SCHEMBL1389171

SCHEMBL1389171

Cc1cc(NS(=O)(=O)c2cccc(C#N)c2)c2[nH]cc(Br)c2c1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CRBN Q96SW2 2/20 0.59
▸ RXFP1 Q9HBX9 1/20 0.48
▸ ACLY P53396 2/20 0.45
▸ GLO1 Q04760 1/20 0.45
▸ SLC40A1 Q9NP59 1/20 0.45
▸ TRIM24 O15164 1/20 0.44
▸ MAPT P10636 1/20 0.44
▸ PTGES2 Q9H7Z7 3/20 0.44
▸ CCKBR P32239 1/20 0.43
▸ PGR P06401 1/20 0.42
▸ BRD4 O60885 1/20 0.41
▸ SGK1 O00141 2/20 0.41
▸ BRD1 O95696 1/20 0.39
▸ BRPF1 P55201 1/20 0.39
▸ PGAM1 P18669 1/20 0.39
▸ CA12 O43570 1/20 0.38
▸ CA1 P00915 1/20 0.38
▸ CA2 P00918 1/20 0.38
▸ CA3 P07451 1/20 0.38
▸ CA6 P23280 1/20 0.38

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
SCHEMBL21218400 0.87 CRBN (0.53) CRBNRXFP1ACLYGLO1SLC40A1
SCHEMBL21218374 0.81 CRBN (0.80) CRBNRXFP1ACLYGLO1SLC40A1
SCHEMBL13049652 0.81 CRBN (0.38) CRBNSLC40A1MAPTCA12CA1
SCHEMBL1389185 0.79 CA1 (0.52) CRBNCA12CA1CA2CA3
SCHEMBL26844497 0.79 CRBN (0.74) CRBNRXFP1ACLYGLO1SLC40A1
SCHEMBL26844443 0.79 CRBN (0.61) CRBNRXFP1ACLYGLO1SLC40A1
SCHEMBL2768168 0.79 SMN1; SMN2 (0.42) CRBNRXFP1MAPTPGRCA12
SCHEMBL26844440 0.77 CRBN (0.59) CRBNRXFP1ACLYGLO1SLC40A1
SCHEMBL3060786 0.77 CRBN (0.71) CRBNRXFP1ACLYGLO1SLC40A1
SCHEMBL21218180 0.75 CRBN (0.78) CRBNRXFP1ACLYGLO1SLC40A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100267754-A1 INTEGRIN EXPRESSION INHIBITOR WAKABAYASHI TOSHIAKI 2010-10-21 — — US claimed
EP-1258252-B1 INTEGRIN EXPRESSION INHIBITORS EISAI R&D MAN CO LTD (JP) 2010-04-21 — — EP claimed
US-6469043-B1 ANTIANGIOGENIC AGENT WITH ANTITUMOR, ANTIMETASTATIC PROPERTIES WHICH SHOWS HIGH SAFETY EISAI CO., LTD. (JP) 2002-10-22 — — US claimed
EP-1074542-A1 SULFONAMIDE-CONTAINING INDOLE COMPOUNDS Eisai Co., Ltd. (JP) 2001-02-07 — — EP claimed
US-7834049-B2 Sulfonamide compound for treating arteriosclerosis, psoriasis, colon cancer, retinal angiogenesis, diabetic retinopathy or inflammatory diseases EISAI R&D MANAGEMENT CO., LTD. (JP) 2010-11-16 — — US disclosed
US-20100267754-A1 INTEGRIN EXPRESSION INHIBITOR WAKABAYASHI TOSHIAKI 2010-10-21 — — US disclosed
JP-2010180229-A SULFONAMIDE-CONTAINING INDOLE COMPOUND EISAI R & D MANAGEMENT CO LTD 2010-08-19 — — JP disclosed
EP-1258252-B1 INTEGRIN EXPRESSION INHIBITORS EISAI R&D MAN CO LTD (JP) 2010-04-21 — — EP disclosed
US-20090269352-A1 ANTITUMOR AGENT COMPRISING SULFONAMIDE-CONTAINING HETEROCYCLIC COMPOUND COMBINED WITH AN ANGIOGENESIS INHIBITOR WAKABAYASHI TOSHIAKI 2009-10-29 — — US disclosed
EP-1742052-A1 Method for testing effect of angiogenesis inhibitor via integrin expression inhibition Eisai Co., Ltd (JP) 2007-01-10 — — EP disclosed
EP-1362601-B1 METHOD OF EXAMINING EFFECT OF ANGIONEGESIS INHIBITOR MEDIATED BY THE INHIBITION OF INTEGRIN EXPRESSION EISAI CO LTD (JP) 2007-01-03 — — EP disclosed
JP-2006312652-A SULFONAMIDE-CONTAINING INDOLE COMPOUND EISAI R & D MANAGEMENT CO LTD 2006-11-16 — — JP disclosed
US-6673787-B2 PYRIMIDINESULFONAMIDE CONTAINING INDOLE COMPOUNDS USED AS ANTIANGIOGENIC AND ANTITUMOR AGENTS EISAI CO., LTD. (JP) 2004-01-06 — — US disclosed
EP-1362601-A1 METHOD OF EXAMINING EFFECT OF ANGIONEGESIS INHIBITOR MEDIATED BY THE INHIBITION OF INTEGRIN EXPRESSION Eisai Co. Ltd (JP) 2003-11-19 — — EP disclosed
US-6638964-B2 Pyridinesulfonamide containing indole compounds used as antiangiogenic and antitumor agents EISAI CO., LTD. (JP) 2003-10-28 — — US disclosed
EP-1258252-A1 INTEGRIN EXPRESSION INHIBITORS Eisai Co., Ltd. (JP) 2002-11-20 — — EP disclosed
US-6469043-B1 ANTIANGIOGENIC AGENT WITH ANTITUMOR, ANTIMETASTATIC PROPERTIES WHICH SHOWS HIGH SAFETY EISAI CO., LTD. (JP) 2002-10-22 — — US disclosed
US-20020128483-A1 Sulfonamide-containing indole compounds EISAI CO., LTD. 2002-09-12 — — US disclosed
US-20020128480-A1 Sulfonamide-containing indole compounds EISAI CO., LTD. 2002-09-12 — — US disclosed
EP-1074542-A1 SULFONAMIDE-CONTAINING INDOLE COMPOUNDS Eisai Co., Ltd. (JP) 2001-02-07 — — 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-20090269352-A1 ANTITUMOR AGENT COMPRISING SULFONAMIDE-CONTAINING HETEROCYCLIC COMPOUND COMBINED WITH AN ANGIOGENESIS INHIBITOR FGF1, FGF2, FGFR1 CRBN 2082/4885RXFP1 2153/4885ACLY 2148/4885
US-20020128480-A1 Sulfonamide-containing indole compounds IDO1, HCCS, VEGFA CRBN 428/4885RXFP1 158/4885ACLY 1933/4885
US-20100267754-A1 INTEGRIN EXPRESSION INHIBITOR ITGB5, ITGB1, ITGB2 CRBN 319/4885RXFP1 1804/4885ACLY 4504/4885
US-20020128483-A1 Sulfonamide-containing indole compounds IDO1, HCCS, VEGFA CRBN 482/4885RXFP1 149/4885ACLY 1794/4885

“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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