SCHEMBL7524657

SCHEMBL7524657

Cc1cc(C(C)(C)C)cc(Sc2cc(C(C)(C)C)cc(C)c2O)c1O

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 5/20 0.47
▸ ALOX15 P16050 4/20 0.47
▸ SMN1; SMN2 Q16637 3/20 0.47
▸ TDP1 Q9NUW8 2/20 0.47
▸ TP53 P04637 2/20 0.47
▸ CYP3A4 P08684 2/20 0.47
▸ TSHR P16473 2/20 0.47
▸ MAPK1 P28482 2/20 0.47
▸ HIF1A Q16665 2/20 0.47
▸ GABRA1 P14867 2/20 0.44
▸ GABRB2 P47870 2/20 0.44
▸ CYP2C19 P33261 3/20 0.42
▸ CYP1A2 P05177 2/20 0.42
▸ CYP2C9 P11712 2/20 0.42
▸ POLB P06746 3/20 0.41
▸ ESR1 P03372 3/20 0.39
▸ ESR2 Q92731 2/20 0.39
▸ CYP2D6 P10635 1/20 0.38
▸ HTR1D P28221 2/20 0.37
▸ HTR1B P28222 1/20 0.37

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
SCHEMBL11988588 0.85 GABRA1 (0.43) ALDH1A1ALOX15SMN1; SMN2TDP1TP53
SCHEMBL16977970 0.82 GABRA1 (0.40) ALDH1A1ALOX15SMN1; SMN2TDP1TP53
SCHEMBL201609 0.81 GABRA1 (0.57) ALDH1A1ALOX15SMN1; SMN2TDP1HIF1A
SCHEMBL3820150 0.81 CA2 (0.46) ALDH1A1ALOX15SMN1; SMN2TDP1TP53
SCHEMBL31131308 0.81 CA2 (0.46) ALDH1A1ALOX15SMN1; SMN2TDP1TP53
SCHEMBL28119481 0.79 GABRA1 (0.55) ALDH1A1ALOX15SMN1; SMN2TDP1HIF1A
SCHEMBL10299829 0.75 SMN1; SMN2 (0.59) ALDH1A1ALOX15SMN1; SMN2TDP1TP53
SCHEMBL70587 0.75 ALDH1A1 (0.50) ALDH1A1ALOX15SMN1; SMN2TDP1TP53
SCHEMBL19732817 0.75 GABRA1 (0.50) ALDH1A1ALOX15SMN1; SMN2TDP1HIF1A
Dimethylamine SCHEMBL8990212 0.75 GABRA1 (0.50) ALDH1A1ALOX15SMN1; SMN2TDP1GABRA1

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 64 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0027620-B1 2,2,6,6-TETRAALKYL-4-PIPERIDYL-BIS-SPIRO-ETHERS AND SYNTHETIC POLYMERS STABILISED THEREWITH ADEKA ARGUS CHEMICAL CO., Ltd. (JP) 1985-07-24 — — EP claimed
US-4305832-A ACETAL DERIVATIVES OF PHENOL SULFIDES, DISULFIDES OR POLYSULFIDES MOBIL OIL CORPORATION (US) 1981-12-15 — — US claimed
US-9834511-B2 Organodiaryl selenoxides and process for preparation thereof EVONIK DEGUSSA GMBH (DE) 2017-12-05 — — US disclosed
EP-3178829-A1 ORGANODIARYL SELENIUM OXIDES AND METHOD FOR THE PRODUCTION THEREOF Evonik Degussa GmbH (DE) 2017-06-14 — — EP disclosed
US-20170158726-A1 ORGANODIARYL SELENOXIDES AND PROCESS FOR PREPARATION THEREOF EVONIK DEGUSSA GMBH (DE) 2017-06-08 — — US disclosed
WO-2012143794-A1 POLYMER STABILIZER SYSTEM FOR POLYMERS CONTAINING HALOGEN GALATA CHEMICALS GMBH (DE) 2012-10-26 — — WO disclosed
US-20070203035-A1 Stabilizing compositions for lubricants LANXESS SOLUTIONS US INC. 2007-08-30 — — US disclosed
US-20070203035-A1 Stabilizing compositions for lubricants LANXESS SOLUTIONS US INC. 2007-08-30 — — US disclosed
EP-0888364-B1 Process to prepare a multidentate phosphite compound DSM NV (NL) 2002-02-06 — — EP disclosed
EP-0888364-A1 PROCESS TO PREPARE A MULTIDENTATE PHOSPHITE COMPOUND DSM N.V. (NL) 1999-01-07 — — EP disclosed
US-5710306-A REACTING A PHOSPHPHOROCHLORODITE WITH HYDOXY COMPOUND CONTAINING FUSED RING AND HYDROHALOGENATION DSM N.V. (NL) 1998-01-20 — — US disclosed
US-4174297-A Polyhydric phenol coester stabilizers ARGUS CHEMICAL CORPORATION (US) 1979-11-13 — — US disclosed
US-4171298-A SUBSTITUTED ORTHO-ALKYLHYDROXYBENZYLPROPANE-1,3-DIOL ESTERS ARGUS CHEMICAL CORPORATION (US) 1979-10-16 — — US disclosed
US-4146517-A FOR SYNTHETIC RESINS AGAINST HEAT ARGUS CHEMICAL CORPORATION (US) 1979-03-27 — — US disclosed
US-4124564-A LIGHT AND HEAT RESISTANCE ARGUS CHEMICAL CORPORATION (US) 1978-11-07 — — US disclosed
US-4115476-A 2,2,6,6-Tetramethyl-4-piperidyl carbonic acid esters of dihydric alcohols and phenols as stabilizers for synthetic polymers ARGUS CHEMICAL CORPORATION (US) 1978-09-19 — — US disclosed
US-4107136-A Synthetic resin stabilizer comprising an organic phosphite and a carbonate ARGUS CHEMICAL CORPORATION (US) 1978-08-15 — — US disclosed
US-4105629-A SYNTHETIC RESIN STABILIZER COMPRISING A THIOETHER ESTER AND HINDERED PHENOLIC CARBONATE ARGUS CHEMICAL CORPORATION (US) 1978-08-08 — — US disclosed
US-4013618-A NITROGEN-CONTAINING STABILIZER TOYOBO CO., LTD. (JA) 1977-03-22 — — US disclosed
US-3957905-A HALOGENATED BISPHENYL COMPOUND, ANTIMONY COMPOUND TOYO BOSEKI KABUSHIKI KAISHA (JA) 1976-05-18 — — 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-20170158726-A1 ORGANODIARYL SELENOXIDES AND PROCESS FOR PREPARATION THEREOF SCLY, SELENOI, GPX4 ALDH1A1 2085/4885ALOX15 1290/4885SMN1; SMN2 3204/4885

“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.

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