2-AMINO-3-[METHYLTHIO]BUTYRIC ACID

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Names

[ CAS No. ]:
443-80-1

[ Name ]:
2-AMINO-3-[METHYLTHIO]BUTYRIC ACID

[Synonym ]:
DL-4-Thiaisoleucine
DL-thiaisoleucine
4-Thiaisoleucine
2-Amino-3-methylmercapto-buttersaeure
MFCD00056745

Chemical & Physical Properties

[ Density]:
1.202g/cm3

[ Boiling Point ]:
280.1ºC at 760 mmHg

[ Molecular Formula ]:
C₅H₁₁NO₂S

[ Molecular Weight ]:
149.21100

[ Flash Point ]:
123.2ºC

[ Exact Mass ]:
149.05100

[ PSA ]:
88.62000

[ LogP ]:
0.85010

[ Vapour Pressure ]:
0.00103mmHg at 25°C

[ Index of Refraction ]:
1.528

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2930909090

Customs

[ HS Code ]: 2930909090

[ Summary ]:
2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Validation of isoleucine utilization targets in Plasmodium falciparum.

Proc. Natl. Acad. Sci. U. S. A. 108 , 1627-1632, (2011)

Intraerythrocytic malaria parasites can obtain nearly their entire amino acid requirement by degrading host cell hemoglobin. The sole exception is isoleucine, which is not present in adult human hemog...

Isopenicillin N synthase binds δ-(L-α-aminoadipoyl)-L-cysteinyl-D-thia-allo-isoleucine through both sulfur atoms.

ChemBioChem. 12 , 1881-1885, (2011)

Isopenicillin N synthase (IPNS) catalyses the synthesis of isopenicillin N (IPN), the biosynthetic precursor to penicillin and cephalosporin antibiotics. IPNS is a non-heme iron(II) oxidase that media...

Incorporation of amino acid analogs interferes with the processing of the asparagine-linked oligosaccharide of the MOPC-46B kappa light chain.

J. Biol. Chem. 257 , 9039-9042, (1982)

The incorporation of the leucine analog, beta-hydroxyleucine, or the isoleucine analog, 4-thiaisoleucine, into the MPOC-46B kappa chain interfered with the processing of the oligosaccharide moiety of ...

2-Amino-3-(methylthio)propansaeure-methylester
2-Amino-3-(1H-indol-3-yl)-butyric acid ethyl ester
2-amino-3-(1(3)H-imidazol-4-yl)-butyric acid
2-amino-3-Methyl-3-sulfino-4-(1H-1,2,3-triazol-1-yl)butyric acid
2-amino-3-fluorobutyric acid
2-AMINO-3-PHENYLBUTANOIC ACID HYDROCHLORIDE
N-(3,4-dimethoxyphenyl)-2-(6-ethoxy-3-(4-methylbenzoyl)-4-oxoquinolin-1(4H)-yl)acetamide
2-(6-ethoxy-3-(4-methylbenzoyl)-4-oxoquinolin-1(4H)-yl)-N-(4-ethoxyphenyl)acetamide
2-(6-ethoxy-3-(4-methylbenzoyl)-4-oxoquinolin-1(4H)-yl)-N-(3-methoxyphenyl)acetamide
N-(3,5-dimethoxyphenyl)-2-[6-ethoxy-3-(4-methylbenzoyl)-4-oxo-1,4-dihydroquinolin-1-yl]acetamide
N-(2,5-dimethoxyphenyl)-2-(6-ethoxy-3-(4-methylbenzoyl)-4-oxoquinolin-1(4H)-yl)acetamide
N-(2,4-dimethoxyphenyl)-2-(6-ethoxy-3-(4-methylbenzoyl)-4-oxoquinolin-1(4H)-yl)acetamide
2-(6-ethoxy-3-(4-methylbenzoyl)-4-oxoquinolin-1(4H)-yl)-N-phenylacetamide
2-(6-ethoxy-3-(4-methylbenzoyl)-4-oxoquinolin-1(4H)-yl)-N-(p-tolyl)acetamide
2-(6-ethoxy-3-(4-methylbenzoyl)-4-oxoquinolin-1(4H)-yl)-N-(4-ethylphenyl)acetamide
N-(3,4-dimethylphenyl)-2-(6-ethoxy-3-(4-methylbenzoyl)-4-oxoquinolin-1(4H)-yl)acetamide

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