SCHEMBL1065719

SCHEMBL1065719

CCS(=O)(=O)O.O=S(=O)(O)CCS(=O)(=O)O

nearest known ligand 0.50

Known targets — ChEMBL curated mechanism

DRD2

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 19)

geneUniProtsupporting neighboursconfidence
PTGS1 P23219 1/20 0.50
PDE4A P27815 1/20 0.50
LMNA P02545 1/20 0.50
SLC6A6 P31641 1/20 0.50
CYP2C19 P33261 1/20 0.50
BLM P54132 1/20 0.50
APP P05067 1/20 0.45
CA5A P35218 2/20 0.36
CA5B Q9Y2D0 2/20 0.36
EPHX2 P34913 1/20 0.32
TSHR P16473 2/20 0.31
CA1 P00915 1/20 0.31
CA2 P00918 1/20 0.31
NT5E P21589 1/20 0.31
CA4 P22748 1/20 0.31
CA6 P23280 1/20 0.31
CA7 P43166 1/20 0.31
CA9 Q16790 1/20 0.31
TDP1 Q9NUW8 1/20 0.31

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
Methyl Alcohol SCHEMBL7651538 0.88 PTGS1 (0.53) PTGS1PDE4ALMNASLC6A6CYP2C19
SCHEMBL21777928 0.88 PTGS1 (0.60) PTGS1PDE4ALMNASLC6A6CYP2C19
SCHEMBL2058760 0.88 CA5A (0.46) PTGS1PDE4ALMNASLC6A6CYP2C19
SCHEMBL126970 0.88
SCHEMBL2622 0.88 PTGS1 (0.60) PTGS1PDE4ALMNASLC6A6CYP2C19
SCHEMBL1904 0.88
SCHEMBL8768770 0.86 LMNA (0.45) PTGS1PDE4ALMNASLC6A6CYP2C19
Methyl Alcohol SCHEMBL23421569 0.84
SCHEMBL22581624 0.84
SCHEMBL20533683 0.84

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-20240158339-A1 TYRAMINE CONTAINING HYDROXYCINNAMIC ACID AMIDE DERIVATIVES AND METHODS OF USE THEREOF Sanford Burnham Prebys Medical Discovery Institute 2024-05-16 US disclosed
EP-3288548-A1 NOVEL PRODRUGS OF DITHIOL MUCOLYTIC AGENTS Parion Sciences, Inc. (US) 2018-03-07 EP disclosed
WO-2016176423-A1 NOVEL PRODRUGS OF DITHIOL MUCOLYTIC AGENTS PARION SCIENCES, INC. (US) 2016-11-03 WO disclosed
US-20150307530-A1 NOVEL MUCOLYTIC AGENTS PARION SCIENCES, INC. (US) 2015-10-29 US disclosed
US-7863286-B2 Stereoisomerically enriched 3-aminocarbonyl bicycloheptene pyrimidinediamine compounds and their uses RIGEL PHARMACEUTICALS, INC. (US) 2011-01-04 US disclosed
US-20070179140-A1 Stereoisomerically Enriched 3-Aminocarbonyl Bicycloheptene Pyrimidinediamine Compounds And Their Uses RIGEL PHARMACEUTICALS, INC. (US) 2007-08-02 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 (3 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-20150307530-A1 NOVEL MUCOLYTIC AGENTS MUC1, MMP8, MMP7 PTGS1 402/4885PDE4A 127/4885LMNA 4248/4885
US-20070179140-A1 Stereoisomerically Enriched 3-Aminocarbonyl Bicycloheptene Pyrimidinediamine Compounds And Their Uses MKI67, PCNA, CCNI PTGS1 1882/4885PDE4A 2948/4885LMNA 3220/4885
US-20240158339-A1 TYRAMINE CONTAINING HYDROXYCINNAMIC ACID AMIDE DERIVATIVES AND METHODS OF USE THEREOF GLS2, LIPC, AADAT PTGS1 2165/4885PDE4A 3160/4885LMNA 2052/4885

“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.