HUHS-015
CAS No. 1453097-13-6
HUHS-015( HUHS015 )
Catalog No. M11950 CAS No. 1453097-13-6
HUHS-015 (HUHS015) is a potent, orally active prostate cancer antigen-1 (PCA-1/ALKBH3) inhibitor with IC50 of 0.67 uM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 60 | In Stock |
|
| 2MG | 36 | In Stock |
|
| 5MG | 58 | In Stock |
|
| 10MG | 83 | In Stock |
|
| 25MG | 147 | In Stock |
|
| 50MG | 243 | In Stock |
|
| 100MG | 411 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameHUHS-015
-
NoteResearch use only, not for human use.
-
Brief DescriptionHUHS-015 (HUHS015) is a potent, orally active prostate cancer antigen-1 (PCA-1/ALKBH3) inhibitor with IC50 of 0.67 uM.
-
DescriptionHUHS-015 (HUHS015) is a potent, orally active prostate cancer antigen-1 (PCA-1/ALKBH3) inhibitor with IC50 of 0.67 uM; significantly suppresses the growth of DU145 cells in vitro and in a mouse xenograft model.
-
In VitroHUHS015 significantly suppresses the growth of DU145 cells, which are human hormone-independent prostate cancer cells.
-
In VivoHUHS015 potently suppresses the growth of DU145 cells in a mouse xenograft model.HUHS015 displays 7.2% bioavailability (BA) in rats after oral administration. Animal Model:Nude miceDosage:32 mg/kg Administration:Subcutaneous injection; daily; 6 days Result:Has inhibitory effect on the growth of subcutaneously implanted DU145, without limiting weight gains after a 6 days continuous administration.
-
SynonymsHUHS015
-
PathwayCell Cycle/DNA Damage
-
TargetDNA Repair Protein
-
RecptorPCA-1/ALKBH3inhibitor
-
Research AreaCancer
-
Indication——
Chemical Information
-
CAS Number1453097-13-6
-
Formula Weight318.3724
-
Molecular FormulaC19H18N4O
-
Purity>98% (HPLC)
-
SolubilityDMSO: ≥ 34 mg/mL
-
SMILESOC1=C(CC2=CC=CC=C2)C(C)=NN1C3=NC4=CC(C)=CC=C4N3
-
Chemical Name1H-Pyrazol-5-ol, 3-methyl-1-(6-methyl-1H-benzimidazol-2-yl)-4-(phenylmethyl)-
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Nakao S, et al. Bioorg Med Chem Lett. 2014 Feb 15;24(4):1071-4.
2. Mabuchi M, et al. In Vivo. 2015 Jan-Feb;29(1):39-43.
molnova catalog
related products
-
RAD51-IN-17
RAD51-IN-17 is a quinazolinone derivative that inhibts homologous recombinase RAD51, effectively inhibits both RAD51 foci formation in response to DNA damage, and proliferation of TNBC cell lines.
-
IBR2
IBR2 is a novel small molecule RAD51 inhibitor that specifically binds to RAD51 and disrupts the BRC repeats of BRCA2/RAD51 interaction with IC50 of 0.11 uM.
-
ML216
ML216 (CID49852229) is a potent, selective inhibitor of DNA unwinding activity of BLM (Bloom's syndrome protein) with IC50 of 2.98 and 0.97 uM for full length BLM and BLM636-1298, respectively.
Cart
sales@molnova.com