SCHEMBL6096493

SCHEMBL6096493

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
SCHEMBL6096311 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 22 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115872882-B Synthesis method of 3-chloro-alanine 中国科学院大连化学物理研究所 2024-05-10 — — CN disclosed
CN-115872882-A Synthetic method of 3-chloro-alanine 中国科学院大连化学物理研究所 2023-03-31 — — CN disclosed
WO-2023280280-A1 FUSED-RING COMPOUND THAT ACTS AS KRAS G12D INHIBITOR 微境生物医药科技(上海)有限公司 2023-01-12 — — WO disclosed
CN-111018728-A Method and device for preparing 3-chloro-alanine hydrochloride by using water as auxiliary agent 暨南大学 2020-04-17 — — CN disclosed
CN-110642736-A Synthesis method of acetamido-3-methyl chloropropionate 湖北宇阳药业有限公司 2020-01-03 — — CN disclosed
EP-3197874-B1 PROCESS FOR SYNTHESIZING ERGOTHIONEINE AND RELATED COMPOUNDS UNIV CAPE TOWN (ZA) 2019-04-24 — — EP disclosed
US-9908854-B2 Process for synthesizing ergothioneine and related compounds UNIVERSITY OF CAPE TOWN (ZA) 2018-03-06 — — US disclosed
US-20170305865-A1 PROCESS FOR SYNTHESIZING ERGOTHIONEINE AND RELATED COMPOUNDS UNIVERSITY OF CAPE TOWN (ZA) 2017-10-26 — — US disclosed
EP-3197874-A1 PROCESS FOR SYNTHESIZING ERGOTHIONEINE AND RELATED COMPOUNDS University of Cape Town (ZA) 2017-08-02 — — EP disclosed
WO-2016046618-A1 PROCESS FOR SYNTHESIZING ERGOTHIONEINE AND RELATED COMPOUNDS UNIVERSITY OF CAPE TOWN (ZA) 2016-03-31 — — WO 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
EP-0219344-B1 VINYL MONOMERS AND DERIVED LIQUID CRYSTALLINE POLYMERS The University of Southern Mississippi (US) 1991-04-17 — — EP disclosed
US-4985522-A Polymers containing pendant urea groups THE UNIVERSITY OF SOUTHERN MISSISSIPPI (US) 1991-01-15 — — US disclosed
US-4906767-A Monomers with urea groups THE UNIVERSITY OF SOUTHERN MISSISSIPPI (US) 1990-03-06 — — US disclosed
US-4793949-A New vinyl monomers capable of forming side-chain liquid crystalline polymers and the resulting polymers UNIVERSITY OF SOUTHERN MISSISSIPPI (US) 1988-12-27 — — US disclosed
EP-0219344-A1 Vinyl monomers and derived liquid crystalline polymers The University of Southern Mississippi (US) 1987-04-22 — — EP disclosed
US-4613658-A Vinyl monomers capable of forming side-chain liquid crystalline polymers and the resulting polymers UNIVERSITY OF SOUTHERN MISSISSIPPI (US) 1986-09-23 — — US disclosed
US-4260681-A Reagent system and method for assaying peptidase enzymes CALBIOCHEM-BEHRING CORP. (US) 1981-04-07 — — US disclosed
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