SCHEMBL19476166

SCHEMBL19476166

COc1ccc(NC(=O)c2cc3ccccc3[nH]2)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 8/20 1.00
RAB9A P51151 7/20 1.00
TP53 P04637 1/20 0.73
LMNA P02545 1/20 0.72
SMN1; SMN2 Q16637 1/20 0.72
EGFR P00533 5/20 0.70
PIK3CA P42336 5/20 0.70
PDGFRB P09619 2/20 0.61
PDGFRA P16234 2/20 0.61
FLT3 P36888 2/20 0.61
CASP3 P42574 2/20 0.59
SENP7 Q9BQF6 2/20 0.59
KDM4E B2RXH2 2/20 0.59
ALDH1A1 P00352 2/20 0.59
PRNP P04156 1/20 0.59
GAA P10253 1/20 0.59
L3MBTL1 Q9Y468 1/20 0.59
MAPT P10636 1/20 0.58
KDM1A O60341 1/20 0.58
RCOR1 Q9UKL0 1/20 0.58

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
SCHEMBL19476082 0.87 NPC1 (0.77) NPC1RAB9ATP53LMNASMN1; SMN2
SCHEMBL9410579 0.85 NPC1 (0.74) NPC1RAB9ATP53LMNASMN1; SMN2
SCHEMBL19476163 0.85 NPC1 (0.78) NPC1RAB9ATP53LMNASMN1; SMN2
SCHEMBL8769590 0.84 NPC1 (0.82) NPC1RAB9ATP53LMNASMN1; SMN2
SCHEMBL27336120 0.84 RAB9A (0.73) NPC1RAB9ATP53LMNASMN1; SMN2
SCHEMBL29475123 0.84 NPC1 (1.00) NPC1RAB9ATP53LMNASMN1; SMN2
SCHEMBL7208136 0.84 NPC1 (1.00) NPC1RAB9ATP53LMNASMN1; SMN2
SCHEMBL2735814 0.83 TP53 (0.76) NPC1RAB9ATP53PDGFRBPDGFRA
SCHEMBL5818325 0.83 NPC1 (0.75) NPC1RAB9ATP53LMNASMN1; SMN2
Hydrochloric Acid SCHEMBL16465542 0.83 NPC1 (0.97) NPC1RAB9ATP53LMNASMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10759765-B2 Heterocyclic carboxylic acid amide ligand and applications thereof in copper catalyzed coupling reaction of aryl halogeno substitute CE PHARM CO., LTD. (CN) 2020-09-01 US disclosed
US-20190127337-A1 HETEROCYCLIC CARBOXYLIC ACID AMIDE LIGAND AND APPLICATIONS THEREOF IN COPPER CATALYZED COUPLING REACTION OF ARYL HALOGENO SUBSTITUTE CE PHARM CO., LTD. (CN) 2019-05-02 US disclosed
EP-3444031-A1 HETEROCYCLIC CARBOXYLIC ACID AMIDE LIGAND AND APPLICATIONS THEREOF IN COPPER CATALYZED COUPLING REACTION OF ARYL HALOGENO SUBSTITUTE Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences (CN) 2019-02-20 EP disclosed
WO-2017177979-A1 HETEROCYCLIC CARBOXYLIC ACID AMIDE LIGAND AND APPLICATIONS THEREOF IN COPPER CATALYZED COUPLING REACTION OF ARYL HALOGENO SUBSTITUTE 中国科学院上海有机化学研究所 2017-10-19 WO 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 (2 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-20190127337-A1 HETEROCYCLIC CARBOXYLIC ACID AMIDE LIGAND AND APPLICATIONS THEREOF IN COPPER CATALYZED COUPLING REACTION OF ARYL HALOGENO SUBSTITUTE AOC1, AOC2, AOC3 NPC1 3545/4885RAB9A 2403/4885TP53 2426/4885
US-10759765-B2 Heterocyclic carboxylic acid amide ligand and applications thereof in copper catalyzed coupling reaction of aryl halogeno substitute AOC1, AOC2, AOC3 NPC1 3545/4885RAB9A 2403/4885TP53 2426/4885

“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.