1075 Results for "

Compound E

" in MedChemExpress (MCE) Product Catalog:
Products (1075)

1075 Results for "Compound E" in MCE Product Catalog:

18
18 Publications Verification
Cat. No.: HY-14176
CAS No.: 209986-17-4
Purity:  99.97%
Synonyms: γ-Secretase-IN-1
Target:  

γ-secretase

Research Areas:  

Cancer

Compound E is a γ-secretase inhibitor. Compound E blocks β-amyloid(40), β-amyloid(42), and Notch γ-secretase cleavage with IC50s of 0.24, 0.37, 0.32 nM, respectively.
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6
6 Cited Publications
Cat. No.: HY-17461
CAS No.: 53-06-5
Synonyms: 17-Hydroxy-11-dehydrocorticosterone; Kendall's Compound E
Cortisone (17-Hydroxy-11-dehydrocorticosterone), an oxidized metabolite of Cortisol (a Glucocorticoid). Cortisone acts as an immunosuppressant and anti-inflammatory agent. Cortisone can partially intervene in binding of Glucocorticoid to Glucocorticoid-receptor at high concentrations .
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4
4 Cited Publications
Cat. No.: HY-N4182
CAS No.: 864232-34-8
Licochalcone E, a flavonoid compound isolated from Glycyrrhiza uralensis, inhibits NF-κB and AP-1 transcriptional activity through the inhibition of AKT and MAPK activation .
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4
4 Cited Publications
Cat. No.: HY-N6966
CAS No.: 102-37-4
Ethyl Caffeate is a natural phenolic compound isolated from Bidens pilosa. Ethyl caffeate suppresses NF-κB activation and its downstream inflammatory mediators, inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), and prostaglandin E2 (PGE2) in vitro or in mouse skin .
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3
3 Cited Publications
Cat. No.: HY-N2963
CAS No.: 90902-21-9
Broussonin E is a phenolic compound and shows anti-inflammatory activity. Broussonin E can suppress inflammation by modulating macrophages activation statevia inhibiting the ERK and p38 MAPK and enhancing JAK2-STAT3 signaling pathway. Broussonin E can be used for the research of inflammation-related diseases such as atherosclerosis .
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3
3 Cited Publications
Cat. No.: HY-16950A
CAS No.: 68392-35-8
Synonyms: Afimoxifene; 4-OHT
(E/Z)-4-Hydroxytamoxifen (Afimoxifene) is a racemic compound of (Z)-4-Hydroxytamoxifen and (E)-4-Hydroxytamoxifen isomers. (E/Z)-4-Hydroxytamoxifen is a selective estrogen receptor modulator with mixed estrogenic and antiestrogenic activity, which is also an active metabolite of Tamoxifen (HY-13757A). (E/Z)-4-Hydroxytamoxifen is an agonist of the G protein-coupled estrogen receptor (GPER) with relatively low affinity (100-1000 nM). (E/Z)-4-Hydroxytamoxifen is promising for research of cyclical mastalgia, such as breast pain, tenderness, and nodularity .
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3
3 Cited Publications
Cat. No.: HY-153034
CAS No.: 2729981-17-1
Purity:  99.74%
Target:  

Proteasome Phosphatase

Research Areas:  

Cancer

LONP1-IN-2 (Compound 9e) is a potent and selective LONP1 inhibitor with an IC50 value of 0.093 μM. LONP1-IN-2 can be used in research of cancer .
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2
2 Cited Publications
Cat. No.: HY-14270
CAS No.: 53882-12-5
Purity:  98.02%
Synonyms: U-42585E free acid
Target:  

Histamine Receptor

Lodoxamide (U-42585E free acid) is an antiallergic compound acting as a mast-cell stabilizer for the treatment of asthma and allergic conjunctivitis.
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2
2 Cited Publications
Cat. No.: HY-129523
CAS No.: 2378258-52-5
Purity:  95.66%
Target:  

PROTACs Ras

Research Areas:  

Cancer

PROTAC K-Ras Degrader-1 (Compound 518) is a PROTAC. PROTAC K-Ras Degrader-1 can effectively degrades K-Ras based on Cereblon E3 ligand, exhibits ≥70% degradation efficacy in SW1573 cells .
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2
2 Cited Publications
Cat. No.: HY-N6954
CAS No.: 76996-27-5
Garcinone C, a xanthone derivative, is a natural compound extracted from Garcinia oblongifolia that is used as an anti-inflammatory, astringency and granulation-promoting medicine, and has potential cytotoxic effects on certain cancers. Garcinone C stimulates the expression levels of ATR and 4E-BP1, arrests the cell cycle, inhibits cell viability of the human Nasopharyngeal carcinoma (NPC) cell lines CNE1, CNE2, HK1 and HONE1 in a time‑ and dose‑dependent manner through inhibition of Hedgehog signaling pathway. Garcinone C is orally active .
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1
1 Cited Publications
Cat. No.: HY-N2543
CAS No.: 23696-85-7
Synonyms: (E/Z)-Damascenone
Damascenone ((E/Z)-Damascenone) is an active compound of Epipremnum pinnatum with anti-inflammatory activity . Damascenone is a mixture complex of E-isomer-Damascenone and Z-isomer Damascenone.
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1
1 Cited Publications
Cat. No.: HY-N2173
CAS No.: 93675-88-8
Forsythoside E is a phenylethanoid glycoside compound. Forsythoside E can be isolated from Shuanghuanglian. Forsythoside E does not induce vascular leakage or promote histamine release in mice. Forsythoside E does not cause pseudo-allergic reactions .
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1
1 Cited Publications
Cat. No.: HY-117762
CAS No.: 137018-55-4
Purity:  98.44%
Synonyms: PNU-83836E
Research Areas:  

Inflammation/Immunology

U-83836E (PNU-83836E) is a compound with anti-inflammatory and antioxidant activities that reduces lung inflammation inhibiting oxidative stress and ROS production. U-83836E has shown potential for studying asthma and lung inflammation in animal models .
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1
1 Cited Publications
Cat. No.: HY-107459
CAS No.: 134036-52-5
Purity:  99.71%
Synonyms: (E/Z)-Tyrphostin AG490; (E/Z)-Tyrphostin B42
Target:  

EGFR STAT JAK

Research Areas:  

Cancer

(E/Z)-AG490 ((E/Z)-Tyrphostin AG490) is a racemic compound of (E)-AG490 and (Z)-AG490 isomers. (E)-AG490 (HY-12000) is a tyrosine kinase inhibitor that inhibits EGFR, Stat-3 and JAK2/3.
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1
1 Cited Publications
Cat. No.: HY-N0060B
CAS No.: 537-98-4
Synonyms: (E)-Coniferic acid
(E)-Ferulic acid is an isomer of ferulic acid, an aromatic compound abundant in plant cell walls. (E)-Ferulic acid causes phosphorylation of β-catenin (β-catenin), leading to proteasome degradation, increasing the expression of pro-apoptotic factor Bax and reducing pro-apoptotic factor Expression of the survival factor survivin. (E)-Ferulic acid can effectively remove reactive oxygen species (ROS) and inhibit lipid peroxidation. (E)-Ferulic acid exerts antiproliferative and antimigratory effects in the human lung cancer cell line H1299.
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1
1 Cited Publications
Cat. No.: HY-109081
CAS No.: 1141397-80-9
Purity:  ≥98.0%
Synonyms: E7727
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

Cedazuridine (E7727) (Compound 7a) is an orally active cytidine deaminase (CDA) inhibitor with an IC50 value of 0.4 μM. Cedazuridine can be used for cancer research .
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1
1 Cited Publications
Cat. No.: HY-135813
CAS No.: 877950-01-1
Purity:  95.05%
Target:  

Bacterial

Research Areas:  

Infection

LtaS-IN-1 (compound 1771) is a potent small-molecule inhibitor of Lipoteichoic acid (LTA) synthesis in multidrug-resistant (MDR) E. faecium and by altering the cell wall morphology. LtaS-IN-1 alone inhibits Enterococcus.spp 28 strains with varying MIC values ranging from 0.5 μg/mL to 64 μg/mL. LtaS-IN-1 combination with antibiotics abolishs multidrug-resistant E. faecium growth almost completely .
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1
1 Cited Publications
Cat. No.: HY-13973A
CAS No.: 603272-51-1
Purity:  99.16%
Target:  

GSK-3

Research Areas:  

Metabolic Disease

GSK-3 inhibitor 1 (compound core 3) is a GSK-3 inhibitor that induces stem/progenitor cell self-renewal (e.g. induces stem/progenitor cell proliferation while maintaining the ability to differentiate into tissue cells in the progeny) .
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1
1 Cited Publications
Cat. No.: HY-153866
CAS No.: 1383376-92-8
Purity:  99.54%
Target:  

Casein Kinase

Research Areas:  

Cancer

CK1-IN-2 (compound Nr.4) is a potent CK1 inhibitor with an IC50 values of 123, 19.8, 26.8, 74.3 nM for CK1a, CK1d, CK1e, p38a, respectively .
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1
1 Cited Publications
Cat. No.: HY-112098
CAS No.: 2417369-94-7
Purity:  96.68%
Research Areas:  

Cancer

PROTAC ERα Degrader-1 comprises an ubiquitin E3 ligase binding group, a linker and a protein binding group. PROTAC ERα Degrader-1 extracts from patent WO2017201449A1, compound P1. PROTAC ERα Degrader-1 is an estrogen receptor-alpha (ERα) degrader.
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