Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
Cilastatin sodium (JP17/USP) | HMS2051L07 | NC00182 | MFCD08459332 | Cilastatin sodium salt | Cilastatin sodium, Bio-X | CILASTATIN Na | MLS001401364 | Sodium;(Z)-7-[(2S)-2-amino-2-carboxyethyl]sulfanyl-2-[[(1S)-2,2-dimethylcyclopropanecarbonyl]amino]hept
Storage
Protected from light,Store at -20°C,Argon charged,Desiccated
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
50mg
C275313-50mg
3
38,90US$
250mg
C275313-250mg
3
109,90US$
1g
C275313-1g
1
313,90US$
5g
C275313-5g
1
1.218,90US$
Enter a quantity for the sizes you want to add.

Descripción general

Store at -20°C. Store under desiccating conditions. The product can be stored for up to 12 months.

Specifications

Sinónimos
Cilastatin sodium (JP17/USP) | HMS2051L07 | NC00182 | MFCD08459332 | Cilastatin sodium salt | Cilastatin sodium, Bio-X | CILASTATIN Na | MLS001401364 | Sodium;(Z)-7-[(2S)-2-amino-2-carboxyethyl]sulfanyl-2-[[(1S)-2, 2-dimethylcyclopropanecarbonyl]amino]hept
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Selective dehydrodipeptidase I inhibitor (K i = 0.11 µM). Inhibits leukotriene D 4 hydrolase (K i = 0.11 µM). Potentiates the antibiotic activity of Imipenem. Shows nephroprotective effects in vivo.
Condiciones de almacenamiento de almacenamiento
Protected from light, Store at -20°C, Argon charged, Desiccated
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Tipo de acción
INHIBITOR
Mecanismo de acción
Renal dipeptidase inhibitor
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.
Pureza
≥98%
Propiedades del producto
ALogP-1
Nombres e identificadores
Sonrisas canónicasCC1(CC1C(=O)NC(=CCCCCSCC(C(=O)O)N)C(=O)[O-])C.[Na+]
IUPAC Namesodium;(Z)-7-[(2R)-2-amino-2-carboxyethyl]sulfanyl-2-[[(1S)-2,2-dimethylcyclopropanecarbonyl]amino]hept-2-enoate
InChIKeyQXPBTTUOVWMPJN-QBNHLFMHSA-M
INCHI1S/C16H26N2O5S.Na/c1-16(2)8-10(16)13(19)18-12(15(22)23)6-4-3-5-7-24-9-11(17)14(20)21;/h6,10-11H,3-5,7-9,17H2,1-2H3,(H,18,19)(H,20,21)(H,22,23);/q;+1/p-1/b12-6-;/t10-,11+;/m1./s1
Isómeros SMILES CC1(C[C@@H]1C(=O)N/C(=C\CCCCSC[C@@H](C(=O)O)N)/C(=O)[O-])C.[Na+]
Peso molecular 380.43
Reaxy-Rn 47692307
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=47692307&ln=

Documentation

📋 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
ClaseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives - N-acyl-alpha amino acids and derivatives
Direct ParentN-acyl-alpha amino acids
Alternative Parents L-cysteine-S-conjugates  L-alpha-amino acids  Medium-chain fatty acids  Cyclopropanecarboxylic acids and derivatives  Dicarboxylic acids and derivatives  Unsaturated fatty acids  Secondary carboxylic acid amides  Carboxylic acid salts  Amino acids  Sulfenyl compounds  Dialkylthioethers  Carboxylic acids  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  Organic sodium salts  Organic zwitterions  Organopnictogen compounds  
Molecular FrameworkAliphatic homomonocyclic compounds
Substituents N-acyl-alpha-amino acid - L-cysteine-s-conjugate - Cysteine or derivatives - Alpha-amino acid - L-alpha-amino acid - Medium-chain fatty acid - Cyclopropanecarboxylic acid or derivatives - Dicarboxylic acid or derivatives - Unsaturated fatty acid - Fatty acid - Fatty acyl - Carboxamide group - Carboxylic acid salt - Amino acid - Secondary carboxylic acid amide - Organic alkali metal salt - Sulfenyl compound - Dialkylthioether - Carboxylic acid - Thioether - Organic sodium salt - Carbonyl group - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Primary aliphatic amine - Hydrocarbon derivative - Amine - Organopnictogen compound - Organic nitrogen compound - Organic oxide - Organic salt - Organic zwitterion - Aliphatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as n-acyl-alpha amino acids. These are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom.
External Descriptors organic sodium salt
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ERG Tbio Transcriptional regulator ERG (5589 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RAN Tchem GTP-binding nuclear protein Ran/Importin subunit beta-1/Snurportin-1 (21853 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TGR Thioredoxin glutathione reductase (28579 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

5 results found

Lot NumberCertificate TypeFechaArticulo
I2202422Certificate of AnalysisJun 11, 2026 C275313
I2202423Certificate of AnalysisJun 11, 2026 C275313
I2202480Certificate of AnalysisJun 11, 2026 C275313
I2202481Certificate of AnalysisJun 11, 2026 C275313
L2411168Certificate of AnalysisJun 11, 2026 C275313
Propiedades químicas y físicas
SolubilidadSoluble in water to 50 mM and in DMSO to 25 mM (with warming)
SensibilidadMoisture & Heat & Light Sensitive
Punto de fusión (°C)>160°C
Peso molecular380.400 g/mol
XLogP3
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count7
Rotatable Bond Count11
Exact Mass380.138 Da
Monoisotopic Mass380.138 Da
Topological Polar Surface Area158.000 Ų
Heavy Atom Count25
Formal Charge0
Complexity525.000
Isotope Atom Count0
Defined Atom Stereocenter Count2
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds1
Covalently-Bonded Unit Count2
Calculadoras de soluciones
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