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Filtered Search Results
Medchemexpress LLC HY-101763A 500mg Medchemexpress, (S,R,S)-AHPC (hydrochloride) CAS:1448189-80-7 Purity:>98%
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Medchemexpress, HY-101763A 500mg (S,R,S)-AHPC (hydrochloride) CAS:1448189-80-7 (S,R,S)-AHPC hydrochloride is the VH032-based VHL ligand used in the recruitment of the von Hippel-Lindau (VHL) protein. (S,R,S)-AHPC hydrochloride can be connected to the ligand for protein (e.g., BCR-ABL1) by a linker to form PROTACs (e.g., GMB-475). GMB-475 induces the degradation of BCR-ABL1 with an IC50 of 1.11 μM in Ba/F3 cells. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Selleck Chemical LLC Paritaprevir (ABT-450) S5404-5mg
Paritaprevir (ABT-450) is a nonstructural (NS) protein 3/4A protease inhibitor
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Strem, An Ascensus Company CAS 1357562-63-0. 50mg. 1-(2S)-1-[(11bS)-26-Dimethyldinaphtho[21-d12-f][132]dioxaphosphepin-4-yloxy]propan-2-yl-3-phenylurea min. 97%. MFCD18827630
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CAS 1357562-63-0. 50mg. 1-(2S)-1-[(11bS)-26-Dimethyldinaphtho[21-d12-f][132]dioxaphosphepin-4-yloxy]propan-2-yl-3-phenylurea min. 97%. MFCD18827630. Molecular Weight 536.56. Molecular Formula C32H29N2O4P. Color/form white pwdr. Strem 15-2204. http//www.strem.com/catalog/v/15-2204/
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Medchemexpress LLC (S,R,S)-AHPC-O-Ph-PEG1-NH2 | 2361117-24-8 | 97.0% | 50 MG
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(S,R,S)-AHPC-O-Ph-PEG1-NH2 is an E3 ligase ligand-linker conjugate that incorporates a VHL ligand for the E3 ubiquitin ligase and a PROTAC linker. It is utilized in PROTAC EED degrader-1 (HY-130614), which is a PROTAC targeting EED with a pKD of 9.02.
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Medchemexpress LLC PROTAC IRAK4 degrader-1 | 2360533-90-8 | 99.8% | 50 MG
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PROTAC IRAK4 degrader-1 (compound I-210) is a Cereblon-based IRAK4 PROTAC. It is composed of an IRAK4 ligand, an E3 ligase ligand, and a PROTAC linker. This product is for research use only.
- Cereblon-based IRAK4 PROTAC
- Composed of an IRAK4 ligand, an E3 ligase ligand, and a PROTAC linker
- Induces IRAK4 protein degradation in OCI-LY-10 cells
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Medchemexpress LLC (S,R,S)-AHPC-phenol-C4-NH2 dihydrochloride | 2376990-26-8 | 99.0% | 632.64 g/mol | C28H43Cl2N5O5S | 5 MG
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(S,R,S)-AHPC-phenol-C4-NH2 dihydrochloride is a von Hippel-Lindau (VHL) ligand building block used in PROTAC and E3 ligase chemistry. Supplied as a high-purity, research-scale solid, it is suitable for synthetic chemistry and ligand design workflows.
- VHL ligand used to recruit the von Hippel-Lindau protein.
- High reported purity (99.01%).
- White to off-white solid physical form.
- Available in small research-scale quantities, including 5 MG.
- Datasheet, certificate of analysis, and safety data sheet available for characterization and handling.
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Medchemexpress LLC HY-17584 10mg , Linaclotide CAS:851199-59-2 Purity:98%
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Medchemexpress, HY-17584 10mg Linaclotide CAS:851199-59-2 Formula:C59H79N15O21S6 Purity:98% Linaclotide is a potent and selective guanylate cyclase C agonist; developed for the treatment of constipation-predominant irritable bowel syndrome (IBS-C) and chronic constipation. Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC Milademetan tosylate hydrate | 2095625-97-9 | 98.9% | 808.74 g/mol | C37H44Cl2FN5O8S | 25 MG
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Milademetan tosylate hydrate is the tosylate hydrate salt of milademetan, an orally active MDM2 inhibitor used in preclinical research. It disrupts the p53-MDM2 interaction, inducing G1 cell cycle arrest and apoptosis, and is investigated for acute myeloid leukemia and various solid tumor models. For research use only.
- Specific MDM2 inhibitor with p53 pathway activity.
- Induces G1 cell cycle arrest and apoptosis in preclinical models.
- High purity reported (98.89%) on the COA.
- Available in small research quantities, including 25 mg packaging.
- Supplied with a datasheet and certificate of analysis for traceability.
- Chemical identifiers: CAS 2095625-97-9; formula C37H44Cl2FN5O8S.
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Medchemexpress LLC CCT251455 | 1400284-80-1 | 99.1% | 503.98 | C26H26ClN7O2 | 10MG
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CCT251455 is a potent, selective inhibitor of mitotic kinase monopolar spindle 1 (MPS1) with an IC50 of 3 nM. It exhibits cellular potency (P-MPS1 IC50 ≈ 0.04 μM; GI50 ≈ 0.16 μM) and shows oral pharmacokinetic activity in mouse and rat, making it suitable for preclinical research into mitotic checkpoint signaling and anticancer mechanisms.
- Potent MPS1 inhibition, IC50 3 nM.
- Demonstrates cellular activity: P-MPS1 IC50 ≈ 0.04 μM and GI50 ≈ 0.16 μM.
- Shows oral pharmacokinetic activity in rodent models.
- High purity for biochemical and cellular assays.
- Available in multiple milligram quantities and as a DMSO solution.
- Storage recommendations provided for powder and solution to preserve stability.
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Sigma Aldrich Fine Chemicals Biosciences Tankyrase 2 849 1166 act
TNKS2 (TRF1-interacting ankyrin-related ADP-ribose polymerase 2) also known as PARP5B tanykyrase-2 or TNKL (GenBank Accession No. NM 025235) amino acids 849-1166 (end) with N-terminal GST-tag MW62kDa expressed in Sf9 cells via a Baculovirus expression system.
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Medchemexpress LLC Bisindolylmaleimide I hydrochloride | 176504-36-2 | MFCD00236429 | 98.4% | 448.94 | C25H25ClN4O2 | 5 MG
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Bisindolylmaleimide I hydrochloride is a cell-permeable, reversible protein kinase C (PKC) inhibitor that also shows activity against GSK-3. It is supplied as a powder for research and analytical use, with reported potency in the low nanomolar range against PKC isoforms and a high reported purity.
- Cell-permeable, reversible PKC inhibitor
- Potent activity: IC50 ≈ 16-20 nM for PKC isoforms
- Also reported to inhibit GSK-3
- High purity (reported 98.4%)
- Supplied as a powder in small analytical pack sizes (for example, 1 mg, 5 mg, 10 mg)
- Recommended storage: powder at 4°C or -20°C; solutions at -20°C or -80°C
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Medchemexpress LLC Bisindolylmaleimide XI hydrochloride | 145333-02-4 | MFCD01319127 | 98.0% | 489.01 g/mol | C28H29ClN4O2 | 1 MG
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Bisindolylmaleimide XI hydrochloride is a bisindolylmaleimide-class small molecule and a potent inhibitor of protein kinase C (PKC) isoforms. It is supplied as the hydrochloride salt for research use and is used in studies of PKC-dependent signaling and cellular pathways.
- Potent PKC inhibitor for biochemical and cellular studies.
- Hydrochloride salt form improves solubility for assay preparation.
- Available in small research pack sizes (1 mg, 5 mg, 10 mg).
- Molecular weight 489.01 g/mol; formula C28H29ClN4O2.
- High purity (98.0%) suitable for research applications.
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Medchemexpress LLC Crocin II | 55750-84-0 | MFCD11111454 | 98.0% | 10 MG
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Crocin II is a natural glycoside isolated from Gardenia jasminoides, supplied as a solid research reagent and analytical standard with reported antioxidant, anticancer, and antidepressant activities. The product is characterized by a molecular weight of 814.82 g/mol, CAS number 55750-84-0, and a recorded purity around 98%. Recommended storage is -20°C and protect from light; solubility in DMSO is approximately 25 mg/mL.
- Natural glycoside isolated from Gardenia jasminoides
- High purity suitable for analytical applications
- Molecular weight 814.82 g/mol and CAS 55750-84-0
- Soluble in DMSO (≈25 mg/mL) for in vitro use
- Storage recommended at -20°C and protect from light
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Medchemexpress LLC Amino-PEG4-Val-Cit-PAB-MMAE | 1492056-71-9 | 99.9% | 1370.71 g/mol | C69H115N11O17 | 25 MG
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Amino-PEG4-Val-Cit-PAB-MMAE is a cleavable 4-unit polyethylene glycol (PEG) linker containing a valine-citrulline (Val-Cit) dipeptide and a para-aminobenzyl (PAB) self-immolative spacer designed for use in antibody-drug conjugate (ADC) synthesis. It provides a hydrophilic spacer, a protease-cleavable linker for controlled payload release, and an amine handle for conjugation to payloads such as MMAE. Supplied as a purified solid for research use and soluble in DMSO.
- Cleavable Val-Cit dipeptide enables protease-mediated payload release.
- PAB self-immolative spacer enables rapid payload release after cleavage.
- Four-unit PEG spacer increases hydrophilicity and solubility.
- Primary amine handle supports site-specific conjugation chemistries.
- High purity and characterized molecular weight for reproducible conjugation.
- Soluble in DMSO at 100 mg/mL for convenient stock preparation.
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Medchemexpress LLC N- t-Boc-Aminooxy-PE | 25MG
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N- t-Boc-Aminooxy-PE | 25MG
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