Cloxacillin

Cloxacillin

SCHEMBL8728823

Cc1onc(-c2ccccc2Cl)c1C(=O)NC1C(=O)N2C1SC(C)(C)[C@@H]2C(=O)O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

mecApbp2pbp4pbpApbpF

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

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
ABCB11 O95342 3/20 1.00
LMNA P02545 4/20 0.84
HPGD P15428 3/20 0.84
CYP1A2 P05177 1/20 0.79
KMT2A Q03164 2/20 0.71
MEN1 O00255 1/20 0.71
TDP1 Q9NUW8 1/20 0.71
SLCO1B3 Q9NPD5 1/20 0.70
SLCO1B1 Q9Y6L6 1/20 0.70
ALDH1A1 P00352 1/20 0.68
SMN1; SMN2 Q16637 1/20 0.68
PTGS1 P23219 1/20 0.55
PDE3A Q14432 1/20 0.55
HRH1 P35367 1/20 0.51
SLC22A8 Q8TCC7 1/20 0.51
CYP2C19 P33261 1/20 0.51

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
Cloxacillin SCHEMBL11404593 1.00 ABCB11 (1.00) ABCB11LMNAHPGDCYP1A2KMT2A
Cloxacillin SCHEMBL11404577 1.00 ABCB11 (1.00) ABCB11LMNAHPGDCYP1A2KMT2A
Cloxacillin SCHEMBL16333855 1.00 ABCB11 (1.00) ABCB11LMNAHPGDCYP1A2KMT2A
Cloxacillin SCHEMBL1625107 1.00 ABCB11 (1.00) ABCB11LMNAHPGDCYP1A2KMT2A
Cloxacillin SCHEMBL31229061 1.00 ABCB11 (1.00) ABCB11LMNAHPGDCYP1A2KMT2A
Cloxacillin SCHEMBL2953 1.00 ABCB11 (1.00) ABCB11LMNAHPGDCYP1A2KMT2A
Cloxacillin SCHEMBL11404582 1.00 ABCB11 (1.00) ABCB11LMNAHPGDCYP1A2KMT2A
Cloxacillin SCHEMBL41014 0.99 ABCB11 (0.98) ABCB11LMNAHPGDCYP1A2KMT2A
Cloxacillin SCHEMBL28547421 0.99 ABCB11 (0.98) ABCB11LMNAHPGDCYP1A2KMT2A
Cloxacillin SCHEMBL5550210 0.98 ABCB11 (0.97) ABCB11LMNAHPGDCYP1A2KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5017566-A Redox systems for brain-targeted drug delivery UNIVERSITY OF FLORIDA (US) 1991-05-21 US claimed
US-5002935-A Inclusion Complexing Hydroxypropylcyclodextrin with a Dihydropyridine-substituted Drug UNIVERSITY OF FLORIDA (US) 1991-03-26 US claimed
EP-0335545-B2 Pharmaceutical formulations for parenteral use UNIV FLORIDA (US) 1998-09-23 EP disclosed
US-5024998-A Administering in aqueous solution with cyclodextrin derivative UNIVERSITY OF FLORIDA (US) 1991-06-18 US disclosed
US-4983586-A Decreasing precipitation at injection site or in lungs or other organs by combining with hydroxypropyl-beta-cyclodextrin UNIVERSITY OF FLORIDA (US) 1991-01-08 US disclosed
EP-0335545-A2 Pharmaceutical formulations for parenteral use UNIVERSITY OF FLORIDA (US) 1989-10-04 EP disclosed