|
V3070
|
A20832 |
40526-96-3 |
A 20832 is a potent inhibitor that inhibits resolvase-promoted site-specific recombination postsynaptically at strand cleavage. |
|
V3073
|
A2315A |
58717-24-1 |
A2315A is a new antibiotics produced by Actinoplanes philippinensis. |
|
V3074
|
A23887 |
61955-05-3 |
A23887(A 23887 or A-23887)is atetracyclic spiro aminewhich has previously been shown to have considerable affinity for dopamine D-2 receptors. |
|
V3076
|
A25822B |
50686-98-1 |
A25822B is anazasterol antifungal agent. |
|
V3080
|
A28086B |
58439-94-4 |
A28086B is an ionophore antibioticstructurally related to narasin, it was derived from fermentation and the structure was elucidated using electron impact and field desorption mass spectrometry. |
|
V3082
|
A28695B |
42617-35-6 |
A28695B is a potent polyether antibiotic that was originally isolated from Streptomyces albus. |
|
V2025
|
A32390A |
61241-59-6 |
A32390A, an isonitrile-containing analog of mannitol, is a new class of antifungal antibiotics. |
|
V3094
|
A331440 |
392338-13-5 |
A331440 is aninverse agonists/antagonists or modulator of theH3 receptor. |
|
V4312
|
ABT-288 |
948845-91-8 |
ABT-288 isa novel, potent and highly selective histamine-3 receptor antagonist which demonstrated efficacy across several preclinical cognitive domains, and safety in healthy subjects and elderly volunteers. |
|
V3742
|
ABT-639 HCl |
1235560-31-2 |
ABT-639hydrochloride (HCl) is a new potent, peripherally acting, selective T-type Ca2+channel blocker that blocks recombinant human T-type (Cav3.2) Ca2+channels in a voltage-dependent fashion (IC50=2 μM) and attenuates low voltage-activated (LVA) currents in rat DRG neurons (IC50=8 μM). |
|
V2462
|
Acetyl Tetrapeptide-11 |
928006-88-6 |
Acetyltetrapeptide 11 is a biologically active peptide with anti-aging activities that has been reported as an ingredient of cosmetics. |
|
V60053
|
Acetyl Tetrapeptide-11 |
928006-88-6 |
Acetyl tetrapeptide 11 is a biologically active peptide with anti-aging (anti-aging) effects that has been reported for use as a cosmetic ingredient. |
|
V4377
|
ADALIMUMAB |
331731-18-1 |
Adalimumab (trade name Humira; also known as Anti-Human TNF-alpha, Human Antibody) is a human monoclonal IgG1 antibody targeting tumour necrosis factor α (TNF-α). |
|
V3938
|
ADU-S100 |
1638241-89-0 |
ADU-S100 (formerly known asMIW-815; MIW815; ML RR-S2 CDA), a cyclic dinucleotide, is a novel and potent agonist of STING (Stimulator of Interferon Genes) with immunomodulatory and anticancer activities. |
|
V0433
|
ALG1001 TFA |
1307293-62-4 |
ALG1001 has been discontinued due to commercial reasons. |
|
V2155
|
AMG-25 |
1003311-62-3 |
AMG-25 (AMG25) is a novel, oral, potent and selective inhibitor of c-Kit with anticancer activity and desirable pharmacokinetic properties. |
|
V2509
|
AP3 Impurity 1 |
77714-98-8 |
AP3 Impurity 1 is a bioactive molecules. |
|
V2510
|
AP3 Impurity 2 |
625834-49-3 |
AP3 Impurity 2 is a bioactive molecules. |
|
V3814
|
Atabecestat (JNJ-54861911) HCl |
1200493-78-2 |
Atabecestat HCl (formerly known as JNJ-54861911 HCl), the hydrochloride salt ofAtabecestat, is a novel potent, oral, and brain-penetrantinhibitor of β-site amyloid precursor protein cleaving enzyme 1 (BACE1), which is an enzyme that is up-regulated in Alzheimer's disease. |
|
V4374
|
ATEZOLIZUMAB |
1380723-44-3 |
Atezolizumab (also known as MPDL3280A; trade name:Tecentriq) is a novel and selective humanized monoclonal IgG1 antibody against programmed death ligand 1 (PD-L1). |