| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
V13338 | Carboxyamidotriazole | 99519-84-3 | Carboxyamidotriazole (RFE-007; L-651582;NSC-609974; CAI)is a novel and potent inhibitor of both cAMP-phosphodiesterases and GMP-phosphodiesterases withanti-tumor and anti-inflammatory activity. |
|
V17563 | Carboxyamidotriazole orotate | 187739-60-2 | Carboxyamidotriazole orotate is the orotate salt form of carboxyamidotriazole (CAI;RFE-007; L-651582;NSC-609974), which is a novel and potent inhibitor of both cAMP-phosphodiesterases and GMP-phosphodiesterases withanti-tumor, antiangiogenicand anti-inflammatory activity. |
|
V16856 | Carfecillin Sodium | 21649-57-0 | CarfecillinSodium (BRL-3475; BRL3475; Carbenicillin Phenyl Sodium), the phenyl ester and sodium salt form of Carbenicillin, is a semi-synthetic penicillin and a prodrug of carboxybenicillin with improved oral absorption. |
|
V31333 | CB-6644 | 2316817-88-4 | CB-6644 is a novel, potent, and selective inhibitor of RUVBL1/2 complex with anticancer activity, blocking the ATPase activity of RUVBL1/2 with an IC50 of 15 nM. |
|
V17730 | CCR2-RA-[R] | 512177-83-2 | CCR2-RA-[R] is a novel and potent CCR2 receptor (C-C chemokine receptor type 2) antagonist (allosteric, IC50 = 103 nM) with anti-inflammatory activity. |
|
V12351 | Cefminox Sodium | 75498-96-3 | Cefminox Sodium (MT-141;Meicelin) is a potent penicillin binding protein inhibitor and asemisynthetic cephamycin with a broad spectrum ofantibacterialactivity. |
|
V17851 | Cefpodoxime Proxetil | 87239-81-4 | Cefpodoxime Proxetil (Doxef;CS-807; U-76252;) is a broad spectrumantibacterial agent that acts bybinding to penicillin binding proteins (PBPs), thus inhibiting peptidoglycan synthesis, leading to disruption ofbacterialcell wall biosynthesis. |
|
V17892 | Centhaquine (Centhaquin; PMZ-2010) | 57961-90-7 | Centhaquine, formerly known as PMZ-2010, is a centrally-acting modulator of adrenergic receptor potentially for the treatment of postoperative pain and for the resuscitation of hypovolemic shock. |
|
V17896 | Cenupatide free base | 1006388-38-0 | Cenupatide is a novel and potent urokinase plasminogen activator receptor (uPAR) inhibitorpotentially for treating disorders associated altered cell migration, such as cancer. |
|
V17921 | Cephalomannine | 71610-00-9 | Cephalomannine is a taxol alkaloid analog that can be extracted from most Cephalotaxus plants. |
|
V17937 | Cetaben | 55986-43-1 | Cetaben is a PPARα-independent peroxisome proliferator. |
|
V17970 | CFLZ-171 TFA salt | 247068-85-5 | CFLZ-171 TFA (CFLZ 171; CFLZ171), the trifluoroacetic acid salt of CFLZ-171, is a key intermediate used for the synthesis of carfilzomib (Kyprolis) which is an irreversible proteasome inhibitor and approved anticancer drug. |
|
V17971 | CFLZ-567 | 868540-16-3 | CFLZ-567 (CFLZ567; CFLZ 567) is a key intermediate for the production of carfilzomib(Kyprolis) which is an irreversible proteasome inhibitor and approved anticancer drug. |
|
V41216 | Chelidonic Acid Monohydrate | 6003-94-7 | Chelidonic acid monohydrate, a naturally occurring heterocyclic organic acid with a pyran skeleton, is isolated fromChelidonium majus andoccurs naturally in plants of the Asparagales order. |
|
V6449 | Chlorothiazide | 58-94-6 | Chlorothiazide is a potent thiazide diuretic withantihypertensive effects. |
|
V18258 | Chromocarb | 4940-39-0 | Chromocarb is a synthetic vasoprotectant. |
|
V18331 | Ciliobrevin D | 1370554-01-0 | Ciliobrevin D is a novel and potent AAA+ ATPase motor cytoplasmic dynein inhibitor, alsoinhibits Hedgehog (Hh) signaling and primary cilia formation and dynein-dependent microtubule gliding and ATPase activity in vitro. |
|
V18342 | Cinchonidine HCl | 524-57-2 | Cinchonidine HCl is a natural cinchona alkaloidwith antimalarial activity. |
|
V18363 | CINPA1 | 102636-74-8 | CINPA1 is a potent and specific constitutive androstane (CAR) inhibitor that does not activate the pregnane X receptor (PXR). |
|
V18374 | Ciraparantag | 1438492-26-2 | Ciraparantag (PER977;Aripazine;PER 977;PER-977) is a novel and potent reversal agent for anticoagulants and heparins. |
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