177 Results for "

dimerization

" in MedChemExpress (MCE) Product Catalog:
Products (177)

177 Results for "dimerization" in MCE Product Catalog:

Cat. No.: HY-111009
CAS No.: 95927-67-6
Purity:  98.30%
Swinholide A is the actin-binding marine polyketide and dimerizes actin with the Kd of ~ 50 nM . Swinholide A is a microfilament disrupting marine toxin that stabilizes actin dimers and severs actin filaments. Swinholide A disrupts the actin cytoskeleton of cells.Antifungal activity .
loading...
    loading...
Cat. No.: HY-122678
CAS No.: 354543-09-2
Purity:  97.13%
Target:  

Survivin Apoptosis

Research Areas:  

Cancer

LQZ-7F, a survivin dimerization inhibitor, induces spontaneous apoptosis and synergizes with Docetaxel in prostate cancer cells. LQZ-7F dose-dependently inhibits survival of both PC-3 and C4-2 cells with IC50s of 2.99 and 2.47 µM, respectively .
loading...
    loading...
Cat. No.: HY-Y0779
CAS No.: 403-42-9
Synonyms: 1-(4-Fluorophenyl)ethan-1-one
4'-Fluoroacetophenone (1-(4-Fluorophenyl)ethan-1-one) is p-fluoroacetophenone, and serves as a substrate for both SNAr dimerization reactions and cross SNAr reactions. 4'-Fluoroacetophenone is also an important intermediate that can be used in the synthesis of other active compounds, such as aromatic diketones .
loading...
    loading...
Cat. No.: HY-126558
CAS No.: 1373154-68-7
Purity:  99.62%
Research Areas:  

Others

GA3-AM is a cell permeable analog of the plant hormone gibberellic acid that acts as a chemical dimerizer or chemical inducer of dimerization .
loading...
    loading...
Cat. No.: HY-114771
CAS No.: 490-20-0
Purity:  99.93%
Target:  

Drug Intermediate

Research Areas:  

Inflammation/Immunology

α-Truxillic acid is form by the dimerization of two molecules of α-trans-cinnamic acid, with anti-inflammatory activities. α-Truxillic acid has no analgesic activity, but its derivatives bound to camphor fragments exhibit significant activity in the peripheral analgesic model (writhing test) .
loading...
    loading...
Cat. No.: HY-P10438
Target:  

Raf

Research Areas:  

Cancer

TAT-Braftide is a peptide inhibitor designed to block the dimerization of BRAF, thereby inhibiting its kinase activity. The destruction of BRAF dimer by TAT-Braftide makes BRAF protein more susceptible to proteasome degradation, directly inhibits the activity of BRAF kinase, and reduces the activation of MAPK signaling pathway. Tat-braftide can be used for the role of RAF kinase in MAPK signaling pathway and for the study of BRAF mutant cancers .
loading...
    loading...
Cat. No.: HY-127041
CAS No.: 88909-96-0
Purity:  98.00%
Target:  

Bacterial

Research Areas:  

Infection

Virstatin inhibits the pili system synthesis and prevents A. baumannii biofilm formation. Virstatin also inhibits dimerization of the transcriptional activator ToxT .
loading...
    loading...
Cat. No.: HY-160783
CAS No.: 2727872-88-8
Target:  

HuR

Research Areas:  

Cancer

SRI-43265 (compound 40) is an inhibitor of human antigen R protein (HuR) dimerization, and HuR multimers have been implicated in cancer and inflammatory pathogenesis .
loading...
    loading...
Cat. No.: HY-122702
CAS No.: 77855-76-6
Purity:  ≥95.0%
Target:  

PROTAC Linkers

Research Areas:  

Others

PEG6-(CH2CO2H)2 is a symmetric PEG PROTAC linker, for the synthesis of Homo-PROTACs which is bivalent small-molecule dimerizers of the VHL E3 ubiquitin ligase to induce self-degradation .
loading...
    loading...
Cat. No.: HY-W004078
CAS No.: 696-60-6
4-Hydroxybenzylamine is a dimerizer and precursor. 4-Hydroxybenzylamine forms cyclic dimers stabilized by O-H/N hydrogen bonds and π-stacking interactions in solution. 4-Hydroxybenzylamine undergoes condensation with formaldehyde to form a 12-atom azacyclophane, facilitated by pre-organization into cyclic dimeric templates .
loading...
    loading...
Cat. No.: HY-176749
CAS No.: 3007689-83-7
Research Areas:  

Neurological Disease

HUP-46 is a BBB-penatrable modulator of αSyn dimerization and autophagy. HUP-46 reduces the ratio of pPP2A/PP2A, increases the autophagy marker LC3BII levels, and decreases αSyn dimerization. HUP-46 can be used for research of neurodegenerative diseases .
loading...
    loading...
Cat. No.: HY-153890
CAS No.: 2137894-98-3
Purity:  96.04%
Research Areas:  

Others

NVOC cage-TMP-Halo is a cell-permeable and photoactivatable protein dimerization inducer. NVOC cage-TMP-Halo can rapidly and reversibly control protein localization in living cells. NVOC cage-TMP-Halo can be used for dynamic cellular processes research .
loading...
    loading...
Cat. No.: HY-12124
CAS No.: 402934-09-2
Purity:  99.51%
Target:  

NO Synthase

Research Areas:  

Cardiovascular Disease

BBS-4 is a potent and selective inducible nitric oxide synthase (NOS2) dimerization inhibitor, with an IC50 of 0.49 nM. BBS-4 can protect mice from the cardiovascular dysfunction of sepsis .
loading...
    loading...
Cat. No.: HY-123335
CAS No.: 217480-25-6
Target:  

Somatostatin Receptor

Research Areas:  

Others

L-796778 is an agonist of the hsst3 receptor. In CHO-K1 cells expressing the hsst3 receptor, L-796778 is a partial agonist that inhibits forskolin (HY-15371)-stimulated cAMP production with an IC50 value of 18 nM .
loading...
    loading...
Cat. No.: HY-100610
CAS No.: 1456602-51-9
Target:  

STAT

Research Areas:  

Cancer

S3I-1757 is a STAT3 inhibitor. S3I-1757 inhibits the phosphorylation and dimerization of STAT3. S3I-1757 can be used for the research of STAT3 hyperactive cancers such as melanoma .
loading...
    loading...
Cat. No.: HY-P991237
CAS No.: 2673271-78-6
Synonyms: HMBD-001

Target:  

EGFR

Research Areas:  

Cancer

Nezutatug (HMBD-001) is a humanized IgG1 monoclonal antibody inhibitor targeting HER3. Nezutatug inhibits the dimerization of HER3 and inhibits the growth, proliferation and other activities of tumor cells. Nezutatug is promising for research of cancers, such as pancreatic cancer and non-small cell lung cancer .
loading...
    loading...
Cat. No.: HY-134269A
Synonyms: 7-deaza-8-bromo-cADPR disodium; 7-deaza-8-bromo-cyclic ADP ribose disodium
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

8-Br-7-CH-cADPR disodium (7-Deaza-8-bromo-cADPR) is a potent cADPR antagonist. 8-Br-7-CH-cADPR disodium shows partial inhibition of calcium elevation caused by sTIR dimerization. 8-Br-7-CH-cADPR disodium significantly decreases Paclitaxel (HY-B0015)-induced axon degeneration .
loading...
    loading...
Cat. No.: HY-150252
CAS No.: 1402453-15-9
Target:  

Others

Research Areas:  

Cancer

ATIC-IN-1(compound 14) is an inhibitor targeting to Aminoimidazole carboxamide ribonucleotide transformylase/inosine monophosphate cyclohydrolase (ATIC) dimerization with a Ki value of 685 nM. ATIC dimerization is crucial for its aminoimidazole carboxamide ribonucleotide (AICAR) transformylase activity. ATIC-IN-1 exhibits anti-tumor activity via reduction in cell numbers and cell division rates .
loading...
    loading...
Cat. No.: HY-W008356
CAS No.: 137553-42-5
Target:  

Drug Intermediate

Research Areas:  

Infection Metabolic Disease

2-Fluoro-4-iodobenzonitrile is a building block, which can be used to synthesize L. infantum trypanothione reductase (Li-TryR) dimerization and oxidoreductase activity inhibitors. 2-Fluoro-4-iodo benzonitrile can also be used to synthesize transient receptor potential ankyrin 1 (TRPA1) antagonists .
loading...
    loading...
Cat. No.: HY-P3223A
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

Biphalin acetate, a BBB-penetrable opioid peptide analog, contains two active enkephalin pharmacophores.Biphalin acetate has high affinity for opioid receptors. Biphalin acetate shows analgesic effect in acute, neuropathic, and chronic animal pain models. Biphalin acetate is also an antiviral, antiproliferative, anti-inflammatory, and neuroprotective agent .
loading...
    loading...