Cephalexin Anhydrous
drug drugOn this page
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
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL1727 |
| Name | Cephalexin Anhydrous |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | yes |
| PubChem CID | 27447 |
| ChEBI | CHEBI:3534 |
| Molecular formula | C16H17N3O4S |
| Molecular weight | 347.4 |
| InChIKey | ZAIPMKNFIOOWCQ-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):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| ADRA1A | 5.24 | AC50 | 5780 | nM | CHEMBL_ACT_25137922 |
| HTR2B | 5.2 | AC50 | 6306 | nM | CHEMBL_ACT_25164106 |
| MAPK1 | 5.1 | Potency | 7943 | nM | CHEMBL_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
| Phase | Trials |
|---|---|
| PHASE4 | 14 |
| PHASE1 | 13 |
| Not specified | 9 |
| PHASE2 | 7 |
| PHASE3 | 5 |
| PHASE2/PHASE3 | 1 |
| PHASE1/PHASE2 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT01912651 | PHASE4 | RECRUITING | The Role of Antibiotics in Full Thickness Skin Graft Survival for Facial Reconstructive Surgery |
| NCT04297592 | PHASE4 | ENROLLING_BY_INVITATION | Antibiotic Prophylaxis in High-Risk Arthroplasty Patients |
| NCT04538053 | PHASE4 | RECRUITING | BonE and Joint Infections - Simplifying Treatment in Children Trial |
| NCT04580472 | PHASE4 | ACTIVE_NOT_RECRUITING | Utility of Single-dose Oral Antibiotic Prophylaxis in Prevention of Surgical Site Infection in Dermatologic Surgery |
| NCT05852262 | PHASE4 | ENROLLING_BY_INVITATION | High-dose Cephalexin for Cellulitis (HI-DOCC) |
| NCT06055712 | PHASE4 | ENROLLING_BY_INVITATION | Antibiotic Prophylaxis in Pediatric Open Fractures |
| NCT00234949 | PHASE4 | COMPLETED | A Study to Compare Cefdinir and Cephalexin for the Treatment of Mild to Moderate Uncomplicated Skin Infections |
| NCT00352612 | PHASE4 | COMPLETED | Comparison of Cephalexin Versus Clindamycin for Suspected CA-MRSA Skin Infections |
| NCT04471246 | PHASE4 | COMPLETED | High-dose vs. Standard-dose Cephalexin for Cellulitis |
| NCT04834310 | PHASE4 | WITHDRAWN | Postoperative Antibiotics Following Primary and Secondary Breast Augmentation |
| NCT05156437 | PHASE4 | TERMINATED | Postoperative Antibiotic Management Duration Following Surgery for Intravenous Drug Abuse (IVDA) Endocarditis (OPTIMAL) |
| NCT05274672 | PHASE4 | WITHDRAWN | Role of Prophylactic Postoperative Antibiotics in HoLEP |
| NCT05977868 | PHASE4 | TERMINATED | Comparing Oral Versus Parenteral Antimicrobial Therapy |
| NCT06127160 | PHASE4 | COMPLETED | Patient-Directed Antimicrobial Duration in Acute Uncomplicated Pyelonephritis |
| NCT00003824 | PHASE3 | TERMINATED | S9809, Ciprofloxacin Compared With Cephalexin in Treating Patients With Bladder Cancer |
| NCT00729937 | PHASE2/PHASE3 | COMPLETED | Strategies Using Off-Patent Antibiotics for Methicillin Resistant S. Aureus STOP MRSA |
| NCT01002911 | PHASE3 | COMPLETED | Prevention of Arrhythmia Device Infection Trial (PADIT Pilot) |
| NCT02809131 | PHASE3 | COMPLETED | Perioperative Antibiotic Therapy to Prevent Cardiac Implantable Electronic Device Infections. |
| NCT04553419 | PHASE3 | UNKNOWN | Antibiotic Treatment Of Staphylococcus Aureus In Stable People With CF |
| NCT04577846 | PHASE3 | UNKNOWN | SSI Rates in Patients Undergoing Mastectomy Without Reconstruction- A Multicenter, Double-blinded RCT. |
| NCT01631617 | PHASE2 | RECRUITING | Effects of Treatments on Atopic Dermatitis |
| NCT05020574 | PHASE2 | RECRUITING | Microbiome and Association With Implant Infections |
| NCT06406114 | PHASE2 | RECRUITING | Optimizing the Diagnostic Approach to Cephalosporin Allergy Testing |
| NCT01029782 | PHASE2 | COMPLETED | Comparison of Intravenous Cefazolin Plus Oral Probenecid With Oral Cephalexin for the Treatment of Cellulitis |
| NCT01595529 | PHASE2 | COMPLETED | The SCOUT Study: Short Course Therapy for Urinary Tract Infections in Children |
| NCT02014558 | PHASE1/PHASE2 | COMPLETED | Dose Escalation Study Investigating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics of ASP2215 in Patients With Relapsed or Refractory Acute Myeloid Leukemia |
| NCT02569866 | PHASE2 | COMPLETED | Antibiotics After Breast Reduction:Clinical Trial With Randomization |
| NCT05664568 | PHASE2 | UNKNOWN | The BLAST- 1 Trial - Cephalexin+Amoxicillin-clavulanate for Tuberculosis |
| NCT07300670 | PHASE1 | RECRUITING | The Effect of Losartan on Cephalexin |
| NCT01073553 | PHASE1 | COMPLETED | Cross-over Study to Prove Bioequivalence Between Two Brands of Cefalexin Capsules |
| NCT01767532 | PHASE1 | COMPLETED | Bioequivalence Study of Cephalexin Suspension 125 |
| NCT01767571 | PHASE1 | COMPLETED | Bioequivalence Study of Cephalexin Suspension 250 |
| NCT01767584 | PHASE1 | COMPLETED | Bioequivalence Study of Cephalexin Tablets 1g |
| NCT02100826 | PHASE1 | COMPLETED | A Study of Cephalexin in Healthy Participants |
| NCT02123446 | PHASE1 | COMPLETED | A Study of Cephalexin Capsules in Healthy Participants |
| NCT02123459 | PHASE1 | COMPLETED | A Study of Cephalexin Suspension in Healthy Participants |
| NCT02123472 | PHASE1 | COMPLETED | A Study of Cephalexin Liquid for Pediatrics in Healthy Adults Participants |
| NCT02490670 | PHASE1 | COMPLETED | A Study of Cephalexin Liquid in Healthy Participants |
| NCT03187106 | PHASE1 | COMPLETED | Prophylactic Antibiotics After Cesarean |
| NCT03802552 | PHASE1 | COMPLETED | Cefadroxil and Cephalexin Drug Levels and Dosing in Pediatric Musculoskeletal Infections |
| NCT04916951 | PHASE1 | COMPLETED | Oral Amoxicillin and Cephalexin PK/PD in Neonates |
| NCT00187759 | Not specified | COMPLETED | Placebo Controlled Study of Antibiotic Treatment of Soft Tissue Infection |
| NCT00676130 | Not specified | COMPLETED | Study of New Antibiotic Regimen for the Treatment of Uncomplicated Cellulitis in Emergency Department Patients |
| NCT01155154 | Not specified | TERMINATED | Antibiotic Prophylaxis for Simple Hand Lacerations |
| NCT01194115 | Not specified | UNKNOWN | Use of 48 Hour Course of Antibiotics to Prevent Surgical Site Infection in Obese Patients Undergoing Cesarean Delivery |
| NCT01501747 | Not specified | COMPLETED | The Placebo Effect May Involve Modulating Drug Bioavailability |
| NCT01823523 | Not specified | UNKNOWN | Orthognathic Surgery and Postoperative Antibiotic Use |
| NCT02911662 | Not specified | TERMINATED | Treatment of Asymptomatic Bacteriuria in Pregnancy |
| NCT03357419 | Not specified | WITHDRAWN | The Effect of Prophylactic Antibiotics on Surgical Site Infection Lower Limb Skin Excisions |
| NCT03736187 | Not specified | UNKNOWN | Antibiotics 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).
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.