3667 Results for "

anticancer activity

" in MedChemExpress (MCE) Product Catalog:
Products (3667)

3667 Results for "anticancer activity" in MCE Product Catalog:

20
20 Cited Publications
Art. -Nr.: HY-10297
CAS. Nr.: 1086062-66-9
Reinheit:  99.94%
Synonyms: GSK2126458; GSK458
Target:  

PI3K mTOR Autophagy

Forschungsgebiete:  

Cancer

Omipalisib (GSK2126458) is an orally active and highly selective inhibitor of PI3K with Kis of 0.019 nM/0.13 nM/0.024 nM/0.06 nM and 0.18 nM/0.3 nM for p110α/β/δ/γ, mTORC1/2, respectively. Omipalisib has anti-cancer activity .
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20
20 Cited Publications
Art. -Nr.: HY-B2163
CAS. Nr.: 472-61-7
Astaxanthin, the red dietary carotenoid, is an orally effective and potent antioxidant. Astaxanthin inhibits NF-κB and down-regulates VEGF in blood glucose. Astaxanthin exerts anti-cancer cell proliferation, increases apoptosis, impairs migration and invasion by activating PPARγ and reducing the expression of STAT3. Astaxanthin also has neuroprotective and anti-inflammatory activity and can be used in studies of cancer, diabetic retinopathy, cardiovascular disease, and in the coloring of animal feed .
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20
20 Cited Publications
Art. -Nr.: HY-N1584B
CAS. Nr.: 1217623-74-9
Synonyms: RU-19110 hydrochloride
Halofuginone hydrochloride (RU-19110 hydrochloride), a Febrifugine derivative, is a competitive prolyl-tRNA synthetase inhibitor with a Ki of 18.3 nM . Halofuginone hydrochloride is a specific inhibitor of type-I collagen synthesis and attenuates osteoarthritis (OA) by inhibition of TGF-β activity . Halofuginone hydrochloride is also a potent pulmonary vasodilator by activating Kv channels and blocking voltage-gated, receptor-operated and store-operated Ca 2+ channels. Halofuginone hydrochloride has anti-malaria, anti-inflammatory, anti-cancer, anti-fibrosis effects .
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19
19 Cited Publications
Art. -Nr.: HY-N0015
CAS. Nr.: 480-10-4
Synonyms: Astragaline; 3-Glucosylkaempferol; Kaempferol 3-β-D-glucopyranoside
Astragalin (Astragaline) a flavonoid with anti-inflammatory, antioxidant, anticancer, bacteriostatic activity. Astragalin inhibits cancer cells proliferation and migration, induces apoptosis. Astragalin is orally active and provides nerve and heart protection, and resistance against and osteoporosis .
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19
19 Cited Publications
Art. -Nr.: HY-N0279
CAS. Nr.: 18956-16-6
Synonyms: Cardamomin; Alpinetin chalcone
Cardamonin can be found from cardamom, and can target various signaling molecules, transcriptional factors, cytokines and enzymes. Cardamonin can inhibit mTOR, NF-κB, Akt, STAT3, Wnt/β-catenin and COX-2. Cardamonin shows anticancer, anti-inflammatory, antimicrobial and antidiabetic activities .
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19
19 Cited Publications
Art. -Nr.: HY-108357
CAS. Nr.: 157-03-9
Reinheit:  99.98%
Synonyms: L-6-Diazo-5-oxonorleucine; DON
Forschungsgebiete:  

Infection Cancer

6-Diazo-5-oxo-L-nor-Leucine (L-6-Diazo-5-oxonorleucine; DON) is a glutamine antagonist that irreversibly inhibits the catabolic effect of glutamine. 6-Diazo-5-oxo-L-nor-Leucine shows good anticancer activity (especially in pancreatic cancer) and reduces the self-renewal potential and metastatic capacity of tumour cells. 6-Diazo-5-oxo-L-nor-Leucine also possesses antibacterial and antiviral activity .
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18
18 Cited Publications
Art. -Nr.: HY-N0376
CAS. Nr.: 551-15-5
Liquiritin, a flavonoid isolated from Glycyrrhiza uralensis, is a potent and competitive AKR1C1 inhibitor with IC50s of 0.62 μM, 0.61 μM, and 3.72μM for AKR1C1, AKR1C2 and AKR1C3, respectively. Liquiritin efficiently inhibits progesterone metabolism mediated by AKR1C1 in vivo . Liquiritin acts as an antioxidant and has neuroprotective, anti-cancer and anti-inflammatory activity .
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17
17 Cited Publications
Art. -Nr.: HY-114429
CAS. Nr.: 2316817-88-4
Reinheit:  99.88%
Target:  

DNA/RNA Synthesis

Forschungsgebiete:  

Cancer

CB-6644 is a selective inhibitor of RUVBL1/2 complex with anti-cancer activity. CB-6644 blocks the ATPase activity of RUVBL1/2 with an IC50 of 15 nM .
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17
17 Cited Publications
Art. -Nr.: HY-14443
CAS. Nr.: 1234480-50-2
Reinheit:  99.48%
Forschungsgebiete:  

Cancer

XMD8-92 is a potent ERK5 (BMK1)/BRD4 inhibitor with Kds of 80 and 190 nM, respectively. XMD8-92 inhibits DCAMKL2, PLK4 and TNK1 with Kds of 190, 600 and 890 nM, respectively. Anti-cancer activity .
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16
16 Cited Publications
Art. -Nr.: HY-102007A
CAS. Nr.: 1131626-47-5
Reinheit:  99.68%
Target:  

HSP

Forschungsgebiete:  

Cancer

Gamitrinib TPP hexafluorophosphate is a Gamitrinib (GA) mitochondrial matrix inhibitor. Gamitrinib TPP hexafluorophosphate is a mitochondrial targeted HSP90 inhibitor with anti-cancer activity.
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16
16 Cited Publications
Art. -Nr.: HY-14615
CAS. Nr.: 23513-14-6
Reinheit:  99.68%
Synonyms: (S)-(+)-[6]Gingerol
[6]-Gingerol is an active compound isolated from Ginger (Zingiber officinale), exhibits a variety of biological activities including anticancer, anti-inflammation, and anti-oxidation.
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16
16 Cited Publications
Art. -Nr.: HY-N0290
CAS. Nr.: 4773-96-0
Mangiferin is a Nrf2 activator. Mangiferin suppresses nuclear translocation of the NF-κB subunits p65 and p50. Mangiferin exhibits antioxidant, antidiabetic, antihyperuricemic, antiviral, anticancer and antiinflammatory activities .
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16
16 Cited Publications
Art. -Nr.: HY-N1067
CAS. Nr.: 6754-58-1
Xanthohumol is one of the principal flavonoids isolated from hops, the inhibitor of diacylglycerol acetyltransferase (DGAT), COX-1 and COX-2, and shows anti-cancer and anti-angiogenic activities. Xanthohumol also has antiviral activity against bovine viral diarrhea virus (BVDV), rhinovirus, HSV-1, HSV-2 and cytomegalovirus (CMV).
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16
16 Cited Publications
Art. -Nr.: HY-N0451
CAS. Nr.: 480-44-4
Synonyms: 5,7-Dihydroxy-4'-methoxyflavone
Acacetin (5,7-Dihydroxy-4'-methoxyflavone) is an orally active flavonoid derived from Dendranthema morifolium. Acacetin docks in the ATP binding pocket of PI3Kγ. Acacetin causes cell cycle arrest and induces apoptosis and autophagy in cancer cells. Acacetin has potent anti-cancer and anti-inflammatory activity and has the potential for pain-related diseases research .
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16
16 Cited Publications
Art. -Nr.: HY-144806
CAS. Nr.: 3033069-84-7
Reinheit:  99.64%
Target:  

PI3K Akt Apoptosis

Forschungsgebiete:  

Cancer

PI3K/AKT-IN-1 is an effective PI3K/AKT dual inhibitor (IC50 of 6.99, 4.01 and 3.36 μM for PI3Kγ, PI3Kδ and AKT, respectively). PI3K/AKT-IN-1 has anticancer activity and acts by inhibiting PI3K/AKT axis and inducing caspase 3 dependent apoptosis .
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15
15 Cited Publications
Art. -Nr.: HY-12484
CAS. Nr.: 896705-16-1
Reinheit:  99.25%
Target:  

DNA/RNA Synthesis

Forschungsgebiete:  

Cancer

BMH-21 is a first-in-class DNA intercalator which inhibits RNA polymerase I (Pol I) transcription. BMH-21 possesses anticancer activity .
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15
15 Cited Publications
Art. -Nr.: HY-N2302
CAS. Nr.: 3351-86-8
Synonyms: all-trans-Fucoxanthin
Fucoxanthin (all-trans-Fucoxanthin) is a marine carotenoid and shows anti-obesity, anti-diabetic, anti-oxidant, anti-inflammatory and anticancer activities .
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15
15 Cited Publications
Art. -Nr.: HY-N0720
CAS. Nr.: 41060-15-5
Neobavaisoflavone, a flavonoid, is isolated from the seeds of Psoralea corylifolia. Neobavaisoflavone exhibits anti-inflammatory, anti-cancer and anti-oxidation activities. Neobavaisoflavone inhibits DNA polymerase at moderate to high concentrations. Neobavaisoflavone also inhibits platelet aggregation .
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15
15 Cited Publications
Art. -Nr.: HY-N0540
CAS. Nr.: 5373-11-5
Synonyms: Luteolin 7-glucoside; Luteolin 7-O-β-D-glucoside
Cynaroside (Luteolin 7-glucoside) is a flavonoid compound that exhibits anti-oxidative capabilities. Cynaroside is also a potent influenza RNA-dependent RNA polymerase inhibitor with an IC50 of 32 nM. Cynaroside also is a promising inhibitor for H2O2-induced apoptosis, has cytoprotection against oxidative stress-induced cardiovascular diseases. Cynaroside also has antibacterial, antifungal and anticancer activities, antioxidant and anti-inflammatory activities .
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15
15 Cited Publications
Art. -Nr.: HY-D0803
CAS. Nr.: 490-91-5
Thymoquinone is an orally active natural product isolated from N. sativa Thymoquinone down-regulates the VEGFR2-PI3K-Akt pathway. Thymoquinone has antioxidant, anti-inflammatory, anticancer, antiviral, anticonvulsant, antifungal, antiviral, antiangiogenic activity and hepatoprotective effects. Thymoquinone can be used to study Alzheimer's disease, cancer, cardiovascular disease, infectious disease and inflammation .
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