SCHEMBL1069753

SCHEMBL1069753

Clc1ccc(C2CN2)cc1

nearest known ligand 0.48

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
SLC6A3 Q01959 8/20 0.48
SLC6A2 P23975 8/20 0.48
SLC6A4 P31645 2/20 0.48
HTR3A P46098 1/20 0.48
LMNA P02545 2/20 0.42
CYP2A6 P11509 1/20 0.42
PRCP P42785 1/20 0.41
CHRNA7 P36544 1/20 0.41
MEN1 O00255 1/20 0.39
ALDH1A1 P00352 1/20 0.39
HPGD P15428 1/20 0.39
KMT2A Q03164 1/20 0.39

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
SCHEMBL4467879 0.84 HTR3A (0.46) SLC6A3SLC6A2SLC6A4HTR3ALMNA
SCHEMBL1673686 0.83 HTR3A (0.53) SLC6A3SLC6A2SLC6A4HTR3APRCP
SCHEMBL263978 0.83 HTR3A (0.53) SLC6A3SLC6A2SLC6A4HTR3APRCP
Hydrochloric Acid SCHEMBL2031988 0.81 HTR3A (0.52) SLC6A3SLC6A2SLC6A4HTR3APRCP
Hydrochloric Acid SCHEMBL1673491 0.81 HTR3A (0.52) SLC6A3SLC6A2SLC6A4HTR3APRCP
Hydrochloric Acid SCHEMBL1673492 0.81 HTR3A (0.52) SLC6A3SLC6A2SLC6A4HTR3APRCP
SCHEMBL170771 0.80 HTR3A (0.50) SLC6A3SLC6A2SLC6A4HTR3ALMNA
SCHEMBL29081932 0.80 HTR3A (0.42) SLC6A3SLC6A2SLC6A4HTR3APRCP
SCHEMBL12549830 0.78 SLC6A3 (0.45) SLC6A3SLC6A2SLC6A4HTR3AALDH1A1
SCHEMBL1673367 0.75 CHRNB2 (0.50) SLC6A3SLC6A2SLC6A4HTR3ALMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2394989-A1 Method for producing a N-substituted aziridine BASF SE (DE) 2011-12-14 EP disclosed
EP-2275408-A1 Method for synthesizing a n-substituted aziridine BASF SE (DE) 2011-01-19 EP disclosed
US-20100191000-A1 METHOD FOR SYNTHESIZING AN N-UNSUBSTITUTED OR N-SUBSTITUTED AZIRIDINE BASF SE (DE) 2010-07-29 US disclosed
CN-101679234-A Method for synthesizing N-unsubstituted or N-substituted aziridine BASF SE 2010-03-24 CN disclosed
EP-2160379-A1 METHOD FOR SYNTHESIZING AN N-UNSUBSTITUTED OR N-SUBSTITUTED AZIRIDINE BASF SE (DE) 2010-03-10 EP disclosed
WO-2008155355-A1 METHOD FOR SYNTHESIZING AN N-UNSUBSTITUTED OR N-SUBSTITUTED AZIRIDINE BASF SE (DE) 2008-12-24 WO disclosed
US-6974874-B2 Reduction of monomer content and stabilization of polyaziridines BAYER MATERIALSCIENCE LLC (US) 2005-12-13 US disclosed
US-6927297-B2 Reduction of monomer content and stabilization of polyaziridines BAYER MATERIALSCIENCE LLC (US) 2005-08-09 US disclosed
US-20040087762-A1 Reduction of monomer content and stabilization of polyaziridines COVESTRO LLC 2004-05-06 US disclosed
US-20040087763-A1 Reduction of monomer content and stabilization of polyaziridines COVESTRO LLC 2004-05-06 US disclosed
EP-0158874-A2 Curable iminated resins from aminoplasts and hydroxylcontaining carboxylic acids PPG INDUSTRIES, INC. (US) 1985-10-23 EP disclosed
US-4293457-A POLYESTER; AMINOPLAST CURING AGENT; THERMOPLASTIC ACRYLIC POLYMER; CELLULOSE ACETATE BUTYRATE, EPOXY RESIN, OR VINYL ESTER-VINYL HALIDE COPOLYMER PPG INDUSTRIES, INC. (US) 1981-10-06 US disclosed
US-4232090-A Sealerless primers PPG INDUSTRIES, INC. (US) 1980-11-04 US disclosed
US-4225480-A Addition interpolymers having improved stability and two-package compositions comprising such interpolymers and polyepoxides PPG INDUSTRIES, INC. (US) 1980-09-30 US disclosed
US-4221885-A COATINGS; ACRYLIC ACID-ESTER COPOLYMERS, IMINATED AND NEUTRALIZED PPG INDUSTRIES, INC. (US) 1980-09-09 US disclosed
US-4187258-A AMINOPLAST CURING AGENT; POLYESTER, POLYETHER, OR POLYURETHANE, THERMOPLASTIC ACRYLIC RESIN PPG INDUSTRIES, INC. (US) 1980-02-05 US disclosed
US-4126596-A INTERPOLYMER CONTAINING CARBOXYL GROUPS, ANIONIC SALT GROUPS AND AMINE GROUPS PPG INDUSTRIES, INC. (US) 1978-11-21 US disclosed
US-4104230-A POLYEPOXIDES, COPOLYMERS CONTAINING PENDANT SALT GROUPS PPG INDUSTRIES, INC. (US) 1978-08-01 US disclosed
US-4018849-A Polyurethane polyol compositions modified with an alkylenimine PPG INDUSTRIES, INC. (US) 1977-04-19 US disclosed
US-3966667-A Preparation of non-aqueous thermosetting acrylic polymer dispersions PPG INDUSTRIES, INC. (US) 1976-06-29 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 (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-20100191000-A1 METHOD FOR SYNTHESIZING AN N-UNSUBSTITUTED OR N-SUBSTITUTED AZIRIDINE CBR1, CBR3, AOC2 SLC6A3 2138/4885SLC6A2 1480/4885SLC6A4 2198/4885

“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.