Interesting facts
Interesting Facts about (2S)-2-amino-3-methyl-3-sulfanyl-butanoic acid
(2S)-2-amino-3-methyl-3-sulfanyl-butanoic acid, commonly known as methionine, is an essential amino acid that plays a crucial role in various biological processes. Here are some fascinating facts about this compound:
- Protein Building Block: Methionine is one of the 20 natural amino acids that are incorporated into proteins. It is typically the first amino acid in the sequence of proteins synthesized during translation.
- Critical for Growth: As an essential amino acid, methionine must be obtained through diet. It is integral for tissue growth and repair, making it particularly important in periods of rapid growth, such as during childhood and pregnancy.
- Role in Metabolism: Methionine participates in the synthesis of other important compounds, such as cysteine and taurine. It also plays a role in the formation of S-adenosylmethionine (SAMe), a key methyl donor involved in numerous biochemical reactions.
- Antioxidant Properties: Methionine has antioxidant properties, which help protect cells from oxidative damage by neutralizing free radicals. This characteristic is significant in the context of aging and various disease processes.
- Source of Sulfur: As a sulfur-containing amino acid, methionine is a vital source of sulfur for the body, which is essential for the synthesis of various biochemical compounds, including certain vitamins and coenzymes.
In the words of famous biochemist Michael J. Rutter, "Methionine represents a vital intersection between nutrition and metabolism, emphasizing the significance of dietary amino acids in human health." This essential amino acid underscores the intricate relationship between our diet and overall well-being.
Understanding the role and function of methionine highlights the interconnectedness of nutrients in biochemistry and provides insight into dietary planning for optimal health.
Synonyms
D-Penicillamine
penicillamine
52-67-5
Cuprimine
D-(-)-Penicillamine
3-Mercapto-D-valine
Depen
(2S)-2-Amino-3-methyl-3-sulfanylbutanoic acid
D-Penamine
Cuprenil
D-Valine, 3-mercapto-
D-Mercaptovaline
(-)-Penicillamine
Mercaptovaline
Penicilamina
Penicillamin
Artamine
Cupripen
Depamine
Kuprenil
Mercaptyl
Pendramine
Perdolat
Trolovol
D-3-Mercaptovaline
(S)-3,3-Dimethylcysteine
Penicillaminum
Sufirtan
beta-Thiovaline
D-beta,beta-Dimethylcysteine
3-sulfanyl-D-valine
beta,beta-Dimethylcysteine
(S)-Penicillamin
(S)-Penicillamine
d,3-Mercaptovaline
Penicillamina
Reduced penicillamine
Reduced D-penicillamine
Dimethylcysteine
(D)-PENICILLAMINE
Sufortan
Penicilamina [INN-Spanish]
Penicillaminum [INN-Latin]
(S)-2-amino-3-mercapto-3-methylbutanoic acid
Metalcaptase
Distamine
Valine, 3-mercapto-, D-
D-Penicilamine
CCRIS 2904
CHEBI:7959
Penicillamina [DCIT]
HSDB 3378
UNII-GNN1DV99GX
3,3-Dimethyl-D-cysteine
GNN1DV99GX
EINECS 200-148-8
MFCD00064302
NSC 81549
alpha-Amino-beta-methyl-beta-mercaptobutyric acid
DTXSID6037069
Penicillamine (Cuprimine)
NSC-81549
CHEMBL1430
DTXCID4017069
D-(-)-2-Amino-3-mercapto-3-methylbutanoic acid
NSC81549
NCGC00024359-04
Penicillamine [USAN:USP:INN:BAN:JAN]
D Penicillamine
Penicilamina (INN-Spanish)
Penicillaminum (INN-Latin)
D 3 Mercaptovaline
PENICILLAMINE (MART.)
PENICILLAMINE [MART.]
PENICILLAMINE (USP-RS)
PENICILLAMINE [USP-RS]
PENICILLAMINE (EP IMPURITY)
PENICILLAMINE [EP IMPURITY]
PENICILLAMINE (EP MONOGRAPH)
PENICILLAMINE [EP MONOGRAPH]
beta,beta Dimethylcysteine
PENICILLAMINE (USP MONOGRAPH)
PENICILLAMINE [USP MONOGRAPH]
Cuprimine (TN)
Penicillamine (USAN:USP:INN:BAN:JAN)
D-beta-Mercaptovaline
Depen (TN)
D(-)PENICILLAMINE HYDROCHLORIDE
SR-01000000262
(2S)-2-amino-3-methyl-3-sulfanyl-butanoic acid
Distamine (*Hydrochloride*)
Kelatin
Atamir
Penicillamine (JAN/USP/INN)
Metalcaptase (*Hydrochloride*)
penicillamine-(d)
3-Thio-D-valine
Penicillamine,(S)
D-Penicillamine API
penicillamine-(racemic)
Spectrum_000283
Penicillamine (Standard)
Spectrum2_001029
Spectrum3_000541
Spectrum4_000470
Spectrum5_001196
PENICILLAMINE [MI]
Epitope ID:113237
PENICILLAMINE [INN]
PENICILLAMINE [JAN]
SCHEMBL4343
PENICILLAMINE [HSDB]
PENICILLAMINE [USAN]
BSPBio_002181
KBioGR_000920
KBioSS_000763
PENICILLAMINE [VANDF]
cid_92173
DivK1c_000314
SPBio_001217
D-Penicillamine, 98-101%
PENICILLAMINE [WHO-DD]
GTPL7264
BDBM39346
HY-B0300R
KBio1_000314
KBio2_000763
KBio2_003331
KBio2_005899
KBio3_001681
M01CC01
NINDS_000314
PENICILLAMINE [ORANGE BOOK]
BCP17247
HY-B0300
STR02534
Tox21_110899
BDBM50217941
s1853
AKOS006237201
CCG-266197
DB00859
FP26792
CAS-52-67-5
IDI1_000314
SMP1_000042
NCGC00018283-01
NCGC00024359-05
NCGC00024359-06
DA-63011
NS00008268
P0147
EN300-52608
C07418
D00496
M06142
P15236
Q421239
SR-01000000262-3
SR-01000000262-4
BRD-K17518951-001-03-0
BRD-K17518951-001-04-8
Z234896485
(2S)-2-amino-3-mercapto-3-methyl-butyric acid;hydrochloride
(2S)-2-amino-3-mercapto-3-methylbutanoic acid;hydrochloride
(2S)-2-azanyl-3-methyl-3-sulfanyl-butanoic acid;hydrochloride
Penicillamine, European Pharmacopoeia (EP) Reference Standard
(2S)-2-amino-3-methyl-3-sulfanylbutanoic acid3-sulfanyl-D-valine
Penicillamine, United States Pharmacopeia (USP) Reference Standard
200-148-8
3-Mercapto-D-valine;(2S)-2-Amino-3-methyl-3-sulfanylbutanoic acid;(S)-3,3-Dimethylcysteine;H-D-Pen-OH
Solubility of (2S)-2-amino-3-methyl-3-sulfanyl-butanoic acid
(2S)-2-amino-3-methyl-3-sulfanyl-butanoic acid, with the chemical formula C5H11NO2S, displays intriguing solubility characteristics due to its unique structural components. This compound features both amino and acidic functional groups, which significantly influences its interaction with solvents.
Key Points on Solubility:
Furthermore, factors such as temperature and pH can also play pivotal roles in the solubility of this compound, potentially altering its solubility profile. As a result, understanding these attributes is crucial for its application in various chemical processes and formulations.