SCHEMBL2833352

SCHEMBL2833352

Fc1cccc(-c2ncc(-c3c[nH]c(Cc4ccncc4)n3)cn2)c1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP11B1 P15538 2/20 0.50
CYP3A4 P08684 2/20 0.50
CYP17A1 P05093 1/20 0.50
CYP11B2 P19099 1/20 0.50
HPGDS O60760 4/20 0.42
IDO1 P14902 2/20 0.40
FYN P06241 1/20 0.39
TP53 P04637 1/20 0.39
HRH3 Q9Y5N1 3/20 0.38
BCHE P06276 1/20 0.38
ACHE P22303 1/20 0.38
GRIN1 Q05586 1/20 0.38
GRIN2B Q13224 1/20 0.38
GSK3B P49841 1/20 0.37
WNT3A P56704 1/20 0.37
HRH4 Q9H3N8 1/20 0.37
PIM1 P11309 1/20 0.36
MAPK13 O15264 1/20 0.36
RAF1 P04049 1/20 0.36
MAPK12 P53778 1/20 0.36

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
SCHEMBL2839487 0.91 IDO1 (0.42) CYP11B1CYP3A4CYP17A1CYP11B2HPGDS
SCHEMBL2840149 0.91 HPGDS (0.47) CYP11B1CYP3A4CYP17A1CYP11B2HPGDS
SCHEMBL2840271 0.89 IDO1 (0.43) HPGDSIDO1HRH3BCHEACHE
SCHEMBL2838285 0.89 HPGDS (0.48) CYP11B1CYP3A4CYP17A1CYP11B2HPGDS
SCHEMBL2837596 0.87 HPGDS (0.49) CYP11B1CYP3A4CYP11B2HPGDSHRH3
SCHEMBL2838171 0.83 HPGDS (0.46) HPGDSIDO1HRH3BCHEACHE
SCHEMBL2837476 0.83 HPGDS (0.42) HPGDSIDO1HRH3BCHEACHE
SCHEMBL2834260 0.82 HPGDS (0.50) CYP11B1CYP3A4CYP17A1CYP11B2HPGDS
SCHEMBL2835441 0.81 HPGDS (0.43) HPGDSIDO1BCHEACHEPIM1
SCHEMBL2843041 0.81 HPGDS (0.48) CYP11B1CYP11B2HPGDSTP53MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2350059-B1 MULTIHETEROARYL COMPOUNDS AS INHIBITORS OF H-PGDS AND THEIR USE FOR TREATING PROSTAGLANDIN D2 MEDIATED DISEASES CAYMAN CHEM CO (US) 2016-03-23 EP disclosed
US-9126973-B2 Multiheteroaryl compounds as inhibitors of H-PGDS and their use for treating prostaglandin D2 mediated diseases CAYMAN CHEMICAL COMPANY, INCORPORATED (US) 2015-09-08 US disclosed
US-20150099748-A1 MULTIHETEROARYL COMPOUNDS AS INHIBITORS OF H-PGDS AND THEIR USE FOR TREATING PROSTAGLANDIN D2 MEDIATED DISEASES CAYMAN CHEMICAL COMPANY, INCORPORATED 2015-04-09 US disclosed
US-8536185-B2 Multiheteroaryl compounds as inhibitors of H-PGDS and their use for treating prostaglandin D2 mediated diseases CAYMAN CHEMICAL COMPANY, INCORPORATED (US) 2013-09-17 US disclosed
US-8450326-B2 2013-05-28 US disclosed
US-20130079375-A1 MULTIHETEROARYL COMPOUNDS AS INHIBITORS OF H-PGDS AND THEIR USE FOR TREATING PROSTAGLANDIN D2 MEDIATED DISEASES CAYMAN CHEMICAL COMPANY, INCORPORATED (US) 2013-03-28 US disclosed
US-20100075990-A1 MULTIHETEROARYL COMPOUNDS AS INHIBITORS OF H-PGDS AND THEIR USE FOR TREATING PROSTAGLANDIN D2 MEDIATED DISEASES CAYMAN CHEMICAL COMPANY (US) 2010-03-25 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 (3 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-20100075990-A1 MULTIHETEROARYL COMPOUNDS AS INHIBITORS OF H-PGDS AND THEIR USE FOR TREATING PROSTAGLANDIN D2 MEDIATED DISEASES HPGDS, PTGIS, PTGES CYP11B1 105/4885CYP3A4 964/4885CYP17A1 1014/4885
US-20130079375-A1 MULTIHETEROARYL COMPOUNDS AS INHIBITORS OF H-PGDS AND THEIR USE FOR TREATING PROSTAGLANDIN D2 MEDIATED DISEASES HPGDS, PTGIS, PTGES CYP11B1 105/4885CYP3A4 964/4885CYP17A1 1014/4885
US-20150099748-A1 MULTIHETEROARYL COMPOUNDS AS INHIBITORS OF H-PGDS AND THEIR USE FOR TREATING PROSTAGLANDIN D2 MEDIATED DISEASES HPGDS, PTGIS, PTGES CYP11B1 105/4885CYP3A4 964/4885CYP17A1 1014/4885

“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.