Determine the necessary mass, volume, or concentration for preparing a solution.
Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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C127044-10mg | 10mg | Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience! | $53.90 | |
C127044-50mg | 50mg | In stock | $107.90 | |
C127044-100mg | 100mg | In stock | $194.90 | |
C127044-250mg | 250mg | In stock | $437.90 | |
C127044-500mg | 500mg | Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience! | $787.90 |
Synonyms | Idelalisib | 870281-82-6 | CAL-101 | Zydelig | GS-1101 | CAL101 | CAL 101 | (S)-2-(1-((9H-Purin-6-yl)amino)propyl)-5-fluoro-3-phenylquinazolin-4(3H)-one | 1146702-54-6 | Idelalisib (CAL-101) | UNII-YG57I8T5M0 | CAL-101 (Idelalisib, GS-1101) | GS 1101 | YG57I8T5M0 | CHEBI:82701 | 5-Flu |
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Specifications & Purity | Moligand™, ≥99% |
Biochemical and Physiological Mechanisms | CAL-101 (GS-1101) is a potent and selective PI3K p110δ inhibitor with an IC50 of 2.5 nM. This compound induces selective cytotoxicity in CLL cells and is independent of IgVH mutational status. CAL--101 also acts as an antagonist in CD40L-mediated CLL cell |
Storage Temp | Store at -20°C |
Shipped In | Ice chest + Ice pads |
Grade | Moligand™ |
Action Type | INHIBITOR |
Mechanism of action | PI3-kinase p110-delta subunit inhibitor |
Note | 10mg卖完停产,不再备货 |
Product Description | CAL-101 (Idelalisib, GS-1101) is a selective p110δ inhibitor with IC50 of 2.5 nM; shown to have 40- to 300-fold greater selectivity for p110δ thanp110α/β/γ, and 400- to 4000-fold more selectivity to p110δ than C2β, hVPS34, DNA-PK and mTOR. |
ALogP | 3.7 |
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IUPAC Name | 5-fluoro-3-phenyl-2-[(1S)-1-(7H-purin-6-ylamino)propyl]quinazolin-4-one |
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INCHI | InChI=1S/C22H18FN7O/c1-2-15(28-20-18-19(25-11-24-18)26-12-27-20)21-29-16-10-6-9-14(23)17(16)22(31)30(21)13-7-4-3-5-8-13/h3-12,15H,2H2,1H3,(H2,24,25,26,27,28)/t15-/m0/s1 |
InChi Key | IFSDAJWBUCMOAH-HNNXBMFYSA-N |
Canonical SMILES | CCC(C1=NC2=C(C(=CC=C2)F)C(=O)N1C3=CC=CC=C3)NC4=NC=NC5=C4NC=N5 |
Isomeric SMILES | CC[C@@H](C1=NC2=C(C(=CC=C2)F)C(=O)N1C3=CC=CC=C3)NC4=NC=NC5=C4NC=N5 |
PubChem CID | 11625818 |
Molecular Weight | 415.43 |
PubChem CID | 11625818 |
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CAS Registry No. | 870281-82-6 |
ChEMBL Ligand | CHEMBL2216870 |
Wikipedia | Idelalisib |
RCSB PDB Ligand | 40L |
PEP | idelalisib |
DrugCentral Ligand | 4878 |
Enter Lot Number to search for COA:
To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section
Lot Number | Certificate Type | Date | Item |
---|---|---|---|
B1525011 | Certificate of Analysis | Jun 05, 2024 | C127044 |
G2203126 | Certificate of Analysis | Apr 07, 2024 | C127044 |
G2203129 | Certificate of Analysis | Apr 07, 2024 | C127044 |
G2203137 | Certificate of Analysis | Apr 07, 2024 | C127044 |
G2203143 | Certificate of Analysis | Apr 07, 2024 | C127044 |
Solubility | DMSO 83 mg/mL Water <1 mg/mL Ethanol 35 mg/mL |
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Pictogram(s) | GHS08 |
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Signal | Danger |
Hazard Statements | H372:Causes damage to organs through prolonged or repeated exposure H360:May damage fertility or the unborn child |
Precautionary Statements | P280:Wear protective gloves/protective clothing/eye protection/face protection. P405:Store locked up. P501:Dispose of contents/container to ... P264:Wash hands [and …] thoroughly after handling. P260:Do not breathe dust/fume/gas/mist/vapors/spray. P270:Do not eat, drink or smoke when using this product. P203:Obtain, read and follow all safety instructions before use. P318:if exposed or concerned, get medical advice. P319:Get medical help if you feel unwell. |
1. Furman RR, Sharman JP, Coutre SE, Cheson BD, Pagel JM, Hillmen P, Barrientos JC, Zelenetz AD, Kipps TJ, Flinn I et al.. (2014) Idelalisib and rituximab in relapsed chronic lymphocytic leukemia.. N Engl J Med, 370 (11): (997-1007). [PMID:24450857] |
2. Lin S, Jin J, Liu Y, Tian H, Zhang Y, Fu R, Zhang J, Wang M, Du T, Ji M et al.. (2019) Discovery of 4-Methylquinazoline Based PI3K Inhibitors for the Potential Treatment of Idiopathic Pulmonary Fibrosis.. J Med Chem, 62 (19): (8873-8879). [PMID:31335136] |