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Synonyms:
UCUF-965
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | UCUF-965 is a positive allosteric modulator of CXCR4. It enhances CXCL12-mediated β-arrestin recruitment and cAMP signaling pathways, thereby activating lymphoblast migration and inducing calcium influx without binding to the orthosteric CXCL12-binding site on CXCR4. In fibroblasts, UCUF-965 reduces levels of miR-15b and miR-29a while increasing miR-146a. Additionally, UCUF-965 promotes angiogenesis and accelerates wound healing in diabetic mice, making it useful for research into diabetic wound healing disorders. |
| In vitro | UCUF-965, within the concentration range of 0.1-10 μM, enhances the recruitment of β-arrestin with an EC50 of 0.02 μM. It functions as a partial agonist of CXCR4-mediated cAMP inhibition in CXCR4-overexpressing CHO cells, with an EC50 of 0.05 μM. UCUF-965, after a 3-hour exposure, induces migration in the human lymphoblastic cell line CEM-CCRF via CXCR4 activation, presenting an EC50 of 0.4 μM. At a concentration of 10 μM, UCUF-965 facilitates CXCR4-mediated calcium influx in the CEM-CCRF cell line. Additionally, a 24-hour treatment with UCUF-965, at 0.1-10 μM, modulates the expression of wound healing-related microRNAs in both diabetic and non-diabetic mouse fibroblasts, decreasing the levels of miR-15b and miR-29a while increasing the level of miR-146a. |
| In vivo | UCUF-965 (10 μM; intradermal injection; single administration) reduces wound healing time in diabetic mice by 36% and enhances angiogenesis. |
| Molecular Weight | 405.52 |
| Formula | C22H23N5OS |
| Cas No. | 2965316-77-0 |
| Smiles | N=1N=C(C=2C=CC=CC2OCC)N3N=C(C=4C=CC(=CC4)N5CCCC5)CSC13 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 µL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 µL Tween 80 and mix well until fully clarified.
3) Add 450 µL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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