1032350-13-2,MFCD14584463
Catalog No.:AA008TF8

1032350-13-2 | 8-(4-(1-Aminocyclobutyl)phenyl)-9-phenyl-[1,2,4]triazolo[3,4-f][1,6]naphthyridin-3(2h)-one dihydrochloride

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
98%
in stock  
$13.00   $9.00
- +
5mg
98%
in stock  
$22.00   $15.00
- +
10mg
98%
in stock  
$41.00   $29.00
- +
100mg
95%
in stock  
$211.00   $148.00
- +
250mg
95%
in stock  
$361.00   $253.00
- +
1g
98%
in stock  
$653.00   $458.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA008TF8
Chemical Name:
8-(4-(1-Aminocyclobutyl)phenyl)-9-phenyl-[1,2,4]triazolo[3,4-f][1,6]naphthyridin-3(2h)-one dihydrochloride
CAS Number:
1032350-13-2
Molecular Formula:
C25H23Cl2N5O
Molecular Weight:
480.3890
MDL Number:
MFCD14584463
SMILES:
O=c1[nH]nc2n1ccc1c2cc(c(n1)c1ccc(cc1)C1(N)CCC1)c1ccccc1.Cl.Cl
Properties
Computed Properties
 
Complexity:
760  
Covalently-Bonded Unit Count:
3  
Heavy Atom Count:
33  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
4  
Rotatable Bond Count:
3  

Downstream Synthesis Route

[1]CurrentPatentAssignee:MERCK&COINC-WO2013/9535,2013,A1Locationinpatent:Paragraph00186;00187

893423-62-6   
MK-2206 

[1]Patent:WO2013/9535,2013,A1

338452-92-9   
MK-2206 

[1]CurrentPatentAssignee:MERCK&COINC-WO2013/9535,2013,A1

[1]CurrentPatentAssignee:CHONGQINGUPGRABIOTECHNOLOGY-US2022/105189,2022,A1Locationinpatent:Paragraph0172

[2]CurrentPatentAssignee:CHONGQINGUPGRABIOTECHNOLOGY-US2022/105189,2022,A1Locationinpatent:Paragraph0172

Literature

Title: Plasticizer Di-(2-Ethylhexyl)Phthalate Induces Epithelial-to-Mesenchymal Transition and Renal Fibrosis In Vitro and In Vivo.

Journal: Toxicological sciences : an official journal of the Society of Toxicology 20180701

Title: Gap junctional intercellular communication and endoplasmic reticulum stress regulate chronic cadmium exposure induced apoptosis in HK-2 cells.

Journal: Toxicology letters 20180515

Title: Airborne nitro-PAHs induce Nrf2/ARE defense system against oxidative stress and promote inflammatory process by activating PI3K/Akt pathway in A549 cells.

Journal: Toxicology in vitro : an international journal published in association with BIBRA 20171001

Title: Akt activation by Ca(2+)/calmodulin-dependent protein kinase kinase 2 (CaMKK2) in ovarian cancer cells.

Journal: The Journal of biological chemistry 20170825

Title: Role of Exchange Protein Directly Activated by Cyclic AMP Isoform 1 in Energy Homeostasis: Regulation of Leptin Expression and Secretion in White Adipose Tissue.

Journal: Molecular and cellular biology 20161001

Title: Taurocholate Induces Cyclooxygenase-2 Expression via the Sphingosine 1-phosphate Receptor 2 in a Human Cholangiocarcinoma Cell Line.

Journal: The Journal of biological chemistry 20151225

Title: Utilization of human nuclear receptors as an early counter screen for off-target activity: a case study with a compendium of 615 known drugs.

Journal: Toxicological sciences : an official journal of the Society of Toxicology 20150601

Title: Effects of AKT inhibition on HGF-mediated erlotinib resistance in non-small cell lung cancer cell lines.

Journal: Journal of cancer research and clinical oncology 20150401

Title: S6 inhibition contributes to isoflurane neurotoxicity in the developing brain.

Journal: Toxicology letters 20150304

Title: The Akt inhibitor MK-2206 enhances the cytotoxicity of paclitaxel (Taxol) and cisplatin in ovarian cancer cells.

Journal: Naunyn-Schmiedeberg's archives of pharmacology 20150101

Title: Elucidating mechanisms of toxicity using phenotypic data from primary human cell systems--a chemical biology approach for thrombosis-related side effects.

Journal: International journal of molecular sciences 20150101

Title: Detection of key enzymes, free radical reaction products and activated signaling molecules as biomarkers of cell damage induced by benzo[a]pyrene in human keratinocytes.

Journal: Toxicology in vitro : an international journal published in association with BIBRA 20140801

Title: PI3K signaling mediates diverse regulation of ATF4 expression for the survival of HK-2 cells exposed to cadmium.

Journal: Archives of toxicology 20140201

Title: Preventing the calorie restriction-induced increase in insulin-stimulated Akt2 phosphorylation eliminates calorie restriction's effect on glucose uptake in skeletal muscle.

Journal: Biochimica et biophysica acta 20121101

Title: A novel PKB/Akt inhibitor, MK-2206, effectively inhibits insulin-stimulated glucose metabolism and protein synthesis in isolated rat skeletal muscle.

Journal: The Biochemical journal 20121001

Title: Phosphatidylinositol 3-kinase/Akt signaling pathway activates the WNK-OSR1/SPAK-NCC phosphorylation cascade in hyperinsulinemic db/db mice.

Journal: Hypertension (Dallas, Tex. : 1979) 20121001

Title: Dual targeting of the Akt/mTOR signaling pathway inhibits castration-resistant prostate cancer in a genetically engineered mouse model.

Journal: Cancer research 20120901

Title: Harnessing the PI3K/Akt/mTOR pathway in T-cell acute lymphoblastic leukemia: eliminating activity by targeting at different levels.

Journal: Oncotarget 20120801

Title: Combination of an allosteric Akt Inhibitor MK-2206 with etoposide or rapamycin enhances the antitumor growth effect in neuroblastoma.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research 20120701

Title: Akt inhibitors MK-2206 and nelfinavir overcome mTOR inhibitor resistance in diffuse large B-cell lymphoma.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research 20120501

Title: The Akt inhibitor MK2206 synergizes, but perifosine antagonizes, the BRAF(V600E) inhibitor PLX4032 and the MEK1/2 inhibitor AZD6244 in the inhibition of thyroid cancer cells.

Journal: The Journal of clinical endocrinology and metabolism 20120201

Title: MK-2206, a novel allosteric inhibitor of Akt, synergizes with gefitinib against malignant glioma via modulating both autophagy and apoptosis.

Journal: Molecular cancer therapeutics 20120101

Title: Inhibition of AKT with the orally active allosteric AKT inhibitor, MK-2206, sensitizes endometrial cancer cells to progestin.

Journal: PloS one 20120101

Title: First-in-man clinical trial of the oral pan-AKT inhibitor MK-2206 in patients with advanced solid tumors.

Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology 20111210

Title: IKBKE protein activates Akt independent of phosphatidylinositol 3-kinase/PDK1/mTORC2 and the pleckstrin homology domain to sustain malignant transformation.

Journal: The Journal of biological chemistry 20111028

Title: The insulin-like growth factor 1 pathway is a potential therapeutic target for low-grade serous ovarian carcinoma.

Journal: Gynecologic oncology 20111001

Title: Next-generation Akt inhibitors provide greater specificity: effects on glucose metabolism in adipocytes.

Journal: The Biochemical journal 20110415

Title: The Akt-specific inhibitor MK2206 selectively inhibits thyroid cancer cells harboring mutations that can activate the PI3K/Akt pathway.

Journal: The Journal of clinical endocrinology and metabolism 20110401

Title: eEF-2 kinase dictates cross-talk between autophagy and apoptosis induced by Akt Inhibition, thereby modulating cytotoxicity of novel Akt inhibitor MK-2206.

Journal: Cancer research 20110401

Title: MK-2206, an allosteric Akt inhibitor, enhances antitumor efficacy by standard chemotherapeutic agents or molecular targeted drugs in vitro and in vivo.

Journal: Molecular cancer therapeutics 20100701

Title: Combination treatment with MEK and AKT inhibitors is more effective than each drug alone in human non-small cell lung cancer in vitro and in vivo.

Journal: PloS one 20100101

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SDS
Related Products of 1032350-13-2
Tags:1032350-13-2 Molecular Formula|1032350-13-2 MDL|1032350-13-2 SMILES|1032350-13-2 8-(4-(1-Aminocyclobutyl)phenyl)-9-phenyl-[1,2,4]triazolo[3,4-f][1,6]naphthyridin-3(2h)-one dihydrochloride
Catalog No.: AA008TF8
1032350-13-2,MFCD14584463
1032350-13-2 | 8-(4-(1-Aminocyclobutyl)phenyl)-9-phenyl-[1,2,4]triazolo[3,4-f][1,6]naphthyridin-3(2h)-one dihydrochloride
Pack Size: 1mg
Purity: 98%
in stock
$13.00 $9.00
Pack Size: 5mg
Purity: 98%
in stock
$22.00 $15.00
Pack Size: 10mg
Purity: 98%
in stock
$41.00 $29.00
Pack Size: 100mg
Purity: 95%
in stock
$211.00 $148.00
Pack Size: 250mg
Purity: 95%
in stock
$361.00 $253.00
Pack Size: 1g
Purity: 98%
in stock
$653.00 $458.00
Quantity
- +
Add to Card
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bulk Quotation Request
Technical Information
Catalog Number: AA008TF8
Chemical Name: 8-(4-(1-Aminocyclobutyl)phenyl)-9-phenyl-[1,2,4]triazolo[3,4-f][1,6]naphthyridin-3(2h)-one dihydrochloride
CAS Number: 1032350-13-2
Molecular Formula: C25H23Cl2N5O
Molecular Weight: 480.3890
MDL Number: MFCD14584463
SMILES: O=c1[nH]nc2n1ccc1c2cc(c(n1)c1ccc(cc1)C1(N)CCC1)c1ccccc1.Cl.Cl
Properties
Complexity: 760  
Covalently-Bonded Unit Count: 3  
Heavy Atom Count: 33  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 4  
Rotatable Bond Count: 3  
Downstream Synthesis Route
1032350-03-0    1032350-13-2 

[1]CurrentPatentAssignee:MERCK&COINC-WO2013/9535,2013,A1Locationinpatent:Paragraph00186;00187

893423-62-6   
MK-2206 

[1]Patent:WO2013/9535,2013,A1

338452-92-9   
MK-2206 

[1]CurrentPatentAssignee:MERCK&COINC-WO2013/9535,2013,A1

1032350-13-2    192055-73-5    2467989-96-2 

[1]CurrentPatentAssignee:CHONGQINGUPGRABIOTECHNOLOGY-US2022/105189,2022,A1Locationinpatent:Paragraph0172

[2]CurrentPatentAssignee:CHONGQINGUPGRABIOTECHNOLOGY-US2022/105189,2022,A1Locationinpatent:Paragraph0172

Literature fold

Title: Plasticizer Di-(2-Ethylhexyl)Phthalate Induces Epithelial-to-Mesenchymal Transition and Renal Fibrosis In Vitro and In Vivo.

Journal: Toxicological sciences : an official journal of the Society of Toxicology20180701

Title: Gap junctional intercellular communication and endoplasmic reticulum stress regulate chronic cadmium exposure induced apoptosis in HK-2 cells.

Journal: Toxicology letters20180515

Title: Airborne nitro-PAHs induce Nrf2/ARE defense system against oxidative stress and promote inflammatory process by activating PI3K/Akt pathway in A549 cells.

Journal: Toxicology in vitro : an international journal published in association with BIBRA20171001

Title: Akt activation by Ca(2+)/calmodulin-dependent protein kinase kinase 2 (CaMKK2) in ovarian cancer cells.

Journal: The Journal of biological chemistry20170825

Title: Role of Exchange Protein Directly Activated by Cyclic AMP Isoform 1 in Energy Homeostasis: Regulation of Leptin Expression and Secretion in White Adipose Tissue.

Journal: Molecular and cellular biology20161001

Title: Taurocholate Induces Cyclooxygenase-2 Expression via the Sphingosine 1-phosphate Receptor 2 in a Human Cholangiocarcinoma Cell Line.

Journal: The Journal of biological chemistry20151225

Title: Utilization of human nuclear receptors as an early counter screen for off-target activity: a case study with a compendium of 615 known drugs.

Journal: Toxicological sciences : an official journal of the Society of Toxicology20150601

Title: Effects of AKT inhibition on HGF-mediated erlotinib resistance in non-small cell lung cancer cell lines.

Journal: Journal of cancer research and clinical oncology20150401

Title: S6 inhibition contributes to isoflurane neurotoxicity in the developing brain.

Journal: Toxicology letters20150304

Title: The Akt inhibitor MK-2206 enhances the cytotoxicity of paclitaxel (Taxol) and cisplatin in ovarian cancer cells.

Journal: Naunyn-Schmiedeberg's archives of pharmacology20150101

Title: Elucidating mechanisms of toxicity using phenotypic data from primary human cell systems--a chemical biology approach for thrombosis-related side effects.

Journal: International journal of molecular sciences20150101

Title: Detection of key enzymes, free radical reaction products and activated signaling molecules as biomarkers of cell damage induced by benzo[a]pyrene in human keratinocytes.

Journal: Toxicology in vitro : an international journal published in association with BIBRA20140801

Title: PI3K signaling mediates diverse regulation of ATF4 expression for the survival of HK-2 cells exposed to cadmium.

Journal: Archives of toxicology20140201

Title: Preventing the calorie restriction-induced increase in insulin-stimulated Akt2 phosphorylation eliminates calorie restriction's effect on glucose uptake in skeletal muscle.

Journal: Biochimica et biophysica acta20121101

Title: A novel PKB/Akt inhibitor, MK-2206, effectively inhibits insulin-stimulated glucose metabolism and protein synthesis in isolated rat skeletal muscle.

Journal: The Biochemical journal20121001

Title: Phosphatidylinositol 3-kinase/Akt signaling pathway activates the WNK-OSR1/SPAK-NCC phosphorylation cascade in hyperinsulinemic db/db mice.

Journal: Hypertension (Dallas, Tex. : 1979)20121001

Title: Dual targeting of the Akt/mTOR signaling pathway inhibits castration-resistant prostate cancer in a genetically engineered mouse model.

Journal: Cancer research20120901

Title: Harnessing the PI3K/Akt/mTOR pathway in T-cell acute lymphoblastic leukemia: eliminating activity by targeting at different levels.

Journal: Oncotarget20120801

Title: Combination of an allosteric Akt Inhibitor MK-2206 with etoposide or rapamycin enhances the antitumor growth effect in neuroblastoma.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research20120701

Title: Akt inhibitors MK-2206 and nelfinavir overcome mTOR inhibitor resistance in diffuse large B-cell lymphoma.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research20120501

Title: The Akt inhibitor MK2206 synergizes, but perifosine antagonizes, the BRAF(V600E) inhibitor PLX4032 and the MEK1/2 inhibitor AZD6244 in the inhibition of thyroid cancer cells.

Journal: The Journal of clinical endocrinology and metabolism20120201

Title: MK-2206, a novel allosteric inhibitor of Akt, synergizes with gefitinib against malignant glioma via modulating both autophagy and apoptosis.

Journal: Molecular cancer therapeutics20120101

Title: Inhibition of AKT with the orally active allosteric AKT inhibitor, MK-2206, sensitizes endometrial cancer cells to progestin.

Journal: PloS one20120101

Title: First-in-man clinical trial of the oral pan-AKT inhibitor MK-2206 in patients with advanced solid tumors.

Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology20111210

Title: IKBKE protein activates Akt independent of phosphatidylinositol 3-kinase/PDK1/mTORC2 and the pleckstrin homology domain to sustain malignant transformation.

Journal: The Journal of biological chemistry20111028

Title: The insulin-like growth factor 1 pathway is a potential therapeutic target for low-grade serous ovarian carcinoma.

Journal: Gynecologic oncology20111001

Title: Next-generation Akt inhibitors provide greater specificity: effects on glucose metabolism in adipocytes.

Journal: The Biochemical journal20110415

Title: The Akt-specific inhibitor MK2206 selectively inhibits thyroid cancer cells harboring mutations that can activate the PI3K/Akt pathway.

Journal: The Journal of clinical endocrinology and metabolism20110401

Title: eEF-2 kinase dictates cross-talk between autophagy and apoptosis induced by Akt Inhibition, thereby modulating cytotoxicity of novel Akt inhibitor MK-2206.

Journal: Cancer research20110401

Title: MK-2206, an allosteric Akt inhibitor, enhances antitumor efficacy by standard chemotherapeutic agents or molecular targeted drugs in vitro and in vivo.

Journal: Molecular cancer therapeutics20100701

Title: Combination treatment with MEK and AKT inhibitors is more effective than each drug alone in human non-small cell lung cancer in vitro and in vivo.

Journal: PloS one20100101

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