SCHEMBL6844950

SCHEMBL6844950

Cc1nc(C)c(Cl)cc1Cl

nearest known ligand 0.52

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.38
CYP3A4 P08684 1/20 0.37
SMN1; SMN2 Q16637 1/20 0.36
MAPT P10636 2/20 0.35
MAPK1 P28482 1/20 0.35
AHR P35869 1/20 0.35
HTT P42858 1/20 0.33
CD44 P16070 1/20 0.33
HRH4 Q9H3N8 1/20 0.32
CHRNB2 P17787 1/20 0.32
CHRNA4 P43681 1/20 0.32
PTPN1 P18031 1/20 0.32
ALDH1A1 P00352 1/20 0.32
MEN1 O00255 1/20 0.32
KMT2A Q03164 1/20 0.32
HPGD P15428 2/20 0.32
TSHR P16473 2/20 0.32
HSD17B10 Q99714 2/20 0.32
CASP1 P29466 1/20 0.32

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
SCHEMBL19674785 0.85 CD44 (0.35) CYP3A4SMN1; SMN2MAPK1HTTCD44
SCHEMBL11154303 0.85 TDP1 (0.39) LMNACYP3A4SMN1; SMN2MAPTMAPK1
SCHEMBL559000 0.81 CD44 (0.37) LMNACYP3A4SMN1; SMN2HTTCD44
SCHEMBL3001668 0.81 LMNA (0.32) LMNAMAPTKMT2AHPGD
SCHEMBL22165264 0.81 HPGD (0.43) LMNACYP3A4SMN1; SMN2MAPTHTT
SCHEMBL29331735 0.81 APP (0.32) SMN1; SMN2MEN1KMT2A
SCHEMBL11294968 0.81 MAPT (0.38) LMNACYP3A4MAPTMAPK1ALDH1A1
SCHEMBL19964756 0.81 CD44 (0.48) LMNACYP3A4SMN1; SMN2CD44ALDH1A1
SCHEMBL11156180 0.79 LMNA (0.31) LMNAKMT2A
SCHEMBL20457096 0.79 SMN1; SMN2 (0.41) SMN1; SMN2MAPTALDH1A1

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 19 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115028576-B Production process of 3, 5-dichloro-2, 6-dimethyl-4-hydroxypyridine 广西金源生物化工实业有限公司 2023-12-01 CN disclosed
CN-115028576-A Production process of 3, 5-dichloro-2, 6-dimethyl-4-hydroxypyridine 广西金源生物化工实业有限公司 2022-09-09 CN disclosed
EP-2691095-B1 IMIDAZOLYL AMIDE COMPOUNDS AND USES RELATED THERETO UNIV EMORY (US) 2017-07-05 EP disclosed
US-9365523-B2 Imidazolyl amide compounds and uses related thereto EMORY UNIVERSITY (US) 2016-06-14 US disclosed
US-20160101104-A1 QUINUCLIDINE COMPOUNDS AS ALPHA-7 NICOTINIC ACETYLCHOLINE RECEPTOR LIGANDS BRISTOL MYERS SQUIBB CO (US) 2016-04-14 US disclosed
US-20150342935-A1 QUINUCLIDINE COMPOUNDS AS ALPHA-7 NICOTINIC ACETYLCHOLINE RECEPTOR LIGANDS BRISTOL MYERS SQUIBB CO (US) 2015-12-03 US disclosed
US-20140221377-A1 Quinuclidine Compounds as Alpha-7 Nicotinic Acetylcholine Receptor Ligands BRISTOL MYERS SQUIBB CO (US) 2014-08-07 US disclosed
US-20140080828-A1 IMIDAZOLYL AMIDE COMPOUNDS AND USES RELATED THERETO CHILDREN'S HEATLHCARE OF ATLANTA, INC. (US) 2014-03-20 US disclosed
US-20130131064-A1 Quinuclidine Compounds as Alpha-7 Nicotinic Acetylcholine Receptor Ligands BRISTOL-MYERS SQUIBB COMPANY (US) 2013-05-23 US disclosed
WO-2011053292-A1 QUINUCLIDINE COMPOUNDS AS ALPHA-7 NICOTINIC ACETYLCHOLINE RECEPTOR LIGANDS BRISTOL-MYERS SQUIBB COMPANY (US) 2011-05-05 WO disclosed
US-4620033-A CATALYST OF NICKEL COMPOUND, IODIDE COMPOUND AND PROMOTER OF TIN COMPOUND AND LITHIUM COMPOUND MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 1986-10-28 US disclosed
US-4544511-A CATALYST CONTAINING NICKEL, HALIDES AND ORGANIC NITROGEN COMPOUND;COCATALYST OF METAL COMPOUND MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 1985-10-01 US disclosed
EP-0035860-B1 PROCESS FOR PRODUCING ETHYLIDENE DIACETATE AND/OR ACETALDEHYDE MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 1984-03-14 EP disclosed
EP-0048174-B1 PROCESS FOR PRODUCING VINYL ACETATE MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 1984-02-22 EP disclosed
EP-0065817-A1 Process for producing carboxylic acids MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 1982-12-01 EP disclosed
EP-0055622-A1 Process for producing acetic anhydride MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 1982-07-07 EP disclosed
EP-0048174-A1 Process for producing vinyl acetate MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 1982-03-24 EP disclosed
EP-0035860-A2 Process for producing ethylidene diacetate and/or acetaldehyde MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 1981-09-16 EP disclosed
US-3938259-A Process for continuous drying of chemical products by milling-fluidisation RICHTER GEDEON VEGYESZETI GYAR RT (HU) 1976-02-17 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 (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-20140080828-A1 IMIDAZOLYL AMIDE COMPOUNDS AND USES RELATED THERETO TPMT, PNP, MTAP LMNA 3734/4885CYP3A4 249/4885SMN1; SMN2 2371/4885
US-20140221377-A1 Quinuclidine Compounds as Alpha-7 Nicotinic Acetylcholine Receptor Ligands CHRNA7, CHRNA5, CHRNA6 LMNA 2215/4885CYP3A4 2815/4885SMN1; SMN2 813/4885
US-20130131064-A1 Quinuclidine Compounds as Alpha-7 Nicotinic Acetylcholine Receptor Ligands CHRNA7, CHRNA5, CHRNA6 LMNA 2215/4885CYP3A4 2815/4885SMN1; SMN2 813/4885
US-20160101104-A1 QUINUCLIDINE COMPOUNDS AS ALPHA-7 NICOTINIC ACETYLCHOLINE RECEPTOR LIGANDS CHRNA7, CHRNA5, CHRNA6 LMNA 2215/4885CYP3A4 2815/4885SMN1; SMN2 813/4885
US-20150342935-A1 QUINUCLIDINE COMPOUNDS AS ALPHA-7 NICOTINIC ACETYLCHOLINE RECEPTOR LIGANDS CHRNA7, CHRNA5, CHRNA6 LMNA 2215/4885CYP3A4 2815/4885SMN1; SMN2 813/4885

“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.