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Thalidomide-O-amido-C8-NH2
Catalog No. A20174 Thalidomide-O-amido-C8-NH2 is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology. 了解更多 -
MAT2A inhibitor 2
Catalog No. A20171 MAT2A inhibitorMAT2A inhibitor 2 is a methionine adenosyltransferase 2A (MAT2A) inhibitor. 了解更多 -
Polymyxin B nonapeptide
Catalog No. A20168 Polymyxin B nonapeptide is a cyclic peptide obtained from Polymyxin B by proteolytic removal of its terminal amino acyl residue. Polymyxin B nonapeptide is less toxic, lacks bactericidal activity, and retains its ability to render gram-negative bacteria susceptible to several antibiotics by permeabilizing their outer membranes. 了解更多 -
Thalidomide-O-amido-PEG3-C2-NH2
Catalog No. A20161 E3 ligase ligand-linker conjugateThalidomide-O-amido-PEG3-C2-NH2 is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and 3-unit PEG linker used in PROTAC technology. 了解更多 -
Jaspamycin
Catalog No. A20153 PKA activatorJaspamycin (7-CN-7-C-Ino) is a potent activator of PKA, binding to the R site (PKAR), with an EC50 of 6.5 nM and Kd of 8 nM in Trypanosoma brucei. Jaspamycin (7-CN-7-C-Ino) does not bind with purified human PKARIα. Anti-parasite activity. 了解更多 -
Thalidomide-O-amido-PEG3-C2-NH2 (TFA)
Catalog No. A20133 E3 ligase ligand-linker conjugateThalidomide-O-amido-PEG3-C2-NH2 TFA is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and 3-unit PEG linker used in PROTAC technology. 了解更多 -
Thalidomide-O-amido-C4-NH2 (TFA)
Catalog No. A20120 E3 ligase ligand-linker conjugateThalidomide-O-amido-C4-NH2 TFA (Cereblon Ligand-Linker Conjugates 6 TFA) is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology. 了解更多 -
DAAO inhibitor-1
Catalog No. A20117 DAAO inhibitorDAAO inhibitor-1 is a potent D-amino acid oxidase (DAAO) inhibitor with an IC50 of 0.12 μM. 了解更多 -
Losmiprofen
Catalog No. A20115 -
Thalidomide-O-amido-C8-NH2 (TFA)
Catalog No. A20108 E3 ligase ligand-linker conjugateThalidomide-O-amido-C8-NH2 TFA (Cereblon Ligand -Linker Conjugates 2 TFA) is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology. 了解更多 -
Taurochenodeoxycholate-3-sulfate
Catalog No. A20105 Taurochenodeoxycholate-3-sulfate is a bile salt found in urine. 了解更多 -
Thalidomide-O-amido-C4-N3
Catalog No. A20097 E3 ligase ligand-linker conjugateThalidomide-O-amido-C4-N3 is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology. 了解更多 -
SB-772077B dihydrochloride
Catalog No. A20090 ROCK inhibitorSB-772077B dihydrochloride is an aminofurazan-based Rho kinase (ROCK) inhibitor with IC50s of 5.6 nM and 6 nM toward ROCK1 and ROCK2, respevtively. 了解更多 -
Pomalidomide-PEG4-C2-NH2
Catalog No. A20076 Pomalidomide-PEG4-C2-NH2 is a synthesized E3 ligase ligand-linker conjugate that incorporates the Pomalidomide based cereblon ligand and 4-unit PEG linker used in PROTAC technology. 了解更多 -
BOS-172722
Catalog No. A20031 MPS1 checkpointBOS-172722 is an inhibitor of monopolar spindle 1 (MPS1) checkpoint with an IC50 of 2 nM. 了解更多 -
mTOR inhibitor-1
Catalog No. A20029 mTOR inhibitormTOR inhibitor-1 is a novel mTOR pathway inhibitor which can suppress cells proliferation and inducing autophagy. 了解更多 -
Aspartyl-alanyl-diketopiperazine
Catalog No. A20027 Aspartyl-alanyl-diketopiperazine (DA-DKP) is an immunomodulatory molecule generated by cleavage and cyclization from the N-terminus of human albumin and can modulate the inflammatory immune response through a molecular pathway implicated in T- lymphocyte anergy. 了解更多 -
Arachidonic acid
Catalog No. A20014 Arachidonic acid is an essential fatty acid and a major constituent of biomembranes. 了解更多 -
N6-(2-Phenylethyl)adenosine
Catalog No. A20011 A1 adenosine receptor agonistN6-(2-Phenylethyl)adenosine is a selective A1 adenosine receptor agonist. 了解更多 -
WAY-213613
Catalog No. A19992 GLT-1/EAAT2 reuptake inhibitorWAY-213613 is a potent, selective nonsubstrate reuptake inhibitor of GLT-1/EAAT2 with IC50 of 85 nM EAAT2. 了解更多 -
MGAT2-IN-1
Catalog No. A19983 MGAT2 inhibitorMGAT2-IN-1 is an orally active inhibitor of monoacylglycerol acyltransferase (MGAT2) with IC50 of 7.8 and 2.4 nM for human and mouse MGAT2, respectively. 了解更多 -
Reproxalap
Catalog No. A19978 RASP sequestering agentReproxalap (ADX-102) is a reactive aldehyde species (RASP) sequestering agent for the treatment of dry eye. Reproxalap (ADX-102) covalently binds aldehydes including malondialdehyde and 4-hydroxynonenal. 了解更多 -
Diethylamino hydroxybenzoyl hexyl benzoate
Catalog No. A19968 photostable UV-A absorberDiethylamino hydroxybenzoyl hexyl benzoate is a photostable UV-A absorber. 了解更多 -
3,4'-Dihydroxyflavone
Catalog No. A19966 3,4'-Dihydroxyflavone (3,4'-DHF) is an oral active flavonoid with antiviral activity against Influenza A virus. 了解更多 -
N-Nonyldeoxynojirimycin
Catalog No. A19963 alpha-glucosidase/alpha-1,6-glucosidase inhibitorN-Nonyldeoxynojirimycin (NN-DNJ) is a potent inhibitor of alpha-glucosidase and alpha-1,6-glucosidase (IC50s, 0.42, 8.4 μM, respectively), inhibits glycogen breakdown. 了解更多 -
Prolylleucine
Catalog No. A19961 Prolylleucine is a dipeptide containing branched-chain amino acids. 了解更多 -
D-myo-Inositol 1,4,5-trisphosphate hexapotassium salt
Catalog No. A19958 D-myo-Inositol 1,4,5-trisphosphate hexapotassium salt is the hexapotassium salt of D-myo-Inositol 1,4,5-trisphosphate (1,4,5-IP3), which is a second messenger that stimulates the discharge of calcium from the endoplasmic reticulum. 了解更多 -
BRD4 degrader AT1
Catalog No. A19956 Brd4 degraderBRD4 degrader AT1 is a highly selective Brd4 degrader based on PROTAC technology, with a Kd of 44 nM for Brd4BD2 in cells. 了解更多 -
4'-Methoxyflavonol
Catalog No. A19955 4'-Methoxyflavonol is a synthesized flavone/flavonol with 1, 2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) bilayers. 了解更多 -
S-methyl-KE-298
Catalog No. A19954 S-methyl-KE-298 is an active metabolite of KE-298. KE-298 inhibits matrix metalloproteinase (MMP-1) production from rheumatoid arthritis (RA) synovial cells. 了解更多 -
ML 145
Catalog No. A19953 GPR35/CXCR8 antagonistML 145 is a selective GPR35/CXCR8 antagonist with an IC50/EC50 of 20.1 nM, but not for the related GPR55 orphan receptor. GPR35 is expressed by various cells of the immune system and it may has potential as a therapeutic target in inflammatory disease. 了解更多 -
UDP-GlcNAc Disodium Salt
Catalog No. A19951 OGT donor substrateUDP-GlcNAc Disodium Salt (UDP-α-D-N-Acetylglucosamine Disodium Salt) is a donor substrate of O-GlcNAc transferase (OGT). 了解更多
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