SCHEMBL2930650

SCHEMBL2930650

c1ccc2oc(-c3nccs3)cc2c1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CYP19A1 P11511 1/20 0.56
▸ RAB9A P51151 6/20 0.51
▸ NPC1 O15118 5/20 0.51
▸ MAPT P10636 5/20 0.51
▸ ADRA2A P08913 2/20 0.50
▸ GRM4 Q14833 1/20 0.49
▸ PDPK1 O15530 1/20 0.46
▸ MAOB P27338 4/20 0.45
▸ ALDH1A1 P00352 4/20 0.45
▸ MAOA P21397 3/20 0.45
▸ KDM4E B2RXH2 3/20 0.45
▸ HPGD P15428 2/20 0.45
▸ HSD17B10 Q99714 2/20 0.45
▸ CYP1A2 P05177 1/20 0.45
▸ CYP2D6 P10635 1/20 0.45
▸ ADRA2B P18089 1/20 0.45
▸ ADRA2C P18825 1/20 0.45
▸ NISCH Q9Y2I1 1/20 0.45
▸ DCTPP1 Q9H773 1/20 0.45
▸ SMN1; SMN2 Q16637 3/20 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
SCHEMBL1204523 0.78 TNKS (0.54) CYP19A1RAB9ANPC1MAOBALDH1A1
SCHEMBL4951498 0.78 GLA (0.62) RAB9ANPC1MAPTMAOBALDH1A1
Hydrochloric Acid SCHEMBL16826561 0.77 GLA (0.60) RAB9ANPC1MAPTMAOBALDH1A1
SCHEMBL29846430 0.75 F2RL3 (0.40) RAB9AMAPTGRM4PDPK1KDM4E
SCHEMBL13801141 0.74 MAPT (0.51) CYP19A1RAB9ANPC1MAPTADRA2A
SCHEMBL30036439 0.73 MAOB (0.63) RAB9ANPC1MAPTADRA2AGRM4
SCHEMBL103158 0.73 MAOB (0.63) RAB9ANPC1MAPTADRA2AGRM4
SCHEMBL17687570 0.73 CYP19A1 (0.64) CYP19A1RAB9ANPC1MAPTADRA2A
SCHEMBL14936927 0.72 MAPT (0.62) CYP19A1RAB9ANPC1MAPTADRA2A
SCHEMBL25441822 0.71 ADORA2A (0.35) CYP19A1RAB9ANPC1MAPTPDPK1

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 50 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-8325265-A — — None — — JP disclosed
JP-10316678-A — — None — — JP disclosed
JP-5202040-A — — None — — JP disclosed
US-20170014384-A1 METHOD FOR INHIBITING TUMOR METASTASIS INFLAMMATION RES CENTER COMPANY LTD (JP) 2017-01-19 — — US disclosed
CN-102847155-B Method for inhibiting tumor metastasis INFLAMMATION RES CT COMPANY LTD 2014-04-16 — — CN disclosed
CN-101022796-B Method for inhibiting tumor metastasis INFLAMMATION RES CT COMPANY LTD 2013-02-27 — — CN disclosed
CN-102847155-A Method for inhibiting tumor metastasis INFLAMMATION RES CT COMPANY LTD 2013-01-02 — — CN disclosed
EP-1997491-B1 Method for inhibiting tumor metastasis INFLAMMATION RES CT COMPANY LT (JP) 2010-09-22 — — EP disclosed
EP-1997491-A1 Method for inhibiting tumor metastasis Inflammation Research Center Company Ltd. (JP) 2008-12-03 — — EP disclosed
US-20080206203-A1 Administering leukotriene antagonist such as pranlukast INFLAMMATION RESEARCH CENTER COMPANY LTD. (JP) 2008-08-28 — — US disclosed
US-5296495-A Antiallergens, antiinflammatory FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1994-03-22 — — US disclosed
JP-H05202040-A THIAZOLYLBENZOFURAN DERIVATIVE FUJISAWA PHARMACEUT CO LTD 1993-08-10 — — JP disclosed
CN-1074444-A New thiazolyl benzofuran derivative, its preparation method and contain the pharmaceutical composition of this derivative FUJISAWA PHARMACEUTICAL CO (JP) 1993-07-21 — — CN disclosed
CN-1074444-A New thiazolyl benzofuran derivative, its preparation method and contain the pharmaceutical composition of this derivative FUJISAWA PHARMACEUTICAL CO (JP) 1993-07-21 — — CN disclosed
CN-1074444-A New thiazolyl benzofuran derivative, its preparation method and contain the pharmaceutical composition of this derivative FUJISAWA PHARMACEUTICAL CO (JP) 1993-07-21 — — CN disclosed
CN-1070910-A New thiazolyl benzofuran derivative, its preparation method and contain the pharmaceutical composition of this derivative FUJISAWA PHARMACEUTICAL CO (JP) 1993-04-14 — — CN disclosed
CN-1070910-A New thiazolyl benzofuran derivative, its preparation method and contain the pharmaceutical composition of this derivative FUJISAWA PHARMACEUTICAL CO (JP) 1993-04-14 — — CN disclosed
CN-1070910-A New thiazolyl benzofuran derivative, its preparation method and contain the pharmaceutical composition of this derivative FUJISAWA PHARMACEUTICAL CO (JP) 1993-04-14 — — CN disclosed
EP-0528337-A1 New thiazolylbenzofuran derivatives, processes for the preparation thereof and pharmaceutical composition comprising the same FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1993-02-24 — — EP disclosed
EP-0528337-A1 New thiazolylbenzofuran derivatives, processes for the preparation thereof and pharmaceutical composition comprising the same FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1993-02-24 — — 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 (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-20080206203-A1 Administering leukotriene antagonist such as pranlukast LTB4R2, LTB4R, LTC4S CYP19A1 3938/4885RAB9A 3888/4885NPC1 1877/4885
US-20170014384-A1 METHOD FOR INHIBITING TUMOR METASTASIS LTB4R, LTB4R2, LTA4H CYP19A1 4090/4885RAB9A 3497/4885NPC1 2159/4885

“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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