M2698
- Product Name
- M2698
- CAS No.
- 1379545-95-5
- Chemical Name
- M2698
- Synonyms
- M2698;M2698, 10 mM in DMSO;M2698 (MSC-2363318A);M2698; M-2698; M 2698; MSC-2363318A; MSC 2363318A; MSC2363318A;(S)-4-(2-(azetidin-1-yl)-1-(4-chloro-3-(trifluoromethyl)phenyl)ethylamino)quinazoline-8-carboxamide;4-{[(1S)-2-(azetidin-1-yl)-1-[4-chloro-3-(trifluoromethyl)phenyl]ethyl]amino}quinazoline-8-carboxamide;8-Quinazolinecarboxamide, 4-[[(1S)-2-(1-azetidinyl)-1-[4-chloro-3-(trifluoromethyl)phenyl]ethyl]amino]-;4-[(S)-2-azetidin-1-yl-1-(4-chloro-3-trifluoromethylphenyl)ethylamino]quinazoline-8-carboxylic acid amide
- CBNumber
- CB23152911
- Molecular Formula
- C21H19ClF3N5O
- Formula Weight
- 449.86
- MOL File
- 1379545-95-5.mol
M2698 Property
- solubility
- DMSO: soluble
- form
- A solid
- color
- White to off-white
- InChIKey
- HXAUJHZZPCBFPN-QGZVFWFLSA-N
- SMILES
- N1=C2C(C=CC=C2C(N)=O)=C(N[C@@H](C2=CC=C(Cl)C(C(F)(F)F)=C2)CN2CCC2)N=C1
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- CS-0019628
- Product name
- M2698
- Purity
- 99.74%
- Packaging
- 5mg
- Price
- $650
- Updated
- 2021/12/16
- Product number
- DC10751
- Product name
- M2698(MSC-2363318A)
- Purity
- >98%
- Packaging
- 100mg
- Price
- $750
- Updated
- 2021/12/16
- Product number
- DC10751
- Product name
- M2698(MSC-2363318A)
- Purity
- >98%
- Packaging
- 250mg
- Price
- $1300
- Updated
- 2021/12/16
M2698 Chemical Properties,Usage,Production
Uses
M2698 (MSC2363318A) is an orally active, ATP competitive, selective p70S6K and Akt dual-inhibitor with IC50s of 1 nM for p70S6K, Akt1 and Akt3. M2698 can cross the blood-brain barrier and has anti-cancer activity[1].
in vivo
M2698 (10-30 mg/kg/day; PO; 28 days) results in dose-dependent inhibition of tumor growth and results in tumor regression with the highest dose of 30 mg/kg[1].
?
M2698 (20 mg/kg/day; PO; 4 days) has a tumor:plasma exposure ratio of 12:1 over 24 hours and leads to increased levels of pAkt in tumor tissue[1].
?
The mean total concentration of M2698 after 16-hour infusion in rats is 1750 ng/g and 175 ng/mL in brain and plasma, respectively[1].
?
M2698 (po; 1, 5, 10, or 20 mg/kg/day; for 7 days) inhibits the phosphorylation of S6 in a dose-proportional manner over time after a single administration or daily treatments over 7 days[1].
| Animal Model: | Female nude mice bearing MDA-MB-468 tumors[1] |
| Dosage: | 10, 20 and 30 mg/kg |
| Administration: | PO; daily; for 28 days |
| Result: | Resulted in dose-dependent inhibition of tumor growth and resulted in tumor regression with the highest dose of 30 mg/kg. |
| Animal Model: | Female SCID Beige mice with MDA-MB-453 xenografted[1] |
| Dosage: | 20 mg/kg (Pharmacokinetic Analysis) |
| Administration: | Daily; for 4 days |
| Result: | Had a tumor:plasma exposure ratio of 12:1 over 24 hours. |
IC 50
p70S6K: 1 nM (IC50); Akt1: 1 nM (IC50); Akt3: 1 nM (IC50)
References
[1] Machl A, et al. M2698 is a potent dual-inhibitor of p70S6K and Akt that affects tumor growth in mouse models of cancer and crosses the blood-brain barrier. Am J Cancer Res. 2016 Mar 15;6(4):806-18. PMID:27186432
M2698 Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from M2698 manufacturers
- Product
- M2698 1379545-95-5
- Price
- US $1.00/KG
- Min. Order
- 1KG
- Purity
- 97%-99.9%
- Supply Ability
- 100kg
- Release date
- 2019-12-25