penicillin G,Na - Moligand™, 1650 U/mg , CAS No.69-57-8

CAS: 69-57-8 Cat. No.: P105489 Formula: C₁₆H₁₇N₂NaO₄S Peso molecolare: 356.37 Numero EC: 200-710-2
Disponibile su ordine
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. 1650 U/mg
Synonyms
CHEBI:51765 | EN300-25914569 | PENICILLIN G, SODIUM SALT | BENZYLPENICILLIN SODIUM [MART.] | HY-B1463 | Penicillin G, sodium | 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-((phenylacetyl)amino)-(2S,5R,6R)-, monosodium salt | C
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
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Size
Germania (EU)
USA*
Price
Qty
5g
P105489-5g
—
Disponibile ≥10
9,46€
25g
P105489-25g
—
4 Disponibile
16,40€
100g
P105489-100g
—
1 Disponibile
49,37€
500g
P105489-500g
—
1 Disponibile
216,85€
Enter a quantity for the sizes you want to add.
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Why this grade

Moligand™, 1650 U/mg Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 52 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Panoramica

application:

Penicillin G sodium salt is used as a β-lactam antibiotic. Penicillin G can be used as a selective agent in several types of isolation media. It has been used to study the diagnostic and therapeutic implications of gentamicin-resistant Enterococcus faecalis sequence type 6 with reduced penicillin susceptibility and in cell culture both alone and combined with streptomycin and other antibiotics.

Specifications

Sinonimi
CHEBI:51765 | EN300-25914569 | PENICILLIN G, SODIUM SALT | BENZYLPENICILLIN SODIUM [MART.] | HY-B1463 | Penicillin G, sodium | 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-((phenylacetyl)amino)-(2S,5R,6R)-, monosodium salt | C
Specifiche e purezza
Moligand™, 1650 U/mg
Meccanismi biochimici e fisiologici
Narrow spectrum β-lactam antibiotic agent. Binds to specific penicillin-binding proteins. Inhibits bacterial cell wall synthesis. Shows bactericidal effects against Gram-positive aerobic organisms in vivo.
Condizioni di conservazione di stoccaggio
Store at 2-8°C,Argon charged
Spedito in
Wet ice
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Grado
Moligand™
Nota
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Line
P105489-5g
Nomi e identificatori
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/508817072
Sorrisi canonici
CC1(C(N2C(S1)C(C2=O)NC(=O)CC3=CC=CC=C3)C(=O)[O-])C.[Na+]
IUPAC Name
sodium;(2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
InChIKey
FCPVYOBCFFNJFS-LQDWTQKMSA-M
INCHI
1S/C16H18N2O4S.Na/c1-16(2)12(15(21)22)18-13(20)11(14(18)23-16)17-10(19)8-9-6-4-3-5-7-9;/h3-7,11-12,14H,8H2,1-2H3,(H,17,19)(H,21,22);/q;+1/p-1/t11-,12+,14-;/m1./s1
Isomeri SMILES
CC1([C@@H](N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CC=C3)C(=O)[O-])C.[Na+]
CAS alternativo
61-33-6
Peso molecolare
356.37
Reaxy-Rn
1038006
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1038006&ln=

Documentazione

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClasseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentN-acyl-alpha amino acids and derivatives
Alternative Parents Penams  Benzene and substituted derivatives  Thiazolidines  Tertiary carboxylic acid amides  Azetidines  Thiohemiaminal derivatives  Propargyl-type 1,3-dipolar organic compounds  Azacyclic compounds  Carboximidic acids  Carboxylic acids  Monocarboxylic acids and derivatives  Dialkylthioethers  Hydrocarbon derivatives  Organic oxides  Organic sodium salts  Carbonyl compounds  Organic zwitterions  Organonitrogen compounds  Organopnictogen compounds  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents N-acyl-alpha amino acid or derivatives - Penam - Monocyclic benzene moiety - Benzenoid - Beta-lactam - Tertiary carboxylic acid amide - Thiazolidine - Azetidine - Carboxamide group - Lactam - Carboximidic acid - Carboximidic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Azacycle - Organic alkali metal salt - Organoheterocyclic compound - Thioether - Hemithioaminal - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Dialkylthioether - Organonitrogen compound - Organooxygen compound - Organic sodium salt - Organic nitrogen compound - Organic oxide - Organic oxygen compound - Organic zwitterion - Organic salt - Hydrocarbon derivative - Organopnictogen compound - Carbonyl group - Aromatic heteropolycyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as n-acyl-alpha amino acids and derivatives. These are compounds containing an alpha amino acid (or a derivative thereof) which bears an acyl group at its terminal nitrogen atom.
External Descriptors organic sodium salt
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
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)
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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
Obiettivi associati (non umani)
blaZ Beta-lactamase (285 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Streptococcus pneumoniae (31063 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
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Ralstonia solanacearum (520 Activities)
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Klebsiella pneumoniae (43867 Activities)
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Staphylococcus aureus (210822 Activities)
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Acinetobacter baumannii (41033 Activities)
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Moraxella catarrhalis (3334 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
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Haemophilus influenzae (8812 Activities)
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Bacillus subtilis (32866 Activities)
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Bacillus thuringiensis (718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Enterococcus faecalis (29875 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bacillus cereus (7522 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc22a20 Solute carrier family 22 member 20 (86 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc22a6 Solute carrier family 22 member 6 (141 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pectobacterium carotovorum (295 Activities)
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Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

25 results found

Lot NumberCertificate TypeDataOggetto
G2227278Certificate of AnalysisMay 19, 2026 P105489
G2227277Certificate of AnalysisMay 19, 2026 P105489
F2616501Certificate of AnalysisMay 18, 2026 P105489
F2616499Certificate of AnalysisMay 18, 2026 P105489
F2616496Certificate of AnalysisMay 18, 2026 P105489
F2616497Certificate of AnalysisMay 18, 2026 P105489
L2530302Certificate of AnalysisDec 13, 2025 P105489
L2530301Certificate of AnalysisDec 13, 2025 P105489
L2530300Certificate of AnalysisDec 13, 2025 P105489
A2220339Certificate of AnalysisOct 29, 2025 P105489
A2220322Certificate of AnalysisOct 29, 2025 P105489
F2117202Certificate of AnalysisApr 03, 2025 P105489
C2517353Certificate of AnalysisMar 07, 2025 P105489
C2517351Certificate of AnalysisMar 07, 2025 P105489
G2508593Certificate of AnalysisMar 07, 2025 P105489
H2324347Certificate of AnalysisAug 07, 2023 P105489
H2324646Certificate of AnalysisAug 07, 2023 P105489
H2324688Certificate of AnalysisAug 07, 2023 P105489
H2324742Certificate of AnalysisAug 07, 2023 P105489
H2325006Certificate of AnalysisAug 07, 2023 P105489
H2325013Certificate of AnalysisAug 07, 2023 P105489
G2227279Certificate of AnalysisJul 12, 2022 P105489
J2423103Certificate of AnalysisJul 12, 2022 P105489
A2220321Certificate of AnalysisDec 15, 2021 P105489
A2220316Certificate of AnalysisDec 15, 2021 P105489
Proprietà chimiche e fisiche
SolubilitàSoluble in water (100 mg/ml), alcohol, glycerol, DMSO (71 mg/ml at 25°C), and ethanol (< 1 mg/ml at 25°C).
Sensibilitàair sensitive
Rotazione specifica [α][α]D 300° (C=2,H2O)
Punto di fusione (°C)209-212°C
Peso molecolare356.400 g/mol
XLogP3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count5
Rotatable Bond Count4
Exact Mass356.081 Da
Monoisotopic Mass356.081 Da
Topological Polar Surface Area115.000 Ų
Heavy Atom Count24
Formal Charge0
Complexity536.000
Isotope Atom Count0
Defined Atom Stereocenter Count3
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Domande frequenti e articoli
Citations of This Product
Calcolatori di soluzioni
Recensioni

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