Basic Description

Synonyms	ceftizoxime \| CEFTIZOXIME [VANDF] \| CEFTIZOXIME [WHO-DD] \| (6R,7R)-7-(((2Z)-2-(2-AMINO-1,3-THIAZOL-4-YL)-2-METHOXYIMINOACETYL)AMINO)-8-OXO-5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID \| BDBM237182 \| Epocelin \| C06890 \| Ceftizoxima \| CHEBI:553473
Specifications & Purity	Moligand™, ≥98%(HPLC)
Shipped In	Normal
Grade	Moligand™
Product Description	Product Description： Ceftizoxime is a bacterial inhibitor which acts by interfering with bacterial cell wall synthesis and inhibiting cross-linking of the peptidoglycan.

Associated Targets(Human)

ESR1 Tclin Estrogen receptor alpha (17718 Activities)

Discover Target: ESR1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

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PGR Tclin Progesterone receptor (8562 Activities)

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ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)

Discover Target: ADRB2

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CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)

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ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)

Discover Target: ADRB1

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HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)

Discover Target: HTR1A

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ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)

Discover Target: ADRA2A

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AR Tclin Androgen Receptor (11781 Activities)

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CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

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DRD2 Tclin Dopamine D2 receptor (23596 Activities)

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MAOA Tclin Monoamine oxidase A (11911 Activities)

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CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)

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DRD1 Tclin Dopamine D1 receptor (9720 Activities)

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PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)

Discover Target: PTGS1

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SLC6A2 Tclin Norepinephrine transporter (10102 Activities)

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HRH2 Tclin Histamine H2 receptor (5428 Activities)

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HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)

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AVPR2 Tclin Vasopressin V2 receptor (2912 Activities)

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ADORA1 Tclin Adenosine A1 receptor (17603 Activities)

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AGTR1 Tclin Type-1 angiotensin II receptor (5176 Activities)

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SLC6A4 Tclin Serotonin transporter (12625 Activities)

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ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)

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PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)

Discover Target: PTGS2

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HRH1 Tclin Histamine H1 receptor (7573 Activities)

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OPRM1 Tclin Mu opioid receptor (19785 Activities)

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PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)

Discover Target: PPARG

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AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)

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SLC6A3 Tclin Dopamine transporter (10535 Activities)

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KCNH2 Tclin HERG (29587 Activities)

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PDE3A Tclin Phosphodiesterase 3A (3309 Activities)

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SLC29A1 Tclin Equilibrative nucleoside transporter 1 (1711 Activities)

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ADRA2C Tclin Alpha-2c adrenergic receptor (4876 Activities)

Discover Target: ADRA2C

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HTR2B Tclin Serotonin 2b (5-HT2b) receptor (10323 Activities)

Discover Target: HTR2B

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EDNRA Tclin Endothelin receptor ET-A (5008 Activities)

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ADORA2A Tclin Adenosine A2a receptor (16305 Activities)

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ADORA3 Tchem Adenosine A3 receptor (15931 Activities)

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BDKRB2 Tclin Bradykinin B2 receptor (3970 Activities)

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HRH3 Tclin Histamine H3 receptor (10389 Activities)

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SLC15A1 Tchem Oligopeptide transporter small intestine isoform (922 Activities)

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CHRNA4 Tclin Neuronal acetylcholine receptor protein alpha-4 subunit (1265 Activities)

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MC3R Tchem Melanocortin receptor 3 (5659 Activities)

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MLNR Tchem Motilin receptor (1724 Activities)

Discover Target: MLNR

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CCKBR Tclin Cholecystokinin B receptor (3550 Activities)

Discover Target: CCKBR

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GHSR Tclin Ghrelin receptor (6229 Activities)

Discover Target: GHSR

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NR1I2 Tchem Pregnane X receptor (6667 Activities)

Discover Target: NR1I2

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Homo sapiens (32628 Activities)

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SLC22A8 Tclin Solute carrier family 22 member 8 (241 Activities)

Discover Target: SLC22A8

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Associated Targets(non-human)

Npy1r Neuropeptide Y receptor type 1 (8 Activities)

Discover Target: Npy1r

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Cckar Cholecystokinin A receptor (90 Activities)

Discover Target: Cckar

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Pde4d Phosphodiesterase 4D (4 Activities)

Discover Target: Pde4d

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Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

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Streptococcus pneumoniae (31063 Activities)

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Pseudomonas aeruginosa (123386 Activities)

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Enterobacter cloacae (7976 Activities)

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Klebsiella pneumoniae (43867 Activities)

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Providencia rettgeri (925 Activities)

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Bacteroides fragilis (1445 Activities)

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Staphylococcus aureus (210822 Activities)

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Escherichia coli (133304 Activities)

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Proteus mirabilis (3894 Activities)

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Serratia marcescens (3237 Activities)

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Haemophilus influenzae (8812 Activities)

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Streptococcus agalactiae (1777 Activities)

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Streptococcus pyogenes (16140 Activities)

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Bacillus subtilis (32866 Activities)

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Mus musculus (284745 Activities)

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Rattus norvegicus (775804 Activities)

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Mammaliicoccus lentus (29 Activities)

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Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	488195842
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488195842
IUPAC Name	(6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
INCHI	InChI=1S/C13H13N5O5S2/c1-23-17-7(5-4-25-13(14)15-5)9(19)16-8-10(20)18-6(12(21)22)2-3-24-11(8)18/h2,4,8,11H,3H2,1H3,(H2,14,15)(H,16,19)(H,21,22)/b17-7-/t8-,11-/m1/s1
InChi Key	NNULBSISHYWZJU-LLKWHZGFSA-N
Canonical SMILES	CON=C(C1=CSC(=N1)N)C(=O)NC2C3N(C2=O)C(=CCS3)C(=O)O
Isomeric SMILES	CO/N=C(/C1=CSC(=N1)N)\C(=O)N[C@H]2[C@@H]3N(C2=O)C(=CCS3)C(=O)O
RTECS	XI0367375
PubChem CID	6533629
Molecular Weight	383.4
Reaxy-Rn	5777502

Database links

PubChem CID	6533629
CAS Registry No.	68401-81-0
ChEMBL Ligand	CHEMBL528
BindingDB Ligand	237182
DrugCentral Ligand	563
PubChem SID	488195842

Certificates

Certificate of Analysis(COA)

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7 results found

Lot Number	Certificate Type	Date	Item
A2331240	Certificate of Analysis	Aug 19, 2022	C153444
K2224030	Certificate of Analysis	Aug 19, 2022	C153444
K2224033	Certificate of Analysis	Aug 19, 2022	C153444
K2224042	Certificate of Analysis	Aug 19, 2022	C153444
K2224258	Certificate of Analysis	Aug 19, 2022	C153444
K2224259	Certificate of Analysis	Aug 19, 2022	C153444
A2331182	Certificate of Analysis	Nov 15, 2021	C153444

Chemical and Physical Properties

Specific Rotation[α]	139° (C=1,0.1mol/L NaOH 3mL+H2O 7mL)
Melt Point(°C)	227°C

Safety and Hazards(GHS)

Pictogram(s)	GHS08, GHS07
Signal	Danger
Hazard Statements	H317:May cause an allergic skin reaction H334:May cause allergy or asthma symptoms or breathing difficulties if inhaled
Precautionary Statements	P261:Avoid breathing dust/fume/gas/mist/vapors/spray. P280:Wear protective gloves/protective clothing/eye protection/face protection. P302+P352:IF ON SKIN: wash with plenty of water. P321:Specific treatment (see ... on this label). P501:Dispose of contents/container to ... P284:[In case of inadequate ventilation] Wear respiratory protection. P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing. P272:Contaminated work clothing should not be allowed out of the workplace. P333+P313:IF SKIN irritation or rash occurs: Get medical advice/attention. P362+P364:Take off contaminated clothing and wash it before reuse. P342+P316:If experiencing respiratory symptoms: Get emergence medical help immediately.
RTECS	XI0367375
Reaxy-Rn	5777502
Merck Index	1951

Alternative Products

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Shuangmin Wu, Wei Shen, Yushuang Chen, Yongli Zhu, Ren Hou, Menghong Dai, Dapeng Peng. (2022) Rapid Determination of Cephalexin in Animal-Derived Food by an Indirect Competitive Enzyme-Linked Immunosorbent Assay. ANALYTICAL LETTERS, 55 (17): (2803-2816). [PMID:] [10.1080/00032719.2022.2072857]
2. Ali M. R., Bacchu M. S., Al-Mamun M. R., Rahman M. M., Ahommed M. S., Aly M. Aly Saad, Khan M. Z. H.. (2021) Sensitive MWCNT/P-Cys@MIP sensor for selective electrochemical detection of ceftizoxime. JOURNAL OF MATERIALS SCIENCE, 56 (22): (12803-12813). [PMID:] [10.1007/s10853-021-06115-6]

References

1. Cui L, Neoh HM, Shoji M, Hiramatsu K. (2009) Contribution of vraSR and graSR point mutations to vancomycin resistance in vancomycin-intermediate Staphylococcus aureus.. Antimicrob Agents Chemother, 53 (3): (1231-4). [PMID:19124662] [10.1021/op500134e]
2. Blaszczak LC, Brown RF, Cook GK, Hornback WJ, Hoying RC, Indelicato JM, Jordan CL, Katner AS, Kinnick MD, McDonald 3rd JH et al.. (1990) Comparative reactivity of 1-carba-1-dethiacephalosporins with cephalosporins.. J Med Chem, 33 (6): (1656-62). [PMID:2342058] [10.1021/op500134e]
3. Shuangmin Wu, Wei Shen, Yushuang Chen, Yongli Zhu, Ren Hou, Menghong Dai, Dapeng Peng. (2022) Rapid Determination of Cephalexin in Animal-Derived Food by an Indirect Competitive Enzyme-Linked Immunosorbent Assay. ANALYTICAL LETTERS, 55 (17): (2803-2816). [PMID:] [10.1080/00032719.2022.2072857]
4. Ali M. R., Bacchu M. S., Al-Mamun M. R., Rahman M. M., Ahommed M. S., Aly M. Aly Saad, Khan M. Z. H.. (2021) Sensitive MWCNT/P-Cys@MIP sensor for selective electrochemical detection of ceftizoxime. JOURNAL OF MATERIALS SCIENCE, 56 (22): (12803-12813). [PMID:] [10.1007/s10853-021-06115-6]

Solution Calculators

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SKU	Size	Availability	Price
C153444-1g	1g	In stock	$36.90
C153444-5g	5g	In stock	$108.90
C153444-25g	25g	In stock	$487.90

Ceftizoxime - >98.0%(HPLC), high purity , CAS No.68401-81-0

Basic Description

Associated Targets(Human)

Associated Targets(non-human)

Mechanisms of Action

Names and Identifiers

Database links

Certificates

Certificate of Analysis(COA)

Chemical and Physical Properties

Safety and Hazards(GHS)

Related Documents

Alternative Products

Citations of This Product

References

Solution Calculators

Molarity Calculator

Dilution Calculator

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