16 Results for "

mTORC1/2

" in MedChemExpress (MCE) Product Catalog:
Products (16)

16 Results for "mTORC1/2" in MCE Product Catalog:

139
139 Publications Verification
Cat. No.: HY-13003
CAS No.: 1222998-36-8
Pureté:  99.28%
Target:  

mTOR Autophagy

Domaines de recherche:  

Cancer

Torin 1 is a potent inhibitor of mTOR with an IC50 of 3 nM. Torin 1 inhibits both mTORC1/2 complexes with IC50 values between 2 and 10 nM. Torin 1 is an effective inducer of autophagy.
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26
26 Cited Publications
Cat. No.: HY-N0112
CAS No.: 27200-12-0
Synonyms: Ampelopsin; Ampeloptin
Dihydromyricetin is a potent inhibitor with an IC50 of 48 μM on dihydropyrimidinase. Dihydromyricetin can activate autophagy through inhibiting mTOR signaling. Dihydromyricetin suppresses the formation of mTOR complexes (mTORC1/2). Dihydromyricetin is also a potent influenza RNA-dependent RNA polymerase inhibitor with an IC50 of 22 μM.
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20
20 Cited Publications
Cat. No.: HY-10297
CAS No.: 1086062-66-9
Pureté:  99.94%
Synonyms: GSK2126458; GSK458
Target:  

PI3K mTOR Autophagy

Domaines de recherche:  

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 [1] .
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8
8 Cited Publications
Cat. No.: HY-12513
CAS No.: 1386874-06-1
Pureté:  99.27%
Synonyms: LY3023414
Target:  

PI3K DNA-PK mTOR Autophagy

Domaines de recherche:  

Cancer

Samotolisib (LY3023414) potently and selectively inhibits class I PI3K isoforms, DNA-PK, and mTORC1/2 with IC50s of 6.07 nM, 77.6 nM, 38 nM, 23.8 nM, 4.24 nM and 165 nM for PI3Kα, PI3Kβ, PI3Kδ, PI3Kγ, DNA-PK and mTOR, respectively. Samotolisib potently inhibits mTORC1/2 at low nanomolar concentrations [1] .
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6
6 Cited Publications
Cat. No.: HY-15272
CAS No.: 1062159-35-6
Pureté:  99.75%
Target:  

mTOR

Domaines de recherche:  

Inflammation/Immunology Cancer

WAY-600 is a potent, ATP-competitive, and selective mTOR inhibitor with an IC50 of 9 nM for recombinant mTOR enzyme. WAY-600 blocks mTOR complex 1/2 (mTORC1/2) assemble and activation.
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4
4 Cited Publications
Cat. No.: HY-100026
CAS No.: 1927857-56-4
Pureté:  98.01%
Target:  

mTOR

Domaines de recherche:  

Cancer

PQR620 is an orally bioavailable and selective brain penetrant inhibitor of mTORC1/2 [1].
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2
2 Cited Publications
Cat. No.: HY-N0656A
CAS No.: 7562-61-0
(+)-Usnic acid is isolated from isolated from lichens, binds at the ATP-binding pocket of mTOR, and inhibits mTORC1/2 activity. (+)-Usnic acid inhibits the phosphorylation of mTOR downstream effectors: Akt (Ser473), 4EBP1, S6K, induces autophay, with anti-cancer and anti-inflammatory activity. (+)-Usnic acid possesses antimicrobial activity against a number of planktonic gram-positive bacteria, including Staphylococcus aureus, Enterococcus faecalis, and Enterococcus faecium [1] .
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Cat. No.: HY-N2517
CAS No.: 15266-35-0
Dihydroevocarpine induces cytotoxicity in acute myeloid leukemia via suppressing the mTORC1/2 activity [1].
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Cat. No.: HY-107365
CAS No.: 1927857-61-1
Pureté:  99.85%
Target:  

PI3K mTOR

Domaines de recherche:  

Cancer

PQR530 is a potent, ATP-competitive, orally bioavailable and brain-penetrant dual pan-PI3K/mTORC1/2 inhibitor, with a subnanomolar Kd toward PI3Kα and mTOR (0.84 and 0.33 nM, respectively). Antitumor activity [1] .
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Cat. No.: HY-N0112R
CAS No.: 27200-12-0
Synonyms: Ampelopsin (Standard); Ampeloptin (Standard)
Dihydromyricetin (Standard) is the analytical standard of Dihydromyricetin. This product is intended for research and analytical applications. Dihydromyricetin is a potent inhibitor with an IC50 of 48 μM on dihydropyrimidinase. Dihydromyricetin can activate autophagy through inhibiting mTOR signaling. Dihydromyricetin suppresses the formation of mTOR complexes (mTORC1/2). Dihydromyricetin is also a potent influenza RNA-dependent RNA polymerase inhibitor with an IC50 of 22 μM.
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Cat. No.: HY-15281
CAS No.: 1223002-54-7
Target:  

mTOR

Domaines de recherche:  

Cancer

QL-IX-55 is a selective ATP-competitive inhibitor of mTORC1/2 with IC50s of 50/50/10-50 nM for Human mTORC1/Yeast mTORC1/Yeast mTORC2, respectively.
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Cat. No.: HY-N0112S
Synonyms: Ampelopsin-d4; Ampeloptin-d4
Dihydromyricetin-d4 (Ampelopsin-d4) is deuterium labeled Dihydromyricetin. Dihydromyricetin is a potent inhibitor with an IC50 of 48 μM on dihydropyrimidinase. Dihydromyricetin can activate autophagy through inhibiting mTOR signaling. Dihydromyricetin suppresses the formation of mTOR complexes (mTORC1/2). Dihydromyricetin is also a potent influenza RNA-dependent RNA polymerase inhibitor with an IC50 of 22 μM.
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Cat. No.: HY-N0656AR
CAS No.: 7562-61-0
(+)-Usnic acid (Standard) is the analytical standard of (+)-Usnic acid. This product is intended for research and analytical applications. (+)-Usnic acid is isolated from isolated from lichens, binds at the ATP-binding pocket of mTOR, and inhibits mTORC1/2 activity. (+)-Usnic acid inhibits the phosphorylation of mTOR downstream effectors: Akt (Ser473), 4EBP1, S6K, induces autophay, with anti-cancer activity [1]. (+)-Usnic acid possesses antimicrobial activity against a number of planktonic gram-positive bacteria, including Staphylococcus aureus, Enterococcus faecalis, and Enterococcus faecium .
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Cat. No.: HY-100026R
CAS No.: 1927857-56-4
Domaines de recherche:  

Cancer

PQR620 (Standard) is the analytical standard of PQR620 (HY-100026). This product is intended for research and analytical applications. PQR620 is an orally bioavailable and selective brain penetrant inhibitor of mTORC1/2 [1].
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Cat. No.: HY-10297R
CAS No.: 1086062-66-9
Synonyms: GSK2126458 (Standard); GSK458 (Standard)
Domaines de recherche:  

Cancer

Omipalisib (Standard) is the analytical standard of Omipalisib (HY-10297). This product is intended for research and analytical applications. 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 [1] .
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Cat. No.: HY-107365R
CAS No.: 1927857-61-1
Domaines de recherche:  

Cancer

PQR530 (Standard) is the analytical standard of PQR530 (HY-107365). This product is intended for research and analytical applications. PQR530 is a potent, ATP-competitive, orally bioavailable and brain-penetrant dual pan-PI3K/mTORC1/2 inhibitor, with a subnanomolar Kd toward PI3Kα and mTOR (0.84 and 0.33 nM, respectively). Antitumor activity [1] .
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