UK-371804
This product is for research use only, not for human use. We do not sell to patients.
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Size | Price | Stock |
---|---|---|
250mg | $1150 | Check With Us |
500mg | $1725 | Check With Us |
1g | $2585 | Check With Us |
Cat #: V3165 CAS #: 256477-09-5 Purity ≥ 98%
Description: UK-371804 is a potent and selective inhibitor of urokinase-type plasmogen activator (uPA) with excellent potency (Ki=10 nM in an enzyme assay) and selectivity profile (4000-fold versus tPA and 2700-fold versus plasmin).
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Molecular Weight (MW) | 385.82 |
---|---|
Molecular Formula | C14H16ClN5O4S |
CAS No. | 256477-09-5 |
Storage | -20℃ for 3 years in powder formr |
-80℃ for 2 years in solvent | |
Solubility In Vitro | DMSO: 42 mg/mL (99.5 mM)r |
Water: <1 mg/mLr | |
Ethanol: <1 mg/mL | |
SMILES Code | CC(C)(NS(=O)(C1=CC2=C(C=C1)C(Cl)=CN=C2/N=C(N)N)=O)C(O)=O |
Synonyms | UK371804; UK-371804; UK 371804; UK-371,804; UK 371,804; UK371,804. |
Protocol | In Vitro | UK-371804 is able to inhibit exogenous uPA in human chronic wound fluid (IC50=0.89 μM). UK-371804 has its excellent enzyme potency (Ki=10 nM) and selectivity profile (4000-fold versus tPA and 2700-fold versus plasmin). |
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In Vivo | In a porcine acute excisional wound model, following topical delivery, UK-371804 is able to penetrate into pig wounds and inhibit exogenous uPA activity with no adverse effect on wound healing parameters. Concentrations of UK-371804 in the dermis are 41.8 μM. |
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 | 2.5919 mL | 12.9594 mL | 25.9188 mL | 51.8376 mL |
5mM | 0.5184 mL | 2.5919 mL | 5.1838 mL | 10.3675 mL |
10mM | 0.2592 mL | 1.2959 mL | 2.5919 mL | 5.1838 mL |
20mM | 0.1296 mL | 0.6480 mL | 1.2959 mL | 2.5919 mL |
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Step Two: Enter the in vivo formulation
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Method for preparing DMSO master liquid:
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,Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation:
Take
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PEG300, mix and clarify, next add
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Tween 80,mix and clarify, next add
µL
ddH2O,mix and clarify.
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