Cephalexin Anhydrous

Cephalexin Anhydrous

SCHEMBL2224252

CC1=C(C(=O)O)N2C(=O)[C@@H](NC(=O)[C@H](N)c3ccccc3)[C@H]2SC1.CC1=C(C(=O)O)N2C(=O)[C@@H](NC(=O)[C@H](N)c3ccccc3)[C@H]2SC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of Cephalexin Anhydrous. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HSD17B10 Q99714 7/20 1.00
MAPT P10636 7/20 1.00
ALDH1A1 P00352 6/20 1.00
KMT2A Q03164 5/20 1.00
CYP3A4 P08684 4/20 1.00
SLC15A2 Q16348 3/20 1.00
HPGD P15428 3/20 1.00
TDP1 Q9NUW8 3/20 1.00
BLM P54132 2/20 1.00
CYP2C19 P33261 2/20 1.00
MAPK1 P28482 2/20 1.00
ADRA1A P35348 1/20 1.00
HTR2B P41595 1/20 1.00
MEN1 O00255 4/20 0.85
LMNA P02545 2/20 0.85
ESR1 P03372 1/20 0.85
SLC22A6 Q4U2R8 1/20 0.85
SLC22A8 Q8TCC7 1/20 0.85
KDM4E B2RXH2 6/20 0.77
CYP2C9 P11712 2/20 0.77

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Cephalexin Anhydrous SCHEMBL8467348 1.00 HSD17B10 (1.00) HSD17B10MAPTALDH1A1KMT2ACYP3A4
Cephalexin Anhydrous SCHEMBL12961263 1.00 HSD17B10 (1.00) HSD17B10MAPTALDH1A1KMT2ACYP3A4
Cephalexin Anhydrous SCHEMBL11985597 1.00 HSD17B10 (1.00) HSD17B10MAPTALDH1A1KMT2ACYP3A4
Cephalexin Anhydrous SCHEMBL11579781 1.00 HSD17B10 (1.00) HSD17B10MAPTALDH1A1KMT2ACYP3A4
Cephalexin Anhydrous SCHEMBL6663551 1.00 HSD17B10 (1.00) HSD17B10MAPTALDH1A1KMT2ACYP3A4
Cephalexin Anhydrous SCHEMBL10713860 1.00 HSD17B10 (1.00) HSD17B10MAPTALDH1A1KMT2ACYP3A4
Cephalexin Anhydrous SCHEMBL6663545 1.00 HSD17B10 (1.00) HSD17B10MAPTALDH1A1KMT2ACYP3A4
Cephalexin Anhydrous SCHEMBL2961 1.00 HSD17B10 (1.00) HSD17B10MAPTALDH1A1KMT2ACYP3A4
Cephalexin Anhydrous SCHEMBL20703090 1.00 HSD17B10 (1.00) HSD17B10MAPTALDH1A1KMT2ACYP3A4
Cephalexin Anhydrous SCHEMBL11569012 1.00 HSD17B10 (1.00) HSD17B10MAPTALDH1A1KMT2ACYP3A4

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 35 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3344325-A1 LOCAL ADMINISTRATION OF DRUGS FOR THE TREATMENT OF ASTHMA Mercator Medsystems, Inc. (US) 2018-07-11 EP disclosed
WO-2017040605-A1 LOCAL ADMINISTRATION OF DRUGS FOR THE TREATMENT OF ASTHMA MERCATOR MEDSYSTEMS, INC. (US) 2017-03-09 WO disclosed
EP-3086646-A2 PLANTS CONTAINING BENEFICIAL ENDOPHYTES Indigo AG, Inc. (US) 2016-11-02 EP disclosed
US-20150211044-A1 QUICK METHOD FOR DETECTING ENYZMES AND MICROORGANISMS BIO-RAD EUROPE GMBH (CH) 2015-07-30 US disclosed
WO-2015100431-A2 PLANTS CONTAINING BENEFICIAL ENDOPHYTES SYMBIOTA, INC. (US) 2015-07-02 WO disclosed
US-9012167-B2 Quick method for detecting enzymes and microorganisms BIO-RAD INNOVATIONS (FR) 2015-04-21 US disclosed
WO-2014028745-A2 A SYSTEM FOR COMPOUNDING AND PACKAGING READY TO RECONSTITUTE DRUG POWDERS OF SOLUTIONS TO A SOLUTION OR TO A SUSPENSION OR TO AN INJECTABLE ARCHON PHARMACEUTICAL CONSULTING LLC (US) 2014-02-20 WO disclosed
US-20130089883-A1 QUICK METHOD FOR DETECTING ENYZMES AND MICROORANISMS BIO-RAD INNOVATIONS (FR) 2013-04-11 US disclosed
EP-2538970-A1 TREATMENT OR PREVENTION OF INFECTION Oral Health Australia Pty Ltd (AU) 2013-01-02 EP disclosed
EP-2534202-A1 POLYMER COMPOSITION Mitsubishi Chemical Europe GmbH (DE) 2012-12-19 EP disclosed
EP-0878229-A2 Process for removal of high-molecular compounds from a process stream CHEMFERM V.O.F. (NL) 1998-11-18 EP disclosed
EP-0869962-A1 PROCESS FOR THE RECOVERY OF A BETA-LACTAM ANTIBIOTIC CHEMFERM V.O.F. (NL) 1998-10-14 EP disclosed
CN-1179779-A Process for recovery of cephalexin CHEMFERM VOF (NL) 1998-04-22 CN disclosed
WO-1996023797-A1 PROCESS FOR THE RECOVERY OF A β-LACTAM ANTIBIOTIC CHEMFERM V.O.F. (NL) 1996-08-08 WO disclosed
US-4965193-A Using beta-lactamase ring-containing substrate whose amide bond is hydrolyzed in the presence of beta-lactamase WASHINGTON RESEARCH FOUNDATION (US) 1990-10-23 US disclosed
WO-1989003889-A1 DETECTION OF MICROBIAL BETA-LACTAMASE WASHINGTON RESEARCH FOUNDATION (US) 1989-05-05 WO disclosed
US-4680390-A CEPHALOSPORINS TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1987-07-14 US disclosed
US-4520194-A BACTERICIDES TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1985-05-28 US disclosed
US-4510138-A 7-[2-(2-Aminothiazol-4-yl)-2-(syn)-methoxyiminoacetamido]cephalosporin derivatives TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1985-04-09 US disclosed
US-4278671-A ANTIBIOTICS, BACTERICIDES TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1981-07-14 US disclosed