289647
3-Amino-4-hydroxybenzoic acid
97%, for peptide synthesis
동의어(들):
4-Hydroxy-3-aminobenzoic acid
로그인조직 및 계약 가격 보기
모든 사진(1)
About This Item
Linear Formula:
H2NC6H3(OH)CO2H
CAS Number:
Molecular Weight:
153.14
Beilstein:
972238
EC Number:
MDL number:
UNSPSC 코드:
12352106
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.22
추천 제품
product name
3-Amino-4-hydroxybenzoic acid, 97%
분석
97%
형태
solid
반응 적합성
reaction type: solution phase peptide synthesis
mp
208 °C (dec.) (lit.)
응용 분야
peptide synthesis
SMILES string
Nc1cc(ccc1O)C(O)=O
InChI
1S/C7H7NO3/c8-5-3-4(7(10)11)1-2-6(5)9/h1-3,9H,8H2,(H,10,11)
InChI key
MRBKRZAPGUCWOS-UHFFFAOYSA-N
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신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
Arylamine N-acetyltransferase responsible for acetylation of 2-aminophenols in Streptomyces griseus.
Hirokazu Suzuki et al.
Journal of bacteriology, 189(5), 2155-2159 (2006-12-13)
An arylamine N-acetyltransferase (NAT) responsible for the N acetylation of exogenous 3-amino-4-hydroxybenzoic acid in Streptomyces griseus was identified and characterized. This enzyme was distinct from other eukaryotic and bacterial NATs in that it acetylated various 2-aminophenol derivatives more effectively than
Hirokazu Suzuki et al.
The Journal of antibiotics, 60(6), 380-387 (2007-07-10)
In grixazone biosynthesis by Streptomyces griseus, a key intermediate 3-amino-4-hydroxybenzoic acid (3,4-AHBA) is converted to another key intermediate 3-amino-4-hydroxybenzaldehyde (3,4-AHBAL). Two genes griC and griD in the grixazone biosynthesis gene cluster were found to be responsible for this conversion, because
Christian Gerecke et al.
Epigenetics, 15(3), 307-322 (2019-09-12)
Mutations in the enzyme isocitrate dehydrogenase 1 (IDH1) lead to metabolic alterations and a sustained formation of 2-hydroxyglutarate (2-HG). 2-HG is an oncometabolite as it inhibits the activity of α-ketoglutarate-dependent dioxygenases such as ten-eleven translocation (TET) enzymes. Inhibitors of mutant
Experience with cheetan in management of HIV infection.
J Chege et al.
East African medical journal, 74(7), 460-461 (1997-07-01)
Hirokazu Suzuki et al.
The Journal of biological chemistry, 281(48), 36944-36951 (2006-09-28)
The shikimate pathway, including seven enzymatic steps for production of chorismate via shikimate from phosphoenolpyruvate and erythrose-4-phosphate, is common in various organisms for the biosynthesis of not only aromatic amino acids but also most biogenic benzene derivatives. 3-Amino-4-hydroxybenzoic acid (3,4-AHBA)
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