SCHEMBL8277341

SCHEMBL8277341

Cc1cc(Cl)c(F)c(C=O)c1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ERN1 O75460 6/20 0.48
ALDH1A1 P00352 6/20 0.40
KDM4E B2RXH2 2/20 0.40
MEN1 O00255 1/20 0.40
MAPT P10636 1/20 0.40
MPI P34949 1/20 0.40
KMT2A Q03164 1/20 0.40
SMN1; SMN2 Q16637 1/20 0.40
SRC P12931 2/20 0.39
TDP1 Q9NUW8 2/20 0.38
CYP1A2 P05177 2/20 0.34
CYP2C19 P33261 2/20 0.34
CYP3A4 P08684 1/20 0.34
CYP2D6 P10635 1/20 0.34
PTPN1 P18031 1/20 0.33
NPSR1 Q6W5P4 1/20 0.33
CYP2C9 P11712 1/20 0.33
HPGD P15428 1/20 0.33
NSD2 O96028 1/20 0.33
POLB P06746 1/20 0.33

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
SCHEMBL16722745 0.79 ERN1 (0.44) ERN1MEN1MAPTKMT2ATDP1
SCHEMBL12526044 0.78 ERN1 (0.47) ERN1ALDH1A1KDM4ESMN1; SMN2TDP1
SCHEMBL30711844 0.78 ERN1 (0.57) ERN1ALDH1A1MAPTTDP1CYP3A4
SCHEMBL12450080 0.78 ERN1 (0.52) ERN1ALDH1A1KDM4EMEN1MAPT
SCHEMBL10325195 0.78 ERN1 (0.52) ERN1ALDH1A1KDM4EMEN1MAPT
SCHEMBL27290171 0.78 ERN1 (0.52) ERN1ALDH1A1KDM4EMEN1MAPT
SCHEMBL17512175 0.78 ERN1 (0.57) ERN1ALDH1A1MAPTTDP1CYP3A4
SCHEMBL29953689 0.78 ERN1 (0.52) ERN1ALDH1A1KDM4EMEN1MAPT
SCHEMBL12449521 0.77 RAPGEF4 (0.36) ALDH1A1MAPTKMT2ATSHR
SCHEMBL8728790 0.76 TDP1 (0.41) ERN1ALDH1A1MEN1KMT2ATDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12012466-B2 Peptide macrocycles against Acinetobacter baumannii HOFFMANN-LA ROCHE INC. (US) 2024-06-18 US disclosed
US-20220411468-A1 PEPTIDE MACROCYCLES AGAINST ACINETOBACTER BAUMANNII HOFFMANN-LA ROCHE INC. (US) 2022-12-29 US disclosed
CN-108350028-B Peptide macrocycles against Acinetobacter baumannii 豪夫迈·罗氏有限公司 2021-12-07 CN disclosed
EP-3368544-B1 PEPTIDE MACROCYCLES AGAINST ACINETOBACTER BAUMANNII HOFFMANN LA ROCHE (CH) 2020-06-17 EP disclosed
US-20180362578-A1 PEPTIDE MACROCYCLES AGAINST ACINETOBACTER BAUMANNII HOFFMANN-LA ROCHE INC. (US) 2018-12-20 US disclosed
EP-3368544-A1 PEPTIDE MACROCYCLES AGAINST ACINETOBACTER BAUMANNII H. Hoffnabb-La Roche Ag (CH) 2018-09-05 EP disclosed
US-10030047-B2 Peptide macrocycles against acinetobacter baumannii HOFFMANN-LA ROCHE INC. (US) 2018-07-24 US disclosed
US-20170233437-A1 PEPTIDE MACROCYCLES AGAINST ACINETOBACTER BAUMANNII HOFFMANN-LA ROCHE INC. (US) 2017-08-17 US disclosed
WO-2017072062-A1 PEPTIDE MACROCYCLES AGAINST ACINETOBACTER BAUMANNII F. HOFFMANN-LA ROCHE AG (CH) 2017-05-04 WO disclosed
US-8642802-B2 Process for the preparation of halogenated benzoic acid derivatives HOFFMANN-LA ROCHE INC. (US) 2014-02-04 US disclosed
US-20120330055-A1 PROCESS FOR THE PREPARATION OF HALOGENATED BENZOIC ACID DERIVATIVES BACHMANN STEPHAN (CH) 2012-12-27 US disclosed
US-8329939-B2 Process for the preparation of halogenated benzoic acid derivatives HOFFMANN-LA ROCHE INC. (US) 2012-12-11 US disclosed
US-20120130121-A1 PROCESS FOR THE PREPARATION OF HALOGENATED BENZOIC ACID DERIVATIVES BACHMANN STEPHAN (CH) 2012-05-24 US 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 (7 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-20220411468-A1 PEPTIDE MACROCYCLES AGAINST ACINETOBACTER BAUMANNII VIP, ARG1, CX3CR1 ERN1 2560/4885ALDH1A1 4290/4885KDM4E 4323/4885
US-20120330055-A1 PROCESS FOR THE PREPARATION OF HALOGENATED BENZOIC ACID DERIVATIVES CYP2F1, GABRA5, CYP3A5 ERN1 3980/4885ALDH1A1 283/4885KDM4E 1209/4885
US-12012466-B2 Peptide macrocycles against Acinetobacter baumannii VIP, ARG1, CX3CR1 ERN1 2560/4885ALDH1A1 4290/4885KDM4E 4323/4885
US-20120130121-A1 PROCESS FOR THE PREPARATION OF HALOGENATED BENZOIC ACID DERIVATIVES CYP2F1, GABRA5, CYP3A5 ERN1 3980/4885ALDH1A1 283/4885KDM4E 1209/4885
US-20180362578-A1 PEPTIDE MACROCYCLES AGAINST ACINETOBACTER BAUMANNII VIP, ARG1, CX3CR1 ERN1 2560/4885ALDH1A1 4290/4885KDM4E 4323/4885
US-20170233437-A1 PEPTIDE MACROCYCLES AGAINST ACINETOBACTER BAUMANNII VIP, ARG1, CX3CR1 ERN1 2560/4885ALDH1A1 4290/4885KDM4E 4323/4885
US-10030047-B2 Peptide macrocycles against acinetobacter baumannii VIP, ARG1, CX3CR1 ERN1 2560/4885ALDH1A1 4290/4885KDM4E 4323/4885

“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.