| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
V61557 | Itruvone(PH10) | 21321-89-1 | Itruvone is an intermediate in the Fenton oxidation process of 17α-ethinylestradiol (EE2). |
|
V62113 | Ivospemin (SBP-101) | 748119-79-1 | Ivospemin is a spermine analog with anti-cancer activities. |
|
V57924 | IZS-L | 1173464-62-4 | IZS-L is an amino acid (AA) derived corrosion inhibitor. |
|
V60357 | IZS-P | 1173464-65-7 | IZS-P is an amino acid (AA)-derived corrosion inhibitor based on green chemistry principles. |
|
V57698 | JA-ACC (Jasmonyl-ACC) | 371778-55-1 | JA-ACC (Jasmonyl-ACC) is an analogue of 1-aminocyclopropane-1-carboxylic acid (ACC). |
|
V60858 | JH-131e-153 | 742104-91-2 | JH-131e-153, a diacylglycerol (DAG)-lactone, is a small molecule activator of Munc13-1 targeting the C1 domain. |
|
V62199 | JH295 hydrate | 2714087-26-8 | JH295 hydrate is a potent, irreversible and selective NIMA-related kinase 2 (Nek2) inhibitor (antagonist) with IC50 of 770 nM. |
|
V57916 | JH530 | 2928616-74-2 | JH530 is a potent inducer of macrovesicular cell death (methuosis) and suppresses the proliferation/growth of triple-negative breast cancer (TNBC) cells by causing complete intracellular vacuolization. |
|
V57501 | JNJ-3790339 | 93076-87-0 | JNJ-3790339, a Ritanserin analogue, is a potent and specific diacylglycerol kinase (DGKα) inhibitor (antagonist) with IC50 of 9.6 μM. |
|
V58728 | JNJ-54119936 | 1599531-55-1 | JNJ-54119936 is a novel RORC inverse agonist (Kd=5.3 nM). |
|
V57030 | JNJ-65355394 | 2230598-99-7 | JNJ-65355394 (Compound 28) is an O-GlcNAc hydrolase (OGA) inhibitor. |
|
V57824 | Joro spider toxin 3 (JSTX-3; Jorotoxin 3) | 112163-33-4 | Joro spider toxin 3 is a GABA agonist. |
|
V64226 | JY-2 | 339103-05-8 | JY-2 is a moderately selective and orally bioactive inhibitor of forkhead transcription factor O1 (FoxO1) with IC50 of 22 μM for inhibiting FoxO1 transcriptional activity. |
|
V70617 | Kainic acid hydrate | 58002-62-3 | Kainic acid hydrate is a potent excitotoxic agent. |
|
V75072 | Kallikrein 5-IN-2 | 2361160-57-6 | Kallikrein 5-IN-2 (compound 21) is a selective Kallikrein KLK5 inhibitor (pIC50=7.1). |
|
V57862 | Kayexalate (sodium polystyrene sulfonate) | 37349-16-9 | Kayexalate, a cation exchange resin, is an orally bioactive plasma potassium inhibitor. |
|
V61920 | KF38789 | 257292-29-8 | KF38789 selectively inhibits/disrupts the binding of P-selectin to PSGL-1. |
|
V62344 | Kgp-IN-1 hydrochloride | 2097865-47-7 | Kgp-IN-1 HCl is an arginine-specific P. gingivalis protease (Rgp) inhibitor. |
|
V61917 | KHK-IN-3 | 2568608-48-8 | KHK-IN-3 (Example 1) is a hexulokinase (KHK) inhibitor that may be utilized in the study of kidney disease, non-alcoholic steatohepatitis (NASH), diabetes and heart failure. |
|
V61488 | Kinetin triphosphate (6-Fu-ATP; KTP) | 1450894-16-2 | Kinetin triphosphate (6-Fu-ATP; KTP) is an ATP analog used to regulate or improve kinase function, and its catalytic efficiency is higher than its endogenous substrate ATP. |
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