5'-[[(3S)-3-AMINO-3-CARBOXYPROPYL]METHYLSULFONIO]-5'-DEOXY-ADENOSINE IODIDE
![5'-[[(3S)-3-AMINO-3-CARBOXYPROPYL]METHYLSULFONIO]-5'-DEOXY-ADENOSINE IODIDE Structure](https://www.chemsrc.com/caspic/439/3493-13-8.png)
5'-[[(3S)-3-AMINO-3-CARBOXYPROPYL]METHYLSULFONIO]-5'-DEOXY-ADENOSINE IODIDE structure
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Common Name | 5'-[[(3S)-3-AMINO-3-CARBOXYPROPYL]METHYLSULFONIO]-5'-DEOXY-ADENOSINE IODIDE | ||
|---|---|---|---|---|
| CAS Number | 3493-13-8 | Molecular Weight | 526.35000 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C15H23IN6O5S | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | N/A | |
| Symbol |
GHS07 |
Signal Word | Warning | |
Use of 5'-[[(3S)-3-AMINO-3-CARBOXYPROPYL]METHYLSULFONIO]-5'-DEOXY-ADENOSINE IODIDES-(5'-Adenosyl)-L-methionine iodide (S-Adenosyl-L-methionine iodide) is an important methyl donor that is found in all living organisms[1]. |
| Name | s-adenosyl-l-methionine iodide salt |
|---|---|
| Synonym | More Synonyms |
| Description | S-(5'-Adenosyl)-L-methionine iodide (S-Adenosyl-L-methionine iodide) is an important methyl donor that is found in all living organisms[1]. |
|---|---|
| Related Catalog | |
| In Vitro | By donating the methyl group, sues that involves perchloric acid extraction has beenSAM is converted into S-adenosyl-L-homocysteine reported by She et al. Separation of SAM and (SAH)[1]. |
| References |
| Molecular Formula | C15H23IN6O5S |
|---|---|
| Molecular Weight | 526.35000 |
| Exact Mass | 526.05000 |
| PSA | 207.93000 |
| Storage condition | −20°C |
| Water Solubility | H2O: 100 mg/mL |
| Symbol |
GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H317 |
| Precautionary Statements | P280 |
| Personal Protective Equipment | Eyeshields;Faceshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
| Hazard Codes | Xi |
| Risk Phrases | 36/37/38 |
| Safety Phrases | 22-24/25 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
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5'-[[(3S)-3-AMI... CAS#:3493-13-8 |
| Literature: Phytochemistry (Elsevier), , vol. 24, # 6 p. 1151 - 1156 |
| Precursor 2 | |
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| DownStream 0 | |
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In vitro and in vivo biotransformation of WMS-1410, a potent GluN2B selective NMDA receptor antagonist.
J. Pharm. Biomed. Anal. 94 , 36-44, (2014) Structural modification of the GluN2B selective NMDA receptor antagonist ifenprodil led to the 3-benzazepine WMS-1410 with similar GluN2B affinity but higher receptor selectivity. Herein the in vitro ... |
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Structure and reaction mechanism of phosphoethanolamine methyltransferase from the malaria parasite Plasmodium falciparum: an antiparasitic drug target.
J. Biol. Chem. 287 , 1426-1434, (2012) In the malarial parasite Plasmodium falciparum, a multifunctional phosphoethanolamine methyltransferase (PfPMT) catalyzes the methylation of phosphoethanolamine (pEA) to phosphocholine for membrane bi... |
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DNA methyltransferases: mechanistic models derived from kinetic analysis.
Crit. Rev. Biochem. Mol. Biol. 47(2) , 97-193, (2012) The sequence-specific transfer of methyl groups from donor S-adenosyl-L-methionine (AdoMet) to certain positions of DNA-adenine or -cytosine residues by DNA methyltransferases (MTases) is a major form... |
| EINECS 222-486-5 |
| SAM iodide salt |
| S-(5'-ADENOSYL)-L-METHIONINE IODIDE |
| S-ADENOSYL METHIONINE IODIDE SALT |
| adomet |
| MFCD00043192 |
| S-(5'-deoxy-5'-adenosyl)methionine iodide |
| S-adenosylmethionine |
| SAM-E IODIDE SALT |
| AdoMet,SAM |
| S-adenosyl-L-methionine iodide |
| S-ADENOSYLMETHIONINE IODIDE |
| S-adenosylmethione |