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Details

Stereochemistry ABSOLUTE
Molecular Formula C6H14NO2S.I
Molecular Weight 291.15
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METHYLMETHIONINE IODIDE

SMILES

[I-].C[S+](C)CC[C@H](N)C(O)=O

InChI

InChIKey=YFDARUPBTIEXOS-JEDNCBNOSA-N
InChI=1S/C6H13NO2S.HI/c1-10(2)4-3-5(7)6(8)9;/h5H,3-4,7H2,1-2H3;1H/t5-;/m0./s1

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including https://www.drugs.com/international/methylmethionine-sulfonium-chloride.html | https://www.ncbi.nlm.nih.gov/pubmed/1362613 | https://www.ncbi.nlm.nih.gov/pubmed/20110751 | https://www.ncbi.nlm.nih.gov/pubmed/26225962

METHYLMETHIONINE (S-Methionine methyl sulfonium, SMMS) chloride is a derivative of methionine metabolism in some plants. Methylmethionine has therapeutic effects on gastrointestinal ulceration potentially via its ability to promote dermal fibroblast migration and growth. The natural derivative Methylmethionine is biosynthesized from L-methionine which is first converted to S-adenosylmethionine. The subsequent conversion, involving replacement of the adenosyl group by a methyl group is catalyzed by the enzyme methionine S-methyltransferase. Methylmethionine is particularly abundant in plants, being more abundant than methionine. S-Methylmethionine is sometimes referred to as vitamin U, but it is not considered a true vitamin. The term was coined in 1950 by Garnett Cheney for uncharacterized anti-ulcerogenic factors in raw cabbage juice that may help speed healing of peptic ulcers.

Originator

Sources: Journal of Bacteriology, Volume 50, Pages 323-31, Journal, 1945

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
The relative contribution of genes operating in the S-methylmethionine cycle to methionine metabolism in Arabidopsis seeds.
2017 May
Patents

Patents

Sample Use Guides

500 mg 4 times daily for 2 weeks
Route of Administration: Oral
Evaluation of in vitro permeation and deposition of SMM (methylmethionine) through hairless mouse skin was carried out by using Keshary- Chien diffusion cells at 32°C, which have 1.77 cm2 of the surface area for diffusion. After sacrificing the hairless mice by cervical dislocation, the dorsal skin was cut to about 3 cm x 3 cm size and the subcutaneous fat was removed. Then, they were fixed between the donor and receptor cells, laying the stratum corneum toward the donor cells. The donor cells contained 2% (w/v) or 5% (w/v) SMM in the 50:50 (v/v) mixture (1.0 mL) of PG and double distilled water (DDW) with or without permeation enhancers, and were covered with parafilm to prevent evaporation. The receptor cells were filled with DDW (13.0 mL) and continuously stirred by magnetic bar. After applying SMM solution on the donor cells, 0.5 mL of the receptor solution was collected at 3, 6, 9, and 12 hr and added immediately with an equal volume of fresh media. SMM in the receptor solutions was analyzed using LC-MS/MS.
Name Type Language
METHYLMETHIONINE IODIDE
Systematic Name English
LOBARTHROSE
Common Name English
L-METHIONINE METHYLSULFONIUM IODIDE
Systematic Name English
SULFONIUM, ((3S)-3-AMINO-3-CARBOXYPROPYL)DIMETHYL-, IODIDE (1:1)
Systematic Name English
METHYLMETHIONINE SULFONIUM IODIDE, L-
Common Name English
METHIONINE METHIODIDE
Common Name English
VITAMIN U IODIDE
Common Name English
Code System Code Type Description
FDA UNII
7O2D9U053L
Created by admin on Fri Dec 15 17:50:17 GMT 2023 , Edited by admin on Fri Dec 15 17:50:17 GMT 2023
PRIMARY
PUBCHEM
145691
Created by admin on Fri Dec 15 17:50:17 GMT 2023 , Edited by admin on Fri Dec 15 17:50:17 GMT 2023
PRIMARY
CAS
3493-11-6
Created by admin on Fri Dec 15 17:50:17 GMT 2023 , Edited by admin on Fri Dec 15 17:50:17 GMT 2023
PRIMARY