177 Results for "

ENT

" in MedChemExpress (MCE) Product Catalog:
Products (177)

177 Results for "ENT" in MCE Product Catalog:

4
4 Cited Publications
Cat. No.: HY-B0181
CAS No.: 645-05-6
Synonyms: ENT-50852; RB-1515; WR-95704
Research Areas:  

Cancer

Altretamine is an alkylating antineoplastic agent.
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3
3 Cited Publications
Cat. No.: HY-W010936
CAS No.: 38048-32-7
Synonyms: NBMPR
Target:  

Adenosine Receptor

Research Areas:  

Neurological Disease

Nitrobenzylthioinosine is an ENT1 transporter inhibitor that binds to ENT1 transporter with high affinity. Nitrobenzylthioinosine is a photoaffinity probe for adenosine uptake sites in brain. Nitrobenzylthioinosine can cross the blood-brain barrier .
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2
2 Cited Publications
Cat. No.: HY-N2112
CAS No.: 79498-31-0
Glaucocalyxin A, an ent-kauranoid diterpene from Rabdosia japonica var., induces apoptosis in osteosarcoma by inhibiting nuclear translocation of Five-zinc finger Glis 1 (GLI1) via regulating PI3K/Akt signaling pathway. Glaucocalyxin A has antitumor effect .
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1
1 Cited Publications
Cat. No.: HY-16468
CAS No.: 148717-90-2
Synonyms: MSI-1256; ENT-01 free acid
Squalamine (MSI-1256) is an aminosterol compound with broad-spectrum antiviral activity. Squalamine makes cells less conducive to certain viral replication by altering the electrostatic interactions in the inner membrane of host cells. Squalamine also has antibacterial and antitumor activities. Squalamine has broad-spectrum antibacterial activity against Gram-negative and Gram-positive bacteria, fungi and protozoa. Squalamine inhibits tumor-related angiogenesis and the growth of human breast cancer cells. Squalamine restores the function of enteric nervous system in Parkinson ,s disease mouse models .
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1
1 Cited Publications
Cat. No.: HY-B1198
CAS No.: 51-03-6
Synonyms: ENT-14250
Research Areas:  

Infection Cancer

Piperonyl butoxide (ENT-14250) is a pesticide synergist and food additive. Piperonyl butoxide has adverse effects on reproduction, development and behavior in mice. Piperonyl butoxide can activate c-Jun and ATF-2 in mouse hepatocytes. Piperonyl butoxide is a liver cancer carcinogen in rats and mice .
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1
1 Cited Publications
Cat. No.: HY-18776
CAS No.: 41552-95-8
Target:  

Adenosine Receptor

Research Areas:  

Neurological Disease

A2AR-agonist-1 is a potent A2AR agonist and ENT1 inhibitor with Ki of 4.39 and 3.47 for A2AR and ENT1.
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1
1 Cited Publications
Cat. No.: HY-N2113
CAS No.: 80508-81-2
Glaucocalyxin B is an ent kaurane diterpenoid isolated from the Chinese traditional medicine Rabdosia japonica with anticancer and antitumor activity; decreases the growth of HL-60 cells with an IC50 of approximately 5.86 μM at 24 h.
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1
1 Cited Publications
Cat. No.: HY-106841
CAS No.: 120770-34-5
Purity:  99.06%
Synonyms: R-75231; R88021
Draflazine (R-75231) is a ENT1 inhibitor. Draflazine (R-75231) completely reverses the hypersensitivity in the complete Freund’s adjuvant (CFA) model of mechanical hyperalgesia and the carrageenan inflammation model of thermal and mechanical hyperalgesia .
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1
1 Cited Publications
Cat. No.: HY-N6833
CAS No.: 1220616-44-3
Rebaudioside M, a glycoside of the ent-kaurene diterpenoid aglycone, is a non-calorie sweetener isolated from Stevia rebaudiana. Rebaudioside M has antidiabetics, antihypertension, anti-inflammatory, antioxidant, anticaries and anticancer benefits. Rebaudioside M is more than 350 times sweeter than sucrose. Rebaudioside M can be used in food and beverage .
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1
1 Cited Publications
Cat. No.: HY-18775
CAS No.: 110505-75-4
Synonyms: Para-topolin riboside
N6-(4-Hydroxybenzyl) adenosine (Para-topolin riboside) is an equilibrative nucleoside transporter 1 (ENT1) inhibitor and a selective agonist of adenosine A2a receptor (A2aR), and also exhibits activity against P2Y12 receptor. N6-(4-Hydroxybenzyl) adenosine reduces ethanol intake and preference, attenuates operant conditioning-induced ethanol place preference, decreases the value of ethanol-related rewards, and inhibits collagen-induced platelet aggregation. N6-(4-Hydroxybenzyl) adenosine can be used in studies related to alcohol use disorder .
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Cat. No.: HY-N7491A
CAS No.: 2056011-05-1
Target:  

Calcium Channel

Research Areas:  

Cancer

ent-(+)-verticilide is a potent and selective inhibitor of cardiac ryanodine receptor (RyR2) calcium release channels with antiarrhythmic activity. ent-(+)-verticilide inhibits RyR2-mediated diastolic Ca2+ leak and exhibits higher potency and a distinct mechanism of action compared with theDantrolene and Tetracaine. ent-(+)-verticilide is a useful tool to investigate the therapeutic potential of targeting RyR2 hyperactivity in heart and brain pathologies .
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Cat. No.: HY-133695S1
ent-Florfenicol amine-d3 is deuterated labeled ent-Florfenicol amine .
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Cat. No.: HY-N16614
CAS No.: 1292294-31-5
Ent-Calquiquelignan E (Compound 8) is a flavonoid lignan compound. Ent-Calquiquelignan E can selectively inhibit diacylglycerol acyltransferase 1 (DGAT1) with an IC50 of 71.5 μM. Ent-Calquiquelignan E can be used for the research of metabolic diseas .
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Cat. No.: HY-P990917
CAS No.: 2572467-73-1
Synonyms: ENT-001

Target:  

Inhibitory Antibodies

Research Areas:  

Inflammation/Immunology

HY-P990917 is an TMEM219-targeting IgG4λ type human antibody, the recommed isotype control is Human IgG4 (S228P) lambda1, Isotype Control (HY-P99987) .
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Cat. No.: HY-90009C
CAS No.: 629652-72-8
Synonyms: ENT-IC-351
Research Areas:  

Cancer

ent-Tadalafil (ent-IC-351), compound (6S,12aS), is a inactive cis-enantiomer of compound (6R,12aS). compound (6R,12aS) is a potent PDE5 inhibitor with an IC50 of 0.090 μM, while ent-Tadalafil is inactive at concentrations up to 10 µM .
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Cat. No.: HY-152472
CAS No.: 2919962-53-9
Purity:  99.16%
Target:  

Trk Receptor

Research Areas:  

Neurological Disease

ENT-C225 is an effective activator of TrkB neurotrophin receptor. ENT-C225 has high effect on activating TrkB receptor (TrkBR), and has good physicochemical properties and neuroprotective properties .
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Cat. No.: HY-164425
CAS No.: 2597832-98-7
Target:  

Phosphatase STAT

Research Areas:  

Metabolic Disease

ENT-03 is a centrally acting mammalian aminosterol. ENT-03 upregulates cFos activation, inhibits PTP1b and induces phosphorylation of STAT3. ENT-03 normalizes blood glucose, induces weight loss. ENT-03 can be used in the research of type 2 diabetes and obesity .
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Cat. No.: HY-118465
CAS No.: 65085-69-0
Synonyms: ENT-PGE2
Research Areas:  

Endocrinology

ent-Prostaglandin E2 (ent-PGE2) is an enantiomer of PGE2 (HY-101952). unlike PGE2, ent-PGE2 is a poor substrate for 15-hydroxyprostaglandin dehydrogenase .
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Cat. No.: HY-135388
CAS No.: 1376614-99-1
Synonyms: ENT-SCH 58235
Target:  

Drug Metabolite

Research Areas:  

Cardiovascular Disease

ent-Ezetimibe (ent-SCH 58235) is the RRS-enantiomer of Ezetimibe. Ezetimibe is a potent cholesterol absorption inhibitor. Ezetimibe is a Niemann-Pick C1-like1 (NPC1L1) inhibitor, and is a potent Nrf2 activator .
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Cat. No.: HY-172515
CAS No.: 1035895-88-5
Research Areas:  

Infection

ent-Oseltamivir, the enantiomer of Oseltamivir (HY-13317), is a neuraminidase (NA) of influenza virus inhibitor. ent-Oseltamivir is promising for research of influenza virus infections .
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