DCC0526 |
Akr1c3-in-14a |
Novel potent and selective aldo-keto reductase 1C3 inhibitor, displaying selectivity for AKR1C3 over other AKR1C enzymes and COX |
|
DCC0527 |
Akti-2 |
Cell-permeable Akt1/2 inhibitor with improved solubility and Ak2 selectivity |
|
DCC0528 |
Al-34662 |
Potent, selective, and efficacious ocular hypotensive serotonin-2 receptor agonist |
|
DCC0529 |
Al-438 |
Non-steroidal selective modulator for the glucocorticoid receptor (GR) |
|
DCC0530 |
Al-661 |
Novel HCV NS5B Polymerase Inhibitor for the Treatment of Chronic Hepatitis C |
|
DCC0531 |
Alalevonadifloxacin Mesylate |
Novel anti-MRSA antibacterial agent, targeting infections caused by Gram-positive bacteria |
|
DCC0532 |
Ala-vpa Conjugate-1 |
α-Linolenic acid-Valproic acid conjugate, not only modulating microglia polarization, but also counteracting neurodegeneration and demyelination and induce oligodendrocyte precursor cell differentiation, by acting on multiple biochemical and epigenetic pa |
|
DCC0533 |
Alazocine |
Potent analgesic, psychotomimetic or hallucinogen, and morphine or opioid antagonist |
|
DCC0534 |
Albicidin |
Potent DNA gyrase inhibitor |
|
DCC0535 |
Albiziabioside A |
Natural antitumor agent, inducing caspase-dependent apoptosis and ferroptosis as a p53 activator through the mitochondrial pathway |
|
DCC0536 |
Albucidin |
Novel nucleoside phytotoxin |
|
DCC0537 |
Alcuronium Chloride |
Neuromuscular blocking (NMB) agent |
|
DCC0538 |
Alda-89 |
Novel activator of ALDH3A1 |
|
DCC0539 |
Aldi-2 |
Potent and specific covalent inhibitor of aldehyde dehydrogenases |
|
DCC0540 |
Aldi-6 Hydrochloride |
Novel ALDH inhibitor, inhibiting ALDH3A1 activity in SCC4 HNSCC xenografts |
|
DCC0541 |
Aldoxorubicin |
Prodrug of the anthracycline antibiotic doxorubicin, binding selectively to the cysteine-34 position of albumin via its maleimide moiety, inhibiting DNA synthesis, and inducing apoptosis |
|
DCC0542 |
Alk/ros1-in-7d |
Potent and selective L1196M ALK and ROS1 dual inhibitor |
|
DCC0543 |
Alk-001
Featured
|
ALK-001 is a vitamin A analog potentially for the treatment of Stargardt’s disease. |
|
DCC0544 |
Alk-gw9662 |
Clickable PPARγ inhibitor |
|
DCC0545 |
Alkyne-a-dsbso
Featured
|
Novel Enrichable and MS-Cleavable Cross-linker to Define Protein-Protein Interactions by Mass Spectrometry |
|
DCC0546 |
Gsk1360707f |
Potent and selective triple reuptake inhibitor |
|
DCC0547 |
Allo-i1e-isoindoline |
Irreversible and selective dipeptidyl peptidase 8 and 9 (DPP-8/9) inhibitor |
|
DCC0548 |
Allo-ile-isoindoline Hcl |
Irreversible and selective dipeptidyl peptidase 8 and 9 (DPP-8/9) inhibitor |
|
DCC0549 |
Alloswitch-1 |
Novel allosteric modulator to control endogenous G protein-coupled receptors with light |
|
DCC0550 |
Alloxan Hydrate [3237-50-1] |
Natural chemical suppressor of mlo-mediated resistance in monocotyledonous barley (Hordeum vulgare) and dicotyledonous Arabidopsis thaliana |
|
DCC0551 |
Allylpyrocatechol |
Antioxidant, attenuating collagen-induced arthritis via attenuation of oxidative stress secondary to modulation of the MAPK, JAK/STAT, and Nrf2/HO-1 pathways |
|
DCC0552 |
Alpha7-pam-3ea |
Novel potent type I positive allosteric modulator (PAM) of human α7 nAChR |
|
DCC0553 |
Alpha-amplexichromanol |
Highly potent, orally effective, and metabolically stable allosteric 5-LOX Inhibitor |
|
DCC0554 |
Alpha-br-tmc |
Novel JAK2/STAT5 inhibitor |
|
DCC0555 |
Alpha-cf3-tmc |
Novel inhibitor of JAK2 and STAT5 phosphorylation in response to interleukin-3 without altering STAT5 mobility in SDS-PAGE |
|