(E)-cefprozil (Q3231623)

17 November 2015

Cefprozil.svg
512 × 224; 11 KB

0 references

mass

389.104542 dalton

1 reference

cefprozil (English)

4 October 2016

1 reference

C₁₈H₁₉N₃O₅S

1 reference

cefprozil (English)

19 November 2016

CC=CC1=C(N2C(C(C2=O)NC(=O)C(C3=CC=C(C=C3)O)N)SC1)C(=O)O

1 reference

cefprozil (English)

19 November 2016

C/C=C/C1=C(N2[C@@H]([C@@H](C2=O)NC(=O)[C@@H](C3=CC=C(C=C3)O)N)SC1)C(=O)O

1 reference

cefprozil (English)

19 November 2016

1.0 gram

route of administration

oral administration

1 reference

https://www.whocc.no/atc_ddd_index/?code=J01DC10

medical condition treated

Escherichia coli infectious disease

1 reference

13 December 2016

1 reference

upper respiratory tract infection

13 December 2016

1 reference

13 December 2016

1 reference

13 December 2016

1 reference

13 December 2016

1 reference

gram-negative bacterial infection

13 December 2016

1 reference

13 December 2016

staphylococcal infection

1 reference

Food and Drug Administration

13 December 2016

14 November 2005

1 reference

Inxight: Drugs Database

2 November 2018

https://drugs.ncats.io/drug/S1SDI2FJIY

https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a547cc0a-6af0-49c7-a5ea-c41684cc36ae

pharyngitis

start time

14 November 2005

approved by

Food and Drug Administration

1 reference

Inxight: Drugs Database

2 November 2018

https://drugs.ncats.io/drug/S1SDI2FJIY

https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a547cc0a-6af0-49c7-a5ea-c41684cc36ae

otitis media

start time

14 November 2005

approved by

Food and Drug Administration

1 reference

Inxight: Drugs Database

2 November 2018

https://drugs.ncats.io/drug/S1SDI2FJIY

https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a547cc0a-6af0-49c7-a5ea-c41684cc36ae

pregnancy category

US pregnancy category B

1 reference

imported from Wikimedia project

1 reference

5 March 2018

2 references

‎WHO Aware Classification

watch

1 reference

2023 ‎AWaRe classification‎

Identifiers

InChI

InChI=1S/C18H19N3O5S/c1-2-3-10-8-27-17-13(16(24)21(17)14(10)18(25)26)20-15(23)12(19)9-4-6-11(22)7-5-9/h2-7,12-13,17,22H,8,19H2,1H3,(H,20,23)(H,25,26)/b3-2+/t12-,13-,17-/m1/s1

1 reference

WDLWHQDACQUCJR-ZAMMOSSLSA-N

cefprozil (English)

19 November 2016

1 reference

cefprozil (English)

WDLWHQDACQUCJR-PBFPGSCMSA-N

19 November 2016

reason for deprecated rank

applies to other chemical entity

intended subject of deprecated statement

(EZ)-cefprozil

1 reference

ChEBI release 2020-09-01

CAS Registry Number

92676-86-3

2 references

Global Substance Registration System

UNII

S1SDI2FJIY

(E)-cefprozil anhydrous (English)

WDLWHQDACQUCJR-ZAMMOSSLSA-N

19 November 2016

InChIKey

8 April 2021

https://commonchemistry.cas.org/detail?cas_rn=92676-86-3

1 reference

(E)-Cefprozil (English)

19 November 2016

1 reference

cefprozil (English)

reason for deprecated rank

19 November 2016

Reaxys registry number

8167198

0 references

ChEBI ID

3506

applies to other chemical entity

intended subject of deprecated statement

1 reference

Cefprozil (English)

19 January 2016

1 reference

DSSTOX compound identifier

CEFPROZIL (English)

19 November 2016

0 references

0 references

1 reference

reason for deprecated rank

Cefprozil (English)

17 November 2015

Cefprozil

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MeSH tree code

D02.065.589.099.249.183

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D02.886.665.074.183

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D03.633.100.300.249.183

0 references

1 reference

26 February 2018

applies to other chemical entity

intended subject of deprecated statement

1 reference

Cefprozil (English)

Human Metabolome Database ID

19 November 2016

0 references

1 reference

Global Substance Registration System

UNII

S1SDI2FJIY

(E)-cefprozil anhydrous (English)

MedlinePlus drug identifier

19 November 2016

a698022

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PatientsLikeMe treatment ID

0 references

1 reference

CEFPROZIL (English)

19 January 2016

0 references

1 reference

1 reference