SCHEMBL3333110

SCHEMBL3333110

CCCCOC(=O)N1CC(N)C1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.54
POLB P06746 1/20 0.54
SMN1; SMN2 Q16637 1/20 0.54
ALDH1A1 P00352 2/20 0.44
GBA2 Q9HCG7 1/20 0.42
ATM Q13315 1/20 0.41
TSHR P16473 3/20 0.39
HPGD P15428 2/20 0.39
GNAI3 P08754 1/20 0.38
GNAO1 P09471 1/20 0.38
GNAI1 P63096 1/20 0.38
BCHE P06276 1/20 0.38
CHRNB2 P17787 1/20 0.38
CHRNA4 P43681 1/20 0.38
HRH2 P25021 1/20 0.38
HRH1 P35367 1/20 0.38
GAA P10253 1/20 0.38
HCAR2 Q8TDS4 1/20 0.37
CYP1A2 P05177 1/20 0.37
CYP3A4 P08684 1/20 0.37

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
SCHEMBL30816157 0.89 LMNA (0.54) LMNAPOLBSMN1; SMN2ALDH1A1GBA2
SCHEMBL27151384 0.89 LMNA (0.54) LMNAPOLBSMN1; SMN2ALDH1A1GBA2
SCHEMBL323088 0.87 SMN1; SMN2 (0.53) LMNAPOLBSMN1; SMN2ALDH1A1GBA2
SCHEMBL2778567 0.87 SMN1; SMN2 (0.53) LMNAPOLBSMN1; SMN2ALDH1A1GBA2
SCHEMBL30367858 0.86 LMNA (0.51) LMNAPOLBSMN1; SMN2ALDH1A1GBA2
SCHEMBL16653986 0.86 LMNA (0.51) LMNAPOLBSMN1; SMN2ALDH1A1GBA2
SCHEMBL29838431 0.86 LMNA (0.46) LMNAPOLBSMN1; SMN2ALDH1A1GBA2
SCHEMBL29838554 0.86 LMNA (0.46) LMNAPOLBSMN1; SMN2ALDH1A1GBA2
SCHEMBL31554325 0.84 POLB (0.50) LMNAPOLBSMN1; SMN2ALDH1A1GBA2
SCHEMBL1404236 0.84 POLB (0.50) LMNAPOLBSMN1; SMN2ALDH1A1GBA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024158872-A1 1,3-INDOLE-PROPANAMIDE INHIBITORS OF SARS-COV-2 PLPRO/NSP3 AND DERIVATIVES THEREOF THE ROCKEFELLER UNIVERSITY (US) 2024-08-02 WO disclosed
WO-2022198905-A1 TRICYCLIC DERIVATIVE AND PREPARATION METHOD THEREFOR AND USE THEREOF 浙江海正药业股份有限公司 2022-09-29 WO disclosed
EP-4055013-A1 WDR5 INHIBITORS AND MODULATORS Vanderbilt University (US) 2022-09-14 EP disclosed
US-11370761-B2 Voltage-dependent T-type calcium channel inhibitor NIPPON CHEMIPHAR CO., LTD. (JP) 2022-06-28 US disclosed
US-11351173-B2 Substituted pyrrolo[1,2-a]pyrimidines and their use in the treatment of medical disorders Bial—R&D Investments, S.A. (PT) 2022-06-07 US disclosed
US-20210177853-A1 SUBSTITUTED PYRROLO[1,2-A]PYRIMIDINES AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDERS BIAL - R&D INVESTMENTS, S.A. (PT) 2021-06-17 US disclosed
US-10751341-B2 Substituted pyrrolo[1,2-a]pyrimidines and their use in the treatment of medical disorders LYSOSOMAL THERAPEUTICS INC. (US) 2020-08-25 US disclosed
WO-2020162471-A1 PYRIDONE DERIVATIVE マルホ株式会社 2020-08-13 WO disclosed
EP-3215509-B1 SUBSTITUTED PYRROLO[1,2-A]PYRIMIDINES AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDERS LYSOSOMAL THERAPEUTICS INC (US) 2020-02-26 EP disclosed
US-20200030331-A1 SUBSTITUTED PYRROLO[1,2-A]PYRIMIDINES AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDERS BIAL - R&D INVESTMENTS, S.A. (PT) 2020-01-30 US disclosed
EP-3215509-A1 SUBSTITUTED PYRROLO[1,2-A]PYRIMIDINES AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDERS Lysosomal Therapeutics Inc. (US) 2017-09-13 EP disclosed
WO-2016073891-A1 SUBSTITUTED PYRROLO[1,2-A]PYRIMIDINES AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDERS LYSOSOMAL THERAPEUTICS INC. (US) 2016-05-12 WO disclosed
US-8669266-B2 Quinoline-carboxamide derivatives as P2Y12 antagonists SANOFI (FR) 2014-03-11 US disclosed
US-20100135999-A1 QUINOLINE-CARBOXAMIDE DERIVATIVES AS P2Y12 ANTAGONISTS SANOFI-AVENTIS (FR) 2010-06-03 US disclosed
EP-2148871-A1 QUINOLINE-CARBOXAMIDE DERIVATIVES AS P2Y12 ANTAGONISTS Sanofi-Aventis (FR) 2010-02-03 EP disclosed
US-7528150-B2 Urea derivatives having vanilloid receptor antagonist activity GLAXO GROUP LIMITED (GB) 2009-05-05 US disclosed
WO-2008128647-A1 QUINOLINE-CARBOXAMIDE DERIVATIVES AS P2Y12 ANTAGONISTS SANOFI-AVENTIS (FR) 2008-10-30 WO disclosed
US-20060178397-A1 Urea derivatives having vanilloid receptor antagonist activity GLAXO GROUP LIMITED (GB) 2006-08-10 US disclosed
EP-1608640-A2 UREA DERIVATIVES HAVING VANILLOID RECEPTOR ANTAGONIST ACTIVITY GLAXO GROUP LIMITED (GB) 2005-12-28 EP disclosed
WO-2004078101-A2 UREA DERIVATIVES HAVING VANILLOID RECEPTOR ANTAGONIST ACTIVITY GLAXO GROUP LIMITED (GB) 2004-09-16 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 (7 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-20060178397-A1 Urea derivatives having vanilloid receptor antagonist activity UTS2R, TRPV1, TACR1 LMNA 3122/4885POLB 3286/4885SMN1; SMN2 4634/4885
US-11351173-B2 Substituted pyrrolo[1,2-a]pyrimidines and their use in the treatment of medical disorders TYMP, PARK7, PNP LMNA 2364/4885POLB 47/4885SMN1; SMN2 30/4885
US-20100135999-A1 QUINOLINE-CARBOXAMIDE DERIVATIVES AS P2Y12 ANTAGONISTS P2RY12, P2RY1, P2RY2 LMNA 977/4885POLB 1874/4885SMN1; SMN2 4406/4885
US-20210177853-A1 SUBSTITUTED PYRROLO[1,2-A]PYRIMIDINES AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDERS TYMP, PARK7, PNP LMNA 2364/4885POLB 47/4885SMN1; SMN2 30/4885
US-10751341-B2 Substituted pyrrolo[1,2-a]pyrimidines and their use in the treatment of medical disorders TYMP, PARK7, PNP LMNA 2364/4885POLB 47/4885SMN1; SMN2 30/4885
US-20200030331-A1 SUBSTITUTED PYRROLO[1,2-A]PYRIMIDINES AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDERS TYMP, PARK7, PNP LMNA 2364/4885POLB 47/4885SMN1; SMN2 30/4885
US-11370761-B2 Voltage-dependent T-type calcium channel inhibitor CACNA1I, CACNA1G, CACNA1H LMNA 3453/4885POLB 4507/4885SMN1; SMN2 2863/4885

“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.