SCHEMBL610772

SCHEMBL610772

O=C1CCCCCN1Cc1ccccc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 1/20 1.00
HRH3 Q9Y5N1 2/20 0.69
ACHE P22303 1/20 0.61
GAA P10253 1/20 0.57
SMN1; SMN2 Q16637 1/20 0.57
MEN1 O00255 2/20 0.54
KMT2A Q03164 2/20 0.54
DDB1 Q16531 1/20 0.51
CRBN Q96SW2 1/20 0.51
ACACB O00763 1/20 0.50
APP P05067 1/20 0.49
MCHR1 Q99705 1/20 0.49
KCNH2 Q12809 1/20 0.48
ALDH1A1 P00352 1/20 0.47
MAPT P10636 1/20 0.47
HSD17B10 Q99714 1/20 0.47
NPC1 O15118 1/20 0.47
RAB9A P51151 1/20 0.47

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
SCHEMBL1626076 1.00 L3MBTL1 (1.00) L3MBTL1HRH3ACHEGAASMN1; SMN2
SCHEMBL7269112 1.00 L3MBTL1 (1.00) L3MBTL1HRH3ACHEGAASMN1; SMN2
SCHEMBL9212361 1.00 L3MBTL1 (1.00) L3MBTL1HRH3ACHEGAASMN1; SMN2
Hydrochloric Acid SCHEMBL12494696 0.98 L3MBTL1 (0.97) L3MBTL1HRH3ACHEGAASMN1; SMN2
SCHEMBL8903528 0.98 L3MBTL1 (0.97) L3MBTL1HRH3ACHEGAASMN1; SMN2
SCHEMBL596252 0.98 L3MBTL1 (0.96) L3MBTL1HRH3ACHEGAASMN1; SMN2
SCHEMBL180739 0.93 L3MBTL1 (0.86) L3MBTL1HRH3ACHEGAASMN1; SMN2
SCHEMBL24938208 0.92 L3MBTL1 (0.84) L3MBTL1HRH3ACHEGAASMN1; SMN2
Hydrochloric Acid SCHEMBL6818365 0.91 L3MBTL1 (0.83) L3MBTL1HRH3ACHEGAASMN1; SMN2
Trifluoroacetic Acid SCHEMBL12493760 0.88 L3MBTL1 (0.78) L3MBTL1HRH3ACHEGAASMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118203558-A Transdermal patch for treating hypertension 天津汉瑞药业有限公司 2024-06-18 CN claimed
JP-55162746-A None JP disclosed
US-20260102396-A1 NEW THERAPEUTIC APPROACH TO LUNG DISEASE UNIV CALIFORNIA (US) 2026-04-16 US disclosed
US-12521389-B2 Therapeutic approach to lung disease THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2026-01-13 US disclosed
US-20220249471-A1 NEW THERAPEUTIC APPROACH TO LUNG DISEASE THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2022-08-11 US disclosed
US-11236087-B2 Highly active pyrazolo-piperidine substituted indole-2-carboxamides active against the hepatitis B virus (HBV) AICURIS GMBH & CO. KG (DE) 2022-02-01 US disclosed
US-11236087-B2 Highly active pyrazolo-piperidine substituted indole-2-carboxamides active against the hepatitis B virus (HBV) AICURIS GMBH & CO. KG (DE) 2022-02-01 US disclosed
US-20210179608-A1 NOVEL, HIGHLY ACTIVE PYRAZOLO-PIPERIDINE SUBSTITUTED INDOLE-2-CARBOXAMIDES ACTIVE AGAINST THE HEPATITIS B VIRUS (HBV) AICURIS GMBH & CO. KG (DE) 2021-06-17 US disclosed
US-20210179608-A1 NOVEL, HIGHLY ACTIVE PYRAZOLO-PIPERIDINE SUBSTITUTED INDOLE-2-CARBOXAMIDES ACTIVE AGAINST THE HEPATITIS B VIRUS (HBV) AICURIS GMBH & CO. KG (DE) 2021-06-17 US disclosed
EP-3704119-A1 NOVEL, HIGHLY ACTIVE PYRAZOLO-PIPERIDINE SUBSTITUTED INDOLE-2-CARBOXAMIDES ACTIVE AGAINST THE HEPATITIS B VIRUS (HBV) AiCuris GmbH & Co. KG (DE) 2020-09-09 EP disclosed
EP-0318798-A2 Method for the preparation of polyesters and their use as binders or binder components in powder lacques BAYER AG (DE) 1989-06-07 EP disclosed
EP-0292840-A2 Cyclic amine derivatives, medicaments containing these compounds and procedure for their preparation Dr. Karl Thomae GmbH (DE) 1988-11-30 EP disclosed
EP-0021552-B1 HEXAHYDROAZEPINE, PIPERIDINE AND PYRROLIDINE DERIVATIVES AND PROCESSES FOR PREPARING THEM JOHN WYETH & BROTHER LIMITED (GB) 1983-01-26 EP disclosed
EP-0003253-B1 HEXAHYDROAZEPINE, PIPERIDINE AND PYRROLIDINE DERIVATIVES AND PROCESSES FOR MAKING AND USING THEM JOHN WYETH & BROTHER LIMITED (GB) 1982-12-22 EP disclosed
US-4296029-A Process for preparing hexahydroazepine, piperidine and pyrrolidine derivatives JOHN WYETH & BROTHER LIMITED (GB) 1981-10-20 US disclosed
EP-0021772-A1 Method of preparing 2-oxo- and 2-unsubstituted-hexahydroazepine derivatives JOHN WYETH & BROTHER LIMITED (GB) 1981-01-07 EP disclosed
EP-0021552-A1 Hexahydroazepine, piperidine and pyrrolidine derivatives and processes for preparing them JOHN WYETH & BROTHER LIMITED (GB) 1981-01-07 EP disclosed
JP-S55162746-A PREPARATION OF AMINE DERIVATIVE GRELAN PHARMACEUT CO LTD 1980-12-18 JP disclosed
US-4197241-A Hexahydroazepine, piperidine and pyrrolidine derivatives JOHN WYETH & BROTHER LIMITED (GB) 1980-04-08 US disclosed
EP-0003253-A1 Hexahydroazepine, piperidine and pyrrolidine derivatives and processes for making and using them JOHN WYETH & BROTHER LIMITED (GB) 1979-08-08 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 (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-20260102396-A1 NEW THERAPEUTIC APPROACH TO LUNG DISEASE CALCRL, CALCA, P2RY10 L3MBTL1 1423/4885HRH3 298/4885ACHE 1982/4885
US-20210179608-A1 NOVEL, HIGHLY ACTIVE PYRAZOLO-PIPERIDINE SUBSTITUTED INDOLE-2-CARBOXAMIDES ACTIVE AGAINST THE HEPATITIS B VIRUS (HBV) CDK2, HCCS, BRD4 L3MBTL1 4303/4885HRH3 1703/4885ACHE 4330/4885
US-11236087-B2 Highly active pyrazolo-piperidine substituted indole-2-carboxamides active against the hepatitis B virus (HBV) HCCS, BRD4, CDK2 L3MBTL1 4244/4885HRH3 1121/4885ACHE 4329/4885

“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.