SCHEMBL2000699

SCHEMBL2000699

NC(=O)NCC1CC1

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL13999422 0.91 TDP1 (0.83) —
SCHEMBL4697448 0.91 TDP1 (0.83) —
SCHEMBL7296555 0.90 — —
SCHEMBL7296108 0.90 TDP1 (0.82) —
SCHEMBL1050014 0.88 TDP1 (0.78) —
SCHEMBL2285048 0.88 TDP1 (0.78) —
SCHEMBL8596242 0.87 TDP1 (0.76) —
SCHEMBL8596237 0.87 TDP1 (0.76) —
SCHEMBL7350548 0.84 TDP1 (0.72) —
SCHEMBL18028783 0.84 TDP1 (0.72) —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20090104116-A1 COMPOUNDS FOR THE INHIBITION OF INTEGRINS AND USE THEREOF JERINI AG (DE) 2009-04-23 — — US claimed
US-20080306067-A1 Modulators of Chemokine Receptor Activity WEIGAND KLAUS 2008-12-11 — — US claimed
EP-1979342-A1 COMPOUNDS FOR THE INHIBITION OF INTEGRINS AND USE THEREOF Jerini AG (DE) 2008-10-15 — — EP claimed
EP-1943235-A1 ARYLUREA DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY Novartis AG (CH) 2008-07-16 — — EP claimed
WO-2007088041-A1 COMPOUNDS FOR THE INHIBITION OF INTEGRINS AND USE THEREOF JERINI AG (DE) 2007-08-09 — — WO claimed
WO-2007048771-A1 ARYLUREA DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY NOVARTIS AG (CH) 2007-05-03 — — WO claimed
CN-117024411-B Isoquinoline as HPK1 inhibitor 豪夫迈·罗氏有限公司 2026-05-19 — — CN disclosed
EP-4655299-A1 NEW COMPOUNDS FOR TREATING STAPHYLOCOCCUS INFECTIONS Ab2 Therapeutics, S. L. (ES) 2025-12-03 — — EP disclosed
EP-4171563-B1 TETRAZOLE DERIVATIVES AS TRPA1 INHIBITORS BOEHRINGER INGELHEIM INT (DE) 2025-08-06 — — EP disclosed
US-20250092019-A1 TETRAZOLE DERIVATIVES AS TRPA1 INHIBITORS BOEHRINGER INGELHEIM INT (DE) 2025-03-20 — — US disclosed
WO-2024156895-A1 NEW COMPOUNDS FOR TREATING STAPHYLOCOCCUS INFECTIONS ABAC Therapeutics, S.L. (ES) 2024-08-02 — — WO disclosed
EP-4406952-A1 NEW COMPOUNDS FOR TREATING STAPHYLOCOCCUS INFECTIONS ABAC THERAPEUTICS, S.L. (ES) 2024-07-31 — — EP disclosed
US-11884652-B2 Tetrazole derivatives as TRPA1 inhibitors BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2024-01-30 — — US disclosed
WO-2007088041-A1 COMPOUNDS FOR THE INHIBITION OF INTEGRINS AND USE THEREOF JERINI AG (DE) 2007-08-09 — — WO disclosed
US-20070179127-A1 Sulfonamide compound ASAHI KASEI PHARMA CORPORATION (JP) 2007-08-02 — — US disclosed
WO-2007048771-A1 ARYLUREA DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY NOVARTIS AG (CH) 2007-05-03 — — WO disclosed
US-20060241115-A1 Compounds and methods of use AMGEN INC. 2006-10-26 — — US disclosed
EP-0389282-B1 Xanthinederivatives, process for their preparation and their pharmaceutical use SMITHKLINE BEECHAM PHARMA GMBH (DE) 2002-02-20 — — EP disclosed
EP-0386683-A2 Xanthine derivatives having bronchodilating activity, a process for the preparation thereof and pharmaceutical compositions containing them POLI INDUSTRIA CHIMICA S.p.A. (IT) 1990-09-12 — — EP disclosed
US-3984568-A Fungicidal cyclopropyl substituted 2-cyanoacetamide derivatives E. I. DU PONT DE NEMOURS AND COMPANY (US) 1976-10-05 — — US disclosed
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