Che cos'è L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2)?

L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2) è un composto chimico registrato con il numero CAS 5934-29-2. Formula bruta: C₆H₁₂ClN₃O₃. Massa molare: 209.63 g/mol. IUPAC: (2S)-2-amino-3-(1H-imidazol-5-yl)propanoic acid;hydrate;hydrochloride.

Qual è il numero CAS di L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2)?

Il numero CAS di L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2) è 5934-29-2 — un identificativo univoco del Chemical Abstracts Service (CAS).

Qual è la formula bruta di L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2)?

Formula bruta: C₆H₁₂ClN₃O₃. Massa molare: 209.63 g/mol. PSA: 93 Å².

Dove acquistare L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2)?

L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2) è disponibile nel nostro negozio. Vedi il prodotto: https://molgod.org/sds-cards/l-histidine-hydrochloride-monohydrate-cas-no-5934-29-cas-5934-29-2-xilong-scientific/

Da dove provengono i dati chimici di L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2)?

I dati chimici di L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2) provengono da fonti autorevoli: PubChem (NIH). PubChem CID: 165377. Conformi al Regolamento CLP (CE 1272/2008), disponibili con licenza CC-BY 4.0.

L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2)

Name: L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2) (CAS 5934-29-2) — set di dati chimici completo
Creator: MolGod
License: https://creativecommons.org/licenses/by/4.0/

Histidine Monohydrochloride Monohydrate

CAS 5934-29-2 · C₆H₁₂ClN₃O₃ · MW 209.63 g/mol

Informazioni su L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2)

L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2) è un composto chimico registrato con il numero CAS 5934-29-2, con formula bruta C₆H₁₂ClN₃O₃, e massa molare di 209.63 g/mol.

La molecola contiene 25 atomi collegati da 23 legami chimici. Il nome sistematico IUPAC completo di questo composto è (2S)-2-amino-3-(1H-imidazol-5-yl)propanoic acid;hydrate;hydrochloride. Il modello 3D interattivo qui sopra permette di visualizzare la disposizione spaziale degli atomi — puoi ruotarlo con il mouse, zoomare con la rotellina e passare tra le modalità di visualizzazione scheletro / Ball & Stick / Space Fill.

Dal punto di vista delle proprietà chimico-fisiche, superficie polare PSA = 93 Å², 5 donatori e 5 accettori di legami a idrogeno. Questi parametri sono fondamentali per valutare la biodisponibilità e l'interazione con le biomolecole.

I dati chimici di questo composto provengono da PubChem (NIH NLM NCBI), uno dei più grandi database chimici al mondo. Tutte le informazioni sono aggiornate automaticamente e arricchite con le traduzioni delle indicazioni di pericolo GHS conformi al Regolamento CLP (CE 1272/2008). Il widget qui sopra può essere utilizzato per scopi educativi, di ricerca e commerciali.

Proprietà chimico-fisiche

Wzór sumaryczny	C₆H₁₂ClN₃O₃
Masa molowa	209.63 g/mol
IUPAC	(2S)-2-amino-3-(1H-imidazol-5-yl)propanoic acid;hydrate;hydrochloride
SMILES	`C1=C(NC=N1)C[C@@H](C(=O)O)N.O.Cl`
InChIKey	`CMXXUDSWGMGYLZ-XRIGFGBMSA-N`
logP (XLogP3)	—
PSA	93 Å²
HBD / HBA	5 / 5
PubChem CID	CID 165377 ↗

Sicurezza GHS

Sygnał: Uwaga

GHS07

Letteratura scientifica

Related literature

16 artykułów · 4 open access · Źródła: PubMed, OpenAlex, Semantic Scholar

📈 Timeline publikacji (16 artykułów)

Wysokość słupka = liczba artykułów w roku. Hover dla szczegółów.

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Comparative Pharmacology of Bombesin Receptor Subtype-3, Nonpeptide Agonist MK-5046, a Universal Peptide Agonist, and Peptide Antagonist Bantag-1 for Human Bombesin Receptors

P. Moreno, S. Mantey, B. Nuche-Berenguer et al. (2013) · Journal of Pharmacology and Experimental Therapeutics

AI Summary
MK-5046 and Bantag-1 have high affinity/selectivity for hBRS-3, an orphan G-protein-coupled receptor of the bombesin (Bn) family whose natural ligand is unknown and which does not bind any natural Bn-peptide with high affinity.

Cytowania: 35Influential: 4Open AccessDOI ↗PubMed ↗PDF ↗

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Preparation, Spectrochemical, and Computational Analysis of L-Carnosine (2-[(3-Aminopropanoyl)amino]-3-(1H-imidazol-5-yl)propanoic Acid) and Its Ruthenium (II) Coordination Complexes in Aqueous Solution

Michael Lee Branham, Parvesh Singh, Krishna Bisetty et al. (2011) · Molecules

Cytowania: 35Open AccessDOI ↗PDF ↗

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Induction of anxiolytic, antidepressant and analgesic effects by Shiff base of (E)-3-(1H-imidazol-4-yl)-2-((2-oxoindolin-3-ylidene)amino)propanoic acid derivatives in diabetic rats

Mohaddese Goleij, Leila Youseftabar-Miri, Maryam Montazeri et al. (2021) · Journal of Diabetes & Metabolic Disorders

Cytowania: 15Open AccessDOI ↗PDF ↗

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SYNTHESIS, CHARACTERIZATION AND THEORETICAL CALCULATION OF 4-(((1H-IMIDAZOL-2-YL)METHYLENE)AMINO)PHENOL

Dilek ELMALI, Kader ÇITAK (2022) · Eskişehir Teknik Üniversitesi Bilim ve Teknoloji Dergisi B - Teorik Bilimler

Open AccessDOI ↗PDF ↗

In‐vitro Aluminum Determination and Preconcentration in Blood of Dialysis Patients Based on Ionic Liquid Dispersive Liquid‐Liquid Biomicroextraction by 2‐Amino‐3‐(1H‐imidazol‐4‐yl)propanoic Acid

H. Shirkhanloo, H. Z. Mousavi, M. Mohamadi (2014) · Journal of the Chinese Chemical Society

Cytowania: 1$ PaywallDOI ↗

Identification ofS-[2-carboxy-1-(1H-imidazol-4-yl)ethyl]-3-mercaptopyruvic acid with a metabolic intermediate betweenS-[2-carboxy-1-(1H-imidazol-4-yl)ethyl]-l-cysteine andS-[2-carboxy-1-(1H-imidazol-4-yl)ethyl]-3-mercaptolactic acid

M. Kinuta, H. Shimizu, N. Masuoka et al. (1997) · Amino Acids

Cytowania: 4$ PaywallDOI ↗

Chemical structure 1. Synthesis of compound 1: 3-{[2-(1H-imidazol-4-yl)ethyl]carbamoyl}propanoic acid.

$ PaywallDOI ↗

Factor XIa in complex with the inhibitor (2S)-6-amino-N-{(1S)-1-[4-(3-amino-2H-indazol-6-yl)-5-chloro-1H-imidazol-2-yl]-2-phenylethyl}-2-ethylhexanamide

A. Wei (2014)

$ PaywallDOI ↗

Propanoic Acid, 3‐((((3S)‐2‐((2S)‐2‐Amino‐3‐(4‐Hydroxy‐2,6‐Dimethylphenyl)‐1‐Oxopropyl)‐1,2,3,4‐Tetrahydro‐3‐Isoquinolinyl)Carbonyl)Amino)‐3‐(1H‐Benzimidazol‐2‐Yl)‐, (3S)‐ 1421‐14‐3

(2012) · Sax's Dangerous Properties of Industrial Materials

$ PaywallDOI ↗

Crystal structure of ((2S)-5-amino-2-((1-n-propyl-1H-imidazol-4-yl) methyl)pentanoic acid) UK396,082 a TAFIa inhibitor, Bound to Activated Porcine Pancreatic carboxypeptidaseB

D.G. Brown, R.S. Moore (2007) · Worldwide Protein Data Bank

$ PaywallDOI ↗

Structure of the DNA duplex d(AAATTT)2 with [N-(3-chloro-4-((4,5-dihydro-1H-imidazol-2-yl)amino)phenyl)-4-((4,5-dihydro-1H-imidazol-2- yl)amino)benzamide] - (drug JNI18)

C.R. Millan, C. Dardonvile, H.P. de Koning et al. (2018)

$ PaywallDOI ↗

Bovine Trypsin 2-[amino(imino)methyl]-2-hydroxyphenoxy]-6-[3-(4,5-dihydro-1H-imidazol-2-yl)phenoxy]pyridine-4-carboxylic Acid (ZK-806688) Complex

M. Whitlow (2000)

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Bovine Trypsin with 1-[2-[5-[amino(imino)methyl]-2-hydroxyphenoxy]-6-[3-(4,5-dihydro-1-methyl-1H-imidazol-2-yl)phenoxy]pyridin-4-yl]piperidine-3-carboxylic Acid (ZK-806974)

M. Whitlow (2000)

$ PaywallDOI ↗

FACTOR XIA IN COMPLEX WITH THE INHIBITOR 1-{(1S)-1-[4-(3-amino-1H-indazol-6-yl)-5-chloro-1H-imidazol-2-yl]-2-phenylethyl}-3-[5-chloro-2-(1H-tetrazol-1-yl)benzyl]urea

A. Wei (2015)

$ PaywallDOI ↗

ChemInform Abstract: Synthesis of 3‐(1‐Methyl‐1H‐imidazol‐2‐ylthio)propanoic Acid and (E)‐3‐(1‐Methyl‐1H‐imidazol‐2‐ylthio)acrylic Acid.

Christopher M. Hattan, Jalil Shojaie, Serrine S. Lau et al. (2013) · ChemInform

$ PaywallDOI ↗

Crystal structure of E.coli Phosphopantetheine Adenylyltransferase (PPAT/CoaD) in complex with 3-((1S,2S)-2-(4-hydroxy-1H-benzo[d]imidazol-2-yl)cyclopentyl)benzoic acid

M. Mamo, B.A. Appleton (2018) · Worldwide Protein Data Bank

$ PaywallDOI ↗

Dane z PubMed (NIH NLM), OpenAlex (CC0), Semantic Scholar (AI2). AI Summary wygenerowane przez Semantic Scholar TLDR. Artykuły z ikoną wymagają płatnego dostępu.

Sinonimi

5934-29-2 · L-Histidine Hydrochloride Monohydrate · L-Histidine hydrochloride hydrate · L-Histidine monohydrochloride monohydrate · L-Histidine HCl hydrate · L-Histidine, monohydrochloride, monohydrate · Histidine monohydrochloride monohydrate · Histidine hydrochloride hydrate · Histidine, monohydrochloride, monohydrate, L- · X573657P6P · histidine hydrochloride monohydrate · L-Histidine hydrochloride hydrate (JP17) · L-HISTIDINE HYDROCHLORIDE HYDRATE [JAN] · HISTIDINE, L-, HYDROCHLORIDE MONOHYDRATE · HISTIDINE, L-, MONOHYDROCHLORIDE MONOHYDRATE

Fonti dei dati

📊 PubChem CID 165377 — NIH
🔬 NIST WebBook — spektroskopia
💊 ChEMBL — bioaktywność

Acquista nel negozio

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