adenosine cyclic phosphate
adenosine, cyclic 3',5'-(hydrogen phosphate)

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  CODE113663 CODE113663
  Product(s):
  60-92-4 cAMP > 99% by HPLC

Name: (4aR,6R,7R,7aS)-6-(6-aminopurin-9-yl)-2-hydroxy-2-oxo-4a,6,7,7a-tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinin-7-ol CAS Number: 60-92-4 3D/inchi Other(deleted CASRN): 11002-78-1 ECHA EINECS - REACH Pre-Reg: 200-492-9 FDA UNII: E0399OZS9N Nikkaji Web: J4.811I Beilstein Number: 0052645 MDL: MFCD00005845 XlogP3-AA: -2.60 (est) Molecular Weight: 329.20960200 Formula: C10 H12 N5 O6 P BioActivity Summary: listing NMR Predictor: Predict (works with chrome, Edge or firefox) Category:cosmetic ingredient for skin conditioning   US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information: Google Scholar: Search Google Books: Search Google Scholar: with word "volatile" Search Google Scholar: with word "flavor" Search Google Scholar: with word "odor" Search Google Patents: Search US Patents: Search EU Patents: Search Pubchem Patents: Search PubMed: Search NCBI: Search   Physical Properties: Assay: 95.00 to 100.00 Food Chemicals Codex Listed: No Melting Point: 219.00 °C. @ 760.00 mm Hg Boiling Point: 701.50 °C. @ 760.00 mm Hg (est) Flash Point: 712.00 °F. TCC ( 378.00 °C. ) (est) Soluble in:   water, 1.364e+005 mg/L @ 25 °C (est)   Organoleptic Properties: Odor and/or flavor descriptions from others (if found).   Cosmetic Information: CosIng: cosmetic data Cosmetic Uses: skin conditioning   Suppliers: Alfa Biotechnology For experimental / research use only. Cyclic AMP 98% BOC Sciences For experimental / research use only. cAMP > 99% by HPLC M.C.Biotec Adenosine Cyclic Phosphate   Safety Information:   Hazards identification   Classification of the substance or mixture GHS Classification in accordance with 29 CFR 1910 (OSHA HCS) None found. GHS Label elements, including precautionary statements   Pictogram   Hazard statement(s) None found. Precautionary statement(s) None found. Oral/Parenteral Toxicity: Not determined Dermal Toxicity: Not determined Inhalation Toxicity: Not determined   Safety in Use Information: Category: cosmetic ingredient for skin conditioning Recommendation for adenosine cyclic phosphate usage levels up to:   not for fragrance use.   Recommendation for adenosine cyclic phosphate flavor usage levels up to:   not for flavor use.   Safety References: EPI System: View ClinicalTrials.gov:search Daily Med:search Chemical Carcinogenesis Research Information System:Search AIDS Citations:Search Cancer Citations:Search Toxicology Citations:Search EPA Substance Registry Services (TSCA):60-92-4 EPA ACToR:Toxicology Data EPA Substance Registry Services (SRS):Registry Laboratory Chemical Safety Summary :6076 National Institute of Allergy and Infectious Diseases:Data (4aR,6R,7R,7aS)-6-(6-aminopurin-9-yl)-2-hydroxy-2-oxo-4a,6,7,7a-tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinin-7-ol Chemidplus:0000060924 RTECS:AU7357600 for cas# 60-92-4   References:   (4aR,6R,7R,7aS)-6-(6-aminopurin-9-yl)-2-hydroxy-2-oxo-4a,6,7,7a-tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinin-7-ol NIST Chemistry WebBook: Search Inchi Pubchem (cid): 6076 Pubchem (sid): 134970712   Other Information: (IUPAC): Atomic Weights of the Elements 2011 (pdf) Videos: The Periodic Table of Videos tgsc: Atomic Weights use for this web site (IUPAC): Periodic Table of the Elements CHEBI: View CHEMBL: View Golm Metabolome Database: Search Metabolomics Database: Search KEGG (GenomeNet): C00575 HMDB (The Human Metabolome Database): HMDB00058 FooDB: FDB001497 YMDB (Yeast Metabolome Database): YMDB00023 Export Tariff Code: 2934.90.5000 VCF-Online: VCF Volatile Compounds in Food ChemSpider: View Wikipedia: View   Potential Blenders and core components note None Found   Potential Uses: None Found   Occurrence (nature, food, other):note   barley seed Search Trop Picture   barley sprout Search Trop Picture   bean field bean Search Trop Picture   carrot Search Trop Picture   Synonyms: (-)- adenosine 3,5-cyclic monophosphate   adenosine 3,5'-cyclic monophosphorate   adenosine 3',5'-(hydrogen phosphate)   adenosine 3',5'-cyclic monophosphate   adenosine 3',5'-cyclic phosphate   adenosine 3',5'-cyclophosphate   adenosine 3',5'-monophosphate cyclic adenosine 3',5'-monophosphate   adenosine 3',5'-phosphate cyclic adenosine 3',5'-phosphate   adenosine 3',5'-phosphate monohydrate   adenosine 3':5'-cyclicmonophosphate   adenosine cyclic 3',5'-(hydrogen phosphate)   adenosine cyclic 3',5'-phosphate   adenosine cyclic monophosphate   adenosine cyclicphosphate 3',5'-cyclic adenosine monophosphate   adenosine-3',5'-cyclicmonophosphate   adenosine-3',5'-cyclophosphate   adenosine, cyclic 3',5'-(hydrogen phosphate)   adenosinecyclicphosphate cyclic 3',5'- adenylate cyclic 3',5'- adenylic acid cyclic adenylic acid (S)-1-C-(7- amino-1H-pyrazolo(4,3-d)pyrimidine-3-yl)-1,4-anhydro-D-ribitol cyclic 3',5'-(hydrogen phosphate) (2R,4aR,6R,7R,7aS)-6-(6- amino-9H-purin-9-yl)tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinine-2,7-diol 2-oxide (4aR,6R,7R,7aS)-6-(6- amino-9H-purin-9-yl)tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinine-2,7-diol 2-oxide 6-(6- amino-9H-purin-9-yl)tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinine-2,7-diol 2-oxide (4aR,6R,7R,7aS)-6-(6- aminopurin-9-yl)-2-hydroxy-2-oxo-4a,6,7,7a-tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinin-7-ol (4aR,6R,7R,7aS)-6-(6- aminopurin-9-yl)-2-oxo-tetrahydro-2-?*5*-furo[3,2-d][1,3,2]dioxaphosphinine-2,7-diol (1S,6R,8R,9R)-8-(6- aminopurin-9-yl)-3,9-dihydroxy-2,4,7-trioxa-3-phosphabicyclo[4.3.0]nonan-3-one 3',5'-cyclic AMP 3'5'-cyclic ester of AMP cyclic 3',5'- AMP cyclic AMP 4H- furo[3,2-d]-1,3,2-dioxaphosphorin-7-ol, 6-(6-amino-9H-purin-9-yl)tetrahydro-2-hydroxy-, 2-oxide, (2R,4aR,6R,7R,7aS)- 4H- furo[3,2-d]-1,3,2-dioxaphosphorin-7-ol, 6-(6-amino-9H-purin-9-yl)tetrahydro-2-hydroxy-, 2-oxide, (4aR,6R,7R,7aS)- cyclic-3',5'-( hydrogen phosphate)adenosine   Articles:   None found yet. 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Notes: an adenine nucleotide containing one phosphate group which is esterified to both the 3'- and 5'-positions of the sugar moiety. it is a second messenger and a key intracellular regulator, functioning as a mediator of activity for a number of hormones, including epinephrine, glucagon, and acth. Cyclic adenosine monophosphate (cAMP) is a second messenger important in many biological processes. cAMP is derived from adenosine triphosphate (ATP) and used for intracellular signal transduction in many different organisms, conveying the cAMP-dependent pathway. (Wikipedia)