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Preclinical Pharmacology Equipment & Supplies

4 equipment items found

Model CTT1403 - PSMA-targeted 177Lu-Labeled Agent for Prostate Cancer

Model CTT1403 - PSMA-targeted 177Lu-Labeled Agent for Prostate Cancer

Manufactured by:Cancer Targeted Technology   based inWoodinville, WASHINGTON (USA)
CTT’s lead therapeutic product, CTT1403, is a PSMA-targeted 177Lu-labeled agent for prostate cancer that can has superior binding characteristics, long circulation half-life, enhanced tumor uptake and unparalleled anti-tumor efficacy. CTT1403 will specifically deliver the radionuclide, 177Lu, minimizing toxic side effects and more effectively treating metastatic prostate cancer and other ...
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InMed - Model INM-755 - Cannabinol Topical Cream for the Treatment of Epidermolysis Bullosa

InMed - Model INM-755 - Cannabinol Topical Cream for the Treatment of Epidermolysis Bullosa

Manufactured by:InMed Pharmaceuticals Inc.   based inVancouver, BRITISH COLUMBIA (CANADA)
INM-755 is a cannabinol topical cream under development for the treatment of epidermolysis bullosa. INM-755 cream for EB is the first, and currently the only, cannabinol formulation being tested in clinical trials as a therapeutic ...
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MedChemExpress - Model Narazaciclib - 1357470-29-1

MedChemExpress - Model Narazaciclib - 1357470-29-1

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
Narazaciclib (ON123300), a strong and brain-penetrant[1] multi-kinase inhibitor, inhibits CDK4 (IC50=3.9 nM), Ark5 (IC50=5 nM), PDGFRβ (IC50=26 nM), FGFR1 (IC50=26 nM), RET (IC50=9.2 nM), and FYN (IC50=11 nM). Single agent Narazaciclib causes a dose-dependent suppression of phosphorylation of Akt as well as activation of Erk in brain tumors[2]. Narazaciclib inhibits CDK6 with an IC50 of 9.82 ...
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MedChemExpress - Model Roflumilast-d4 - 1398065-69-4

MedChemExpress - Model Roflumilast-d4 - 1398065-69-4

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
Roflumilast-d4 is the deuterium labeled Roflumilast. Roflumilast is a selective PDE4 inhibitor with IC50s of 0.7, 0.9, 0.7, and 0.2 nM for PDE4A1, PDEA4, PDEB1, and PDEB2, respectively, without affecting PDE1, PDE2, PDE3 or PDE5 isoenzymes from various ...
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