SCHEMBL5198324

SCHEMBL5198324

BrSc1ccc2c(c1)CCCO2

nearest known ligand 0.43

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
DYRK1A Q13627 3/20 0.43
DYRK1B Q9Y463 2/20 0.43
CLK1 P49759 1/20 0.43
CTNNB1 P35222 7/20 0.42
WNT3A P56704 7/20 0.42
NOTUM Q6P988 1/20 0.41
PRKCI P41743 1/20 0.41
RIPK1 Q13546 1/20 0.38
GSK3B P49841 3/20 0.34
KEAP1 Q14145 1/20 0.34
NFE2L2 Q16236 1/20 0.34
TRIM24 O15164 1/20 0.34
BRD1 O95696 1/20 0.34
BRPF1 P55201 1/20 0.34
DYRK2 Q92630 1/20 0.33

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
SCHEMBL5440454 0.86 KCNH2 (0.37) DYRK1ADYRK1BCLK1CTNNB1WNT3A
SCHEMBL11519067 0.84 DYRK1A (0.44) DYRK1ADYRK1BCLK1CTNNB1WNT3A
SCHEMBL8560705 0.79 DYRK1A (0.41) DYRK1ADYRK1BCLK1CTNNB1WNT3A
SCHEMBL8139356 0.77 CTNNB1 (0.51) DYRK1ADYRK1BCLK1CTNNB1WNT3A
SCHEMBL7762954 0.76 CTNNB1 (0.47) DYRK1ADYRK1BCLK1CTNNB1WNT3A
SCHEMBL4854354 0.76 LMNA (0.50) DYRK1ADYRK1BCLK1CTNNB1WNT3A
SCHEMBL8566959 0.73 NOTUM (0.41) DYRK1ADYRK1BCLK1CTNNB1WNT3A
SCHEMBL10693468 0.72 CTNNB1 (0.47) DYRK1ADYRK1BCLK1CTNNB1WNT3A
SCHEMBL23653205 0.72 DYRK1A (0.46) DYRK1ADYRK1BCLK1CTNNB1WNT3A
SCHEMBL459693 0.72 CTNNB1 (0.49) DYRK1ADYRK1BCLK1CTNNB1WNT3A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260001886-A1 ENPP1 INHIBITORS I RE VENTURES I LLC (US) 2026-01-01 US disclosed
WO-2025233863-A1 ENPP1 INHIBITORS RE VENTURES I, LLC (US) 2025-11-13 WO disclosed
CN-119384413-A Anilino-pyrazole derivatives, compositions and methods thereof 昂胜医药有限公司 2025-01-28 CN disclosed
EP-1700855-B1 A process for the preparation of tazarotene FIDIA FARMACEUTICI (IT) 2015-05-06 EP disclosed
US-20070275968-A1 Substituted Biphenyl Derivative SANKYO COMPANY, LIMITED (JP) 2007-11-29 US disclosed
US-7273937-B2 Process for the preparation of Tazarotene SOLMAG S.P.A. (IT) 2007-09-25 US disclosed
EP-1798229-A1 SUBSTITUTED BIPHENYL DERIVATIVE Sankyo Company, Limited (JP) 2007-06-20 EP disclosed
US-20060205950-A1 Process for the preparation of Tazarotene SOLMAG S.P.A. (IT) 2006-09-14 US disclosed
EP-1700855-A1 A process for the preparation of tazarotene SOLMAG S.p.A. (IT) 2006-09-13 EP disclosed
EP-1031572-A1 PYRIDYLPYRROLE DERIVATIVES Sankyo Company Limited (JP) 2000-08-30 EP disclosed
US-5162546-A ACETYLENES DISUBSTITUTED WITH A PHENYL GROUP AND A 2-SUBSTITUTED CHROMANYL, THIOCHROMANYL OR 1,2,3,4-TETRAHYDROQUINOLINYL GROUP HAVING RETINOID-LIKE ACTIVITY ALLERGAN, INC. (US) 1992-11-10 US disclosed
WO-1992006084-A1 CHROMANS AND THIOCHROMANS WITH RETINOID-LIKE ACTIVITY ALLERGAN, INC. (US) 1992-04-16 WO disclosed
WO-1992006092-A1 ACETYLENES DISUBSTITUTED WITH A HETEROAROMATIC GROUP AND A 2-SUBSTITUTED CHROMANYL, THIOCHROMANYL OR 1,2,3,4-TETRAHYDROQUINOLINYL GROUP HAVING RETINOID-LIKE ACTIVITY ALLERGAN, INC. (US) 1992-04-16 WO disclosed
US-5053523-A Chemical intermediate for compounds having retinoic acid-like activity ALLERGAN, INC. (US) 1991-10-01 US disclosed
US-5045551-A Acetylenes disubstituted with a heteroaromatic group and a 2-substituted chromanyl, thiochromanyl or 1,2,3,4-tetrahydroquinolinyl group having retinoid-like activity ALLERGAN, INC. (US) 1991-09-03 US disclosed
US-5023341-A Acetylene thiochroman ALLERGAN, INC. (US) 1991-06-11 US disclosed
EP-0419132-A2 Process and intermediates for preparing compounds having a disubstituted acetylene moiety and retinoic acid-like biological activity ALLERGAN, INC. (US) 1991-03-27 EP disclosed
EP-0419130-A2 Acetylenes disubstituted with a heteroaromatic group and A 2-substituted chromanyl, thiochromanyl or 1,2,3,4- tetrahydroquinolinyl group having retinoid-like activity ALLERGAN, INC. (US) 1991-03-27 EP disclosed
EP-0419131-A2 Acetylenes disubstituted with a phenyl group and a 2-substituted chromanyl, thiochromanyl or 1,2,3,4-tetrahydroquinolinyl group having retinoid-like activity ALLERGAN, INC. (US) 1991-03-27 EP disclosed
US-4980369-A ANTIARTHRITIC AGENTS, SKIN DISORDERS, ANTIULCER AGENTS, WOUND HEALING AGENTS ALLERGAN, INC. (US) 1990-12-25 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-20060205950-A1 Process for the preparation of Tazarotene DHPS, COASY, STS DYRK1A 1435/4885DYRK1B 1325/4885CLK1 3440/4885
US-20260001886-A1 ENPP1 INHIBITORS I ENPP1, ENPP2, ENPP3 DYRK1A 3504/4885DYRK1B 3712/4885CLK1 2266/4885
US-20070275968-A1 Substituted Biphenyl Derivative COL2A1, COL1A1, FGFR3 DYRK1A 2084/4885DYRK1B 1902/4885CLK1 4024/4885

“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.