8 results for "Insulin and Insulin-like Receptor Inhibitors" in Products

Insulin and Insulin-like Receptor Inhibitors

Insulin receptors (IRs) and insulin-like growth factor receptors (IGFRs) are formed from two subunits, each of which is comprised of an extracellular α-subunit and a transmembrane β-subunit with intracellular tyrosine kinase activity. IR homodimers are activated by insulin and, in adults, mediate an increase in glucose uptake through upregulation of GLUT4 expression. Two isoforms of the IR exist: fetal IR-A and adult IR-B.

IGF1R homodimers are activated by IGF-I and IGF-II and ...

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Selective IGF1R inhibitor

Alternate Names: Picropodophyllin
Chemical Name: (5R,5aS,8aR,9R)-5,8,8a,9-Tetrahydro-9-hydroxy-5-(3,4,5-trimethoxyphenyl)-furo[3',4':6,7]naphtho[2,3-d]-1,3-dioxol-6(5aH)-one
Purity: ≥97%
Selective IGF1R inhibitor
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High affinity insulin-like growth factor-I binding protein IGFBP inhibitor

Chemical Name: 1-(3,4-Dihydroxybenzoyl)-6,7-dihydroxy-3-isoquinolinecarboxylic acid
Purity: ≥98%
High affinity insulin-like growth factor-I binding protein IGFBP inhibitor
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IGF1R inhibitor

Chemical Name: N-(5-Chloro-2-methoxyphenyl)-N'-(2-methyl-4-quinolinyl)urea
Purity: ≥98%
IGF1R inhibitor
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Dual IR/IGF1R inhibitor

Chemical Name: 4-[[(2S)-2-(3-Chlorophenyl)-2-hydroxyethyl]amino]-3-[7-methyl-5-(4-morpholinyl)-1H-benzimidazol-2-yl]-2(1H)-pyridinone
Purity: ≥98%
Dual IR/IGF1R inhibitor
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Potent IR and IGF1R inhibitor; also inhibits anaplastic lymphoma kinase (ALK)

Chemical Name: 2-[[2-[[1-[(Dimethylamino)ethanoyl]-5-(methyloxy)-2,3-dihydro-1H-indol-6-yl]amino]-7H-pyrrolo[2,3-d]pyrimidin-4-yl]amino]-6-fluoro-N-methylbenzamide
Purity: ≥98%
Potent IR and IGF1R inhibitor; also inhibits anaplastic lymphoma kinase (ALK)
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ATP-competitive inhibitor of IGF1R

Chemical Name: 5-[3-(Phenylmethoxy)phenyl]-7-[trans-3-(1-pyrrolidinylmethyl)cyclobutyl]-7H-pyrrolo[2,3-d]pyrimidin-4-amine
Purity: ≥98%
ATP-competitive inhibitor of IGF1R
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Highly potent ALK inhibitor; also potently inhibits IR, IGF1R, STK22D and FLT3

Alternate Names: LDK378
Chemical Name: 5-Chloro-N4-[2-[(1-methylethyl)sulfonyl]phenyl]-N2-[5-methyl-2-(1-methylethoxy)-4-(4-piperidinyl)phenyl]-2,4-pyrimidinediamine
Purity: ≥98%
Highly potent ALK inhibitor; also potently inhibits IR, IGF1R, STK22D and FLT3
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Potent and selective dual inhibitor of the IGF-1 receptor and insulin receptor

Chemical Name: cis-3-[8-Amino-1-(2-phenyl-7-quinolinyl)imidazo[1,5-a]pyrazin-3-yl]-1-methylcyclobutanol
Purity: ≥98%
Potent and selective dual inhibitor of the IGF-1 receptor and insulin receptor
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