SCHEMBL12588926

SCHEMBL12588926

CN(C)p1oc2ccc3ccccc3c2c2c(o1)c(COCc1cc3ccccc3c3c1op(N(C)C)oc1ccc4ccccc4c13)cc1ccccc12

nearest known ligand 0.35

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
▸ KMT2A Q03164 3/20 0.35
▸ KDM4E B2RXH2 7/20 0.34
▸ ATM Q13315 1/20 0.32
▸ MAPT P10636 3/20 0.32
▸ ALDH1A1 P00352 3/20 0.32
▸ MEN1 O00255 2/20 0.31
▸ POLB P06746 1/20 0.31
▸ RAD52 P43351 1/20 0.31
▸ HPGD P15428 2/20 0.31
▸ LMNA P02545 1/20 0.31
▸ HTT P42858 1/20 0.31
▸ NPSR1 Q6W5P4 1/20 0.31
▸ AHR P35869 1/20 0.31
▸ ABCG2 Q9UNQ0 1/20 0.31
▸ GAA P10253 1/20 0.30
▸ NPC1 O15118 1/20 0.30
▸ RAB9A P51151 1/20 0.30
▸ PAX8 Q06710 1/20 0.30
▸ TDP1 Q9NUW8 1/20 0.30

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
SCHEMBL12588930 0.89 KMT2A (0.34) KMT2AKDM4EMAPTALDH1A1NPSR1
SCHEMBL12588934 0.88 KDM4E (0.33) KMT2AKDM4EATMMAPTALDH1A1
SCHEMBL11988006 0.82 ALDH1A1 (0.35) KMT2AKDM4EATMMAPTALDH1A1
SCHEMBL973485 0.81 HNF4A (0.40) KMT2AKDM4EATMMAPTALDH1A1
SCHEMBL29424688 0.81 HNF4A (0.40) KMT2AKDM4EATMMAPTALDH1A1
SCHEMBL12588944 0.78 KDM4E (0.33) KDM4EAHRABCG2NPC1RAB9A
SCHEMBL14382011 0.74 KDM4E (0.34) KMT2AKDM4EMAPTALDH1A1HPGD
SCHEMBL2847420 0.71 CYP1A2 (0.38) KMT2AKDM4EATMALDH1A1POLB
SCHEMBL14001440 0.71 KMT2A (0.40) KMT2AKDM4EATMMAPTALDH1A1
SCHEMBL12570267 0.71 SMN1; SMN2 (0.43) KDM4EMAPTALDH1A1HPGDLMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10752625-B2 Method of making tetrahydronaphthyridinyl nonanoic acid compounds SCIFLUOR LIFE SCIENCES, INC. (US) 2020-08-25 — — US disclosed
US-20190194195-A1 METHOD OF MAKING TETRAHYDRONAPHTHYRIDINYL NONANOIC ACID COMPOUNDS FELIQS CORPORATION (JP) 2019-06-27 — — US disclosed
US-10253025-B2 Method of making tetrahydronaphthyridinyl nonanoic acid compounds SCIFLUOR LIFE SCIENCES, INC. (US) 2019-04-09 — — US disclosed
US-7964743-B2 Catalyst for asymmetric synthesis, ligand for use therein, and process for producing optically active compound through asymmetric synthesis reaction using them JAPAN SCIENCE AND TECHNOLOGY AGENCY (JP) 2011-06-21 — — US disclosed
US-7964743-B2 Catalyst for asymmetric synthesis, ligand for use therein, and process for producing optically active compound through asymmetric synthesis reaction using them JAPAN SCIENCE AND TECHNOLOGY AGENCY (JP) 2011-06-21 — — US disclosed
US-20090156849-A1 Catalyst for Asymmetric Synthesis, Ligand for Use Therein, and Process for Producing Optically Active Compound through Asymmetric Synthesis Reaction Using Them JAPAN SCIENCE AND TECHNOLOGY AGENCY (JP) 2009-06-18 — — US disclosed
US-20090156849-A1 Catalyst for Asymmetric Synthesis, Ligand for Use Therein, and Process for Producing Optically Active Compound through Asymmetric Synthesis Reaction Using Them JAPAN SCIENCE AND TECHNOLOGY AGENCY (JP) 2009-06-18 — — US disclosed
EP-1854802-A1 CATALYST FOR ASYMMETRIC SYNTHESIS, LIGAND FOR USE THEREIN, AND PROCESS FOR PRODUCING OPTICALLY ACTIVE COMPOUND THROUGH ASYMMETRIC SYNTHESIS REACTION USING THEM Japan Science and Technology Agency (JP) 2007-11-14 — — 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 (4 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-20190194195-A1 METHOD OF MAKING TETRAHYDRONAPHTHYRIDINYL NONANOIC ACID COMPOUNDS NISCH, SLC10A1, AANAT KMT2A 3422/4885KDM4E 4287/4885ATM 4755/4885
US-20090156849-A1 Catalyst for Asymmetric Synthesis, Ligand for Use Therein, and Process for Producing Optically Active Compound through Asymmetric Synthesis Reaction Using Them ME1, ATIC, ADH1A KMT2A 3016/4885KDM4E 3842/4885ATM 3596/4885
US-10752625-B2 Method of making tetrahydronaphthyridinyl nonanoic acid compounds NISCH, SLC10A1, AANAT KMT2A 3422/4885KDM4E 4287/4885ATM 4755/4885
US-10253025-B2 Method of making tetrahydronaphthyridinyl nonanoic acid compounds NISCH, SLC10A1, AANAT KMT2A 3422/4885KDM4E 4287/4885ATM 4755/4885

“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.

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