SCHEMBL240715

SCHEMBL240715

Clc1cccc(OBOc2cccc(Cl)c2)c1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
WDR5 P61964 1/20 0.44
LMNA P02545 1/20 0.43
MAPK1 P28482 1/20 0.43
HTT P42858 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.43
ALDH1A1 P00352 1/20 0.41
TSHR P16473 1/20 0.41
SLC6A4 P31645 3/20 0.41
CYP1A2 P05177 2/20 0.41
CYP2C9 P11712 2/20 0.41
CYP2C19 P33261 2/20 0.41
SLC6A2 P23975 2/20 0.41
SLC6A3 Q01959 2/20 0.41
CYP2D6 P10635 1/20 0.41
DRD2 P14416 1/20 0.41
DRD4 P21917 1/20 0.41
RHEB Q15382 2/20 0.40
KCNH2 Q12809 1/20 0.40
OGG1 O15527 1/20 0.40
KMT2A Q03164 1/20 0.40

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
SCHEMBL28642433 0.82 CYP1A2 (0.37) WDR5LMNAMAPK1HTTSMN1; SMN2
SCHEMBL10102796 0.82 WDR5 (0.50) WDR5LMNAMAPK1HTTSMN1; SMN2
SCHEMBL21409 0.78 MAOB (0.61) MAOBRXRARXRBRXRG
SCHEMBL29924283 0.77 RHEB (0.52) WDR5LMNAMAPK1HTTSMN1; SMN2
SCHEMBL6206121 0.77 RHEB (0.52) WDR5LMNAMAPK1HTTSMN1; SMN2
SCHEMBL1855228 0.75
SCHEMBL16890555 0.75 RHEB (0.50) WDR5LMNAMAPK1HTTSMN1; SMN2
SCHEMBL177674 0.74 TSHR (0.47) ALDH1A1TSHRCYP2C19
SCHEMBL10715309 0.73 MAPT (0.54) WDR5SMN1; SMN2ALDH1A1TSHRSLC6A4
SCHEMBL535619 0.73

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 1333 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119978389-A Boron-containing oligomer for aging-resistant high-transparency addition-type silicon rubber, and preparation method and application thereof 中国科学院化学研究所 2025-05-13 CN claimed
EP-4280882-A2 MATERIALS AND METHODS FOR EXTENDING SHELF-LIFE OF FOODS JP LABORATORIES, INC. (US) 2023-11-29 EP claimed
US-11426393-B2 Prolyl hydroxylase inhibitors and methods of use AKEBIA THERAPEUTICS, INC. (US) 2022-08-30 US claimed
WO-2022159439-A2 MATERIALS AND METHODS FOR EXTENDING SHELF-LIFE OF FOODS JP LABORATORIES, INC. (US) 2022-07-28 WO claimed
CN-110483291-B Synthesis method of (E) -beta-aryl-beta, gamma-unsaturated ester compound 安阳师范学院 2021-09-10 CN claimed
US-20210137901-A1 PROLYL HYDROXYLASE INHIBITORS AND METHODS OF USE KREOS CAPITAL VII (UK) LIMITED (GB) 2021-05-13 US claimed
US-9233967-B2 Process for the preparation of sitagliptin and intermediate compounds CIPLA LIMITED (IN) 2016-01-12 US claimed
US-20150197523-A1 PROCESS FOR THE PREPARATION OF SITAGLIPTIN AND INTERMEDIATE COMPOUNDS CIPLA LIMITED (IN) 2015-07-16 US claimed
EP-2882752-A1 PROCESS FOR THE PREPARATION OF SITAGLIPTIN AND INTERMEDIATE COMPOUNDS Cipla Limited (IN) 2015-06-17 EP claimed
US-8921299-B2 Detergents having acceptable color THE PROCTER & GAMBLE COMPANY (US) 2014-12-30 US claimed
WO-2014023930-A1 PROCESS FOR THE PREPARATION OF SITAGLIPTIN AND INTERMEDIATE COMPOUNDS CIPLA LIMITED (IN) 2014-02-13 WO claimed
US-7919618-B2 Preparing (3'-chloro-biphenyl-4-yl)-(1-pyrimidin-2-yl-piperidin-4-yl)-methanone, or a salt or solvate thereof by contacting (3'-chloro-biphenyl-4-yl)-piperidine-4-yl-methanone with 2-chloropyrimidine in base; cataysis using bis(triphenylphosphine)palladium(II) dichloride; nervous system disorders LEXICON PHARMACEUTICALS, INC. (US) 2011-04-05 US claimed
EP-2084144-B1 SYNTHESIS OF PIPERAZINES, PIPERIDINES AND RELATED COMPOUNDS LEXICON PHARMACEUTICALS INC (US) 2011-02-23 EP claimed
EP-2084144-A2 SYNTHESIS OF PIPERAZINES, PIPERIDINES AND RELATED COMPOUNDS Lexicon Pharmaceuticals, Inc. (US) 2009-08-05 EP claimed
US-20080177070-A1 Synthesis of piperazines, piperidines and related compounds OXFORD FINANCE LLC, AS COLLATERAL AGENT 2008-07-24 US claimed
WO-2008019279-A2 SYNTHESIS OF PIPERAZINES, PIPERIDINES AND RELATED COMPOUNDS LEXICON PHARMACEUTICALS, INC. (US) 2008-02-14 WO claimed
US-12641999-B2 Composition for organic optoelectronic device, organic optoelectronic device and display device SAMSUNG SDI CO., LTD. (KR) 2026-05-26 US disclosed
EP-3856179-B1 MONOACYLGLYCEROL LIPASE MODULATORS JANSSEN PHARMACEUTICA NV (BE) 2026-05-13 EP disclosed
US-5455252-A Antiinflammatory agent, immunosuppressant, antiallergen, skin disorders, bronchodilator, analgesic SYNTEX (U.S.A.) INC. (US) 1995-10-03 US disclosed
WO-1994022852-A1 QUINOLINES AS TYPE IV PHOSPHODIESTERASE INHIBITORS SYNTEX (U.S.A.) INC. (US) 1994-10-13 WO 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-11426393-B2 Prolyl hydroxylase inhibitors and methods of use HIF1AN, EGLN3, HIF1A WDR5 4262/4885LMNA 2347/4885MAPK1 2780/4885
US-12641999-B2 Composition for organic optoelectronic device, organic optoelectronic device and display device NR2E3, OXER1, NR0B2 WDR5 2629/4885LMNA 2771/4885MAPK1 846/4885
US-20210137901-A1 PROLYL HYDROXYLASE INHIBITORS AND METHODS OF USE HIF1AN, EGLN3, HIF1A WDR5 4262/4885LMNA 2347/4885MAPK1 2780/4885
US-20080177070-A1 Synthesis of piperazines, piperidines and related compounds CTPS2, PLP2, DHPS WDR5 512/4885LMNA 3221/4885MAPK1 2844/4885
US-20150197523-A1 PROCESS FOR THE PREPARATION OF SITAGLIPTIN AND INTERMEDIATE COMPOUNDS DPP4, DPP7, DPP9 WDR5 2942/4885LMNA 2767/4885MAPK1 2018/4885

“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.