21 Results for "

E-isomer

" in MedChemExpress (MCE) Product Catalog:
Products (21)

21 Results for "E-isomer" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-14971A
CAS No.: 681281-88-9
Purity:  99.40%
Synonyms: AKTIV
Target:  

Akt

Research Areas:  

Cancer

Akt inhibitor-IV (AKTIV) acts as a PI3K-Akt inhibitor at the E isomer (HY-14971), with potent cytotoxicity .
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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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Cat. No.: HY-18719D
CAS No.: 114828-90-9
Synonyms: E-Endoxifen
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

Endoxifen E-isomer (E-Endoxifen), an E-isomer of Endoxifen, is an impurity in Endoxifen Z-isomer agent substance. Endoxifen E-isomer exhibits antiestrogenic effects .
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Cat. No.: HY-13851
CAS No.: 1180676-33-8
Purity:  98.83%
Target:  

PDK-1

Research Areas:  

Others

PS47 is an inactive E-isomer of PS48. PS48 is an activator of PDK1. PS47 can be used as a negative control for PS48 .
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Cat. No.: HY-18719C
CAS No.: 1197194-61-8
Synonyms: E-Endoxifen hydrochloride
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

Endoxifen E-isomer hydrochloride (E-Endoxifen hydrochloride), an E-isomer of Endoxifen, is an impurity in Endoxifen Z-isomer agent substance. Endoxifen E-isomer hydrochloride exhibits antiestrogenic effects .
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Cat. No.: HY-15870A
CAS No.: 1386982-70-2
Purity:  99.68%
Target:  

AP-1

Research Areas:  

Inflammation/Immunology Cancer

(6E)-SR 11302 is a E-isomer of SR 11302. SR 11302 is an activator protein-1 (AP-1) transcription factor inhibitor. SR 11302 is a retinoid that specifically inhibits AP-1 activity without activating the transcription of retinoic acid response element (RARE) .
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Cat. No.: HY-133068A
CAS No.: 110642-42-7
Target:  

COMT

Research Areas:  

Metabolic Disease

(E)-5-Hydroxyferulic acid is the E-isomer of 5-Hydroxyferulic acid (HY-133068). 5-hydroxyferulic acid is a hydroxycinnamic acid and is a metabolite of the phenylpropanoid pathway. 5-Hydroxyferulic acid is a precursor in the biosynthesis of sinapic acid and is also a COMT non-esterifed substrat .
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Cat. No.: HY-17536A
CAS No.: 1421923-86-5
Synonyms: (E)-KPT-330
Target:  

CRM1

Research Areas:  

Cancer

(E)-Selinexor ((E)-KPT-330) is the E-isomer of Selinexor (HY-17536). Selinexor is the selective, orally active CRM1 inhibitor .
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Cat. No.: HY-112762A
Purity:  99.21%
Target:  

Arenavirus

Research Areas:  

Infection

(E)-LHF-535 is the E-isomer of LHF-535. LHF-535 is an antiviral agent extracted from patent WO2013123215A2, Compound 38, has EC50s of <1 μM, <1 μM, <1 μM, and 1-10 μM for Lassa, Machupo, Junin, and VSVg virus, respectively .
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Cat. No.: HY-N2543R
CAS No.: 23696-85-7
Synonyms: (E/Z)-Damascenone (Standard)
Damascenone (Standard) is the analytical standard of Damascenone. This product is intended for research and analytical applications. 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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Cat. No.: HY-N15691A
CAS No.: 283176-41-0
(E)-Tadehaginoside is the E-isomer of Tadehaginoside (HY-N15691). Tadehaginoside, a phenylpropanoid glycoside, is a regulator of lipogenesis and glucose consumption. Tadehaginoside has antioxygenic property. Tadehaginoside mediates liver protection against oxidative stress injury and inflammation by regulating Nrf2 and NF-κB signaling pathways in hepatocytes. Tadehaginoside can be used for the study of obesity and diabetes .
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Cat. No.: HY-124414S
CAS No.: 1346606-80-1
4'-Hydroxytamoxifen-d6 (contains up to 10% E isomer) is deuterium labeled 4'-Hydroxy Tamoxifen. 4'-Hydroxytamoxifen is a metabolite of Tamoxifen.
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Cat. No.: HY-W926789
CAS No.: 195611-82-6
Target:  

Estrogen Receptor/ERR

Research Areas:  

Metabolic Disease Cancer

(E)-GW7604 is the (E)-isomer of GW7604, an antiestrogen and a metabolite of GW5638 (HY-112746), which is a high-affinity estrogen receptor (ER) antagonist .
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Cat. No.: HY-N0359A
CAS No.: 212891-05-9
Synonyms: (E)-Cynarine; (E)-Plemocil
(E)-Cynarin ((E)-Cynarine) is the E-isomer of Cynarin (HY-N0359). Cynarin is an anti-asphyxiant with multiple biological activities, possessing antioxidant, antihistamine, and antiviral activities, etc.
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Cat. No.: HY-19394A
CAS No.: 606932-81-4
Target:  

PPAR

Research Areas:  

Metabolic Disease

(E)-CLX-0921 is the E-isomer of CLX-0921 (HY-19394). CLX-0921 is an orally active PPARγ agonist with an IC50 of 1.54 μM. CLX-0921 has a potent antihyperglycemic activity, and can be used for the study of type 2 diabetes .
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Cat. No.: HY-16511A
CAS No.: 1191101-18-4
Synonyms: (E)-WX-671
Target:  

Ser/Thr Protease

Research Areas:  

Cancer

(E)-Upamostat ((E)-WX-671) is an E-isomer of Upamostat (HY-16511). Upamostat (WX-671), a prodrug of WX-UK1, is an orally active serine protease inhibitor .
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Cat. No.: HY-113691
CAS No.: 102565-09-3
Target:  

Lipoxygenase

Research Areas:  

Others

(E)-L-652343 is a compound with potent cyclooxygenase and 5-lipoxygenase inhibitory activity. (E)-L-652343 can effectively inhibit the synthesis of products of these two pathways in vivo. (E)-L-652343 showed high sensitivity and specificity in the detection of geometric isomers in canine and human plasma. (E)-L-652343 showed selective metabolism in vivo, and the elimination rate of the E isomer was faster than that of the Z isomer .
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Cat. No.: HY-123066A
CAS No.: 1263143-51-6
Target:  

Drug Isomer

Research Areas:  

Others

(E)-DIDS monohydrate sodium is the E-isomer of DIDS monohydrate sodium (HY-123066). DIDS is a hRAD51 inhibitor with an IC50 value of 90 μM. DIDS exhibits significant inhibitory activity against HIV-1 integrase with an IC50 value of 5 μM .
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Cat. No.: HY-16511AS
Synonyms: (E)-WX-671-d5
(E)-Upamostat-d5 ((E)-WX-671-d5) is the deuterium labeled (E)-Upamostat (HY-16511A). (E)-Upamostat ((E)-WX-671) is an E-isomer of Upamostat (HY-16511). Upamostat (WX-671), a prodrug of WX-UK1, is an orally active serine protease inhibitor .
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Cat. No.: HY-17603A
CAS No.: 1388225-72-6
Synonyms: (E)-TSR-011
Research Areas:  

Cancer

(E)-Belizatinib ((E)-TSR-011)) (compound 36), the (E)-isomer of Belizatinib (HY-17603), is a potent, selective and orally active anaplastic lymphoma kinase (ALK) Inhibitor with an enzymatic IC50 of 0.005 μM and a cellular IC50 of 0.048 μM. (E)-Belizatinib shows >61-fold selectivity over JAK2, SRC, and IGF1R. (E)-Belizatinib shows favorable potency and PK characteristics in rats and dogs. (E)-Belizatinib can be used for ALK-driven cancer research .
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