SCHEMBL188971

SCHEMBL188971

CN(C)CCCOc1ccc(N)cc1

nearest known ligand 0.69

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 4/20 0.69
ALDH1A1 P00352 3/20 0.69
SMN1; SMN2 Q16637 2/20 0.69
HRH3 Q9Y5N1 4/20 0.65
LSS P48449 1/20 0.62
KEAP1 Q14145 1/20 0.55
NFE2L2 Q16236 1/20 0.55
TDP1 Q9NUW8 2/20 0.53
TSHR P16473 1/20 0.52
LTA4H P09960 1/20 0.50
CYP1A2 P05177 1/20 0.50
CYP3A4 P08684 1/20 0.50
CYP2D6 P10635 1/20 0.50
CYP2C9 P11712 1/20 0.50
CYP2C19 P33261 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
Hydrochloric Acid SCHEMBL3657036 0.98 KDM4E (0.67) KDM4EALDH1A1SMN1; SMN2HRH3LSS
SCHEMBL3367452 0.94 KDM4E (0.70) KDM4EALDH1A1SMN1; SMN2HRH3LSS
SCHEMBL56571 0.90 KEAP1 (0.67) KDM4EALDH1A1SMN1; SMN2HRH3LSS
SCHEMBL9671156 0.89 KDM4E (0.83) KDM4EALDH1A1SMN1; SMN2HRH3LSS
Hydrochloric Acid SCHEMBL3570082 0.88 KEAP1 (0.65) KDM4EALDH1A1SMN1; SMN2HRH3KEAP1
Hydrochloric Acid SCHEMBL56159 0.88 KEAP1 (0.65) KDM4EALDH1A1SMN1; SMN2HRH3KEAP1
SCHEMBL14547108 0.83 KEAP1 (0.54) KDM4EALDH1A1SMN1; SMN2HRH3LSS
SCHEMBL19026551 0.82 HRH3 (0.77) KDM4EALDH1A1SMN1; SMN2HRH3LSS
SCHEMBL2022333 0.82 KCNH2 (0.56) KDM4EALDH1A1SMN1; SMN2HRH3KEAP1
SCHEMBL8226392 0.82 KDM4E (0.71) KDM4EALDH1A1SMN1; SMN2HRH3LSS

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120081789-A Pyrazole derivative with antitumor activity and preparation method and application thereof 天津匠新致成科技有限公司 2025-06-03 CN disclosed
EP-3388435-B1 PYRROLOBENZODIAZEPINES AND TARGETED CONJUGATES SEAGEN INC (US) 2023-05-03 EP disclosed
US-11273154-B2 Azole compounds as ubiquitin-specific protease USP7 inhibitors PROGENRA, INC. (US) 2022-03-15 US disclosed
EP-3390370-B1 BIS-TRIAZOLE COMPOUNDS WITH ANTI-BIOFILM AND ANTI-CORROSION PROPERTIES UNIV DE TOULON (FR) 2021-02-03 EP disclosed
EP-1836174-B2 ARYL NITROGEN-CONTAINING BICYCLIC COMPOUNDS AND THEIR USE AS KINASE INHIBITORS AMGEN INC (US) 2019-10-02 EP disclosed
EP-1836174-B2 ARYL NITROGEN-CONTAINING BICYCLIC COMPOUNDS AND THEIR USE AS KINASE INHIBITORS AMGEN INC (US) 2019-10-02 EP disclosed
WO-2018160944-A1 AZOLE COMPOUNDS AS UBIQUITIN-SPECIFIC PROTEASE USP7 INHIBITORS PROGENRA, INC. (US) 2018-09-07 WO disclosed
WO-2018090939-A1 8,9-DIHYDROIMIDAZOLE[1,2-A]PYRIMIDO[5,4-E]PYRIMIDINE-5(6H)-KETONE COMPOUND 上海瑛派药业有限公司 2018-05-24 WO disclosed
EP-1732543-B1 TETRACYCLIC CARBOLINE DERATIVES FOR INHIBITING ANGIOGENESIS PTC THERAPEUTICS INC (US) 2017-05-10 EP disclosed
EP-2961750-A1 SUBSTITUTED 7-OXO-PYRIDO [2, 3-D]PYRIMIDINES AND THEIR USE FOR THE TREATMENT OF EGFR / ERBB2 RELATED DISORDERS Amgen Inc. (US) 2016-01-06 EP disclosed
WO-2003024967-A2 INDOLIZINES AS KINASE PROTEIN INHIBITORS AVENTIS PHARMA S.A. (FR) 2003-03-27 WO disclosed
US-6515027-B1 Ligands, agonists or antagonists, of the CC chemokine receptor CC-CKR5 SMITHKLINE BEECHAM CORP. 2003-02-04 US disclosed
US-6319918-B1 FOR LYMPHOMA OR SOLID TUMORS TREATMENT BOEHRINGER INGELHEIM PHARMA KG (DE) 2001-11-20 US disclosed
CN-1303374-A Substituted indolinones, process for their preparation and their use as pharmaceutical compositions BOEHRINGER INGELHEIM PHARMA (DE) 2001-07-11 CN disclosed
EP-1100779-A1 SUBSTITUTED INDOLINONES, THE PRODUCTION THEREOF AND THEIR USE AS MEDICAMENTS Boehringer Ingelheim Pharma KG (DE) 2001-05-23 EP disclosed
WO-1999062882-A1 SUBSTITUTED INDOLINONES, THE PRODUCTION THEREOF AND THEIR USE AS MEDICAMENTS BOEHRINGER INGELHEIM PHARMA KG (DE) 1999-12-09 WO disclosed
US-5801170-A Heterocyclic biphenylylamides useful as 5HT1D antagonists SMITHKLINE BEECHAM PLC (GB) 1998-09-01 US disclosed
EP-0733048-A1 HETEROCYCLIC BIPHENYLYLAMIDES USEFUL AS 5HT1D ANTAGONISTS SMITHKLINE BEECHAM PLC (GB) 1996-09-25 EP disclosed
WO-1995015954-A1 HETEROCYCLIC BIPHENYLYLAMIDES USEFUL AS 5HT1D ANTAGONISTS SMITHKLINE BEECHAM PLC (GB) 1995-06-15 WO disclosed
US-3994900-A 6-(Or 8)-[[(substituted amino)alkyl]oxy(or thio)]-3,4-dihydro-4-phenyl-2(1H)-quinolinones E. R. SQUIBB & SONS, INC. (US) 1976-11-30 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-11273154-B2 Azole compounds as ubiquitin-specific protease USP7 inhibitors USP7, USP1, USP2 KDM4E 513/4885ALDH1A1 2210/4885SMN1; SMN2 4723/4885

“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.