Sigma A6730 - Small Molecule (ID:10035-109)
HMS LINCS ID: | 10035-109 |
Name: | Sigma A6730 |
Alternative Names: | KIN001-102; AKT inhibitor VIII; Akt1/2 kinase inhibitor |
LINCS ID: | LSM-1035 |
PubChem CID: | 10196499 |
ChEBI ID: | |
ChEMBL ID: | 258844 |
Molecular Mass: | 551.24 |
InChi: | InChI=1S/C34H29N7O/c42-34-39-26-8-4-5-9-31(26)41(34)25-14-16-40(17-15-25)20-22-10-12-24(13-11-22)33-32(23-6-2-1-3-7-23)37-29-18-27-28(36-21-35-27)19-30(29)38-33/h1-13,18-19,21,25H,14-17,20H2,(H,35,36)(H,39,42) |
InChi Key: | BIWGYFZAEWGBAL-UHFFFAOYSA-N |
SMILES: | C1CN(CCC1N2C3=CC=CC=C3NC2=O)CC4=CC=C(C=C4)C5=NC6=CC7=C(C=C6N=C5C8=CC=CC=C8)N=CN7 |
Relevant Citations: | |
Comments: | |
Date Publicly Available: | |
Most Recent Update: | 2016-04-04 |
Target Affinity:
(see Study 20000)Target Affinity Spectrum Value | HUGO Gene Name |
---|---|
AKT1 | |
2 (equivalent to 100 nM ≤ Kd < 1µM) | AKT2, CAMK1, MYLK |
3 (equivalent to 1µM ≤ Kd < 10 µM) | AKT3 |
10 (confirmed non-binding) |
Batch Information for HMSL10035-109-2:
HMS LINCS Batch ID: | 10035-109-2 |
Provider: | Sigma-Aldrich |
Provider Batch ID: | |
Salt: | 109 |
Molecular Formula: | C34H29N7O.xC2HF3O2.yH2O |
Molecular Weight: | |
Purity: | |
Purification Method: | |
Chemical Synthesis Reference: | |
Comments: | |
Date Publicly Available: | 2012-11-14 |
Most Recent Update: | 2016-12-02 |
(Kd <100 nM)