Cefaclor Anhydrous

Cefaclor Anhydrous

SCHEMBL6155629

NC(C(=O)NC1C(=O)N2C(C(=O)O)=C(Cl)CSC12)c1ccccc1

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 Cefaclor 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
ALDH1A1 P00352 7/20 1.00
HSD17B10 Q99714 7/20 1.00
MAPT P10636 7/20 1.00
KMT2A Q03164 6/20 1.00
KDM4E B2RXH2 5/20 1.00
MEN1 O00255 5/20 1.00
CYP3A4 P08684 4/20 1.00
HPGD P15428 3/20 1.00
TDP1 Q9NUW8 3/20 1.00
SLC15A2 Q16348 3/20 1.00
CYP2C9 P11712 2/20 1.00
LMNA P02545 2/20 1.00
NR1I2 O75469 1/20 1.00
ADORA3 P0DMS8 1/20 1.00
CTDSP1 Q9GZU7 1/20 1.00
HIF1A Q16665 1/20 1.00
CYP2C19 P33261 2/20 0.77
BLM P54132 1/20 0.77
MAPK1 P28482 1/20 0.77
ADRA1A P35348 1/20 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
Cefaclor Anhydrous SCHEMBL49912 1.00 ALDH1A1 (1.00) ALDH1A1HSD17B10MAPTKMT2AKDM4E
Cefaclor Anhydrous SCHEMBL33540 1.00 ALDH1A1 (1.00) ALDH1A1HSD17B10MAPTKMT2AKDM4E
Cefaclor Anhydrous SCHEMBL8626211 1.00 ALDH1A1 (1.00) ALDH1A1HSD17B10MAPTKMT2AKDM4E
Cefaclor Anhydrous SCHEMBL8524989 1.00 ALDH1A1 (1.00) ALDH1A1HSD17B10MAPTKMT2AKDM4E
Cefaclor Anhydrous SCHEMBL8943624 1.00 ALDH1A1 (1.00) ALDH1A1HSD17B10MAPTKMT2AKDM4E
Cefaclor Anhydrous SCHEMBL16072812 1.00 ALDH1A1 (1.00) ALDH1A1HSD17B10MAPTKMT2AKDM4E
Cefaclor Anhydrous SCHEMBL8478823 1.00 ALDH1A1 (1.00) ALDH1A1HSD17B10MAPTKMT2AKDM4E
Cefaclor Anhydrous SCHEMBL1006419 1.00 ALDH1A1 (1.00) ALDH1A1HSD17B10MAPTKMT2AKDM4E
Cefaclor Anhydrous SCHEMBL8626208 1.00 ALDH1A1 (1.00) ALDH1A1HSD17B10MAPTKMT2AKDM4E
Cefaclor Anhydrous SCHEMBL27281884 1.00 ALDH1A1 (1.00) ALDH1A1HSD17B10MAPTKMT2AKDM4E

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 14 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20190352691-A1 PATHOGEN DETECTION UNIVERSITY OF NOTRE DAME DU LAC (US) 2019-11-21 US disclosed
EP-2528589-B1 STABLE EFERVESCENT FORMULATIONS COMPRISING CEFACLOR BILGIC MAHMUT (TR) 2017-08-16 EP disclosed
US-20160368878-A1 REDUCTION-TRIGGERED ANTIBACTERIAL SIDEROMYCINS NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2016-12-22 US disclosed
US-20160319322-A1 PATHOGEN DETECTION UNIVERSITY OF NOTRE DAME DU LAC (US) 2016-11-03 US disclosed
EP-2181330-B2 COMPOSITIONS AND MEANS FOR DIAGNOSING MICROBIAL INFECTIONS STATENS SERUMINSTITUT (DK) 2016-08-31 EP disclosed
EP-2181330-B1 COMPOSITIONS AND MEANS FOR DIAGNOSING MICROBIAL INFECTIONS STATENS SERUMINSTITUT (DK) 2013-11-20 EP disclosed
EP-0523585-B1 Improvements in or relating to beta lactam production SANDOZ AG (CH) 2005-02-02 EP disclosed
EP-1043978-B1 PHOSPHOLIPID-COATED MICROCRYSTALS FOR THE SUSTAINED RELEASE OF PHARMACOLOGICALLY ACTIVE COMPOUNDS AND METHODS OF THEIR MANUFACTURE AND USE IDEXX LAB INC (US) 2004-06-09 EP disclosed
US-6423338-B1 PHOSPHATIDES AND MICROCRYSTALS IDEXX PHARMACEUTICALS, INC. 2002-07-23 US disclosed
US-6180136-B1 USEFUL FOR TREATING RESPIRATORY DISEASES, INFECTIONS, INFLAMMATION, AND PAIN IN VARIETY OF MAMMALS; ALSO ABLE TO SHARPLY REDUCE TOXICITY OF DRUG COMPOUNDS IDEXX LABORATORIES, INC. 2001-01-30 US disclosed
EP-1043978-A1 PHOSPHOLIPID-COATED MICROCRYSTALS FOR THE SUSTAINED RELEASE OF PHARMACOLOGICALLY ACTIVE COMPOUNDS AND METHODS OF THEIR MANUFACTURE AND USE IDEXX LABORATORIES, INC. (US) 2000-10-18 EP disclosed
WO-2000027369-A1 PHOSPHOLIPID-COATED MICROCRYSTALS FOR THE SUSTAINED RELEASE OF PHARMACOLOGICALLY ACTIVE COMPOUNDS AND METHODS OF THEIR MANUFACTURE AND USE IDEXX LABORATORIES, INC. (US) 2000-05-18 WO disclosed
US-5608055-A Beta lactam production BIOCHEMIE GESELLSCHAFT M.B.H. (AT) 1997-03-04 US disclosed
EP-0523585-A2 Improvements in or relating to beta lactam production BIOCHEMIE Gesellschaft m.b.H. (AT) 1993-01-20 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20160368878-A1 REDUCTION-TRIGGERED ANTIBACTERIAL SIDEROMYCINS HAMP, SLC40A1, FTH1 ALDH1A1 4009/4885HSD17B10 1192/4885MAPT 3298/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.