8-Chloro-arabinoadenosine

Modify Date: 2024-01-10 15:42:27

8-Chloro-arabinoadenosine Structure
8-Chloro-arabinoadenosine structure
Common Name 8-Chloro-arabinoadenosine
CAS Number 769872-68-6 Molecular Weight N/A
Density N/A Boiling Point N/A
Molecular Formula N/A Melting Point N/A
MSDS N/A Flash Point N/A

 Use of 8-Chloro-arabinoadenosine


8-Chloro-arabinoadenosine is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].

 Names

Name 8-Chloro-arabinoadenosine

 8-Chloro-arabinoadenosine Biological Activity

Description 8-Chloro-arabinoadenosine is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].
Related Catalog
References

[1]. Robak T, Robak P. Purine nucleoside analogs in the treatment of rarer chronic lymphoid leukemias. Curr Pharm Des. 2012;18(23):3373-88.  

 Chemical & Physical Properties

No Any Chemical & Physical Properties
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.
Top Suppliers:I want be here
Related Compounds: More...
8-chloro-7-methoxymethoxy-2,2-dimethyl-10H-[1,3]dioxolo[4,5-b]phenothiazine
61588-52-1
8-chloro-2,3-dimethyl-4-phenyl-3,4-dihydro-1H-[1]benzothiolo[3,2-c]pyridine,hydrochloride
70547-09-0
8-chloro-6-(2-chlorophenyl)-3a,4-dihydro-1-methyl-4H-imidazo[1,5-a][1,4]benzodiazepine
59467-76-4
8-chloro-5-fluoroquinoline
917251-76-4
8-Chloro-3-methoxy-11-(1-methyl-4-piperidinyl)-6,11-dihydro-5H-benzo[5,6]-cyclohepta[1,2-b]pyridin-11-ol
165739-71-9
8-Chloro-2,6,6a,7,8,9,10,10a-octahydro-10-isocyano-6,6,9-trimethyl-9-oxiranylnaphth[1,2,3-cd]indole
106865-65-0
8-Chloro-2'-deoxyguanosine
437715-62-3
8-Chloro-5-isoquinolinesulfonic acid
1246816-17-0
8-chloro-1,7-naphthyridine
13058-77-0
1-{[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-hydroxybutanamido]methyl}cyclohexane-1-carboxylic acid
2172268-04-9
1-benzyl-3-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylbutanamido]pyrrolidine-3-carboxylic acid
2171790-22-8
2-[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-hydroxybutanamido]-1-methylcyclopentane-1-carboxylic acid
2172268-21-0
3-[N-benzyl-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2-methoxypropanamido]propanoic acid
2171950-33-5
4-bromo-1-(oxolan-3-ylmethyl)-1H-imidazole
2171990-59-1
3-{N-benzyl-1-[5-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-1,2-oxazol-3-yl]formamido}propanoic acid
2171887-77-5
rac-2-[(1R,2S)-2-[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)oxolane-3-amido]cyclopentyl]acetic acid
2227976-30-7
1-[(2S)-3-cyclopropyl-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanoyl]-2-ethylpyrrolidine-3-carboxylic acid
2171352-78-4
2-({1-[(3S)-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanoyl]piperidin-4-yl}oxy)acetic acid
2171277-36-2
3-[N-methyl3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)cyclobutaneamido]oxolane-3-carboxylic acid
2171418-02-1