SCHEMBL2570798

SCHEMBL2570798

COC(=O)c1c(-c2ccccc2)noc1C(=O)O

nearest known ligand 0.86

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
PTGS1 P23219 3/20 0.71
ALDH1A1 P00352 6/20 0.60
POLB P06746 1/20 0.55
LMNA P02545 3/20 0.51
RAB9A P51151 1/20 0.51
SMN1; SMN2 Q16637 2/20 0.51
KDM4E B2RXH2 1/20 0.51
TP53 P04637 1/20 0.51
HPGD P15428 1/20 0.51
PTBP1 P26599 1/20 0.51
GAA P10253 2/20 0.50
GABRA1 P14867 1/20 0.50
GABRG2 P18507 1/20 0.50
GABRB3 P28472 1/20 0.50
GABRA5 P31644 1/20 0.50
GABRA3 P34903 1/20 0.50
MEN1 O00255 1/20 0.50
KMT2A Q03164 1/20 0.50

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
SCHEMBL2568217 0.92 PTGS1 (0.73) PTGS1ALDH1A1POLBLMNARAB9A
SCHEMBL2565750 0.91 PTGS1 (0.68) PTGS1ALDH1A1POLBLMNARAB9A
SCHEMBL2570531 0.88 PTGS1 (0.67) PTGS1ALDH1A1POLBLMNARAB9A
SCHEMBL4088587 0.84 ALDH1A1 (0.59) PTGS1ALDH1A1POLBLMNARAB9A
SCHEMBL2565912 0.84 PTPN1 (0.58) PTGS1ALDH1A1POLBLMNASMN1; SMN2
SCHEMBL12374641 0.83 PTGS1 (1.00) PTGS1ALDH1A1POLBLMNARAB9A
SCHEMBL4683450 0.83 PTGS1 (0.73) PTGS1ALDH1A1POLBLMNASMN1; SMN2
SCHEMBL408224 0.82 POLB (0.49) PTGS1ALDH1A1POLBRAB9ASMN1; SMN2
SCHEMBL12997955 0.82 LMNA (0.74) PTGS1ALDH1A1POLBLMNARAB9A
SCHEMBL2567463 0.82 PTGS1 (0.51) PTGS1ALDH1A1SMN1; SMN2KDM4EGAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8354398-B2 Substituted isoxazole compounds BRISTOL-MYERS SQUIBB COMPANY (US) 2013-01-15 US disclosed
US-8354398-B2 Substituted isoxazole compounds BRISTOL-MYERS SQUIBB COMPANY (US) 2013-01-15 US disclosed
US-20110300165-A1 SUBSTITUTED ISOXAZOLE COMPOUNDS The Board of TRustees of the University of Illinoi University of Illinios (US) 2011-12-08 US disclosed
US-20110300165-A1 SUBSTITUTED ISOXAZOLE COMPOUNDS The Board of TRustees of the University of Illinoi University of Illinios (US) 2011-12-08 US disclosed
US-20110300165-A1 SUBSTITUTED ISOXAZOLE COMPOUNDS The Board of TRustees of the University of Illinoi University of Illinios (US) 2011-12-08 US disclosed
EP-2382212-A1 SUBSTITUTED OXADIAZOLE DERIVATIVES AS S1P AGONISTS IN THE TREATMENT OF AUTOIMMUNE AND INFLAMMATORY DISEASES Bristol-Myers Squibb Company (US) 2011-11-02 EP disclosed
WO-2010085581-A1 SUBSTITUTED OXADIAZOLE DERIVATIVES AS S1P AGONISTS IN THE TREATMENT OF AUTOIMMUNE AND INFLAMMATORY DISEASES BRISTOL-MYERS SQUIBB COMPANY (US) 2010-07-29 WO 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-20110300165-A1 SUBSTITUTED ISOXAZOLE COMPOUNDS S1PR4, S1PR3, S1PR1 PTGS1 1441/4885ALDH1A1 1558/4885POLB 3843/4885

“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.