nidurufin is a potent cell cycle inhibitor (antagonist) with anti-tumor effects. |
|
V26501 | Nigrescigenin | 6785-70-2 | Nigrescigenin is a novel and potent cardenolide agent |
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