19 Results for "

DIM

" in MedChemExpress (MCE) Product Catalog:
Products (19)

19 Results for "DIM" in MCE Product Catalog:

12
12 Publications Verification
Cat. No.: HY-15758
CAS No.: 1968-05-4
Purity:  99.89%
Synonyms: DIM; Arundine; HB 236
3,3'-Diindolylmethane is a strong, pure androgen receptor (AR) antagonist.
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9
9 Cited Publications
Cat. No.: HY-112055
CAS No.: 151358-47-3
Purity:  99.05%
Research Areas:  

Cancer

DIM-C-pPhOH is a nuclear receptor 4A1 (NR4A1) antagonist. DIM-C-pPhOH inhibits cancer cell growth and mTOR signaling, induce apoptosis and cellular stress. DIM-C-pPhOH reduces cell proliferation with IC50 values of 13.6 μM and 13.0 μM for ACHN cells and 786-O cells, respectively .
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2
2 Cited Publications
Cat. No.: HY-19808
CAS No.: 178946-89-9
Synonyms: DIM-C-pPhCl
C-DIM12 is a potent, orally active Nurr1 modulator. C-DIM12 inhibits the tumor growth and autophagy, and induces the cell apoptosis. C-DIM12 has anti-inflammatory and neuroprotective effects, and can be used for cancer and neurological disease study .
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1
1 Cited Publications
Cat. No.: HY-112056
CAS No.: 151358-48-4
Purity:  99.47%
DIM-C-pPhCO2Me is a nuclear receptor 4A1 (NR4A1) antagonist. DIM-C-pPhCO2Me induces Apoptosis. DIM-C-pPhCO2Me decreases PAX3-FOXO1A, N-Myc, Rassf4, MyoD1, Grem1, and DAPK1 proteins. DIM-C-pPhCO2Me decreases expression of TXNDC5 and IDH1, induces markers of ER stress (CHOP, ATF4 and p-PERK). DIM-C-pPhCO2Me inhibits renal cell carcinoma, breast cancer. DIM-C-pPhCO2Me can also be used in rhabdomyosarcoma research .
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1
1 Cited Publications
Cat. No.: HY-111492
CAS No.: 33985-68-1
Purity:  99.41%
Research Areas:  

Cancer

DIM-C-pPhOCH3 is a Nur77 agonist. Nerve growth factor-induced Bα (NGFI-Bα, Nur77) is an orphan nuclear receptor.
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Cat. No.: HY-15758R
CAS No.: 1968-05-4
Synonyms: DIM (Standard); Arundine (Standard); HB 236 (Standard)
3,3'-Diindolylmethane (Standard) is the analytical standard of 3,3'-Diindolylmethane. This product is intended for research and analytical applications. 3,3'-Diindolylmethane is a strong, pure androgen receptor (AR) antagonist.
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Cat. No.: HY-49223
CAS No.: 1620837-47-9
Target:  

ADC Linkers

Research Areas:  

Cancer

diMal-O-CH2COOH is a cleavable ADC linker.
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Cat. No.: HY-149310
CAS No.: 2743448-32-8
Research Areas:  

Metabolic Disease

Dim16 is a dual PCSK9 inhibitor and HMG-CoAR inhibitor, with an IC50 of 0.8 nM against human PCSK9 and an IC50 of 146.8 μM against HMG-CoAR. Dim16 disrupts the PCSK9-LDLR protein-protein interaction, inhibits the catalytic activity of HMG-CoAR, enhances cellular uptake of extracellular LDL, and suppresses PCSK9-induced platelet aggregation. Dim16 can be used in research related to hypercholesterolemia .
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Cat. No.: HY-151786
CAS No.: 2408993-33-7
Target:  

ADC Linkers

Research Areas:  

Others

Fmoc-L-Lys(Pentynoyl-DIM)-OH is a click chemistry reagent containing an azide. Fmoc-L-Lys(Pentynoyl-DIM)-OH can be used as a SPPS building block for the “helping hand” strategy for purification of highly insoluble peptides. Solubilizing residues are attached to the Lys side-chains using Click-chemistry. The solubilizing tag can be removed with 1M hydrazine or hydroxylamine solution . It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups.
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Cat. No.: HY-175248
Target:  

PSMA

Research Areas:  

Cancer

PSMA-DIM is a dimeric PSMA ligand with a Kd of 37.09 nM for LNCaP cells. PSMA-DIM can be radiolabeled with [ 68Ga]Ga to form [ 68Ga]Ga-PSMA-DIM. [ 68Ga]Ga-PSMA-DIM can effectively distinguish between cells and animal models with different expression levels of PSMA. [ 68Ga]Ga-PSMA-DIM exhibits high LNCaP cells uptake and tumor uptake peak values. PSMA-DIM can be used for the study of prostate cancer (PCa) .
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Cat. No.: HY-159715
CAS No.: 2820155-36-8
Target:  

Liposome

Research Areas:  

Others

Lipid DIM1 is an ionizable lipid that can be used for the generation of lipid nanoparticles (LNPs). Lipid DIM1 is a carrier for both siRNA and mRNA .
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Cat. No.: HY-169581
CAS No.: 94944-80-6
Research Areas:  

Cancer

DIM-C-pPhtBu is an orally active endoplasmic reticulum stress activator. DIM-C-pPhtBu induces mitochondrial and lysosome dysfunction, excessive mitosis, ROS production, and unfolded protein response-mediated cell death in neck cancer cells. DIM-C-pPhtBu has antitumor activity .
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Cat. No.: HY-151787
CAS No.: 2408993-39-3
Target:  

ADC Linkers

Research Areas:  

Others

Fmoc-L-Lys(N3-Aca-DIM)-OH is a click chemistry reagent containing an azide group. Used as a SPPS building-block for the “helping hand” strategy for purification of highly insoluble peptides. Solubilizing residues are attached to the Lys side-chains using Click-chemistry. The solubilizing tag can be removed with 1M hydrazine or hydroxylamine solution . It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups.
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Cat. No.: HY-N12703
CAS No.: 1519015-73-6
Category:  

Animals Phenols Polyphenols

Target:  

Others

N-Acetyldopamine dimmers A (Compound (+)-2) can be isolated from the cast-off shell of the cicada of Cryptotympana sp. N-Acetyldopamine dimmers A increases collagen and α-SMA expression .
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Cat. No.: HY-179528
CAS No.: 2595179-74-9
DIM-3,5-Cl2 is an inverse NR4A1/NR4A2 agonist with KD values of 7.7 μM and 12.0 μM for NR4A1 and NR4A2, respectively. DIM-3,5-Cl2 acts as an inverse agonist to downregulate pro-oncogenic and proendometriotic gene products, and as an agonist to enhance NR4A1/2/Sp1/Sp4-mediated CD71 transactivation. DIM-3,5-Cl2 induces ferroptosis via ROS formation, lipoperoxidation, MDA production, and reduced GPX4, SLC7A11 expression. DIM-3,5-Cl2 induces apoptosis via PARP and caspase-3 cleavage, reduced BCL-2 expression, and inhibits cancer cell viability. DIM-3,5-Cl2 can be used for the research of triple negative breast cancer, endometriosis, and colorectal cancer .
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Cat. No.: HY-149310A
CAS No.: 2743448-41-9
Research Areas:  

Metabolic Disease

Dim16 hydrochloride is a dual PCSK9 inhibitor and HMG-CoAR inhibitor, with an IC50 of 0.8 nM against human PCSK9 and an IC50 of 146.8 μM against HMG-CoAR. Dim16 hydrochloride disrupts the PCSK9-LDLR protein-protein interaction, inhibits the catalytic activity of HMG-CoAR, enhances cellular uptake of extracellular LDL, and suppresses PCSK9-induced platelet aggregation. Dim16 hydrochloride can be used in research related to hypercholesterolemia .
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Cat. No.: HY-P77270
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Thioredoxin-like protein 4B; DIM1-like protein; DIM2; DLP
Species:  
Source:  
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Cat. No.: HY-P77269
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Thioredoxin-like protein 4A; DIM1 protein homolog; DIM1; TXNL4
Species:  
Source:  
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Cat. No.: HY-E71369
Research Areas:  

Others

18S rRNA (adenine1779-N6/adenine1780-N6)-Dimethyltransferase (EC 2.1.1.183): dIM1 is involved in pre-rRNA processing.
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