SCHEMBL5459757

SCHEMBL5459757

Cc1ccc(S(=O)(=O)[O-])cc1.Cc1oc2ccccc2[n+]1C

nearest known ligand 0.42

Known targets — ChEMBL curated mechanism

CHRM1CHRM2CHRM3CHRM4CHRM5SLC6A2dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of None. 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 5/20 0.42
KDM4E B2RXH2 2/20 0.42
NPSR1 Q6W5P4 1/20 0.42
RXFP1 Q9HBX9 1/20 0.42
SMN1; SMN2 Q16637 4/20 0.41
PKM P14618 1/20 0.41
HPGD P15428 1/20 0.41
GAA P10253 2/20 0.40
PIK3CD O00329 1/20 0.37
PIK3CA P42336 1/20 0.37
PIK3CB P42338 1/20 0.37
PIK3CG P48736 1/20 0.37
LMNA P02545 3/20 0.36
CYP3A4 P08684 2/20 0.36
CYP2D6 P10635 1/20 0.36
MAPK1 P28482 1/20 0.36
THPO P40225 1/20 0.36
CA12 O43570 4/20 0.36
CA9 Q16790 4/20 0.36
HTT P42858 2/20 0.36

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
SCHEMBL7481019 0.83 ALDH1A1 (0.39) ALDH1A1KDM4ENPSR1RXFP1SMN1; SMN2
SCHEMBL31169578 0.83 CA12 (0.38) ALDH1A1KDM4ENPSR1RXFP1SMN1; SMN2
SCHEMBL1833906 0.82 KDM4E (0.41) ALDH1A1KDM4ENPSR1RXFP1SMN1; SMN2
Iodide SCHEMBL1874401 0.79 PTPN1 (0.35) ALDH1A1KDM4ELMNACYP3A4CYP2D6
SCHEMBL10424501 0.78 TP53 (0.47) ALDH1A1KDM4ESMN1; SMN2HPGDGAA
SCHEMBL7491820 0.76 ALDH1A1 (0.51) ALDH1A1KDM4ENPSR1RXFP1SMN1; SMN2
SCHEMBL7491818 0.76 ALDH1A1 (0.51) ALDH1A1KDM4ENPSR1RXFP1SMN1; SMN2
SCHEMBL1656260 0.75 ALDH1A1 (0.41) ALDH1A1KDM4ENPSR1RXFP1SMN1; SMN2
SCHEMBL3396649 0.74 KDM4E (0.41) ALDH1A1KDM4ENPSR1RXFP1SMN1; SMN2
SCHEMBL3180420 0.73 GAA (0.62) ALDH1A1KDM4ESMN1; SMN2PKMHPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20070281363-A1 Reporter molecules based on squaric, croconic, and/or rhodizonic acid; photoluminescence Terpetschnig, Ewald (US) 2007-12-06 US disclosed
US-6143434-A HIGH LUMINANCE AND A HIGH LUMINESCENT EFFICIENCY AT A LOW DRIVING VOLTAGE AND HAS EXCELLENT STABILITY IN REPETITIONS OF USE FUJI PHOTO FILM CO., LTD. (JP) 2000-11-07 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 (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-20070281363-A1 Reporter molecules based on squaric, croconic, and/or rhodizonic acid; photoluminescence SPR, SRRT, SQLE ALDH1A1 2350/4885KDM4E 2948/4885NPSR1 2668/4885

“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.