Cephalexin Anhydrous

drug
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Also known as AlsporinAnhydrous cephalexinCarnosporinCefadrosCefaleksinCefalexinCefalexin anhydrousCefalexinaCefalexineCephamastenDurantelEfalexinFelexinGarasinIwalexinKefloridinaLilly-66873MamalexinNSC-758162

Summary

Cephalexin Anhydrous (CHEMBL1727) is an approved small-molecule antibacterial drug.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • Clinical trials: 50
  • Chemistry: 347.4 Da · C16H17N3O4S

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1727
NameCephalexin Anhydrous
TypeSmall molecule
Max phase4
FDA approvedyes
PubChem CID27447
ChEBICHEBI:3534
Molecular formulaC16H17N3O4S
Molecular weight347.4
InChIKeyZAIPMKNFIOOWCQ-UEKVPHQBSA-N

SMILES: CC1=C(N2[C@@H]([C@@H](C2=O)NC(=O)[C@@H](C3=CC=CC=C3)N)SC1)C(=O)O

IUPAC name: (6R,7R)-7-[[(2R)-2-amino-2-phenylacetyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

ChEBI definition: A semisynthetic first-generation cephalosporin antibiotic having methyl and β-(2R)-2-amino-2-phenylacetamido groups at the 3- and 7- of the cephem skeleton, respectively. It is effective against both Gram-negative and Gram-positive organisms, and is used for treatment of infections of the skin, respiratory tract and urinary tract.

Pharmacological roles (ChEBI): antibacterial drug.

Also known as: Alsporin, Anhydrous cephalexin, Carnosporin, Cefadros, Cefaleksin, Cefalexin, Cefalexin anhydrous, Cefalexina, Cefalexine, Cephalexin anhydrous, Cephamasten, Durantel

Parent form; salt/anhydrous children: CHEMBL1200366, CHEMBL1200544

Patent coverage: 18,458 distinct patent families (59,411 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Broader ChEMBL bioactivity targets: 11 (assay-derived). Sample: Tyrosyl-DNA phosphodiesterase 1, Microtubule-associated protein tau, Fructose-bisphosphate aldolase, 4’-phosphopantetheinyl transferase ffp, 15-hydroxyprostaglandin dehydrogenase [NAD(+)], Solute carrier family 15 member 2, 5-hydroxytryptamine receptor 2B, Alpha-1A adrenergic receptor, Solute carrier family 15 member 2, Aldehyde dehydrogenase 1A1, Mitogen-activated protein kinase 1.

Bioactivity

ChEMBL activities: 3 potent at pChembl ≥ 5 of 16 total. Top 100 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
ADRA1A5.24AC505780nMCHEMBL_ACT_25137922
HTR2B5.2AC506306nMCHEMBL_ACT_25164106
MAPK15.1Potency7943nMCHEMBL_ACT_4701491

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

0 indication records carry no mapped disease name (EFO/MeSH-only); none shown.

Clinical trials

Total trials: 50.

Phase distribution

PhaseTrials
PHASE414
PHASE113
Not specified9
PHASE27
PHASE35
PHASE2/PHASE31
PHASE1/PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01912651PHASE4RECRUITINGThe Role of Antibiotics in Full Thickness Skin Graft Survival for Facial Reconstructive Surgery
NCT04297592PHASE4ENROLLING_BY_INVITATIONAntibiotic Prophylaxis in High-Risk Arthroplasty Patients
NCT04538053PHASE4RECRUITINGBonE and Joint Infections - Simplifying Treatment in Children Trial
NCT04580472PHASE4ACTIVE_NOT_RECRUITINGUtility of Single-dose Oral Antibiotic Prophylaxis in Prevention of Surgical Site Infection in Dermatologic Surgery
NCT05852262PHASE4ENROLLING_BY_INVITATIONHigh-dose Cephalexin for Cellulitis (HI-DOCC)
NCT06055712PHASE4ENROLLING_BY_INVITATIONAntibiotic Prophylaxis in Pediatric Open Fractures
NCT00234949PHASE4COMPLETEDA Study to Compare Cefdinir and Cephalexin for the Treatment of Mild to Moderate Uncomplicated Skin Infections
NCT00352612PHASE4COMPLETEDComparison of Cephalexin Versus Clindamycin for Suspected CA-MRSA Skin Infections
NCT04471246PHASE4COMPLETEDHigh-dose vs. Standard-dose Cephalexin for Cellulitis
NCT04834310PHASE4WITHDRAWNPostoperative Antibiotics Following Primary and Secondary Breast Augmentation
NCT05156437PHASE4TERMINATEDPostoperative Antibiotic Management Duration Following Surgery for Intravenous Drug Abuse (IVDA) Endocarditis (OPTIMAL)
NCT05274672PHASE4WITHDRAWNRole of Prophylactic Postoperative Antibiotics in HoLEP
NCT05977868PHASE4TERMINATEDComparing Oral Versus Parenteral Antimicrobial Therapy
NCT06127160PHASE4COMPLETEDPatient-Directed Antimicrobial Duration in Acute Uncomplicated Pyelonephritis
NCT00003824PHASE3TERMINATEDS9809, Ciprofloxacin Compared With Cephalexin in Treating Patients With Bladder Cancer
NCT00729937PHASE2/PHASE3COMPLETEDStrategies Using Off-Patent Antibiotics for Methicillin Resistant S. Aureus STOP MRSA
NCT01002911PHASE3COMPLETEDPrevention of Arrhythmia Device Infection Trial (PADIT Pilot)
NCT02809131PHASE3COMPLETEDPerioperative Antibiotic Therapy to Prevent Cardiac Implantable Electronic Device Infections.
NCT04553419PHASE3UNKNOWNAntibiotic Treatment Of Staphylococcus Aureus In Stable People With CF
NCT04577846PHASE3UNKNOWNSSI Rates in Patients Undergoing Mastectomy Without Reconstruction- A Multicenter, Double-blinded RCT.
NCT01631617PHASE2RECRUITINGEffects of Treatments on Atopic Dermatitis
NCT05020574PHASE2RECRUITINGMicrobiome and Association With Implant Infections
NCT06406114PHASE2RECRUITINGOptimizing the Diagnostic Approach to Cephalosporin Allergy Testing
NCT01029782PHASE2COMPLETEDComparison of Intravenous Cefazolin Plus Oral Probenecid With Oral Cephalexin for the Treatment of Cellulitis
NCT01595529PHASE2COMPLETEDThe SCOUT Study: Short Course Therapy for Urinary Tract Infections in Children
NCT02014558PHASE1/PHASE2COMPLETEDDose Escalation Study Investigating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics of ASP2215 in Patients With Relapsed or Refractory Acute Myeloid Leukemia
NCT02569866PHASE2COMPLETEDAntibiotics After Breast Reduction:Clinical Trial With Randomization
NCT05664568PHASE2UNKNOWNThe BLAST- 1 Trial - Cephalexin+Amoxicillin-clavulanate for Tuberculosis
NCT07300670PHASE1RECRUITINGThe Effect of Losartan on Cephalexin
NCT01073553PHASE1COMPLETEDCross-over Study to Prove Bioequivalence Between Two Brands of Cefalexin Capsules
NCT01767532PHASE1COMPLETEDBioequivalence Study of Cephalexin Suspension 125
NCT01767571PHASE1COMPLETEDBioequivalence Study of Cephalexin Suspension 250
NCT01767584PHASE1COMPLETEDBioequivalence Study of Cephalexin Tablets 1g
NCT02100826PHASE1COMPLETEDA Study of Cephalexin in Healthy Participants
NCT02123446PHASE1COMPLETEDA Study of Cephalexin Capsules in Healthy Participants
NCT02123459PHASE1COMPLETEDA Study of Cephalexin Suspension in Healthy Participants
NCT02123472PHASE1COMPLETEDA Study of Cephalexin Liquid for Pediatrics in Healthy Adults Participants
NCT02490670PHASE1COMPLETEDA Study of Cephalexin Liquid in Healthy Participants
NCT03187106PHASE1COMPLETEDProphylactic Antibiotics After Cesarean
NCT03802552PHASE1COMPLETEDCefadroxil and Cephalexin Drug Levels and Dosing in Pediatric Musculoskeletal Infections
NCT04916951PHASE1COMPLETEDOral Amoxicillin and Cephalexin PK/PD in Neonates
NCT00187759Not specifiedCOMPLETEDPlacebo Controlled Study of Antibiotic Treatment of Soft Tissue Infection
NCT00676130Not specifiedCOMPLETEDStudy of New Antibiotic Regimen for the Treatment of Uncomplicated Cellulitis in Emergency Department Patients
NCT01155154Not specifiedTERMINATEDAntibiotic Prophylaxis for Simple Hand Lacerations
NCT01194115Not specifiedUNKNOWNUse of 48 Hour Course of Antibiotics to Prevent Surgical Site Infection in Obese Patients Undergoing Cesarean Delivery
NCT01501747Not specifiedCOMPLETEDThe Placebo Effect May Involve Modulating Drug Bioavailability
NCT01823523Not specifiedUNKNOWNOrthognathic Surgery and Postoperative Antibiotic Use
NCT02911662Not specifiedTERMINATEDTreatment of Asymptomatic Bacteriuria in Pregnancy
NCT03357419Not specifiedWITHDRAWNThe Effect of Prophylactic Antibiotics on Surgical Site Infection Lower Limb Skin Excisions
NCT03736187Not specifiedUNKNOWNAntibiotics for Prevention of SSI in Obese Women Undergoing CS

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No CPIC/DPWG dosing guideline, but PharmGKB curates 1 clinical and 2 variant annotation(s) for this drug (gene-keyed; see PharmGKB).

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.