SGC707
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 |
|---|---|---|
| 500mg | $1250 | Check With Us |
| 1g | $1850 | Check With Us |
| 5g | $4680 | Check With Us |
: Cat #: V0383 CAS #: 1687736-54-4 Purity ≥ 98%
Description: SGC707 (SGC-707) is a novel, cell-permeable and allosteric PRMT3 inhibitor (protein arginine methyltransferase 3 inhibitor) with potential anticancer activity.
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- Physicochemical and Storage Information
- Protocol
- Related Biological Data
- Stock Solution Preparation
- Quality Control Documentation
| Molecular Weight (MW) | 298.34 |
|---|---|
| Molecular Formula | C16H18N4O2 |
| CAS No. | 1687736-54-4 |
| Storage | -20℃ for 3 years in powder formr |
| -80℃ for 2 years in solvent | |
| Solubility In Vitro | DMSO: 59 mg/mL (197.7 mM)r |
| Water: <1 mg/mLr | |
| Ethanol: 59 mg/mL (197.7 mM) | |
| SMILES Code | O=C(NCC(N1CCCC1)=O)NC2=CC3=C(C=NC=C3)C=C2 |
| Synonyms | SGC707; SGC 707; SGC-707 |
| Protocol | In Vitro | SGC707 (0-10 μM; 6 h) binds to PRMT3 in both HEK293 and A549 cells. |
|---|---|---|
| In Vivo | SGC707 (intraperitoneal injection; 10 mg/kg; 3 times per week; 3 w) treatment reduces hepatic steatosis and plasma triglyceride levels and induces pruritus in Western-type diet-fed LDL receptor knockout mice. |
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 | 3.3519 mL | 16.7594 mL | 33.5188 mL | 67.0376 mL |
| 5mM | 0.6704 mL | 3.3519 mL | 6.7038 mL | 13.4075 mL |
| 10mM | 0.3352 mL | 1.6759 mL | 3.3519 mL | 6.7038 mL |
| 20mM | 0.1676 mL | 0.8380 mL | 1.6759 mL | 3.3519 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.