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Filtered Search Results
Medchemexpress LLC HY-122816 5mg Medchemexpress, HLY78 CAS:854847-61-3 Purity:>98%
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Medchemexpress, HY-122816 5mg HLY78 CAS:854847-61-3 HLY78 is an activator of the Wnt/β-catenin signaling pathway, which targets the DIX domain of Axin and potentiates the Axin-LRP6 association to promote Wnt signaling transduction [1] . 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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eMolecules 4884-25-7 | 2-Cyclopentylcyclopentan-1-ol | Oakwood Chemical | MFCD00045407 | 154.253 | C10H18O | 98.000 | OC1CCCC1C1CCCC1 | 100mg | 537710309
2-Cyclopentylcyclopentan-1-ol | Oakwood Chemical | 4884-25-7 | MFCD00045407 | 154.253 | C10H18O | 98.000 | OC1CCCC1C1CCCC1 | 100mg | 537710309
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Matrix Scientific (3,4-DIMETHOXYPHENYL)ACETIC-25
(3,4-dimethoxyphenyl)acetic Acid Mf C10h12o4 Mw 196.20 Cas 93-40-3 Mdl MFCD00004335
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Medchemexpress LLC HY-16582A 10mg Medchemexpress, Sonidegib CAS:956697-53-3 Purity:>98%
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Medchemexpress, HY-16582A 10mg Sonidegib CAS:956697-53-3 Sonidegib (Erismodegib) is a potent and selective Smo antagonist with IC50 of 1.3 nM and 2.5 nM for mouse and human Smo in binding assay, respectively. 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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eMolecules 529489-04-1 | Ambeed | (4S4S5S5S)-22-(1-Methylethylidene)bis(45-dihydro-45-diphenyloxazole) | 100mg | 600828703 | A1219908 | 486.615 | C33H30N2O2
Ambeed | (4S4S5S5S)-22-(1-Methylethylidene)bis(45-dihydro-45-diphenyloxazole) | 100mg | 600828703 | A1219908 | 529489-04-1 | 486.615 | C33H30N2O2
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eMolecules 1965309-26-5 | trans-2-Benzyl-1,2,3,3a,4,9b-hexahydro-pyrrolo[3,4-c]quinoline-5-carboxylic acid tert-butyl ester | J & W PharmLab LLC728.978 | C46H56N4O4 | 97.000 | CC(C)(C)OC(=O)N1C[C@@H]2CN(Cc3ccccc3)C[C@H]2c2ccccc12.CC(C)(C)OC(=O)N1C[C@H]2CN(Cc3ccccc3)C[C@@H]2c2ccccc12 | 25mg | 4...
trans-2-Benzyl-1,2,3,3a,4,9b-hexahydro-pyrrolo[3,4-c]quinoline-5-carboxylic acid tert-butyl ester | J & W PharmLab LLC | 1965309-26-5728.978 | C46H56N4O4 | 97.000 | CC(C)(C)OC(=O)N1C[C@@H]2CN(Cc3ccccc3)C[C@H]2c2ccccc12.CC(C)(C)OC(=O)N1C[C@H]2CN(Cc3ccccc3)C[C@@H]2c2ccccc12 | 25mg | 491380115
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Medchemexpress LLC Phenoxyethanol | 122-99-6 | 10MM/1ML
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Phenoxyethanol is a broad-spectrum antimicrobial agent utilized in various applications, including cosmetics, vaccines, and textiles. It functions by acting as an uncoupling agent in oxidative phosphorylation and competitively inhibiting malate dehydrogenase.
- Exhibits antimicrobial activity against gram-positive bacteria and fungi (C. albicans).
- Enhances microbial uptake of low molecular weight substances.
- Can be used for vaccine preparation.
- Serves as a preservative in diverse products.
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eMolecules 350683-68-0 | (4-Cyclohexyloxy-phenyl)-hydrazine hydrochloride | J & W PharmLab LLC | MFCD28155370 | 242.750 | C12H19ClN2O | 96.000 | Cl.NNc1ccc(OC2CCCCC2)cc1 | 1g | 271112734
(4-Cyclohexyloxy-phenyl)-hydrazine hydrochloride | J & W PharmLab LLC | 350683-68-0 | MFCD28155370 | 242.750 | C12H19ClN2O | 96.000 | Cl.NNc1ccc(OC2CCCCC2)cc1 | 1g | 271112734
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Medchemexpress LLC DM4-SMe | 796073-68-2 | MFCD28400104 | 100.0% | 826.46 | C39H56ClN3O10S2 | 5 MG
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DM4-SMe is a tubulin-inhibiting cytotoxic metabolite used in antibody-drug conjugate (ADC) research and ADC metabolism studies. It is a metabolite of antibody-maytansin conjugates (AMCs), can be linked to antibodies via disulfide or thioether bonds, and is reported to be oxidized and detoxified by human liver microsomes. DM4-SMe inhibits KB cells with an IC50 of 0.026 nM.
- Used as an ADC payload and metabolite for research applications.
- Acts as a microtubule/tubulin inhibitor.
- Reported KB cell IC50 of 0.026 nM.
- Available in small research pack sizes, including 5 mg.
- For research use only; not for human or clinical use.
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Medchemexpress LLC Dm4-sme | 796073-68-2 | 98.0% | 826.46 g/mol | C39H56ClN3O10S2 | 10 MG
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DM4-SMe is a cytotoxic maytansinoid metabolite and microtubule/tubulin inhibitor used as an antibody-drug conjugate (ADC) payload in laboratory research. Supplied as a powder in small mass quantities, it is intended for in vitro and conjugation studies.
- Cytotoxic maytansinoid metabolite and tubulin inhibitor.
- Suitable as an ADC payload or for conjugation studies.
- Supplied as a powder in small mass quantities for research use.
- CAS number 796073-68-2 for unambiguous identification.
- Reported molecular weight 826.46 g/mol and formula C39H56ClN3O10S2.
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Chem-Impex International, Inc. o-Phenyl chlorothiocarbonate | MFCD00004920 | 5G
o-Phenyl chlorothiocarbonate, MFCD00004920, 5G
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Medchemexpress LLC Mast cell degranulating peptide | 32908-73-9 | 98.3% | 2,587.22 g/mol | C110H192N40O24S4 | 5MG
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Peptide 401 is a mast cell-degranulating peptide derived from bee venom, supplied lyophilized for research use. It is suitable for studies of mast cell activation, histamine release, and vascular permeability in cellular and animal models, and is provided in small pack sizes for experimental work.
- Sequence: Ile-Lys-Cys-Asn-Cys-Lys-Arg-His-Val-Ile-Lys-Pro-His-Ile-Cys-Arg-Lys-Ile-Cys-Gly-Lys-Asn-NH2.
- Molecular weight: 2587.22 g/mol.
- Chemical formula: C110H192N40O24S4.
- Purity: 98.3%.
- Solubility: water 2.08 mg/mL; ultrasonic assistance recommended.
- Storage: powder -80°C (2 years) or -20°C (1 year); in solution -80°C (6 months) or -20°C (1 month).
- Available pack sizes: 1 mg, 5 mg, 10 mg.
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eMolecules 134332-50-6 | Medchem Express | Galanthamine N-Oxide | 1mg | 716993934 | HY-N7263 | 303.358 | C17H21NO4
Ambeed | (S)-1-Benzyl 2-methyl 4-oxopyrrolidine-12-dicarboxylate | 250mg | 588341431 | A132265 | 16217-15-5 | MFCD09608116 | 277.276 | C14H15NO5
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Medchemexpress LLC Lin28 inhibitor LI71 enantiomer | 956189-58-5 | 99.7% | 335.40 g·mol⁻1 | C21H21NO3 | 5MG
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LIN28 inhibitor LI71 enantiomer is the less active stereoisomer of a small-molecule LIN28 inhibitor used for research on LIN28-driven cancer biology and RNA-binding protein function. It disrupts LIN28:let-7 binding (reported IC50 ≈ 7 μM) and abolishes LIN28-mediated oligouridylation of the let-7 precursor (reported IC50 ≈ 27 μM); it has also been reported to affect parasite cold shock protein interactions with DNA and tubulin.
- High purity suitable for research applications
- Cell-permeable small molecule for cellular assays
- Disrupts LIN28:let-7 binding (IC50 ≈ 7 μM)
- Abolishes LIN28-mediated oligouridylation of let-7 precursor (IC50 ≈ 27 μM)
- Offered in multiple milligram pack sizes for experimental flexibility
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Medchemexpress LLC SJG-136 | 232931-57-6 | 99.5% | 556.61 | C31H32N4O6 | 50 MG
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SJG-136 is a pyrrolobenzodiazepine-class DNA cross-linking agent supplied as a research reagent. It exhibits potent antitumor activity and an XL50 of 45 nM against pBR322 DNA. The compound is a solid (white to yellow), with formula C31H32N4O6, molecular weight 556.61, and reported purity of 99.47%.
- Pyrrolobenzodiazepine DNA cross-linker with potent antitumor activity.
- XL50 for pBR322 DNA: 45 nM.
- CAS number 232931-57-6.
- Chemical formula C31H32N4O6; molecular weight 556.61.
- Purity reported as 99.47% (certificate of analysis available).
- Appearance: solid, white to yellow.
- Available in multiple package sizes including 50 mg and solution formats.
- Associated documentation available: datasheet, SDS, COA, HNMR, LCMS.
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