β-Alanine - BioReagent, suitable for cell culture, suitable for insect cell culture, high purity , CAS No.107-95-9

Item Number
A431363
Grouped product items
SKUSizeAvailabilityPrice Qty
A431363-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$110.90
A431363-100g
100g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$111.90

Basic Description

SynonymsALANINE, BETA | Alanine, beta- | BETA ALANINE [USP-RS] | EC 203-536-5 | HY-N0230 | omega-Aminopropionate | Q310919 | b-Aminopropanoic acid | .BETA.-ALANINE [MI] | 11P2JDE17B | b-Aminopropionate | 3-Aminopropionsaeure | MFCD00008200 | b-Aminopropanoate | b
Specifications & PurityMoligand™, BioReagent, for cell culture, for insect cell culture
Biochemical and Physiological Mechanismsβ-Alanine, a β−amino acid, is a component of pantothenic acid and the rate-limiting amino acid in the biosynthesis of the histidinyl antioxidant dipeptides carnosine and anserine. Endogenous β-amino acid that is a nonselective agonist at glycine receptors
GradeBioReagent, for cell culture, for insect cell culture, Moligand™
Product Description

An N-blocked form of alanine.

Associated Targets(Human)

MRGPRD Tchem Mas-related G-protein coupled receptor member D (3 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
SLC6A1 Tclin GABA transporter 1 (308 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRIN1 Tclin Glutamate (NMDA) receptor subunit zeta 1 (122 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A11 Tchem GABA transporter 3 (176 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RGS4 Tchem Regulator of G-protein signaling 4 (13867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC36A1 Tchem Proton-coupled amino acid transporter 1 (102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Slc6a13 GABA transporter 2 (37 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc6a11 GABA transporter 4 (930 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
lef Anthrax lethal factor (7585 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
panC Pantothenate synthetase (234 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

IUPAC Name 3-aminopropanoic acid
INCHI InChI=1S/C3H7NO2/c4-2-1-3(5)6/h1-2,4H2,(H,5,6)
InChi Key UCMIRNVEIXFBKS-UHFFFAOYSA-N
Canonical SMILES C(CN)C(=O)O
Isomeric SMILES C(CN)C(=O)O
WGK Germany 3
PubChem CID 239
Molecular Weight 89.09
Beilstein 906793
Reaxy-Rn 906793

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

Chemical and Physical Properties

Melt Point(°C)205°C

Safety and Hazards(GHS)

WGK Germany 3
Reaxy-Rn 906793
Merck Index 205

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Citations of This Product

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2. Wei Hu, Jingchun Huang, Junwen Wang, Di Xie, Zhenqi Wang, Yu Qiao, Minghou Xu.  (2024)  Benign-by-design N-doped activated carbon from wasted aqueous assisted hydrochar of leftover rice for efficient H2S removal.  FUEL,  358  (31): (130233).  [PMID:10734105] [10.1016/j.fuel.2023.130233]
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7. Kaiyang Shi, Man Zhou, Fulin Wang, Xiangwei Li, Weiya Huang, Kangqiang Lu, Kai Yang, Changlin Yu.  (2023)  Perylene diimide/iron phthalocyanine Z-scheme heterojunction with strong interfacial charge transfer through π-π interaction: Efficient photocatalytic degradation of tetracycline hydrochloride.  CHEMOSPHERE,  329  (138617).  [PMID:37037355] [10.1016/j.chemosphere.2023.138617]
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9. Hai-Bin Qin, Jun-Ping Zhou, Bo Zhang, Zhi-Qiang Liu, Yu-Guo Zheng.  (2022)  Combing with redox regulation via quorum-sensing system and fermentation strategies for improving D-pantothenic acid production.  PROCESS BIOCHEMISTRY,  121  (681).  [PMID:] [10.1016/j.procbio.2022.08.012]
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21. Xiao Y. Luo, Xiao Y. Lv, Gui L. Shi, Qin Meng, Hao R. Li, Cong M. Wang.  (2018)  Designing amino-based ionic liquids for improved carbon capture: One amine binds two CO2.  AICHE JOURNAL,  65  (1): (230-238).  [PMID:] [10.1002/aic.16420]
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Solution Calculators