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16
Angiogenesis
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BTK
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8
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19
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10
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20
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Products starting with 'A'
or product name starting with:
A
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571250
A2315A
A2315A is an antibiotic.
466284
A2-32-01
featured
A2-32-01 is a HsClpP antagonist.
571093
A23887
A23887 is a potentially neuroleptic tetracyclic spiro amine that has affinity for ...
576136
A-2545
A-2545 is an antiarrhythmic drug.
571077
A-25794
A 25794 is an antibiotic that may have antidepressant properties.
571086
A25822B
A25822B is an antifungal agent. It is an azasterol that may decrease the ratio of ...
571249
A 26771B
A 26771B is a macrolide lactone antibiotic.
571080
A 269A
A 269A is an antibiotic that is believed to be the same as LL-BL 136; it is isolat...
571095
A 274
A 274 is a highly aromatic, monosubstituted phenol antioxidant generated during di...
556009
A2793
new
featured
A2793 is an inhibitor of TRESK (IC50 value of 6.8 μM for mTRESK). A2793 inhibited ...
571090
A28086B
A28086B is an ionophore antibiotic related to narasin and salinomycin.
525223
A-286501
A-286501 is a novel orally active adenosine kinase inhibitor (IC50=0.47 nM). A-28...
571084
A28695B
A28695B is a polyether antibiotic isolated from Streptomyces albus.
531346
A286982
new
featured
A286982 is an inhibitor that blocks the integrin-ligand interaction between leukoc...
563731
A2A-IN-1
A2A-IN-1 is a potent and selective antagonist of A2A receptor.
574042
A2AR agonist-1
featured
A2AR agonist-1 is an agonist of the adenosine A2A receptor and an inhibitor of equ...
563063
A2B57
A2B57 is a SIRT2-selective inhibitor.
598133
A2-Binding peptide
A2-Binding peptide has a substitution of lysine at position 62 of MP 57-68, K62, K...
571247
A(2)C
A(2)C is a biochemical.
571113
A 30312
A 30312 is a biochemical that may specifically overcome multidrug resistance witho...
531347
A-304121
A-304121 is a histamine H(3) receptor.
571103
A 30641
A 30641 is an epidithioketopiperazine with antifungal activity. It is a metabolite...
571105
A 31472
A 31472 is a tetracyclic spiro amine that has affinity for dopamine D-2 receptors....
571115
A-315675
A-315675 is a potent anti-infuenza agent. It is a neuramidase inhibitor that respo...
571116
A-317491
A-317491 is a potent and selective non-nucleotide antagonist of P2X3 and P2X2/3 re...
526701
A-317491 sodium
featured
A-317491 is a potent and selective non-nucleotide antagonist of P2X3 and P2X2/3 re...
531349
A-317567
A-317567 is an ASIC-3 inhibitor.
531350
A-317920
A-317920 is an inverse agonist radioligand.
573571
A-320436
A-320436 is an H3 receptor antagonist that may affect cognition.
571104
A32390A
A32390A is an antibiotic inhibitor that shows antimicrobial activity against fungi...
584987
A 33
featured
A 33 is a potent and selective PDE4B inhibitor.
531351
A331440
A331440 is an L-histidine and histamine H3 receptor modulator.
563111
A-331440 2HCl
A-331440 2HCl is a histamine H3 receptor antagonist.
464176
A3-32-01
A3-32-01 is a β-lactone hClpP inhibitor.
571108
A 33853
A 33853 is an antibiotic isolated from culture broth of Streptomyces sp. It is a t...
466046
A33903
A33903 is a 1,4-benzodiazepine analog that is being studied as a potential inhibit...
531352
A-349821
A-349821 is an H3 receptor agonist radioligand.
526079
A-350619 hydrochloride
featured
A-350619 hydrochloride is an activator of soluble guanylyl cyclase (sGC).
407998
A-357300
A-357300 is a potent, selective, reversible MetAP2 inhibitor with IC50 of 0.12 uM....
407285
A-366
featured
A-366 is a potent inhibitor of G9a/GLP with IC50 3 nM and > 100-fold selectivity o...
524101
A-366833
A-366833 is a drug developed by Abbott which acts a novel nicotinic acetylcholine ...
561527
A-371191
A-371191 is a novel Bcl-XL antagonist. Bcl-XL is one of the anti-apoptotic Bcl-2 f...
574541
A 37203
A 37203 is a selective D3 receptor antagonist.
531353
A-381393
featured
A-381393 is a potent and selective agonist of the dopamine D4 receptor.
561526
A-385358
A-385358 is an inhibitor of Bcl-XL, a novel target for the treatment of many cance...
571114
A 39355
A 39355 may specifically overcome multidrug resistance without the serious hypoten...
407490
A-395 hydrochloride
featured
A-395 is a potent and selective EED inhibitor. A-395 includes potent binding to EE...
527839
A3 HCl
featured
A3 HCl is an inhibitor of PKA, PKC, and casein kinase I and II, and MLCK.
565651
A-410099.1 free base
A-410099.1 is a novel potent xiap antagonist
584794
A 410099.1 HCl
featured
A 410099.1 is a high affinity XIAP antagonist that is active in vivo.
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