No Product Specs
Selleck Chemicals LLC Products
10058-F4 10058-F4 is a c-Myc inhibitor that specificallly inhibits the c-Myc-Max interaction and prevents transactivation of c-Myc target gene
10-Hydroxycamptothecin 10-Hydroxycamptothecin (10-HCPT, 10-hydroxy-CPT, OHCPT, NSC107124) is a DNA topoisomerase I inhibitor with potent anti-tumor
1-Azakenpaullone 1-Azakenpaullone is a potent and selective GSK-3β inhibitor with IC50 of 18 nM, >100-fold selectivity over CDK1/cyclin B and CDK5/p25.
1-Hexadecanol 1-Hexadecanol is a fatty alcohol used to make other chemicals.
3-Aminobenzamide 3-Aminobenzamide is a competitive PARP inhibitor with Ki of 1.8 μM.
3-Deazaneplanocin A (DZNeP) 3-deazaneplanocin A (DZNeP), an analog of adenosine, is a competitive inhibitor of S-adenosylhomocysteine hydrolase with
3-Indolebutyric acid(IBA) 3-Indolebutyric acid(IBA)
3-Methyladenine 3-Methyladenine (3-MA) is a selective autophagy and phosphoinositide 3-kinase (PI3K) inhibitor for Vps34 and PI3Kγ with IC50 of 25 μM
4μ8C 4μ8C is a potent and selective IRE1 Rnase inhibitor with IC50of 76 nM.
4E1RCat 4E1RCat is a dual inhibitor of eIF4E:eIF4G and eIF4E:4E-BP1 interaction, and inhibits the binding of eIF4G to eIF4E with IC50 of 3.2 μM.
4SC-202 4SC-202 is a selective class I HDAC inhibitor with IC50 of 1.20 μM, 1.12 μM, and 0.57 μM for HDAC1, HDAC2, and HDAC3, respectively. Also
5-Aminolevulinic acid hydrochloride 5-Aminolevulinic acid hydrochloride
6H05 6H05 is a selective, and allosteric inhibitor of oncogenic K-Ras(G12C).
7-Aminocephalosporanic acid 7-Aminocephalosporanic acid
A 205804 A-205804 is a potent and selective inhibitor of E-selectin and ICAM-1 expression with IC50 of 20 nM and 25 nM respectively.
A 922500 A 922500
A-438079 HCl A-438079 HCl is a potent, and selective P2X7 receptor antagonist with pIC50 of 6.9.
A-803467 A-803467 is a selective NaV1.8 channel blocker with IC50 of 8 nM.
Abacavir sulfate Target:Reverse Transcriptase
Abiraterone Acetate Abiraterone Acetate
Abscisic Acid (Dormin） Abscisic Acid is a plant hormone, which is involved in many plant developmental processes, modulates ion homeostasis and
ABT-199 (GDC-0199) ABT-199 (GDC-0199) is a Bcl-2-selective inhibitor with Ki of <0.01 nM, >4800-fold more selective versus Bcl-xL and Bcl-w, and no
Acebutolol HCl Acebutolol is a β-adrenergic receptors antagonist used in the treatment of hypertension, angina pectoris and cardiac arrhythmias.
Aceclidine HCl Aceclidine is a parasympathomimetic miotic agent used to decreases intraocular pressure.
Aclacinomycin A Aclacinomycin A inhibits chymotrypsin-like activity of eukaryotic 20 S proteasome or multicatalytic proteinase complex (MPC), inhibits
Aclidinium Bromide Aclidinium Bromide inhibits human muscarinic AChR M1, M2, M3, M4 and M5 with Ki of 0.1 nM, 0.14 nM, 0.14 nM, 0.21 nM and 0.16 nM,
Adefovir dipivoxil Adefovir dipivoxil
Adrenalone HCl Target:Adrenergic Receptor
AEBSF HCl AEBSF HCl is a broad spectrum, irreversible serine protease inhibitor.
Afatinib (BIBW2992) Dimaleate Afatinib (BIBW2992) Dimaleate irreversibly inhibits EGFR/HER2 including EGFR(wt), EGFR(L858R), EGFR(L858R/T790M) and
AFP antibody Alpha-fetoprotein (AFP) is a 65 kDa glycoprotein found in the serum of the mammalian fetal liver, yolk sac and GI tract. Expression of
Afuresertib (GSK2110183) Afuresertib (GSK2110183) is a potent, orally bioavailable Akt inhibitor with Ki of 0.08 nM, 2 nM, and 2.6 nM for Akt1, Akt2,
AG 18 (Tyrphostin 23) AG 18 inhibits EGFR with IC50 of 35 μM.
AG-1024 AG-1024 (Tyrphostin) is a specific IGF-1R/IR inhibitor with IC50 of 0.4 μM and 0.1 μM, respectively.
AGI-5198 AGI-5198 is the first highly potent and selective inhibitor of IDH1 R132H/R132C mutants with IC50 of 0.07 μM/0.16 μM.
AGI-6780 AGI-6780 is a potent and selective inhibitor of IDH2 R140Q mutant with IC50 of 23 nM.
AGK2 AGK2 is a potent, and selective SIRT2 inhibitor with IC50 of 3.5 μM.
Akt antibody Akt, also referred to as PKB or Rac, plays a critical role in controlling survival and apoptosis. [1-3] This protein kinase is activated
Alendronate sodium Alendronate sodium
Alfuzosin HCl Alfuzosin HCl
Aliskiren hemifumarate Aliskiren hemifumarate
Allopurinol sodium Allopurinol sodium
Allylthiourea Allylthiourea is a metabolic inhibitor that selective inhibits ammonia oxidation.
Almorexant HCl Almorexant HCl is an orally active, dual orexin receptor antagonist with IC50 of 6.6 nM and 3.4 nM for OX1 and OX2 receptor,
Alogliptin (SYR-322) Alogliptin(SYR-322) is a potent, selective inhibitor of DPP-4 with IC50 of < 10 nM.
Altrenogest Target:Estrogen/progestogen Receptor
Alverine Citrate Alverine citrate is a drug used for functional gastrointestinal disorders.
AM251 AM251 is a cannabinoid 1 receptor antagonist with IC50 of 8.9 μM.
Amantadine hydrochloride Amantadine hydrochloride
Ambroxol HCl Ambroxol HCl is a potent inhibitor of the neuronal Na+ channels with IC50 of 35.2 μM and 22.5 μM for tonic and phasic block, respectively.
Amfebutamone hydrochloride Amfebutamone hydrochloride
Amfenac Sodium Monohydrate Amfenac Sodium monohydrate is a non-steroidal analgesic anti-inflammatory drug with acetic acid moiety.
AMG 900 AMG 900
AMG-517 AMG 517 is a potent and selective TRPV1 antagonist, antagonizes capsaicin, proton, and heat activation of TRPV1 with IC50 of 0.76 nM, 0.62 nM
Amifostine Amifostine is the first approved radioprotective drug, used to decrease the risk of kidney problems caused by treatment with cisplatin.
Amikacin hydrate Amikacin hydrate
Amikacin sulfate Amikacin sulfate binds to 16S rRNA (bacterial 30S ribosome), causing misreading of mRNA and supressing proteins synthesis.
Amiloride hydrochloride Amiloride hydrochloride
Aminocaproic acid Aminocaproic acid
Aminothiazole Aminothiazole can be used as a thyroid inhibitor and it has antibacterial activity.
Amitriptyline HCl Target:5-HT Receptor
Amlodipine besylate Amlodipine besylate
Ammonium Glycyrrhizinate Ammonium Glycyrrhizinate
Amorolfine Hydrochloride Amorolfine Hydrochloride
Amoxapine Amoxapine is a tricyclic dibenzoxazepine (an N-aryl piperazine) which acts similarly to several other tricyclic antidepressants, amoxapine
Amphotericin B Amphotericin B
Ampicillin sodium Ampicillin is a beta-lactam antibiotic that is part of the aminopenicillin family.
Ampicillin Trihydrate Ampicillin Trihydrate is a β-lactam antibiotic, which inhibits bacterial cell-wall synthesis (peptidoglycan cross-linking) by
Ampiroxicam Ampiroxicam is a nonselective cyclooxygenase inhibitor uesd as anti-inflammatory drug.
Amprolium HCl Amprolium chloride is a thiamin antagonist, which prevents carbohydrate synthesis by blocking thiamine uptake.
ANA-12 ANA-12 is a selective TrkB antagonist with Kd of 10 nM and 12 μM for the high and low affinity sites, respectively.
Anacardic Acid Anacardic Acid is a potent inhibitor of p300 and p300/CBP-associated factor histone acetyltranferases, which also has antibacterial
Anagrelide hydrochloride Target:PDE
Angiotensin Angiotensin is an oligopeptide and causes blood vessels to constrict, and drives blood pressure up.
Anidulafungin (LY303366) Anidulafungin (LY303366), an echinocandin derivative, inhibits glucan synthase activity, used as an antifungal drug.
Anisomycin Anisomycin is an antibiotic, which inhibits protein synthesis, and also act as a JNK activator.
Antazoline HCl Antazoline HCl is a first generation antihistamine, binding to the histamine H1 receptor and blocking the action of endogenous
Anti-cancer Compound Library A unique collection of 349 anti-cancer compounds under clinical trials
Anti-diabetic Compound Library A unique collection of 31 small molecules affecting the development of diabetes.
Anti-infection Compound Library A unique collection of 134 anti-infective small molecules with biological activity of antibiotics,antifungal
AP26113 AP26113 is a potent ALK inhibitor for ALK, FER, ROS/ROS1, FLT3 and FES/FPS with IC50 of 0.62 nM, 1.3 nM, 1.9 nM, 2.1 nM and 3.4 nM,
Apicidin (OSI-2040) Apicidin is a potent nonselective HDAC inhibitor with IC50 of 0.7 nM.
APO866 (FK866) C24H29N3O2
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