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Filtered Search Results
Sigma Aldrich Fine Chemicals Biosciences 1-Methyl-1-cyclohexene 97% | 591-49-1 | MFCD00001548 | 5G
1-Methyl-1-cyclohexene 97% | Purity: 97% | Mol Wt: 96.17 | 591-49-1 | MFCD00001548 | 5G
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Medchemexpress LLC β-Carotene | 7235-40-7 | 536.87 | 100 MG
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β-Carotene (Provitamin A) is a carotenoid compound and a naturally-occurring precursor to vitamin A. It acts as a modulator of reactive oxygen species (ROS), possessing both antioxidant and anti-inflammatory activities. Its role can vary, acting as either an antioxidant or a prooxidant, depending on its inherent properties and the redox potential of its biological environment.
- Naturally-occurring precursor to vitamin A
- Modulator of reactive oxygen species (ROS)
- Possesses antioxidant and anti-inflammatory activities
- Can act as an antioxidant or prooxidant depending on environment
- Induces apoptosis in breast cancer cells
- Demonstrates anticancer activities
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eMolecules 3-CYCLOPENTENE-1-OL 25G
5000165807 3-CYCLOPENTENE-1-OL 25G
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Medchemexpress LLC Antitumor agent-159 10mg | 1611446-66-2 | 10 MG
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Antitumor agent-159 is a mitochondria-targeting small-molecule research compound that downregulates cardiolipin, inhibits proliferation of MDA-MB-231 cancer cells, arrests the cell cycle at sub-G1, and induces apoptosis. It has demonstrated antitumor efficacy in MDA-MB-231 xenograft models. Molecular formula: C24H36ClF3N2O3; molecular weight: 493.00 g·mol⁻¹.
- Targets mitochondria and reduces cardiolipin levels.
- Inhibits proliferation of MDA-MB-231 cancer cells.
- Arrests the cell cycle at sub-G1 and induces apoptosis.
- Demonstrated in vivo efficacy in MDA-MB-231 xenograft models.
- Intended for use in in vitro and in vivo antitumor research.
- Reported purity: 99.0% (certificate of analysis).
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Medchemexpress LLC DJ-V-159 | 2253744-53-3 | 99.9% | 502.37 | 1 ML
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DJ-V-159 is an agonist for G protein-coupled receptor family C group 6 member A (GPRC6A). It activates ERK and stimulates cAMP production in GPRC6A expressing HEK-293 cells. Additionally, it stimulates insulin secretion in mouse beta-cell MIN-6 cells and reduces blood glucose levels in wild-type mice.
- Activates ERK in HEK-293 cells transfected with GPRC6A.
- Stimulates cAMP production in GPRC6A expressing HEK-293 cells.
- Stimulates insulin secretion in mouse beta-cell MIN-6 cells.
- Reduces blood glucose levels in wild-type mice at a dose of 10 mg/kg.
- Appearance: solid, white to off-white.
- Soluble in DMSO (25 mg/mL).
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Sigma Aldrich Fine Chemicals Biosciences Beta-Carotene | 7235-40-7 | MFCD00001556 | 5 g
Beta-Carotene | Purity: ≥93% | Mol Wt: 536.87 | 7235-40-7 | MFCD00001556 | 5 g
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Sigma Aldrich Fine Chemicals Biosciences beta-Carotene synthetic, >=93% (UV), powder | 7235-40-7 | MFCD00001556 | 10G
beta-Carotene synthetic, >=93% (UV), powder | Purity: >=93% (UV) | Mol Wt: 536.87 | 7235-40-7 | MFCD00001556 | 10G
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eMolecules AstaTech / 2-ETHYL-1-HEXENE / 1g / 718058557 / D90439 / 95.000 / 1632-16-2 / MFCD00027242 / 112.216 / C8H16
AstaTech / 2-ETHYL-1-HEXENE / 1g / 718058557 / D90439 / 95.000 / 1632-16-2 / MFCD00027242 / 112.216 / C8H16
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Abcam 15-cis-phytoene
Intermediate in the biosynthesis of carotenoids
The product is subject to the following: Abcam Restricted Use Statement
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Medchemexpress LLC ETC-159 | 1638250-96-0 | 99.1% | 391.38 | 25 MG
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ETC-159 (ETC-1922159) is a potent, orally available PORCN inhibitor. It inhibits β-catenin reporter activity with an IC50 of 2.9 nM. It blocks the secretion and activity of all Wnts and shows robust activity in multiple cancer models driven by high Wnt signaling. This product is highly efficacious in molecularly defined colorectal cancers (CRCs) with R-spondin translocations.
- Potent, orally available PORCN inhibitor.
- Inhibits β-catenin reporter activity.
- Blocks secretion and activity of Wnts.
- Robust activity in multiple cancer models.
- Highly efficacious in colorectal cancers with R-spondin translocations.
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Cayman Chemical cIs-PetroselInIc AcId 1g
A monounsaturated fatty acid and isomer of oleic acid; major component of plant lipids; rats fed a diet containing it have a reduction in arachidonic acid levels and an increase in linoleic acid levels in the heart, liver, and blood; has been used in a composite membrane to study plant uptake; has been used in the synthesis of new biosurfactants (sophorolipids)
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AccuStandard, Inc CIS 1 3 DICHLOROPROPENE
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NC3362185 CIS 1 3 DICHLOROPROPENE
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Strem, An Ascensus Company CAS# 629-20-9. 1g. Cyclooctatetraene, 98% COT. MFCD00004161
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CAS# 629-20-9. 1g. Cyclooctatetraene, 98% COT. MFCD00004161. Molecular Weight: 104.15. Molecular Formula: C8H8. Color/form: pale yellow liq. Strem# 06-0350. http://www.strem.com/catalog/v/06-0350/
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Chemscene ChemScene | 1,4-Diethynylbenzene | 10G | CS-W016563 | 0.98 | 935-14-8| MFCD00078375 | 126.16
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ChemScene | 1,4-Diethynylbenzene | 10G | CS-W016563 | 0.98 | 935-14-8| MFCD00078375 | 126.16
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Medchemexpress LLC VE-821 | 1232410-49-9 | 99.7% | 368.41 | 10 MM 1 ML
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VE-821 is a potent ATP-competitive inhibitor of ATR with a Ki/IC50 of 13 nM/26 nM. It exhibits excellent selectivity for ATR with minimal cross-reactivity against related PIKKs. This compound significantly enhances the sensitivity of pancreatic cancer cells to radiation and Gemcitabine, making it suitable for studies on DNA damage response and cancer therapy.
- Potent ATP-competitive inhibitor of ATR.
- Exhibits excellent selectivity for ATR.
- Enhances sensitivity of pancreatic cancer cells to radiation and Gemcitabine.
- Inhibits radiation-induced G2/M arrest in cancer cells.
- Soluble in DMSO (50 mg/mL).
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