Mevociclib (SY-1365)
This product is for research use only, not for human use. We do not sell to patients.
For small sizes, please check our retail website as below: www.invivochem.com
Size | Price | Stock |
---|---|---|
100mg | $1950 | To Be Confirmed |
200mg | $2975 | To Be Confirmed |
500mg | $4600 | To Be Confirmed |
Cat #: V4641 CAS #: 1816989-16-8 Purity ≥ 98%
Description: Mevociclib (formerly SY-1365; SY1365) is a novel, potent, highly selective and covalent/irreversible inhibitor of CDK7 (Cyclin-dependent kinase 7) with anticancer activity.
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- Physicochemical and Storage Information
- Protocol
- Related Biological Data
- Stock Solution Preparation
- Quality Control Documentation
Molecular Weight (MW) | 587.12 |
---|---|
Molecular Formula | C31H35ClN8O2 |
CAS No. | 1816989-16-8 |
Storage | -20℃ for 3 years in powder formr |
-80℃ for 2 years in solvent |
Protocol | In Vitro | Mevociclib has inhibitory effect on CDK7/CycH/MAT1, IC50 is 20 nM. Mevociclib is a highly selective covalent CDK7 inhibitor that induces apoptosis leukemia cells but has no role in non-malignant cells. Mevociclib shows activity in breast, ovarian, colorectal, and lung cancer cells, which exhibit low nM EC50 and rapid induction of apoptosis. |
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In Vivo | Mevociclib (20mg/kg; iv; biw; for 35 days) inhibition of tumor growth in an in vivo model of TNBC. Mevociclib induces unique transcriptional features. |
These protocols are for reference only. InvivoChem does not
independently validate these methods.
Solvent volume to be added | Mass (the weight of a compound) | |||
---|---|---|---|---|
Mother liquor concentration | 1mg | 5mg | 10mg | 20mg |
1mM | 1.7032 mL | 8.5161 mL | 17.0323 mL | 34.0646 mL |
5mM | 0.3406 mL | 1.7032 mL | 3.4065 mL | 6.8129 mL |
10mM | 0.1703 mL | 0.8516 mL | 1.7032 mL | 3.4065 mL |
20mM | 0.0852 mL | 0.4258 mL | 0.8516 mL | 1.7032 mL |
The molarity calculator equation
Mass(g) = Concentration(mol/L) × Volume(L) × Molecular Weight(g/mol)
Mass
=
Concentration
×
Volume
×
Molecular Weight*
The dilution calculator equation
Concentration(start)
×
Volume(start)
=
Concentration(final)
×
Volume(final)
This equation is commonly abbreviated as: C1 V1 = C2 V2
Concentration(start)
C1
×
Volume(start)
V1
=
Concentration(final)
C2
×
Volume(final)
V2
Step One: Enter information below
Dosage mg/kg
Average weight of animals g
Dosing volume per animal µL
Number of animals
Step Two: Enter the in vivo formulation
%DMSO
+
%
+
%Tween 80
+
%ddH2O
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 add
µL
PEG300, mix and clarify, next add
µL
Tween 80,mix and clarify, next add
µL
ddH2O,mix and clarify.
Note:
- (1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
- (2) Be sure to add the solvent(s) in order.