AS-605240
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MedKoo CAT#: 200296

CAS#: 648450-29-7

Description: AS605240 is a selective PI3Kgamma inhibitor, has been proved effective on several inflammatory diseases. Orally administration of AS605240 significantly prevented lung inflammation and reduced collagen deposition. AS605240 also inhibited augmented expression of TNF-alpha and IL-1beta induced by bleomycin instillation. AS605240 may be a useful in treating inflammation diseases. AS605240 may represent a promising novel agent for the future therapy of pulmonary fibrosis.

Chemical Structure

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AS-605240
CAS# 648450-29-7
Product data Instruction

Theoretical Analysis

MedKoo Cat#: 200296
Name: AS-605240
CAS#: 648450-29-7
Chemical Formula: C12H7N3O2S
Exact Mass: 257.03
Molecular Weight: 257.270
Elemental Analysis: C, 56.02; H, 2.74; N, 16.33; O, 12.44; S, 12.46

Price and Availability

Size Price Availability Quantity
50mg USD 400 2 Weeks
100mg USD 650
200mg USD 950 2 Weeks
500mg USD 1850 2 Weeks
1g USD 2950 2 Weeks
2g USD 5450 2 Weeks
Bulk inquiry

Synonym: AS 605240; AS605240; AS-605240.

IUPAC/Chemical Name: (E)-5-(quinoxalin-6-ylmethylene)thiazolidine-2,4-dione

InChi Key: SQWZFLMPDUSYGV-UXBLZVDNSA-N

InChi Code: InChI=1S/C12H7N3O2S/c16-11-10(18-12(17)15-11)6-7-1-2-8-9(5-7)14-4-3-13-8/h1-6H,(H,15,16,17)/b10-6+

SMILES Code: O=C(NC/1=O)SC1=C\C2=CC=C3N=CC=NC3=C2

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: Soluble in DMSO, not in water

Shelf Life: >2 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.9001

More Info:

Product Data:
Product Data
Instruction:
View handling instruction
Biological target: AS-605240 is a specific and orally active inhibitor of the PI3Kγ, with an IC50 of 8 nM, and a Ki of 7.8 nM.
In vitro activity: T-cells were stimulated in the presence of HLA-matched (DR401+) antigen-presenting-cells and a specific GAD65-peptide at different concentrations of the PI3Kγ-inhibitor, AS605240. As shown in Fig 4 proliferation of the T-cell-clone was significantly reduced when cultured in the presence of AS605240, even at low concentrations of the drug suggesting relevance of this pathway in T-cell activation and proliferation in human autoreactive-T-cells. Reference: PLoS One. 2017; 12(1): e0169695. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5231340/
In vivo activity: Treatment with AS605240 at indicated doses (5, 15 and 25 mg/kg) significantly (p < 0.01 and p < 0.001) decreased escape latency compared with the STZ group. The standard donepezil treated group showed similar effects as compared with 25 mg/kg of AS605240 treated group (p < 0.001). Similar effects were observed in the spatial probe test with the platform removed. STZ treated rats had a significantly (p < 0.001) decreased amount of time spent in the target quadrant than the control group rats. However, the amount of time spent in the target quadrant by the rats in the AS605240 treated groups was much longer than that in the STZ group (Figure 3B(Fig. 3), p < 0.01 and p < 0.001), supporting a protective effect on learning and memory. Reference: EXCLI J. 2020; 19: 71–85. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7003642/

Solubility Data

Solvent Max Conc. mg/mL Max Conc. mM
Solubility
DMSO 1.7 6.76
DMF 0.2 0.78

Preparing Stock Solutions

The following data is based on the product molecular weight 257.27 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol: 1. Azzi J, Thueson L, Moore R, Abdoli R, Reijonen H, Abdi R. PI3Kγ Deficient NOD-Mice Are Protected from Diabetes by Restoring the Balance of Regulatory to Effector-T-Cells. PLoS One. 2017 Jan 12;12(1):e0169695. doi: 10.1371/journal.pone.0169695. PMID: 28081180; PMCID: PMC5231340. 2. Silveira AB, Laranjeira AB, Rodrigues GO, Leal PC, Cardoso BA, Barata JT, Yunes RA, Zanchin NI, Brandalise SR, Yunes JA. PI3K inhibition synergizes with glucocorticoids but antagonizes with methotrexate in T-cell acute lymphoblastic leukemia. Oncotarget. 2015 May 30;6(15):13105-18. doi: 10.18632/oncotarget.3524. PMID: 25869207; PMCID: PMC4537002. 3. Alluri R, Ambati SR, Routhu K, Kopalli SR, Koppula S. Phosphoinositide 3-kinase inhibitor AS605240 ameliorates streptozotocin-induced Alzheimer's disease like sporadic dementia in experimental rats. EXCLI J. 2020 Jan 6;19:71-85. doi: 10.17179/excli2019-1997. PMID: 32038117; PMCID: PMC7003642. 4. Shang S, Liu L, Wu X, Fan F, Hu E, Wang L, Ding Y, Zhang Y, Lu X. Inhibition of PI3Kγ by AS605240 Protects tMCAO Mice by Attenuating Pro-Inflammatory Signaling and Cytokine Release in Reactive Astrocytes. Neuroscience. 2019 Sep 1;415:107-120. doi: 10.1016/j.neuroscience.2019.06.001. Epub 2019 Jun 11. PMID: 31195053.
In vitro protocol: 1. Azzi J, Thueson L, Moore R, Abdoli R, Reijonen H, Abdi R. PI3Kγ Deficient NOD-Mice Are Protected from Diabetes by Restoring the Balance of Regulatory to Effector-T-Cells. PLoS One. 2017 Jan 12;12(1):e0169695. doi: 10.1371/journal.pone.0169695. PMID: 28081180; PMCID: PMC5231340. 2. Silveira AB, Laranjeira AB, Rodrigues GO, Leal PC, Cardoso BA, Barata JT, Yunes RA, Zanchin NI, Brandalise SR, Yunes JA. PI3K inhibition synergizes with glucocorticoids but antagonizes with methotrexate in T-cell acute lymphoblastic leukemia. Oncotarget. 2015 May 30;6(15):13105-18. doi: 10.18632/oncotarget.3524. PMID: 25869207; PMCID: PMC4537002.
In vivo protocol: 1. Alluri R, Ambati SR, Routhu K, Kopalli SR, Koppula S. Phosphoinositide 3-kinase inhibitor AS605240 ameliorates streptozotocin-induced Alzheimer's disease like sporadic dementia in experimental rats. EXCLI J. 2020 Jan 6;19:71-85. doi: 10.17179/excli2019-1997. PMID: 32038117; PMCID: PMC7003642. 2. Shang S, Liu L, Wu X, Fan F, Hu E, Wang L, Ding Y, Zhang Y, Lu X. Inhibition of PI3Kγ by AS605240 Protects tMCAO Mice by Attenuating Pro-Inflammatory Signaling and Cytokine Release in Reactive Astrocytes. Neuroscience. 2019 Sep 1;415:107-120. doi: 10.1016/j.neuroscience.2019.06.001. Epub 2019 Jun 11. PMID: 31195053.

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1: Azzi J, Moore RF, Elyaman W, Mounayar M, El Haddad N, Yang S, Jurewicz M, Takakura A, Petrelli A, Fiorina P, Ruckle T, Abdi R. The novel therapeutic effect of phosphoinositide 3-kinase-γ inhibitor AS605240 in autoimmune diabetes. Diabetes. 2012 Jun;61(6):1509-18. doi: 10.2337/db11-0134. Epub 2012 Mar 8. PubMed PMID: 22403300; PubMed Central PMCID: PMC3357271.

2: Song LF, Jiang W, Qing Y, Hu XH, Li Y, Tong QY, Wu XH. [The antagonistic effect of PI3K-gamma inhibitor AS605240 on cardiac hypertrophy and cardiac fibrosis induced by isoproterenol in rats]. Sichuan Da Xue Xue Bao Yi Xue Ban. 2011 Jul;42(4):471-4. Chinese. PubMed PMID: 21866628.

3: Wei X, Han J, Chen ZZ, Qi BW, Wang GC, Ma YH, Zheng H, Luo YF, Wei YQ, Chen LJ. A phosphoinositide 3-kinase-gamma inhibitor, AS605240 prevents bleomycin-induced pulmonary fibrosis in rats. Biochem Biophys Res Commun. 2010 Jun 25;397(2):311-7. doi: 10.1016/j.bbrc.2010.05.109. Epub 2010 May 26. PubMed PMID: 20510675.

4: Jin K, Song LF, He CM, Wang ZL, Hu XH, Wu XH. [Intervention effect of PI3Kgamma inhibitor AS605240 on autoimmune myocarditis in mice]. Sichuan Da Xue Xue Bao Yi Xue Ban. 2009 Sep;40(5):817-20, 825. Chinese. PubMed PMID: 19950590.