SCHEMBL2338368

SCHEMBL2338368

Clc1ccc(OCC2CO2)c(Cl)c1

nearest known ligand 0.54

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.49
GLA P06280 1/20 0.49
TDP1 Q9NUW8 3/20 0.47
TSHR P16473 2/20 0.47
TP53 P04637 1/20 0.47
CYP3A4 P08684 1/20 0.47
SMN1; SMN2 Q16637 1/20 0.47
HIF1A Q16665 1/20 0.47
S1PR4 O95977 4/20 0.45
HPGD P15428 1/20 0.43
HTT P42858 1/20 0.43
DRD4 P21917 3/20 0.42
DRD2 P14416 1/20 0.42

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
SCHEMBL7962011 1.00 ALDH1A1 (0.49) ALDH1A1GLATDP1TSHRTP53
SCHEMBL7962015 1.00 ALDH1A1 (0.49) ALDH1A1GLATDP1TSHRTP53
SCHEMBL29847389 1.00 ALDH1A1 (0.49) ALDH1A1GLATDP1TSHRTP53
SCHEMBL2230996 0.89 TTR (0.45) ALDH1A1GLATSHRTP53CYP3A4
SCHEMBL30161198 0.89 TTR (0.45) ALDH1A1GLATSHRTP53CYP3A4
SCHEMBL9840397 0.87 KDM4E (0.44) ALDH1A1GLATDP1TSHRSMN1; SMN2
SCHEMBL2337120 0.86 ALDH1A1 (0.49) ALDH1A1GLATDP1TSHRTP53
SCHEMBL9803136 0.85 ALDH1A1 (0.59) ALDH1A1GLATDP1TSHRTP53
SCHEMBL2122103 0.83 ALDH1A1 (0.46) ALDH1A1GLATDP1TSHRTP53
SCHEMBL4294711 0.83 ALDH1A1 (0.46) ALDH1A1GLATDP1TSHRTP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0308328-B1 (BENZYL-PIPERIDINO)-1-PROPANOL-2 DERIVATIVES, THEIR PREPARATION, THEIR USE AS MICROBICIDES AND COMPOSITIONS CONTAINING THEM SANOFI (FR) 1991-12-04 EP claimed
EP-0086256-B1 1-(2,4-DICHLOROPHENOXY)-3-(3,4-DIMETHOXY-BETA-PHENETHYLAMINO)-PROPAN-2-0L, PROCESSES FOR ITS PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING IT VEB Arzneimittelwerk Dresden (DD) 1985-08-21 EP claimed
EP-0086256-A1 1-(2,4-Dichlorophenoxy)-3-(3,4-dimethoxy-beta-phenethylamino)-propan-2-0l, processes for its preparation and pharmaceutical compositions containing it VEB Arzneimittelwerk Dresden (DD) 1983-08-24 EP claimed
US-4246189-A FOR EASE OF MATERIALS HANDLING DEUTSCHE GOLD- UND SILBER-SCHEIDEANSTALT VORMALS ROESSLER (DE) 1981-01-20 US claimed
US-20240166602-A1 SUBSTITUTED DIARYL COMPOUND AS WELL AS PREPARATION METHOD AND APPLICATION THEREOF SHANDONG FIRST MEDICAL UNIV & SHANDONG ACADEMY OF MEDICAL SCIENCES (CN) 2024-05-23 US disclosed
WO-2022262350-A1 SUBSTITUTED DIARYL COMPOUND, AND PREPARATION METHOD THEREFOR AND USE THEREOF 山东第一医科大学(山东省医学科学院) 2022-12-22 WO disclosed
US-20190092727-A1 Piperidine Compounds, Pharmaceutical Composition Comprising The Same And Its Use SK BIOPHARMACEUTICALS CO., LTD. (KR) 2019-03-28 US disclosed
US-10144709-B2 Piperidine compounds, pharmaceutical composition comprising the same and its use SK BIOPHARMACEUTICALS CO., LTD. (KR) 2018-12-04 US disclosed
CN-105646331-B Piperidine compounds, the medical composition and its use containing the compound 爱思开生物制药株式会社 2018-07-03 CN disclosed
US-20170275250-A1 PIPERIDINE COMPOUNDS, PHARMACEUTICAL COMPOSITION COMPRISING THE SAME AND ITS USE SK BIOPHARMACEUTICALS CO LTD (KR) 2017-09-28 US disclosed
US-9676718-B2 Piperidine compounds, pharmaceutical composition comprising the same and its use SK BIOPHARMACEUTICALS CO., LTD. (KR) 2017-06-13 US disclosed
US-9593102-B2 Piperidine compounds, pharmaceutical composition comprising the same and its use SK BIOPHARMACEUTICALS CO., LTD. (KR) 2017-03-14 US disclosed
US-4269838-A ADRENERGIC BLOCKING AGENTS; ANTIARRHYTHMIA AND HYPOTENSIVE AGENTS NIPPON SHINYAKU CO. LTD. (JP) 1981-05-26 US disclosed
US-4256756-A ADRENERGIC BLOCKING AGENTS, ANTIDEPRESSANTS BOEHRINGER INGELHEIM GMBH (DE) 1981-03-17 US disclosed
US-4255430-A ANDRENERGIC RECEPTOR BLOCKING AGENTS BOEHRINGER INGELHEIM GMBH (DE) 1981-03-10 US disclosed
US-4246189-A FOR EASE OF MATERIALS HANDLING DEUTSCHE GOLD- UND SILBER-SCHEIDEANSTALT VORMALS ROESSLER (DE) 1981-01-20 US disclosed
US-4212877-A ANTIDEPRESSANTS, ADRENERGIC BLOCKING AGENTS BOEHRINGER INGELHEIM GMBH (DE) 1980-07-15 US disclosed
US-4110472-A CEREBROVASCULAR INSUFFICIENCY, PSYCHOSTIMULATION BAYER AKTIENGESELLSCHAFT (DE) 1978-08-29 US disclosed
US-4048100-A Polyhalogenated polyols and foamed polyurethanes prepared from them THE DOW CHEMICAL COMPANY (US) 1977-09-13 US disclosed
US-4036973-A BACTERICIDES AND ANTIPROTOZOA AGENTS SYNTEX (U.S.A.) INC. (US) 1977-07-19 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 (4 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-20170275250-A1 PIPERIDINE COMPOUNDS, PHARMACEUTICAL COMPOSITION COMPRISING THE SAME AND ITS USE PGC, VIP, PIGO ALDH1A1 365/4885GLA 3931/4885TDP1 3850/4885
US-10144709-B2 Piperidine compounds, pharmaceutical composition comprising the same and its use PGC, VIP, PIGO ALDH1A1 365/4885GLA 3931/4885TDP1 3850/4885
US-20190092727-A1 Piperidine Compounds, Pharmaceutical Composition Comprising The Same And Its Use PGC, VIP, PIGO ALDH1A1 365/4885GLA 3931/4885TDP1 3850/4885
US-20240166602-A1 SUBSTITUTED DIARYL COMPOUND AS WELL AS PREPARATION METHOD AND APPLICATION THEREOF DLD, H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, DHODH ALDH1A1 903/4885GLA 3800/4885TDP1 4010/4885

“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.