Home Indole and Oxindoles 114719-57-2
114719-57-2,MFCD04036980
Catalog No.:AA000F0P

114719-57-2 | Pyrido[1,2-a:3,4-b']diindol-5-ium, 12,13-dihydro-13-oxo-, chloride

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  • Technical Information
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Technical Information
Catalog Number:
AA000F0P
Chemical Name:
Pyrido[1,2-a:3,4-b']diindol-5-ium, 12,13-dihydro-13-oxo-, chloride
CAS Number:
114719-57-2
Molecular Formula:
C18H11ClN2O
Molecular Weight:
306.7457
MDL Number:
MFCD04036980
SMILES:
O=C1c2c3[nH]c4c(c3cc[n+]2c2c1cccc2)cccc4.[Cl-]
NSC Number:
622398
Properties
Computed Properties
 
Complexity:
451  
Covalently-Bonded Unit Count:
2  
Heavy Atom Count:
22  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  

Literature

Title: A marine sponge alkaloid derivative 4-chloro fascaplysin inhibits tumor growth and VEGF mediated angiogenesis by disrupting PI3K/Akt/mTOR signaling cascade.

Journal: Chemico-biological interactions 20170925

Title: Chemistry and biology of fascaplysin, a potent marine-derived CDK-4 inhibitor.

Journal: Mini reviews in medicinal chemistry 20120601

Title: Fascaplysin as a specific inhibitor for CDK4: insights from molecular modelling.

Journal: PloS one 20120101

Title: 3-bromohomofascaplysin A, a fascaplysin analogue from a Fijian Didemnum sp. ascidian.

Journal: Bioorganic & medicinal chemistry 20111115

Title: Fascaplysin exert anti-tumor effects through apoptotic and anti-angiogenesis pathways in sarcoma mice model.

Journal: European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences 20110717

Title: Direct effects of fascaplysin on human umbilical vein endothelial cells attributing the anti-angiogenesis activity.

Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie 20101001

Title: Silver catalyzed cascade synthesis of alkaloid ring systems: concise total synthesis of fascaplysin, homofascaplysin C and analogues.

Journal: Chemical communications (Cambridge, England) 20100707

Title: Antimalarial and antitubercular nostocarboline and eudistomin derivatives: synthesis, in vitro and in vivo biological evaluation.

Journal: Bioorganic & medicinal chemistry 20100215

Title: [Anti-proliferation of human cervical cancer HeLa cell line by fascaplysin through apoptosis induction].

Journal: Yao xue xue bao = Acta pharmaceutica Sinica 20090901

Title: Fascaplysin-inspired diindolyls as selective inhibitors of CDK4/cyclin D1.

Journal: Bioorganic & medicinal chemistry 20090815

Title: Recent research in selective cyclin-dependent kinase 4 inhibitors for anti-cancer treatment.

Journal: Current medicinal chemistry 20090101

Title: Design, synthesis and biological evaluation of new tryptamine and tetrahydro-beta-carboline-based selective inhibitors of CDK4.

Journal: Bioorganic & medicinal chemistry 20080815

Title: A systematic interaction map of validated kinase inhibitors with Ser/Thr kinases.

Journal: Proceedings of the National Academy of Sciences of the United States of America 20071218

Title: Fascaplysin, a selective CDK4 inhibitor, exhibit anti-angiogenic activity in vitro and in vivo.

Journal: Cancer chemotherapy and pharmacology 20070301

Title: Synthesis, crystal structure and biological activity of beta-carboline based selective CDK4-cyclin D1 inhibitors.

Journal: Organic & biomolecular chemistry 20061221

Title: Inhibition of cancer cell growth by cyclin dependent kinase 4 inhibitors synthesized based on the structure of fascaplysin.

Journal: Bioorganic chemistry 20061001

Title: Limited redundancy in phosphorylation of retinoblastoma tumor suppressor protein by cyclin-dependent kinases in acute lymphoblastic leukemia.

Journal: The American journal of pathology 20060901

Title: CA224, a non-planar analogue of fascaplysin, inhibits Cdk4 but not Cdk2 and arrests cells at G0/G1 inhibiting pRB phosphorylation.

Journal: Bioorganic & medicinal chemistry letters 20060815

Title: Design, synthesis and biological activity of new CDK4-specific inhibitors, based on fascaplysin.

Journal: Organic & biomolecular chemistry 20060307

Title: A common protein fold topology shared by flavonoid biosynthetic enzymes and therapeutic targets.

Journal: Journal of natural products 20060101

Title: New fascaplysin-based CDK4-specific inhibitors: design, synthesis and biological activity.

Journal: Chemical communications (Cambridge, England) 20040807

Title: Cytotoxic alkaloids from the marine sponge Thorectandra sp.

Journal: Natural product research 20040601

Title: Comparison of fascaplysin and related alkaloids: a study of structures, cytotoxicities, and sources.

Journal: Journal of natural products 20040501

Title: Langerhans cell histiocytosis immunohistochemical expression of fascin, a dendritic cell marker.

Journal: American journal of clinical pathology 20020901

Title: DNA binding properties of the marine sponge pigment fascaplysin.

Journal: Bioorganic & medicinal chemistry 20010401

Title: Inhibition of cyclin-dependent kinase 4 (Cdk4) by fascaplysin, a marine natural product.

Journal: Biochemical and biophysical research communications 20000907

Title: A new bioactive sesterterpene and antiplasmodial alkaloids from the marine sponge hyrtios cf. erecta.

Journal: Journal of natural products 20000601

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Tags:114719-57-2 Molecular Formula|114719-57-2 MDL|114719-57-2 SMILES|114719-57-2 Pyrido[1,2-a:3,4-b']diindol-5-ium, 12,13-dihydro-13-oxo-, chloride