SCHEMBL10070835

SCHEMBL10070835

c1ccc(N2CCOCCOCCOCCOCC2)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 1.00
AKR1C3 P42330 2/20 0.60
PKM P14618 1/20 0.60
TSHR P16473 1/20 0.60
CYP2C9 P11712 1/20 0.60
CYP2C19 P33261 1/20 0.60
ALDH1A1 P00352 5/20 0.59
MAPT P10636 4/20 0.59
MEN1 O00255 2/20 0.59
HTT P42858 2/20 0.59
KMT2A Q03164 2/20 0.59
NPC1 O15118 2/20 0.59
RAB9A P51151 2/20 0.59
CYP1A2 P05177 1/20 0.59
KMO O15229 1/20 0.56
AR P10275 2/20 0.55
SMN1; SMN2 Q16637 3/20 0.54
HTR3E A5X5Y0 1/20 0.54
HTR3B O95264 1/20 0.54
ADRB1 P08588 1/20 0.54

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
SCHEMBL11203977 1.00 LMNA (1.00) LMNAAKR1C3PKMTSHRCYP2C9
SCHEMBL10070687 1.00 LMNA (1.00) LMNAAKR1C3PKMTSHRCYP2C9
SCHEMBL13809379 1.00 LMNA (1.00) LMNAAKR1C3PKMTSHRCYP2C9
SCHEMBL254812 0.97 LMNA (0.95) LMNAAKR1C3PKMTSHRCYP2C9
SCHEMBL3948094 0.97 LMNA (0.95) LMNAAKR1C3PKMTSHRCYP2C9
SCHEMBL2555823 0.97 LMNA (0.95) LMNAAKR1C3PKMTSHRCYP2C9
SCHEMBL4408839 0.95 LMNA (0.91) LMNAAKR1C3PKMTSHRCYP2C9
SCHEMBL184087 0.95 LMNA (0.91) LMNAAKR1C3PKMTSHRCYP2C9
Hydrochloric Acid SCHEMBL9131024 0.95 LMNA (0.91) LMNAAKR1C3PKMTSHRCYP2C9
Ammonia Solution, Strong SCHEMBL4262260 0.95 LMNA (0.91) LMNAAKR1C3PKMTSHRCYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3940806-B1 METHOD OF MODIFYING THE STRUCTURE OF PEROVSKITE FILMS ECOLE POLYTECHNIQUE FED LAUSANNE EPFL (CH) 2023-08-16 EP claimed
CN-116759632-A Crown ether lithium salt compound and perovskite lithium battery thereof 美能能源技术(苏州)有限公司 2023-09-15 CN disclosed
EP-3940806-B1 METHOD OF MODIFYING THE STRUCTURE OF PEROVSKITE FILMS ECOLE POLYTECHNIQUE FED LAUSANNE EPFL (CH) 2023-08-16 EP disclosed
US-20210249714-A1 Lithium Air Secondary Battery NIPPON TELEGRAPH AND TELEPHONE CORPORATION (JP) 2021-08-12 US disclosed
US-11059995-B2 Film forming composition MERCK PATENT GMBH (DE) 2021-07-13 US disclosed
US-20200377761-A1 FILM FORMING COMPOSITION MERCK PATENT GMBH (DE) 2020-12-03 US disclosed
US-9257651-B2 Organic electroluminescence element and method for manufacturing organic electroluminescence element KONICA MINOLTA HOLDINGS, INC. (JP) 2016-02-09 US disclosed
US-20130087778-A1 ORGANIC ELECTROLUMINESCENCE ELEMENT AND METHOD FOR MANUFACTURING ORGANIC ELECTROLUMINESCENCE ELEMENT KONICA MINOLTA HOLDINGS, INC. (JP) 2013-04-11 US disclosed
US-20130087778-A1 ORGANIC ELECTROLUMINESCENCE ELEMENT AND METHOD FOR MANUFACTURING ORGANIC ELECTROLUMINESCENCE ELEMENT KONICA MINOLTA HOLDINGS, INC. (JP) 2013-04-11 US disclosed
WO-2012040204-A2 CYTOSOLIC FLUORESCENT ION INDICATORS ASANTE RESEARCH, LLC (US) 2012-03-29 WO disclosed
US-7541462-B2 Triaminophosphine ligands for carbon-nitrogen and carbon-carbon bond formation IOWA STATE UNIVERSITY RESEARCH FOUNDATION, INC. (US) 2009-06-02 US disclosed
US-20080139806-A1 TRIAMINOPHOSPHINE LIGANDS FOR CARBON-NITROGEN AND CARBON-CARBON BOND FORMATION IOWA STATE UNIVERSITY RESEARCH FOUNDATION, INC.. 2008-06-12 US disclosed
US-7385058-B1 Triaminophosphine ligands for carbon-nitrogen and carbon-carbon bond formation IOWA STATE UNIVERSITY RESEARCH FOUNDATION, INC. (US) 2008-06-10 US disclosed
EP-0171401-A1 PLATINUM AND CROWN ETHER COMPLEXES WITH ANTINEOPLASTIC ACTIVITY AND DRUG CONTAINING THEM Medac Gesellschaft für klinische Spezialpräparate mbH (DE) 1986-02-19 EP disclosed
WO-1985003078-A1 PLATINUM AND CROWN ETHER COMPLEXES WITH ANTINEOPLASTIC ACTIVITY AND DRUG CONTAINING THEM MEDAC GESELLSCHAFT FÜR KLINISCHE SPEZIALPRÄPARATE (DE) 1985-07-18 WO disclosed
EP-0054668-B1 PROCESS FOR THE PREPARATION OF IODO-ORGANYL-ALKOXY SILANES Degussa Aktiengesellschaft (DE) 1985-01-16 EP disclosed
US-4362885-A Process for the manufacture of (iodoorganyl)alkoxysilanes DEGUSSA AKTIENGESELLSCHAFT (DE) 1982-12-07 US disclosed
EP-0054668-A2 Process for the preparation of iodo-organyl-alkoxy silanes Degussa Aktiengesellschaft (DE) 1982-06-30 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-20080139806-A1 TRIAMINOPHOSPHINE LIGANDS FOR CARBON-NITROGEN AND CARBON-CARBON BOND FORMATION ABL1, AOC1, NPPA LMNA 3290/4885AKR1C3 2899/4885PKM 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.