SCHEMBL4425113

SCHEMBL4425113

COc1ccccc1-c1ccc(C)cc1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SYK P43405 2/20 0.56
ALDH1A1 P00352 3/20 0.54
MAPK1 P28482 2/20 0.54
L3MBTL1 Q9Y468 2/20 0.54
GAA P10253 2/20 0.54
NPC1 O15118 1/20 0.54
MAPT P10636 1/20 0.54
RAB9A P51151 1/20 0.54
SMN1; SMN2 Q16637 1/20 0.54
PTPRC P08575 1/20 0.53
PTPN1 P18031 1/20 0.53
XDH P47989 1/20 0.53
APP P05067 1/20 0.50
CA12 O43570 1/20 0.50
CA1 P00915 1/20 0.50
CA2 P00918 1/20 0.50
CA4 P22748 1/20 0.50
CA7 P43166 1/20 0.50
CA9 Q16790 1/20 0.50
CA14 Q9ULX7 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
SCHEMBL11982695 0.86 SYK (0.46) SYKALDH1A1MAPK1L3MBTL1GAA
SCHEMBL29628910 0.85 PTPRC (0.53) SYKALDH1A1MAPK1L3MBTL1GAA
SCHEMBL21102048 0.85 PTPRC (0.53) SYKALDH1A1MAPK1L3MBTL1GAA
SCHEMBL24106783 0.84 ALDH1A1 (0.55) ALDH1A1L3MBTL1GAANPC1RAB9A
SCHEMBL11499533 0.84 SYK (0.53) SYKALDH1A1MAPK1L3MBTL1GAA
SCHEMBL21471580 0.84 PTPRC (0.47) SYKALDH1A1MAPK1L3MBTL1GAA
SCHEMBL294721 0.84 ALDH1A1 (0.58) ALDH1A1MAPK1L3MBTL1GAANPC1
SCHEMBL30136447 0.84 ALDH1A1 (0.58) ALDH1A1MAPK1L3MBTL1GAANPC1
SCHEMBL1704521 0.83 ABL1 (0.62) SYKALDH1A1MAPK1L3MBTL1MAPT
SCHEMBL5690752 0.83 SQOR (0.55) SYKALDH1A1L3MBTL1NPC1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025111511-A2 REVERSIBLY REACTIVE AFFINITY SELECTION MASS SPECTROMETRY AND USES THEREOF CALICO LIFE SCIENCES LLC (US) 2025-05-30 WO disclosed
EP-3242875-B1 4,5-DIHYDROIMIDAZOLE DERIVATIVES AND THEIR USE AS HISTONE DEMETHYLASE (KDM2B) INHIBITORS GENENTECH INC (US) 2022-02-23 EP disclosed
WO-2022036063-A2 COMPOSITIONS AND METHODS FOR TREATING PROLIFERATIVE DISEASES THE BROAD INSTITUTE, INC. (US) 2022-02-17 WO disclosed
EP-3943490-A1 1-CYANO-PYRROLIDINE COMPOUNDS AS USP30 INHIBITORS Mission Therapeutics Limited (GB) 2022-01-26 EP disclosed
US-11091488-B2 1-cyano-pyrrolidine derivatives as inhibitors of USP30 MISSION THERAPEUTICS LIMITED (GB) 2021-08-17 US disclosed
US-11066365-B2 1-cyano-pyrrolidine compounds as USP30 inhibitors MISSION THERAPEUTICS LIMITED (GB) 2021-07-20 US disclosed
US-11053198-B2 1-cyano-pyrrolidine compounds as USP30 inhibitors MISSION THERAPEUTICS LIMITED (GB) 2021-07-06 US disclosed
EP-3842427-A1 1-CYANO-PYRROLIDINE COMPOUNDS AS USP30 INHIBITORS Mission Therapeutics Limited (GB) 2021-06-30 EP disclosed
US-10689345-B2 1-cyano-pyrrolidine compounds as USP30 inhibitors MISSION THERAPEUTICS LIMITED (GB) 2020-06-23 US disclosed
US-20200181086-A1 1-CYANO-PYRROLIDINE COMPOUNDS AS USP30 INHIBITORS MISSION THERAPEUTICS LIMITED (GB) 2020-06-11 US disclosed
US-20020137974-A1 Catalysis using phosphine oxide and sulfoxide compounds DUPONT POLYMERS, INC. 2002-09-26 US disclosed
EP-1235764-A1 CATALYSIS USING PHOSPHINE OXIDE COMPOUNDS E.I. DU PONT DE NEMOURS AND COMPANY (US) 2002-09-04 EP disclosed
US-6395916-B1 AMINE, PHOSPHINE LIGANDS MASSACHUSETTS INSTITUTE OF TECHNOLOGY 2002-05-28 US disclosed
WO-2002000574-A2 CATALYSIS USING PHOSPHINE OXIDE AND SULFOXIDE COMPOUNDS E. I. DU PONT DE NEMOURS AND COMPANY (US) 2002-01-03 WO disclosed
US-6307087-B1 USE OF CATALYSTS COMPRISING THESE LIGANDS IN TRANSITION METAL-CATALYZED CARBON-HETEROATOM AND CARBON-CARBON BOND-FORMING REACTIONS. MASSACHUSETTS INSTITUTE OF TECHNOLOGY 2001-10-23 US disclosed
US-6291722-B1 CONTACTING GRIGNARD REAGENT OF FORMULA R.SUP.7--MGX WITH AN ARYL COMPOUND OF THE FORMULA R.SUP.1--X IN THE PRESENCE OF A CATALYTIC AMOUNT OF COORDINATION COMPRISING TRASITION METAL COMPLEXED TO PHOSPHINE OXIDE TO PREPARE BISARYL COMPOUND E. I. DU PONT DE NEMOURS AND COMPANY 2001-09-18 US disclosed
WO-2001040147-A1 CATALYSIS USING PHOSPHINE OXIDE COMPOUNDS E.I. DU PONT DE NEMOURS AND COMPANY (US) 2001-06-07 WO disclosed
EP-1097158-A2 LIGANDS FOR METALS AND METAL-CATALYZED PROCESSES MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2001-05-09 EP disclosed
US-6124462-A PREPARING ARYLAMINE AND BIARYLS E. I. DU PONT DE NEMOURS AND COMPANY (US) 2000-09-26 US disclosed
WO-2000002887-A2 LIGANDS FOR METALS AND METAL-CATALYZED PROCESSES MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2000-01-20 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 (6 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-11091488-B2 1-cyano-pyrrolidine derivatives as inhibitors of USP30 USP30, USP1, USP20 SYK 3801/4885ALDH1A1 787/4885MAPK1 1265/4885
US-11066365-B2 1-cyano-pyrrolidine compounds as USP30 inhibitors USP30, USP20, USP10 SYK 2638/4885ALDH1A1 1172/4885MAPK1 3020/4885
US-20020137974-A1 Catalysis using phosphine oxide and sulfoxide compounds TST, GSS, ARSA SYK 1712/4885ALDH1A1 2774/4885MAPK1 1057/4885
US-11053198-B2 1-cyano-pyrrolidine compounds as USP30 inhibitors USP30, USP20, USP10 SYK 2615/4885ALDH1A1 1264/4885MAPK1 1601/4885
US-20200181086-A1 1-CYANO-PYRROLIDINE COMPOUNDS AS USP30 INHIBITORS USP30, USP20, USP10 SYK 2387/4885ALDH1A1 1220/4885MAPK1 1536/4885
US-10689345-B2 1-cyano-pyrrolidine compounds as USP30 inhibitors USP30, USP20, USP10 SYK 2615/4885ALDH1A1 1264/4885MAPK1 1601/4885

“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.