SCHEMBL6307204

SCHEMBL6307204

C=CCOc1ccccc1CN

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 3/20 0.53
▸ KDM4E B2RXH2 3/20 0.53
▸ TSHR P16473 2/20 0.49
▸ MAPT P10636 3/20 0.49
▸ L3MBTL1 Q9Y468 1/20 0.49
▸ HPGD P15428 1/20 0.49
▸ MAPK1 P28482 1/20 0.49
▸ HSD17B10 Q99714 1/20 0.49
▸ LIG1 P18858 1/20 0.46
▸ NPC1 O15118 1/20 0.44
▸ HTT P42858 1/20 0.44
▸ RAB9A P51151 1/20 0.44
▸ GAA P10253 1/20 0.44
▸ SLC22A1 O15245 1/20 0.41
▸ LMNA P02545 1/20 0.41
▸ CYP1A2 P05177 1/20 0.41
▸ ADRB2 P07550 1/20 0.41
▸ ADRB1 P08588 1/20 0.41
▸ HTR1A P08908 1/20 0.41
▸ CYP2D6 P10635 1/20 0.41

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
Alcohol SCHEMBL27332773 0.93 ALDH1A1 (0.51) ALDH1A1KDM4ETSHRMAPTL3MBTL1
SCHEMBL2150775 0.84 ALDH1A1 (0.55) ALDH1A1KDM4ETSHRMAPTL3MBTL1
SCHEMBL3766260 0.84 MAPT (0.49) ALDH1A1KDM4ETSHRMAPTL3MBTL1
SCHEMBL14151108 0.82 ALDH1A1 (0.54) ALDH1A1KDM4ETSHRMAPTL3MBTL1
SCHEMBL5085750 0.82 ALDH1A1 (0.54) ALDH1A1KDM4ETSHRMAPTL3MBTL1
SCHEMBL23680099 0.81 KDM4E (0.55) ALDH1A1KDM4ETSHRMAPTL3MBTL1
1,2-Diallyloxybenzene SCHEMBL366516 0.81 HPGD (0.60) ALDH1A1KDM4ETSHRMAPTL3MBTL1
1,2-Diallyloxybenzene SCHEMBL29768784 0.81 HPGD (0.60) ALDH1A1KDM4ETSHRMAPTL3MBTL1
SCHEMBL7334313 0.81 ALDH1A1 (0.53) ALDH1A1KDM4ETSHRMAPTL3MBTL1
SCHEMBL9259701 0.81 ALDH1A1 (0.56) ALDH1A1KDM4ETSHRMAPTL3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4597903-A Process for the direct preparation of N,N-disubstituted derivatives for 4,13-diaza-18-crown-6 UNIVERSITY OF MARYLAND (US) 1986-07-01 — — US claimed
EP-3854789-A1 MACROCYCLIC COMPOUNDS USEFUL AS CHITINASE INHIBITORS CYGNET BIOSCIENCES B.V. (CW) 2021-07-28 — — EP disclosed
US-10071975-B2 Macrocyclic amidinourea derivatives, methods of preparation and uses thereof as chitinase inhibitors CYGNET BIOSCIENCES B.V. (CW) 2018-09-11 — — US disclosed
EP-3010896-B1 NEW MACROCYCLIC AMIDINOUREA DERIVATIVES, METHODS OF PREPARATION AND USES THEREOF AS CHITINASE INHIBITORS CYGNET BIOSCIENCES B V (CW) 2017-11-01 — — EP disclosed
EP-3010896-B1 NEW MACROCYCLIC AMIDINOUREA DERIVATIVES, METHODS OF PREPARATION AND USES THEREOF AS CHITINASE INHIBITORS CYGNET BIOSCIENCES B V (CW) 2017-11-01 — — EP disclosed
EP-3114129-A1 IMIDAZOPYRIDINE MACROCYCLES AS INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION VIIV Healthcare UK (No.5) Limited (GB) 2017-01-11 — — EP disclosed
US-9409922-B2 Imidazopyridine macrocycles as inhibitors of human immunodeficiency virus replication BRISTOL-MYERS SQUIBB COMPANY (US) 2016-08-09 — — US disclosed
US-20160137617-A1 NEW MACROCYCLIC AMIDINOUREA DERIVATIVES, METHODS OF PREPARATION AND USES THEREOF AS CHITINASE INHIBITORS CYGNET BIOSCIENCES B.V. 2016-05-19 — — US disclosed
US-20160137617-A1 NEW MACROCYCLIC AMIDINOUREA DERIVATIVES, METHODS OF PREPARATION AND USES THEREOF AS CHITINASE INHIBITORS CYGNET BIOSCIENCES B.V. 2016-05-19 — — US disclosed
US-20160137617-A1 NEW MACROCYCLIC AMIDINOUREA DERIVATIVES, METHODS OF PREPARATION AND USES THEREOF AS CHITINASE INHIBITORS CYGNET BIOSCIENCES B.V. 2016-05-19 — — US disclosed
EP-0705831-B1 Cycloalkano-indole- and -azaindole derivatives BAYER AG (DE) 2003-12-03 — — EP disclosed
US-20030149073-A1 Cycloalkano-indole and -azaindole derivatives MULLER ULRICH (DE) 2003-08-07 — — US disclosed
US-6479503-B2 SUCH AS 2-(S/R)-2-(4-(2,4-DIMETHYL-5,6,7,8-TETRAHYDRO-ALPHA-CARBOLIN-9-YL)METHYL -PHENYL)-2-CYCLOPENTYL-ACETIC ACID N-((R)PHENYLGLYCINOAMIDE) FOR TREATING ATHEROSCLEROSIS BAYER AKTIENGESELLSCHAFT (DE) 2002-11-12 — — US disclosed
US-20020147209-A1 Cycloalkano-indole and -azaindole derivatives MUELLER ULRICH (DE) 2002-10-10 — — US disclosed
US-20020055635-A1 Cycloalkano-indole and -azaindole derivatives MULLER ULRICH (DE) 2002-05-09 — — US disclosed
US-6265431-B1 ANTICHOLESTEROL DRUGS BAYER AKTIENGESELLSCHAFT (DE) 2001-07-24 — — US disclosed
US-6245775-B1 ANTICHOLESTEROL AGENTS; CARDIOVASCULAR DISORDERS BAYER AKTIENGESELLSCHAFT (DE) 2001-06-12 — — US disclosed
US-5684014-A FOR TREATING ATHEROSCLEROSIS BAYER AKTIENGESELLSCHAFT (DE) 1997-11-04 — — US disclosed
CN-1130631-A Cycloalkano-indole and-azaindole derivatives BAYER AG (DE) 1996-09-11 — — CN disclosed
EP-0705831-A2 Cycloalkano-indole- and -azaindole derivatives BAYER AG (DE) 1996-04-10 — — EP 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 (5 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-20160137617-A1 NEW MACROCYCLIC AMIDINOUREA DERIVATIVES, METHODS OF PREPARATION AND USES THEREOF AS CHITINASE INHIBITORS CHIT1, CHIA, ENGASE ALDH1A1 4141/4885KDM4E 3681/4885TSHR 1973/4885
US-20030149073-A1 Cycloalkano-indole and -azaindole derivatives AADAC, IDO1, AADAT ALDH1A1 1034/4885KDM4E 2676/4885TSHR 3042/4885
US-10071975-B2 Macrocyclic amidinourea derivatives, methods of preparation and uses thereof as chitinase inhibitors CHIT1, CHIA, PEPD ALDH1A1 3977/4885KDM4E 3542/4885TSHR 2280/4885
US-20020147209-A1 Cycloalkano-indole and -azaindole derivatives AADAC, IDO1, AADAT ALDH1A1 1034/4885KDM4E 2676/4885TSHR 3042/4885
US-20020055635-A1 Cycloalkano-indole and -azaindole derivatives ADRB3, AADAT, INMT ALDH1A1 1445/4885KDM4E 3593/4885TSHR 2697/4885

“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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