SCHEMBL2771691

SCHEMBL2771691

CN(C)Cc1ccc(C(=O)Cl)cc1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ HRH3 Q9Y5N1 2/20 0.52
▸ LSS P48449 4/20 0.48
▸ ALDH1A1 P00352 3/20 0.47
▸ POLB P06746 1/20 0.47
▸ MAPT P10636 1/20 0.47
▸ SMN1; SMN2 Q16637 1/20 0.47
▸ TSHR P16473 1/20 0.46
▸ HDAC6 Q9UBN7 2/20 0.46
▸ HDAC3 O15379 1/20 0.46
▸ MCHR1 Q99705 2/20 0.45
▸ TAAR1 Q96RJ0 2/20 0.45
▸ PYCR1 P32322 1/20 0.43
▸ NOS3 P29474 1/20 0.43
▸ NOS1 P29475 1/20 0.43
▸ NOS2 P35228 1/20 0.43
▸ HDAC1 Q13547 1/20 0.42
▸ HTT P42858 1/20 0.42
▸ RAB9A P51151 1/20 0.42
▸ SLC6A2 P23975 1/20 0.41
▸ SLC6A4 P31645 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
Hydrochloric Acid SCHEMBL9834919 0.98 HRH3 (0.50) HRH3LSSALDH1A1POLBMAPT
SCHEMBL25137173 0.83 HRH3 (0.56) HRH3LSSALDH1A1MAPTTSHR
SCHEMBL12734915 0.81 PYCR1 (0.62) HRH3LSSALDH1A1POLBMAPT
SCHEMBL65825 0.81 ALDH1A1 (0.59) HRH3LSSALDH1A1POLBMAPT
SCHEMBL31556890 0.80 HRH3 (0.56) HRH3ALDH1A1MAPTHDAC6MCHR1
SCHEMBL5393101 0.80 HDAC8 (0.64) HRH3ALDH1A1POLBMAPTSMN1; SMN2
SCHEMBL2913661 0.79 HRH3 (0.52) HRH3LSSALDH1A1TSHRHDAC6
Trimethylammonium SCHEMBL19042854 0.79 CA1 (0.55) ALDH1A1POLBMAPTSMN1; SMN2TSHR
Hydrochloric Acid SCHEMBL5065552 0.79 ALDH1A1 (0.57) HRH3LSSALDH1A1POLBMAPT
SCHEMBL7159528 0.79 ALDH1A1 (0.57) HRH3LSSALDH1A1POLBMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-104689809-B Preparation and application of positive charge type polysaccharide derivative chiral stationary phase 台州学院 2017-04-26 — — CN claimed
CN-104689809-A Preparation and application of positive charge type polysaccharide derivative chiral stationary phase UNIV TAIZHOU 2015-06-10 — — CN claimed
US-12509446-B2 FYN and VEGFR2 kinase inhibitors ROTTAPHARM BIOTECH S.R.L. (IT) 2025-12-30 — — US disclosed
WO-2025073682-A1 METHOD FOR THE KETONE FUNCTIONALISATION OF POLYETHYLENES AND COPOLYMERS CONTAINING ETHYLENE UNITS AND 1,3-DIENE UNITS COMPAGNIE GENERALE DES ETABLISSEMENTS MICHELIN (FR) 2025-04-10 — — WO disclosed
CN-115279747-B FYN and VEGFR2 kinase inhibitors 罗达制药生物技术有限责任公司 2024-11-05 — — CN disclosed
EP-4073057-B1 NEW FYN AND VEGFR2 KINASE INHIBITORS Rottapharm Biotech Srl (IT) 2023-11-29 — — EP disclosed
EP-4073057-B1 NEW FYN AND VEGFR2 KINASE INHIBITORS Rottapharm Biotech Srl (IT) 2023-11-29 — — EP disclosed
EP-3303415-B1 VISIBLE-LIGHT PHOTOINITIATORS AND USES THEREOF ALCON INC (CH) 2022-12-28 — — EP disclosed
CN-115279747-A Novel fYN and VEGFR2 kinase inhibitors 罗达制药生物技术有限责任公司 2022-11-01 — — CN disclosed
EP-4073057-A1 NEW FYN AND VEGFR2 KINASE INHIBITORS Rottapharm Biotech S.r.l. (IT) 2022-10-19 — — EP disclosed
EP-3708562-B1 METHOD FOR PRODUCING SEMICARBAZIDE COMPOUND TOKUYAMA CORP (JP) 2022-08-17 — — EP disclosed
EP-0623592-B1 Peptide analogs as irreversible interleukin-1beta protease inhibitors VERTEX PHARMA (US) 2001-06-27 — — EP disclosed
US-5985838-A TREATING INFECTIOUS DISEASE, RESPIRATORY DISEASE, INFLAMMATORY CONDITIONS, IMMUNE-BASED DISEASE, AUTO-IMMUNE DISEASE, BONE DISEASE, AND TUMORS VERTEX PHARMACEUTICALS, INC. (US) 1999-11-16 — — US disclosed
US-5843905-A Peptidic phosphinyloxymethyl ketones as interleukin-1β-converting enzyme inhibitors VERTEX PHARMACEUTICALS, INCORPORATED (US) 1998-12-01 — — US disclosed
EP-0644197-B1 Peptidic phosphinyloxymethyl ketones as interleukin-1beta-converting enzyme inhibitors VERTEX PHARMA (US) 1998-09-09 — — EP disclosed
US-5677283-A α-heteroaryloxymethyl ketones as interleukin - 1 β converting enzyme inhibitors SANOFI (FR) 1997-10-14 — — US disclosed
US-5585357-A Heteroaryloxymethyl ketones as interleukin-1βconverting enzyme inhibitors SANOFI WINTHROP INC. (US) 1996-12-17 — — US disclosed
EP-0644198-A1 Alpha-heteroaryloxymethyl ketones as interleukin-1beta converting enzyme inhibitors STERLING WINTHROP INC. (US) 1995-03-22 — — EP disclosed
EP-0644197-A1 Peptidic phosphinyloxymethyl ketones as interleukin-1beta-converting enzyme inhibitors STERLING WINTHROP INC. (US) 1995-03-22 — — EP disclosed
EP-0623592-A1 Peptide analogs as irreversible interleukin-1beta protease inhibitors STERLING WINTHROP INC. (US) 1994-11-09 — — 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 (1 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-12509446-B2 FYN and VEGFR2 kinase inhibitors FYN, LCK, LYN HRH3 2608/4885LSS 3797/4885ALDH1A1 4279/4885

“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.

Send feedback