10100 Results for "

oral controlled-release dosage forms

" in MedChemExpress (MCE) Product Catalog:
Products (10100)

10100 Results for "oral controlled-release dosage forms" in MCE Product Catalog:

76
76 Cited Publications
Cat. No.: HY-100388A
CAS No.: 2200214-93-1
Purity:  99.87%
Target:  

SHP2 Phosphatase

Research Areas:  

Cancer

SHP099 hydrochloride is a potent, selective and orally available SHP2 inhibitor with an IC50 of 70 nM .
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75
75 Cited Publications
Cat. No.: HY-12075
CAS No.: 700874-71-1
Purity:  99.72%
Research Areas:  

Cancer

LY2109761 is an orally active, selective TGF-β receptor type I/II inhibitor with Kis of 38 nM and 300 nM, respectively.
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75
75 Cited Publications
Cat. No.: HY-13226
CAS No.: 700874-72-2
Purity:  99.84%
Synonyms: LY2157299
Target:  

TGF-β Receptor

Research Areas:  

Cancer

Galunisertib (LY2157299) is an oral and selective TGF-β receptor type I (TGF-βRI) kinase inhibitor with an IC50 of 56 nM.
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75
75 Cited Publications
Cat. No.: HY-B0318
CAS No.: 443-48-1
Metronidazole is an orally active nitroimidazole antibiotic. Metronidazole can cross blood brain barrier. Metronidazole can be used for the research of anaerobic infections .
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75
75 Cited Publications
Cat. No.: HY-B0318A
CAS No.: 69198-10-3
Synonyms: SC 326421
Metronidazole hydrochloride (SC 326421) is an orally active nitroimidazole antibiotic, can be used to research anaerobic infections. Metronidazole hydrochloride can cross blood brain barrier and results inflammation and skeletal muscle contraction under long-term application .
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74
74 Cited Publications
Cat. No.: HY-B0589
CAS No.: 134523-00-5
Atorvastatin is an orally active HMG-CoA reductase inhibitor, has the ability to effectively decrease blood lipids. Atorvastatin inhibits human SV-SMC proliferation and invasion with IC50s of 0.39 μM and 2.39 μM, respectively .
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73
73 Cited Publications
Cat. No.: HY-10422
CAS No.: 1009298-09-2
Purity:  99.60%
Target:  

mTOR Autophagy Apoptosis

Research Areas:  

Cancer

AZD-8055 is a potent, selective, and orally bioavailable ATP-competitive mTOR kinase inhibitor with an IC50 of 0.8 nM. AZD-8055 inhibits both mTORC1 and mTORC2 .
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72
72 Cited Publications
Cat. No.: HY-108257
CAS No.: 134523-01-6
Purity:  99.76%
Atorvastatin sodium is an orally active HMG-CoA reductase inhibitor, has the ability to effectively decrease blood lipids. Atorvastatin sodium inhibits human SV-SMC proliferation and invasion with IC50s of 0.39 μM and 2.39 μM, respectively .
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71
71 Cited Publications
Cat. No.: HY-19323
CAS No.: 1352226-88-0
Synonyms: AZD6738
Target:  

ATM/ATR

Research Areas:  

Cancer

Ceralasertib (AZD6738) is an orally active and bioavailable inhibitor of ATR kinase with an IC50 of 1 nM.
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68
68 Cited Publications
Cat. No.: HY-13426
CAS No.: 808118-40-3
Purity:  99.92%
Synonyms: FG-4592
Research Areas:  

Infection Cancer

Roxadustat is an orally active hypoxia-inducible factor prolyl-hydroxylase (PHD) inhibitor (HIF-PHI) that promotes erythropoiesis through increasing endogenous erythropoietin, improving iron regulation, and reducing hepcidin .
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65
65 Cited Publications
Cat. No.: HY-15145A
CAS No.: 2468639-77-0
Purity:  99.19%
Target:  

Sirtuin Autophagy

Research Areas:  

Metabolic Disease

SRT 1720 dihydrochloride is a selective and orally active activator of SIRT1 with an EC50 of 0.10 μM, and shows less potent activities on SIRT2 and SIRT3 .
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65
65 Cited Publications
Cat. No.: HY-15145
CAS No.: 2060259-60-9
Purity:  99.37%
Target:  

Sirtuin Autophagy

Research Areas:  

Metabolic Disease

SRT 1720 monohydrochloride is a selective and orally active activator of SIRT1 with an EC50 of 0.10 μM, and shows less potent activities on SIRT2 and SIRT3 .
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64
64 Cited Publications
Cat. No.: HY-B0389
CAS No.: 50-99-7
Synonyms: Glucose; D-(+)-Glucose; Dextrose
D-Glucose is the naturally occurring form of glucose and the most abundant monosaccharide. D-Glucose is a critical components of the general metabolism, and serve as critical signaling molecules in relation to both cellular metabolic status and biotic or abiotic stress response .
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63
63 Cited Publications
Cat. No.: HY-13064
CAS No.: 934660-93-2
Purity:  99.81%
Synonyms: GDC-0973; XL518
Target:  

MEK Apoptosis

Research Areas:  

Cancer

Cobimetinib (GDC-0973, RG7420) is a potent, selective and oral MEK1 inhibitor with an IC50 of 4.2 nM for MEK1.
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61
61 Cited Publications
Cat. No.: HY-100347
CAS No.: 1629138-41-5
Purity:  99.40%
Target:  

TGF-beta/Smad

Research Areas:  

Neurological Disease

SRI-011381 is an orally active TGF-β signaling agonist, exhibits neuroprotective effects .
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61
61 Cited Publications
Cat. No.: HY-100347A
CAS No.: 2070014-88-7
Purity:  99.55%
Target:  

TGF-beta/Smad

Research Areas:  

Neurological Disease

SRI-011381 hydrochloride is an orally active TGF-β signaling agonist, exhibits neuroprotective effects, with blood-brain barrier permeability .
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60
60 Cited Publications
Cat. No.: HY-50855B
CAS No.: 1309357-15-0
Synonyms: CX-4945 sodium salt
Target:  

Casein Kinase Autophagy

Research Areas:  

Cancer

Silmitasertib sodium salt is an orally bioavailable, highly selective and potent CK2 inhibitor, with IC50 values of 1 nM against CK2α and CK2α'.
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60
60 Cited Publications
Cat. No.: HY-50855
CAS No.: 1009820-21-6
Synonyms: CX-4945
Target:  

Casein Kinase Autophagy

Research Areas:  

Cancer

Silmitasertib (CX-4945) is an orally bioavailable, highly selective and potent CK2 inhibitor, with IC50 values of 1 nM against CK2α and CK2α'.
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59
59 Cited Publications
Cat. No.: HY-16950
CAS No.: 68047-06-3
Synonyms: (Z)-4-Hydroxytamoxifen; trans-4-Hydroxytamoxifen; (Z)-Afimoxifene
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

4-Hydroxytamoxifen ((Z)-4-Hydroxytamoxifen) is an orally active, selective estrogen receptor modulator (SERM). 4-Hydroxytamoxifen ((Z)-4-Hydroxytamoxifen) is also the active metabolic form of Tamoxifen (HY-13757A) in vivo and can be used to induce gene knockout in transgenic mice expressing CreER .
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59
59 Cited Publications
Cat. No.: HY-10396
CAS No.: 254750-02-2
Purity:  99.81%
Synonyms: PF 03491390; IDN-6556
Target:  

Caspase Flavivirus

Research Areas:  

Infection Neurological Disease Cancer

Emricasan (PF 03491390) is an orally active and irreversible pan-caspase inhibitor. Emricasan inhibits Zika virus (ZIKV)-induced increases in caspase-3 activity and protected human cortical neural progenitors .
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