SCHEMBL6096311

SCHEMBL6096311

COC(=O)[C@H](N)CCl

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
SCHEMBL6096493 1.00 — —
SCHEMBL6950087 1.00 — —
Hydrochloric Acid SCHEMBL9731799 0.98 — —
Hydrochloric Acid SCHEMBL6096305 0.98 — —
Hydrochloric Acid SCHEMBL652660 0.98 — —
SCHEMBL2385218 0.81 — —
Hydrochloric Acid SCHEMBL29060562 0.79 LTA4H (0.36) —
Methylene Chloride SCHEMBL29028670 0.79 KIF11 (0.35) —
Hydrochloric Acid SCHEMBL2386334 0.79 LTA4H (0.36) —
SCHEMBL8894673 0.79 SMN1; SMN2 (0.42) —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106146327-A A kind of synthetic method of D-Cycloserine intermediate 浙江海正药业股份有限公司 2016-11-23 — — CN claimed
US-20260001924-A1 NEMO COILED COIL MIMICS AND METHODS OF USING SAME NEW YORK UNIVERSITY (US) 2026-01-01 — — US disclosed
US-12371461-B2 Nemo coiled coil mimics and methods of using same NEW YORK UNIVERSITY (US) 2025-07-29 — — US disclosed
EP-3303367-B1 STABILIZED MINIMAL COILED-COIL MIMETICS UNIV NEW YORK (US) 2025-06-18 — — EP disclosed
WO-2024130161-A2 NOVEL CAMPTOTHECIN DERIVATIVES AND CONJUGATES THEREOF BIONECURE THERAPEUTICS INC (US) 2024-06-20 — — WO disclosed
US-20240190930-A1 NEMO COILED COIL MIMICS AND METHODS OF USING SAME UNIV NEW YORK (US) 2024-06-13 — — US disclosed
US-20240124539-A1 CROSSLINKED HELIX DIMER MIMICS OF SOS AND METHODS OF USING SAME NEW YORK UNIVERSITY 2024-04-18 — — US disclosed
US-11891422-B2 NEMO coiled coil mimics and methods of using same NEW YORK UNIVERSITY (US) 2024-02-06 — — US disclosed
US-20240034753-A1 THERAPEUTIC PEPTIDES COHBAR, INC. 2024-02-01 — — US disclosed
US-11753445-B2 Therapeutic peptides COHBAR, INC. (US) 2023-09-12 — — US disclosed
WO-2018064098-A1 THERAPEUTIC MOTS-C RELATED PEPTIDES COHBAR, INC. (US) 2018-04-05 — — WO disclosed
WO-2016201007-A1 STABILIZED MINIMAL COILED-COIL MIMETICS NEW YORK UNIVERSITY (US) 2016-12-15 — — WO disclosed
CN-106146327-A A kind of synthetic method of D-Cycloserine intermediate 浙江海正药业股份有限公司 2016-11-23 — — CN disclosed
CN-104710324-B A kind of method synthesizing scheme for lacosamide 华润双鹤药业股份有限公司 2016-08-31 — — CN disclosed
CN-104710324-A Lacosamide synthesis method CHINA RESOURCES DOUBLE CRANE PHARMACEUTICAL CO LTD 2015-06-17 — — CN disclosed
US-7109352-B2 Process for producing optically active amino acid derivatives KANEKA CORPORATION (JP) 2006-09-19 — — US disclosed
US-20050143586-A1 Process for producing optically active amino acid derivatives KANEKA CORPORATION (JP) 2005-06-30 — — US disclosed
US-6720449-B2 N-PROTECTING AN OPTICALLY ACTIVE 3-HALOALANINE DERIVATIVE FOLLOWED BY CYCLIZATION FOR AZIRIDINE-2-CARBOXYLIC ACID DERIVATIVES KANEKA CORPORATION (JP) 2004-04-13 — — US disclosed
US-20030032814-A1 Process for preparing optically active amino acid derivatives KANEKA CORPORATION (JP) 2003-02-13 — — US disclosed
EP-1179530-A1 PROCESSES FOR PREPARING OPTICALLY ACTIVE AMINO ACID DERIVATIVES Kaneka Corporation (JP) 2002-02-13 — — EP disclosed
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