CRT0066101
- Product Name
- CRT0066101
- CAS No.
- 1883545-60-5
- Chemical Name
- CRT0066101
- Synonyms
- CS-2578;CRT0066101 hcl;CRT0066101 2HCL;CRT0066101 (CRT-0066101;CRT0066101 dihydrochloride;2-[4-[[(2R)-2-aminobutyl]amino]-2-pyrimidinyl]-4-(1-methyl-1H-pyrazol-4-yl)phenol dihydrochloride;Inhibitor,CRT-0066101 dihydrochloride,CRT0066101,CRT0066101 dihydrochloride,Protein kinase D,CRT-0066101,CRT 0066101,PKD,inhibit
- CBNumber
- CB63164875
- Molecular Formula
- C18H23ClN6O
- Formula Weight
- 374.87
- MOL File
- 1883545-60-5.mol
CRT0066101 Property
- storage temp.
- Store at -20°C
- solubility
- insoluble in H2O; ≥15.65 mg/mL in DMSO; ≥4.49 mg/mL in EtOH with ultrasonic
- form
- solid
- color
- Off-white to light yellow
N-Bromosuccinimide Price
- Product number
- C782018
- Product name
- CRT0066101
- Packaging
- 5mg
- Price
- $280
- Updated
- 2021/12/16
- Product number
- A8679
- Product name
- CRT0066101
- Packaging
- 10mg
- Price
- $150
- Updated
- 2021/12/16
- Product number
- A8679
- Product name
- CRT0066101
- Packaging
- 10mM(in 1mL DMSO)
- Price
- $180
- Updated
- 2021/12/16
- Product number
- A8679
- Product name
- CRT0066101
- Packaging
- 100mg
- Price
- $1800
- Updated
- 2021/12/16
- Product number
- DC20928
- Product name
- CRT0066101
- Purity
- >98%
- Packaging
- 1g
- Price
- $2500
- Updated
- 2021/12/16
CRT0066101 Chemical Properties,Usage,Production
Biological Activity
crt 0066101 is a specific inhibitor of all pkd isoforms. increasingly studies reveals that pkd family members play an important role in regulating several cellular processes and activities, including chromatin organization, golgi function, gene expression, cell survival, adhesion, motility, differentiation, dna synthesis and proliferation. by suppressing pkd, crt 0066101 is supposed to ameliorate symptoms of pancreatic cancer. [1]
in vitro
in panc-1 cell line based assays, crt0066101 was reported to reduce bromodeoxyuridine incorporation; increase cell apoptosis; suppress neurotensin-induced pkd1/2 activation; block neurotensin-induced hsp27 phosphorylation; interrupt pkd1-mediated nf-κb activation as well as down-regulate expression of nf-κb-dependent proliferative and pro-survival proteins. [1]
in vivo
in panc-1 subcutaneous xenograft model, orally administration of crt0066101 at the dosage of 80 mg/kg/d for 24 days significantly suppressed pancreatic cancer growth. moreover, when crt0066101 reached its peak concentration (12 μmol/l) in tumor model, the expression of activated pkd1/2 in the treated tumor explants was substantially decreased. it was concluded that crt0066101 given orally at 80 mg/kg/d for 21 days in panc-1 orthotropic model suppressed tumor growth potently in vivo. [1]
target
| Target | Value |
| PKD1 (Cell-free assay) | 1 nM |
| PKD3 (Cell-free assay) | 2 nM |
| 2.5 nM |
IC 50
a potent protein kinase d (pkd) antagonist with the ic50 of 1, 2.5 and 2 nm for pkd1, pkd2, pkd3 respectively.
storage
Store at -20°C
References
[1]harikumar kb, kunnumakkara1 ab, ochi n, tong z, deorukhkar a, sung b, kelland l, jamieson s, sutherland r, raynham t, charles m, bagherzadeh a, foxton c, boakes a, farooq m, maru d, diagaradjane p, matsuo y, smith j, gelovani j, krishnan s, aggarwal bb, rozengurt e, ireson cr, and guha s. a novel small-molecule inhibitor of protein kinase d blocks pancreatic cancer growth in vitro and in vivo. mol cancer ther. 2010 may. 9(5): 113646.
CRT0066101 Preparation Products And Raw materials
Raw materials
Preparation Products
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