SCHEMBL19476174

SCHEMBL19476174

O=C(Nc1ncccc1S(=O)(=O)c1cccnc1)c1ccccc1

nearest known ligand 0.70

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 3/20 0.70
RAB9A P51151 3/20 0.70
MEN1 O00255 2/20 0.70
KMT2A Q03164 2/20 0.70
NAMPT P43490 7/20 0.55
ALDH1A1 P00352 1/20 0.53
PTGS2 P35354 1/20 0.50
CYP3A4 P08684 2/20 0.48
KCNK3 O14649 1/20 0.47
POLB P06746 1/20 0.46
LMNA P02545 2/20 0.44
HTT P42858 1/20 0.44
CYP2C9 P11712 1/20 0.44
KDM4E B2RXH2 1/20 0.44
MAPT P10636 1/20 0.44
MAPK1 P28482 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
GAA P10253 1/20 0.44
SNCA P37840 1/20 0.44

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
SCHEMBL19476155 0.91 NPC1 (0.83) NPC1RAB9AMEN1KMT2ANAMPT
SCHEMBL19476169 0.79 RAB9A (0.64) NPC1RAB9AMEN1KMT2AALDH1A1
SCHEMBL15647894 0.73 PTGS2 (0.83) MEN1KMT2ANAMPTALDH1A1PTGS2
SCHEMBL161057 0.71 CYP3A4 (0.81) MEN1KMT2ANAMPTALDH1A1PTGS2
SCHEMBL164829 0.71 NAMPT (1.00) NPC1RAB9AMEN1KMT2ANAMPT
SCHEMBL18640729 0.70 LMNA (0.56) NAMPTALDH1A1KCNK3LMNAHTT
SCHEMBL30648563 0.70 RAB9A (0.88) NPC1RAB9AMEN1KMT2APOLB
SCHEMBL571346 0.69 SIRT2 (0.60) NPC1RAB9AALDH1A1KCNK3LMNA
SCHEMBL23566394 0.69 USP2 (0.68) NPC1RAB9AMEN1KMT2AALDH1A1
SCHEMBL3820618 0.69 HTT (0.66) NPC1RAB9AMEN1KMT2AALDH1A1

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 3 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
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 2403/4885MEN1 3912/4885
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 2403/4885MEN1 3912/4885

“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.