SCHEMBL1919937

SCHEMBL1919937

Nc1c(C(=O)O)sc2ccccc12

nearest known ligand 0.73

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ LIMK1 P53667 2/20 0.73
▸ IKBKB O14920 1/20 0.73
▸ KDM4E B2RXH2 2/20 0.65
▸ MEN1 O00255 1/20 0.65
▸ ALDH1A1 P00352 1/20 0.65
▸ GLA P06280 1/20 0.65
▸ GAA P10253 1/20 0.65
▸ MAPT P10636 1/20 0.65
▸ HPGD P15428 1/20 0.65
▸ ALOX15 P16050 1/20 0.65
▸ KMT2A Q03164 1/20 0.65
▸ ATM Q13315 1/20 0.65
▸ HSD17B10 Q99714 1/20 0.65
▸ MCL1 Q07820 5/20 0.62
▸ GABRA1 P14867 1/20 0.59
▸ GABRA5 P31644 1/20 0.59
▸ PRNP P04156 1/20 0.49
▸ RXFP1 Q9HBX9 1/20 0.49
▸ OGG1 O15527 1/20 0.47
▸ PTPN2 P17706 1/20 0.45

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
SCHEMBL6609258 0.85 LIMK1 (1.00) LIMK1IKBKBKDM4EMEN1ALDH1A1
SCHEMBL16581218 0.84 GABRA1 (0.77) LIMK1IKBKBKDM4EMEN1ALDH1A1
SCHEMBL15766514 0.83 LIMK1 (0.71) LIMK1IKBKBKDM4EMEN1ALDH1A1
SCHEMBL29285354 0.80 OGG1 (0.69) LIMK1IKBKBKDM4EMEN1ALDH1A1
SCHEMBL30173777 0.79 KDM4E (1.00) LIMK1IKBKBKDM4EMEN1ALDH1A1
SCHEMBL3828429 0.79 ALDH1A1 (0.67) LIMK1IKBKBKDM4EMEN1ALDH1A1
SCHEMBL1101766 0.79 KDM4E (1.00) LIMK1IKBKBKDM4EMEN1ALDH1A1
SCHEMBL16581289 0.79 GABRA1 (0.74) LIMK1IKBKBKDM4EMEN1ALDH1A1
SCHEMBL941112 0.78 MCL1 (0.65) LIMK1IKBKBKDM4EMEN1ALDH1A1
SCHEMBL29664668 0.78 MCL1 (0.65) LIMK1IKBKBKDM4EMEN1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025093589-A1 HETEROARYL AMIDE DERIVATIVES AS SODIUM CHANNEL INHIBITORS CHIESI FARMACEUTICI S.P.A. (IT) 2025-05-08 — — WO disclosed
CN-112851732-B Method for synthesizing On-DNA 2-carboxyl-3-amino arylthiophene compound 成都先导药物开发股份有限公司 2023-03-07 — — CN disclosed
CN-112851732-A Method for synthesizing On-DNA 2-carboxyl-3-amino arylthiophene compound 成都先导药物开发股份有限公司 2021-05-28 — — CN disclosed
US-9955689-B2 Method for promoting plant growth SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2018-05-01 — — US disclosed
US-9955689-B2 Method for promoting plant growth SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2018-05-01 — — US disclosed
US-9955689-B2 Method for promoting plant growth SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2018-05-01 — — US disclosed
US-20160322585-A1 CONDENSED CYCLIC COMPOUND AND ORGANIC LIGHT EMITTING DEVICE INCLUDING THE SAME SAMSUNG SDI CO., LTD. (KR) 2016-11-03 — — US disclosed
US-20150289506-A1 METHOD FOR PROMOTING PLANT GROWTH SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2015-10-15 — — US disclosed
US-20150289506-A1 METHOD FOR PROMOTING PLANT GROWTH SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2015-10-15 — — US disclosed
US-20150289506-A1 METHOD FOR PROMOTING PLANT GROWTH SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2015-10-15 — — US disclosed
WO-2002000653-A2 FUSED CYCLIC COMPOUNDS AS MODULATORS OF NUCLEAR HORMONE RECEPTOR FUNCTION BRISTOL-MYERS SQUIBB COMPANY (US) 2002-01-03 — — WO disclosed
EP-0942911-A1 BENZOPYRANOPYRROLE AND BENZOPYRANOPYRIDINE ALPHA-1 ADRENERGIC COMPOUNDS Abbott Laboratories (US) 1999-09-22 — — EP disclosed
WO-1998024791-A1 BENZOPYRANOPYRROLE AND BENZOPYRANOPYRIDINE ALPHA-1 ADRENERGIC COMPOUNDS ABBOTT LABORATORIES (US) 1998-06-11 — — WO disclosed
EP-0817635-A1 USE OF THIAZEPINE, OXAZEPINE AND DIAZEPINE COUMPOUNDS FOR INHIBITING HIV, HERPESVIRUS AND SUPPRESSING THE IMMUNE SYSTEM WARNER-LAMBERT COMPANY LLC (US) 1998-01-14 — — EP disclosed
EP-0772612-A1 4-HYDROXY-3-PHENYL-INDENO(1,2-B)PYRIDINE-2(1H)-ONE DERIVATIVES AS NMDA ANTAGONISTS Aventis Pharma S.A. (FR) 1997-05-14 — — EP disclosed
EP-0749434-A1 BENZOTHIOPHENE, BENZOFURAN AND INDOLETHIAZEPINONES, OXAZEPINONES AND DIAZEPINONES AS INHIBITORS OF CELL ADHESION AND AS INHIBITORS OF HIV WARNER-LAMBERT COMPANY (US) 1996-12-27 — — EP disclosed
WO-1996029077-A1 USE OF THIAZEPINE, OXAZEPINE AND DIAZEPINE COUMPOUNDS FOR INHIBITING HIV, HERPESVIRUS AND SUPPRESSING THE IMMUNE SYSTEM WARNER-LAMBERT COMPANY (US) 1996-09-26 — — WO disclosed
WO-1996002536-A1 4-HYDROXY-3-PHENYL-INDENO(1,2-B)PYRIDINE-2(1H)-ONE DERIVATIVES AS NMDA ANTAGONISTS RHONE-POULENC RORER S.A. (FR) 1996-02-01 — — WO disclosed
WO-1995024408-A1 BENZOTHIOPHENE, BENZOFURAN AND INDOLETHIAZEPINONES, OXAZEPINONES AND DIAZEPINONES AS INHIBITORS OF CELL ADHESION AND AS INHIBITORS OF HIV WARNER-LAMBERT COMPANY (US) 1995-09-14 — — WO disclosed
US-4257942-A New water-insoluble azo dyes AZIENDE COLORI NAZIONALI AFFINI ACNA S.P.A. (IT) 1981-03-24 — — 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 (2 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-20150289506-A1 METHOD FOR PROMOTING PLANT GROWTH FGF2, BROX, BOLA2; BOLA2B LIMK1 4672/4885IKBKB 2375/4885KDM4E 778/4885
US-20160322585-A1 CONDENSED CYCLIC COMPOUND AND ORGANIC LIGHT EMITTING DEVICE INCLUDING THE SAME CRY1, CRY2, CCNE2 LIMK1 1225/4885IKBKB 2327/4885KDM4E 3045/4885

“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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