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Displaying drugs 10301 - 10325 of 10874 in total
Urocortin 2 has been investigated for the basic science of Heart Failure and Cardiovascular Disease.
Investigational
Matched Description: … Urocortin 2 has been investigated for the basic science of Heart Failure and Cardiovascular Disease. …
KW-6356 is a selective antagonist of adenosine A2A receptors developed by Kyowa Kirin.
Experimental
Matched Description: … KW-6356 is a selective antagonist of adenosine A2A receptors developed by Kyowa Kirin.[L43822] …
Zafiride is a human tumor necrosis factor coupled to the C terminus of CNGRCG peptide.
Investigational
Matched Description: … Zafiride is a human tumor necrosis factor coupled to the C terminus of CNGRCG peptide. …
KT-253 is a selective heterobifunctional small molecule degrader of mouse double minute 2 (MDM2).
Investigational
Matched Description: … KT-253 is a selective heterobifunctional small molecule degrader of mouse double minute 2 (MDM2). …
PRG-A01 is a novel inhibitor of Cu, Zn-superoxide dismutase (SOD1) misfolding and aggregation.
Investigational
Matched Description: … PRG-A01 is a novel inhibitor of Cu, Zn-superoxide dismutase (SOD1) misfolding and aggregation. …
Helium He-3 is under investigation in clinical trial NCT00846014 (Asthma Exacerbation and Helium-3 MRI).
Investigational
Matched Description: … Helium He-3 is under investigation in clinical trial NCT00846014 (Asthma Exacerbation and Helium-3 MRI …
GLPG-0259 is under investigation in clinical trial NCT01024517 (GLPG0259 Solid Formulation Bioavailability and Food Effect).
Investigational
Matched Description: … GLPG-0259 is under investigation in clinical trial NCT01024517 (GLPG0259 Solid Formulation Bioavailability …
MCMV5322A is an anticytomegalovirus monoclonal IgG1 antibody used in combination with MCMV3068A to form RG7667.
Investigational
Matched Description: … MCMV5322A is an anticytomegalovirus monoclonal IgG1 antibody used in combination with [MCMV3068A] to …
Veverimer is under investigation in clinical trial NCT03390842 (Long-term Safety Extension to Study TRCA-301).
Investigational
Matched Description: … Veverimer is under investigation in clinical trial NCT03390842 (Long-term Safety Extension to Study TRCA …
Alphameprodine is an opioid analgesic classified by the United States Drug Enforcement Administration under Schedule I of illegal substances. The stereoisomer betameprodine is similarly classified, however alphameprodine is more widely used (both are referred to as Meprodine). Alphameprodine is a structural analogue of meperidine. It exerts physiological effects characteristic of...
Experimental
Illicit
Matched Description: … Alphameprodine is a structural analogue of meperidine. ... an opioid analgesic classified by the United States Drug Enforcement Administration under Schedule I of ... It exerts physiological effects characteristic of opioids, such as analgesia, euphoria and sedation, …
The anti-obesity drug, V24343, acts by targeting the CB1 receptor in the brain and suppressing a person's appetite.
Investigational
Matched Description: … The anti-obesity drug, V24343, acts by targeting the CB1 receptor in the brain and suppressing a person's …
A selective androgen receptor modulator with minimal prostate hypertrophic activity, enhances lean body mass in male rats and stimulates sexual behavior in female rats.
Experimental
Matched Description: … male rats and stimulates sexual behavior in female rats. ... selective androgen receptor modulator with minimal prostate hypertrophic activity, enhances lean body mass in
A sulfonamide antimicrobial used for urinary tract infections and in veterinary medicine.
Vet approved
Matched Description: … A sulfonamide antimicrobial used for urinary tract infections and in veterinary medicine. …
Dinitolmide is a fodder additive for prophylaxis against coccidiosis infections in poultry.
Experimental
Vet approved
Matched Description: … Dinitolmide is a fodder additive for prophylaxis against coccidiosis infections in poultry. …
Liafensine is under investigation in clinical trial NCT00892840 (Multiple-Ascending Dose Study).
Investigational
Matched Iupac: … 6-[(4S)-2-methyl-4-(naphthalen-2-yl)-1,2,3,4-tetrahydroisoquinolin-7-yl]pyridazin-3-amine …
Matched Description: … Liafensine is under investigation in clinical trial NCT00892840 (Multiple-Ascending Dose Study). …
Lunasine is under investigation in clinical trial NCT02709330 (ALS Reversals - Lunasin Regimen).
Investigational
Matched Description: … Lunasine is under investigation in clinical trial NCT02709330 (ALS Reversals - Lunasin Regimen). …
JAK4D is a first-in-class thyrotropin-releasing hormone (TRH)-based compound.
Investigational
Matched Description: … JAK4D is a first-in-class thyrotropin-releasing hormone (TRH)-based compound. …
Amniotic epithelial cells (AEC) are multipotent stem-like cells derived from the basement collagenous membrane of the human amnion, the layer of the placenta closest to the fetus.[A220183,T823] These cells are potential candidates for allogeneic cell therapy and regenerative medicine due to their potential for differentiation and multiplication.
Investigational
Matched Description: … the human amnion, the layer of the placenta closest to the fetus. ... epithelial cells (AEC) are multipotent stem-like cells derived from the basement collagenous membrane of
Estrane-3,17-dione is a potent inhibitor of isomerase.
Experimental
Matched Description: … Estrane-3,17-dione is a potent inhibitor of isomerase. …
MK-886 is an experimental inhibitor of leukotriene synthesis.
Experimental
Matched Description: … MK-886 is an experimental inhibitor of leukotriene synthesis. …
A version of tabituximab barzuxetan radiolabeled with yttrium-90.
Investigational
Matched Description: … A version of [tabituximab barzuxetan] radiolabeled with yttrium-90. …
Zeranol is a non-steroidal estrogen agonist. It is a mycotoxin, derived from fungi in the Fusarium family, and may be found as a contaminant in fungus-infected crops. It is 3-4x more potent as an estrogen agonist than the related compound zearalenone.
Experimental
Vet approved
Matched Description: … It is a mycotoxin, derived from fungi in the Fusarium family, and may be found as a contaminant in fungus-infected …
JPC-3210 is a potent antimalarial agent. It is an erythrocytic schizonticide with potent in vitro antimalarial activity against multidrug-resistant Plasmodium falciparum lines, low cytotoxicity, potent in vivo efficacy against murine malaria, and favourable preclinical pharmacokinetics including a lengthy plasma elimination half-life.
Experimental
Matched Description: … _Plasmodium falciparum_ lines, low cytotoxicity, potent in vivo efficacy against murine malaria, and ... It is an erythrocytic schizonticide with potent in vitro antimalarial activity against multidrug-resistant …
The pyranose form of D-quinovose with an α-configuration at the anomeric position .
Experimental
Matched Description: … The pyranose form of D-quinovose with an α-configuration at the anomeric position . …
Bryostatin 1 has been investigated for the treatment of HIV Infection and Alzheimer's Disease.
Investigational
Matched Description: … Bryostatin 1 has been investigated for the treatment of HIV Infection and Alzheimer's Disease. …
Displaying drugs 10301 - 10325 of 10874 in total