598 Results for "

MCF

" in MedChemExpress (MCE) Product Catalog:
Products (598)

598 Results for "MCF" in MCE Product Catalog:

Art. -Nr.: HY-P5629
CAS. Nr.: 579474-25-2
Target:  

Bacterial

Forschungsgebiete:  

Infection

MCF is an antimicrobial peptide derived from bee venom. MCF has activity against E.coli W 160-37, S.aureus 8530 and B.subtilis, the MIC values are 35-45 μg/ml, 25-35 μg/ml and 15-25 μg/ml .
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192
192 Publications Verification
Art. -Nr.: HY-N0565
CAS. Nr.: 564-25-0
Doxycycline, an antibiotic, is an orally active and broad-spectrum metalloproteinase (MMP) inhibitor . Doxycycline shows antibacterial activity and anti-cancer cell proliferation activity .
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192
192 Publications Verification
Art. -Nr.: HY-N0565A
CAS. Nr.: 10592-13-9
Doxycycline hydrochloride, an antibiotic, is an orally active and broad-spectrum metalloproteinase (MMP) inhibitor . Doxycycline hydrochloride shows antibacterial activity and anti-cancer cell proliferation activity. Doxycycline hydrochloride can be used to construct gene expression regulation models .
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192
192 Publications Verification
Art. -Nr.: HY-N0565B
CAS. Nr.: 24390-14-5
Synonyms: Doxycycline hydrochloride hemiethanolate hemihydrate; WC2031
Doxycycline hyclate, an antibiotic, is an orally active and broad-spectrum metalloproteinase (MMP) inhibitor. Doxycycline hyclate shows antibacterial activity and anti-cancer cell proliferation activity. Doxycycline hyclate can be used to construct gene expression regulation models .
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143
143 Cited Publications
Art. -Nr.: HY-13636
CAS. Nr.: 129453-61-8
Reinheit:  99.92%
Synonyms: ICI 182780; ZD 9238; ZM 182780
Fulvestrant (ICI 182780) is a pure antiestrogen and a potent estrogen receptor (ER) antagonist with an IC50 of 9.4 nM. Fulvestrant is also a GPR30 agonist. Fulvestrant effectively inhibits the growth of ER-positive MCF-7 cells with an IC50 of 0.29 nM. Fulvestrant also induces autophagy and has antitumor efficacy .
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13
13 Cited Publications
Art. -Nr.: HY-134964
CAS. Nr.: 451491-47-7
Reinheit:  99.93%
Forschungsgebiete:  

Neurological Disease Cancer

CTB is a potent p300 histone acetyltransferase activator . CTB can effectively induce apoptosis in MCF-7 cells .
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13
13 Cited Publications
Art. -Nr.: HY-13734
CAS. Nr.: 141400-58-0
Reinheit:  99.87%
Synonyms: IV-2
Target:  

Apoptosis

Forschungsgebiete:  

Cancer

PX-12(IV-2) is an irreversible inhibitor of Thioredoxin-1 (Trx-1); inhibits the growth of MCF-7 and HT-29 cells with IC50 values of 1.9 and 2.9 μM, respectively.
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6
6 Cited Publications
Art. -Nr.: HY-13668
CAS. Nr.: 192441-08-0
Reinheit:  98.83%
Synonyms: PaTrin-2
Target:  

DNA Methyltransferase

Forschungsgebiete:  

Cancer

Lomeguatrib is a O 6-methylguanine-DNA methyltransferase (MGMT) inhibitor, with IC50s of 9 nM in cell-free assay and ~6?nM in MCF-7 cells.
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6
6 Cited Publications
Art. -Nr.: HY-112721
CAS. Nr.: 313380-27-7
Reinheit:  99.65%
Target:  

FOXM1 DNA/RNA Synthesis

Forschungsgebiete:  

Cancer

FDI-6 is an inhibitor of FOXM1. FDI-6 binds directly to FOXM1 protein, to displace FOXM1 from genomic targets in MCF-7 breast cancer cells, and induce concomitant transcriptional down-regulation.
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4
4 Cited Publications
Art. -Nr.: HY-B1029
CAS. Nr.: 17230-88-5
Target:  

PKC Apoptosis Tyrosinase

Forschungsgebiete:  

Endocrinology Cancer

Danazol inhibits the proliferation of cancer cell MDA-MB-231 and MCF-7 with IC50 of 65 µg/mL and 31 µg/mL. Danazol arrests the cell cycle at G1 phase, induces apoptosis in MDA-MB-231 through PKCα signaling pathway .
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3
3 Cited Publications
Art. -Nr.: HY-Y0598
CAS. Nr.: 614-47-1
Synonyms: Benzylideneacetophenone
trans-Chalcone, isolated from Aronia melanocarpa skin, is a biphenolic core structure of flavonoids precursor. trans-Chalcone is a potent fatty acid synthase (FAS) and α-amylase inhibitor. trans-Chalcone causes cellcycle arrest and induces apoptosis in the breastcancer cell line MCF-7. trans-Chalcone has antifungal and anticancer activity .
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3
3 Cited Publications
Art. -Nr.: HY-119358
CAS. Nr.: 6402-36-4
Reinheit:  99.85%
Traumatic Acid is a wound healing agent and a cytokinin (phytohormone). Traumatic Acid enhances the biosynthesis of collagen in cultured human skin fibroblasts. Traumatic Acid inhibits MCF-7 breast cancer cells viability and enhances apoptosis and oxidative stress. Traumatic Acid can be used in studies of cancer, circulatory disorders (including arterial hypertension), and skin diseases associated with oxidative stress and impaired collagen biosynthesis .
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3
3 Cited Publications
Art. -Nr.: HY-147081
CAS. Nr.: 301636-59-9
Reinheit:  99.52%
Synonyms: AGRO-100
Forschungsgebiete:  

Cancer

AS 1411 (AGRO-100) is an oligonucleotide aptamer targeting nucleoproteins. AS 1411 inhibits tumor cell proliferation by affecting the activity of nucleoprotein-containing complexes and can be used as a carrier to precisely deliver nanoparticles, oligonucleotides and small molecules to cancer cells. AS 1411 reduces PRMT5 expression to inhibit tumor growth in DU145 prostate cancer cells. AS 1411 works by blocking the binding of nucleoproteins to bcl-2 mRNA in MCF-7 breast cancer cells. AS 1411-coupled Jin nanospheres can inhibit breast cancer cell proliferation in vitro and in mouse models, has the ability to cross the blood-brain barrier with low tissue toxicity .
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3
3 Cited Publications
Art. -Nr.: HY-147081A
Synonyms: AGRO-100 sodium
Forschungsgebiete:  

Cancer

AS 1411 (AGRO-100) sodium is an oligonucleotide aptamer targeting nucleoproteins. AS 1411 sodium inhibits tumor cell proliferation by affecting the activity of nucleoprotein-containing complexes and can be used as a carrier to precisely deliver nanoparticles, oligonucleotides and small molecules to cancer cells. AS 1411 sodium reduces PRMT5 expression to inhibit tumor growth in DU145 prostate cancer cells. S 1411 sodium works by blocking the binding of nucleoproteins to bcl-2 mRNA in MCF-7 breast cancer cells. S 1411 sodium-coupled Jin nanospheres can inhibit breast cancer cell proliferation in vitro and in mouse models, has the ability to cross the blood-brain barrier with low tissue toxicity
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2
2 Cited Publications
Art. -Nr.: HY-13686
CAS. Nr.: 196868-63-0
Reinheit:  99.85%
Target:  

IGF-1R Apoptosis

Forschungsgebiete:  

Cancer

PQ401 is a potent inhibitor of IGF-IR signaling. PQ401 inhibits IGF-I-stimulated IGF-IR autophosphorylation with an IC50 of 12.0 μM in a series of studies in MCF-7 cells. PQ401 is effective at inhibiting IGF-I-stimulated growth of MCF-7 cells (IC50, 6 μM). PQ401 is a potential agent for breast and other IGF-I-sensitive cancers. PQ401 induces caspase-mediated apoptosis .
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2
2 Cited Publications
Art. -Nr.: HY-B0812
CAS. Nr.: 5965-83-3
Synonyms: SSA dihydrate
5-Sulfosalicylic acid dihydrate is a sulfonated salicylic acid derivative. 5-Sulfosalicylic acid dihydrate is effective against the breast cancer cell line, MCF-7, with less toxicity . 5-Sulfosalicylic acid dihydrate has antioxidant activities .
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2
2 Cited Publications
Art. -Nr.: HY-110193
CAS. Nr.: 1357349-91-7
Reinheit:  99.71%
Target:  

RET

Forschungsgebiete:  

Cancer

SPP-86 is a potent and selective cell permeable inhibitor of RET tyrosine kinase, with an IC50 of 8 nM. SPP-86 inhibits RET-induced phosphatidylinositide 3-kinases (PI3K)/Akt and MAPK signaling, also inhibits RET-induced estrogen receptorα (ERα) phosphorylation in MCF7 cells . SPP-86 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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1
1 Cited Publications
Art. -Nr.: HY-111846
CAS. Nr.: 1351169-29-3
Reinheit:  98.92%
Forschungsgebiete:  

Cancer

PROTAC ERα Degrader-2 is a ERα PROTAC degrader. PROTAC ERα Degrader-2 significantly down-regulates the level of ERα in MCF-7 cells .
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1
1 Cited Publications
Art. -Nr.: HY-121149
CAS. Nr.: 82413-20-5
Reinheit:  99.89%
Synonyms: 3-Hydroxytamoxifen
Forschungsgebiete:  

Cancer

Droloxifene, a Tamoxifen derivative, is an orally active and selective estrogen receptor modulator. Droloxifene shows antiestrogenic and anti-implantation effects. Droloxifene induces p53 expression and apoptosis in MCF-7 cells. Droloxifene prevents bone loss in ovariectomized rats .
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1
1 Cited Publications
Art. -Nr.: HY-N3316
CAS. Nr.: 67884-12-2
Martynoside protects ex vivo bone marrow cells from 5-fluorouracil (5-FU)-induced cell death and inflammation response by down-regulating the TNF signaling pathway .Martynoside is a potent antiestrogen in MCF-7 cells, increasing IGFBP3 levels
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