research use only
Cat.No.S9610
| Related Targets | Bcl-2 Caspase Ferroptosis p53 Apoptosis related Synthetic Lethality STAT TNF-alpha Ras KRas |
|---|---|
| Other PD-1/PD-L1 Inhibitors | AUNP-12 BMS-202 BMS-1 PD-1/PD-L1 Inhibitor 3 BMS-1166 INCB086550 SR 0987 CA-170 (AUPM-170) Sanguisorbae Radix Extract GS-4224 |
| Molecular Weight | 594.65 | Formula | C35H34N2O7 |
Storage (From the date of receipt) | 3 years -20°C powder |
|---|---|---|---|---|---|
| CAS No. | 2113650-03-4 | -- | Storage of Stock Solutions |
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| Synonyms | N/A | Smiles | CC1=CC(=C(C=C1OCC2=C(C(=CC=C2)C3=CC4=C(C=C3)OCCO4)C)OCC5=CC(=CC=C5)C#N)CNC(CO)C(=O)O | ||
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In vitro |
DMSO
: 50 mg/mL
(84.08 mM)
Water : Insoluble Ethanol : Insoluble |
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In vivo |
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Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)
Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)
Calculation results:
Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )
Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.
Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such as vortex, ultrasound or hot water bath can be used to aid dissolving.
| Targets/IC50/Ki |
PD-1/PD-L1
(Cell-free assay) 253 nM(EC50)
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| In vitro |
BMS-1001 alleviates the inhibitory effect of the soluble PD-L1 on the T-cell receptor-mediated activation of T-lymphocytes. This compound is effective in attenuating the inhibitory effect of the cell surface-associated PD-L1. |
References |
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