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Filtered Search Results
Aobchem AOBCHEM
5001031627 ETHYL 3- 3-BROMO-4-METHOXYPHEN
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Aobchem AOBCHEM
5001054023 1- 3- SEC-BUTYL -2-METHOXYPHEN
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Aobchem AOBCHEM
5001056389 2E -4- 3-CHLORO-4-METHOXYPHEN
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MEDCHEMEXPRESS LLC FIMEPINOSTAT 5MG
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501872903 FIMEPINOSTAT 5MG
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MEDCHEMEXPRESS LLC HJB97 5MG
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501872389 HJB97 5MG
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MEDCHEMEXPRESS LLC TELOTRISTAT 5MG
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501872793 TELOTRISTAT 5MG
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MEDCHEMEXPRESS LLC PROTAC BET DEGRADER-2 5MG
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501872511 PROTAC BET DEGRADER-2 5MG
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eMolecules 933052-52-9 | Ambeed | (2-Morpholinophenyl)boronic acid | 1g | 525142093 | A232631 | MFCD03095109 | 207.04 | C10H14BNO3
Ambeed | (2-Morpholinophenyl)boronic acid | 1g | 525142093 | A232631 | 933052-52-9 | MFCD03095109 | 207.040 | C10H14BNO3
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Medchemexpress LLC LP-261 | 915412-67-8 | 99.9% | C22H19N3O4S | 50 MG
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LP-261 is a potent, orally active anti-mitotic agent that inhibits tubulin polymerization in vitro with an EC50 of 3.2 μM. It has shown the ability to inhibit the growth of human non-small-cell lung tumors (NCI-H522) in vivo and is used in cancer research.
- Potent and orally active anti-mitotic agent.
- Inhibits tubulin polymerization in vitro.
- Shows potent G2/M block activity in various cell lines (MCF-7, H522, Jurkat, SW-620, BXPC-3, and PC-3) with IC50 values ranging from 0.01 μM to 0.38 μM.
- Effectively inhibits tumor growth in a human non-small-cell lung tumor xenograft model in NCr-nu mice, with a 96% reduction in mean tumor volume at 50 mg/kg.
- Displays rapid oral adsorption with a Tmax of 2.0 hours in rats.
- Exhibits moderate elimination rate with a terminal half-life of 1.4 hours in rats.
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eMolecules 15018-56-1 | 5-Bromo-6-methyluracil | MFCD00049045 | 1g
Medchem Express | beta-Mangostin | 5mg | 446275559 | HY-N0941 | 20931-37-7 | MFCD00951751 | 424.493 | C25H28O6
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Cambridge Isotope Laboratories URACIL (5-D, 98%), 0.25 G, 24897-50-5
URACIL (5-D, 98%), 0.25 G, 24897-50-5
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Medchemexpress LLC 5,6-Dihydro-5-methyluracil | 696-04-8 | 50 MG
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5,6-Dihydro-5-methyluracil (Dihydrothymine) is an intermediate breakdown product of thymine, found in animals or plants. It can be toxic at abnormally high levels.
- Endogenous metabolite
- Molecular weight: 128.13
- Formula: C5H8N2O2
- Appearance: Solid
- Color: White to off-white
- Initial source: Endogenous metabolite, human gut microbiota metabolites
- Shipping: Room temperature in continental US; may vary elsewhere
- Storage: 4°C, sealed storage, away from moisture
- In solvent storage: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
- Purity: 99.88%
- Chemical structure: O=C1NC(C(C)CN1)=O
- Structure classification: Others
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Medchemexpress LLC Dapaconazole | 1269726-67-1 | 99.8% | 415.24 | 50 MG
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Dapaconazole is an antifungal agent known for its ability to inhibit sterol 14α-demethylase cytochrome P450 activity. This compound has demonstrated efficacy in inhibiting key fungal enzymes and has been investigated in clinical trials for conditions such as Tinea Cruris and Tinea Pedis. It is characterized by high purity and specific chemical properties.
- Inhibits sterol 14α-demethylase cytochrome P450 activity
- Investigated in clinical trials for antifungal applications
- High purity
- Solid appearance
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eMolecules 1394854-52-4 | Medchem Express | GSK-J2 | 10mg | 446266239 | HY-15648A | MFCD27991274 | 389.459 | C22H23N5O2
Ambeed | tert-Butyl 1-bromo-2-oxo-691215-tetraoxa-3-azaoctadecan-18-oate | 250mg | 649270162 | A677171 | 1807521-00-1 | MFCD28505519 | 442.347 | C17H32BrNO7
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Chem-Impex International, Inc. Cytosine | 71-30-7 | MFCD00006034 | 25G
Cytosine, 71-30-7, MFCD00006034, 25G
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