SCHEMBL5401022

SCHEMBL5401022

CC(=O)OC1CC(COCc2ccccc2)N(S(=O)(=O)c2ccc3ccccc3c2)C1

nearest known ligand 0.44

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
MMP9 P14780 2/20 0.44
CCR4 P51679 5/20 0.41
BDKRB2 P30411 2/20 0.41
MMP1 P03956 1/20 0.41
MMP2 P08253 1/20 0.41
MMP3 P08254 1/20 0.41
MMP13 P45452 1/20 0.41
AKR1C3 P42330 3/20 0.40
AKR1C1 Q04828 1/20 0.40
ALDH1A1 P00352 1/20 0.39
LMNA P02545 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
MME P08473 2/20 0.39
ACE P12821 2/20 0.39
ECE1 P42892 2/20 0.39
KMT2A Q03164 1/20 0.38
LOX P28300 1/20 0.38
ELANE P08246 1/20 0.38
MCL1 Q07820 1/20 0.38

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
SCHEMBL5421525 0.92 MMP9 (0.41) MMP9CCR4BDKRB2MMP1MMP2
SCHEMBL5401021 0.92 MMP9 (0.41) MMP9CCR4BDKRB2MMP1MMP2
SCHEMBL5405158 0.87 CASP3 (0.44) AKR1C3AKR1C1ALDH1A1LMNASMN1; SMN2
SCHEMBL5414263 0.87 MMP9 (0.41) MMP9CCR4BDKRB2MMP1MMP2
SCHEMBL5414258 0.87 MMP9 (0.41) MMP9CCR4BDKRB2MMP1MMP2
SCHEMBL5415738 0.86 MMP9 (0.41) MMP9CCR4BDKRB2MMP1MMP2
SCHEMBL5412857 0.84 MMP1 (0.43) MMP9CCR4MMP1MMP2MMP3
SCHEMBL6859145 0.84 CCR4 (0.41) MMP9CCR4MMP1MMP2MMP3
SCHEMBL7688651 0.84 CCR4 (0.41) MMP9CCR4MMP1MMP2MMP3
SCHEMBL5410253 0.82 ECE1 (0.48) MMP9CCR4AKR1C3ALDH1A1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7189756-B2 Pyrrolidine derivatives HOFFMAN-LA ROCHE INC. (US) 2007-03-13 US disclosed
US-20040242672-A1 Useful as inhibitors of metalloproteases, e.g. zinc proteases; effective in treating disease states associated with vasoconstriction such as high blood pressure, coronary disorders, cardiac insufficiency, renal and myocardial ischaemia, renal insufficiency, dialysis, cerebral ischaemia AEBI JOHANNES (CH) 2004-12-02 US disclosed
US-6790860-B2 USEFUL AS INHIBITORS OF METALLOPROTEASES, E.G. ZINC PROTEASES; EFFECTIVE IN TREATING DISEASE STATES ASSOCIATED WITH VASOCONSTRICTION HOFFMANN-LA ROCHE INC. 2004-09-14 US disclosed
US-20030199569-A1 Pyrrolidine derivatives AEBI JOHANNES (CH) 2003-10-23 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 (2 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-20030199569-A1 Pyrrolidine derivatives PREP, PEPD, MMP3 MMP9 35/4885CCR4 1718/4885BDKRB2 370/4885
US-20040242672-A1 Useful as inhibitors of metalloproteases, e.g. zinc proteases; effective in treating disease states associated with vasoconstriction such as high blood pressure, coronary disorders, cardiac insufficiency, renal and myocardial ischaemia, renal insufficiency, dialysis, cerebral ischaemia MMP1, PEPD, MMP25 MMP9 7/4885CCR4 4267/4885BDKRB2 615/4885

“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.