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Filtered Search Results
Medchemexpress LLC HY-114176 100mg Medchemexpress, (S,R,S)-AHPC-C3-NH2 CAS:2245697-83-8 Purity:>98%
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Medchemexpress, HY-114176 100mg (S,R,S)-AHPC-C3-NH2 CAS:2245697-83-8 (S,R,S)-AHPC-C3-NH2 is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and a linker used in PROTAC technology. 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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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000380276 MITO-APOCYNIN C11 25MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000380214 N-BOC-SITAGLIPTIN 100MG
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Medchemexpress LLC Benzyloxycarbonyl-alanyl-glutamyl-valyl-aspartic acid fluoromethyl ketone | 1135688-47-9 | MFCD03453601 | >=95.0% | 610.63 | C28H39FN4O10 | 5MG
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Z-AEVD-FMK is a cell-permeable, fluoromethyl ketone-derivatized peptide that irreversibly inhibits caspase-10 and related caspases. It prevents Bid activation and downstream caspase cascade events and is supplied as a crystalline solid for laboratory research use only.
- Irreversible caspase-10 inhibitor with FMK warhead.
- Cell-permeable peptide suitable for intracellular studies.
- CAS number 1135688-47-9; molecular formula C28H39FN4O10.
- Molecular weight approximately 610.6 Da.
- Purity ≥95% (reported by distributor).
- Soluble in DMSO at ~10 mg/mL; supplied as a crystalline solid.
- For research use only; not for human or veterinary applications.
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Medchemexpress LLC RAC -NSC305787 HYD | 100MG
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RAC -NSC305787 HYD | 100MG
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![Enzo Life Sciences ET A receptor antagonist [BQ-123]. sodium salt (1mg). CAS: 136553-81-6](https://assets.fishersci.com/TFS-Assets/CCG/product-images/ENZOLOGO.png-250.jpg)
Enzo Life Sciences ET A receptor antagonist [BQ-123]. sodium salt (1mg). CAS: 136553-81-6
Highly potent and selective ETA antagonist. Formula: C31H42N6O7 . Na. MW: 633.7. Purity: ≥96%. Solubility: Soluble in water. Long Term Storage: -20°C. Use/Stability: Stable for at least 3 years after receipt when stored at -20°C. Stock solutions are stable for up to 3 months when stored at -20°C.
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Enzo Life Sciences L-161-982 (5 mg). CAS: 147776-06-5
A potent and selective prostaglandin EP4 receptor antagonist. Purity: ≥98% (HPLC). Solubility: Soluble in DMSO (25 mg/ml). Long Term Storage: -20°C.
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Apexbio Technology LLC N-Ethylmaleimide (NEM) 128-53-0 1g
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N-Ethylmaleimide (CAS 128-53-0) is a small molecule commonly utilized in biochemical research as a selective alkylating agent for sulfhydryl groups on cysteine residues in proteins By irreversibly modifying thiol groups N-Ethylmaleimide disrupts the function of enzymes and other proteins that depend on free cysteines for activity or structural integrity This property enables researchers to investigate thiol-dependent biochemical pathways study protein conformational changes and elucidate redox regulation mechanisms Its application extends to proteomics enzymology and the analysis of intracellular signaling processes involving cysteine-mediated modifications
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000428131 TERT-BUTOXYCARBONYL 500G
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eMolecules 3-(Pyrrolidin-1-ylmethyl)benzoic acid, HCl | 887922-93-2 | 250MG | Purity: 95%
Combi-Blocks | 3-(Pyrrolidin-1-ylmethyl)benzoic acid, HCl | 250MG | 887922-93-2 | MFCD08690301
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Medchemexpress LLC (Rac)-5-Hydroxymethyl Tolterodine | 200801-70-3 | 99.05% | C22H31NO2 | 1 G
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(Rac)-5-Hydroxymethyl Tolterodine, an active metabolite of Tolterodine, acts as a muscarinic acetylcholine receptor (mAChR) antagonist. It exhibits Ki values ranging from 2.3 nM to 2.9 nM for M1-M5 receptors and is used in overactive bladder research.
- Competitively inhibits carbachol-induced contraction in guinea-pig isolated urinary bladder strips (KB of 0.84 nM; pA2 of 9.14).
- Shows significant binding to muscarinic receptors in most tissues (in vivo), with prolonged bladder duration.
- Targets mAChR1, mAChR3, mAChR4, mAChR5.
- Soluble in DMSO (100 mg/mL) and various aqueous/oil-based solutions (≥ 2.5 mg/mL).
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Medchemexpress LLC (Rac)-5-Hydroxymethyl Tolterodine | 200801-70-3 | 99.1% | C22H31NO2 | 500 MG
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(Rac)-5-Hydroxymethyl Tolterodine, also known as (Rac)-Desfesoterodine, is an active metabolite of Tolterodine. It acts as a mAChR antagonist, targeting M1-M5 receptors with specific Ki values ranging from 2.3 nM to 2.9 nM. This compound is primarily utilized in research related to overactive bladder. It presents as a solid, white to off-white substance.
- Functions as a mAChR antagonist
- Targets M1, M2, M3, M4, and M5 receptors
- Used for overactive bladder research
- Solid, white to off-white appearance
- Molecular weight of 341.50
- Inhibits carbachol-induced contraction in guinea-pig urinary bladder strips
- Exhibits significant muscarinic receptor binding activity
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Cayman Chemical 9 Z 12 Z 15 Z 18 Z 21 ZTetrac
A very long-chain polyunsaturated fatty acid; has been used to study the desaturation and elongation of ω-3 polyunsaturated fatty acids; found at low levels in mouse brain and spleen and levels decrease in the brain and spleen of old and exceptionally old mice
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Medchemexpress LLC Protac ERRα degrader-3 | 2306388-65-6 | 98.8% | 956.99 g·mol⁻¹ | C47H50F6N6O7S | 5 MG
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PROTAC ERRα Degrader-3 is a small-molecule proteolysis-targeting chimera (PROTAC) that selectively induces ubiquitin-dependent degradation of estrogen-related receptor alpha (ERRα) in biochemical and cell-based assays. It is intended for research use to probe ERRα function and to study PROTAC-mediated target degradation; users should consult the batch COA and SDS for analytical and safety data.
- Selectively degrades ERRα in cellular assays.
- Enables studies of targeted protein degradation mechanisms.
- Suitable for biochemical and cell-based research applications.
- Provided with batch-specific purity and analytical data.
- Stable when stored at -20 °C according to supplier guidance.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000656119 C11 BODIPY 505/515 M 5MG
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