ABT 702 Dihydrochloride
- CAS No.
- 1188890-28-9
- Chemical Name:
- ABT 702 Dihydrochloride
- Synonyms
- CS-2726;ABT702 hcl;ABT-702;ABT702;ABT 702;ABT-702 dihydrochloride, 10 mM in DMSO;5-(3-Bromophenyl)-7-(6-morpholinopyridin-3-yl)pyrido[2,3-d]pyrimidin-4-amine dihydrochloride;Pyrido[2,3-d]pyrimidin-4-amine, 5-(3-bromophenyl)-7-[6-(4-morpholinyl)-3-pyridinyl]-, hydrochloride (1:2);ABT702 dihydrochloride,ABT702,ADK,Inhibitor,inhibit,ABT 702,ABT-702,Adenosine Kinase,ABT 702 dihydrochloride
- CBNumber:
- CB83354238
- Molecular Formula:
- C22H19N6OBr.2HCl
- Molecular Weight:
- 0
- MDL Number:
- MOL File:
- Mol file
SAFETY
Risk and Safety Statements
Symbol(GHS) | ![]() GHS07 |
---|---|
Signal word | Warning |
Hazard statements | H302-H315-H319-H335 |
Precautionary statements | P261-P305+P351+P338 |
ABT 702 Dihydrochloride price More Price(21)
Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
---|---|---|---|---|---|---|---|
TRC | A112435 | ABT702Dihydrochloride | 1188890-28-9 | 10mg | $280 | 2021-12-16 | Buy |
AK Scientific | 9463CW | AdenosineKinaseInhibitor | 1188890-28-9 | 100mg | $460 | 2021-12-16 | Buy |
ChemScene | CS-0025018 | ABT-702dihydrochloride 96.36% | 1188890-28-9 | 5mg | $150 | 2021-12-16 | Buy |
ChemScene | CS-0025018 | ABT-702dihydrochloride 96.36% | 1188890-28-9 | 50mg | $750 | 2021-12-16 | Buy |
ChemScene | CS-0025018 | ABT-702dihydrochloride 96.36% | 1188890-28-9 | 100mg | $1100 | 2021-12-16 | Buy |
ABT 702 Dihydrochloride Chemical Properties,Uses,Production
Biological Activity
adenosine (ado) is an endogenous homeostatic inhibitory neuromodulator that reduces cellular excitability at sites of tissue injury and inflammation. inhibition of adenosine kinase (ak), the primary metabolic enzyme for ado, selectively increases ado concentrations at sites of tissue trauma and enhances the analgesic and antiinflammatory actions of ado. abt 702 is a novel, potent nonnucleoside ak inhibitor.
in vitro
abt 702 was active both in inhibiting ak (ic50 ) 1.7 nm) and ado phosphorylation in the intact cells (ic50 ) 50 nm). abt 702 was also highly selective for ak inhibition as compared to other sites of ado action including ada, ado receptors, and ado transport sites [1].
in vivo
abt 702 had dose-dependent antinociceptive and antiinflammatory actions in a variety of animal models of nociceptive, inflammatory, and neuropathic pain. abt 702 is the first of a novel class of potent, selective, non-nucleoside, orally active ak inhibitors that have potent antinociceptive effects in animal models [1].
IC 50
1.7 nm for adenosine kinase
References
[1] lee ch, jiang m, cowart m, gfesser g, perner r, kim kh, gu yg, williams m, jarvis mf, kowaluk ea, stewart ao, bhagwat ss. discovery of 4-amino-5-(3-bromophenyl)-7-(6-morpholino-pyridin-3-yl)pyrido[2,3-d]pyrimidine, an orally active, non-nucleoside adenosine kinase inhibitor.. j med chem. 2001 jun 21;44(13):2133-8.
ABT 702 Dihydrochloride Preparation Products And Raw materials
Raw materials
Preparation Products
Supplier | Tel | Country | ProdList | Advantage | |
---|---|---|---|---|---|
ATK CHEMICAL COMPANY LIMITED | +undefined-21-51877795 | ivan@atkchemical.com | China | 32965 | 60 |
BOC Sciences | +1-631-485-4226 | inquiry@bocsci.com | United States | 19553 | 58 |
HANGZHOU CLAP TECHNOLOGY CO.,LTD | 86-571-88216897,88216896 13588875226 | sales@hzclap.com | CHINA | 6312 | 58 |
InvivoChem | +1-708-310-1919 +1-13798911105 | sales@invivochem.cn | United States | 6391 | 58 |
TargetMol Chemicals Inc. | support@targetmol.com | United States | 38631 | 58 | |
Wuhan Topule Biopharmaceutical Co., Ltd | +8618327326525 | masar@topule.com | China | 8467 | 58 |
Aladdin Scientific | +1-+1(833)-552-7181 | sales@aladdinsci.com | United States | 57505 | 58 |
Shanghai Boyle Chemical Co., Ltd. | sales@boylechem.com | China | 2922 | 55 | |
Dalian Meilun Biotech Co., Ltd. | 0411-62910999 13889544652 | sales@meilune.com | China | 4727 | 58 |
Shanghai Lollane Biological Technology Co.,Ltd. | 021-52996696,15000506266 15000506266 | China | 4571 | 55 |
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