SCHEMBL365047

SCHEMBL365047

N#CCC1CC1

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
SCHEMBL24197645 1.00 JAK2 (0.33) —
SCHEMBL13907209 1.00 JAK2 (0.33) —
SCHEMBL2162286 1.00 JAK2 (0.33) —
Bromide SCHEMBL30923588 0.97 — —
SCHEMBL27350836 0.97 — —
Hydrochloric Acid SCHEMBL30503012 0.97 — —
Acetonitrile SCHEMBL7798831 0.91 — —
SCHEMBL2974620 0.88 — —
SCHEMBL938283 0.87 — —
SCHEMBL1437260 0.87 — —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118702597-A Fmoc-3-cyclopropyl-L-valine synthesis method 吉尔多肽生物制药(大连市)有限公司 2024-09-27 — — CN claimed
WO-2024196936-A2 LOCALIZED HIGH CONCENTRATION ELECTROLYTE AND LITHIUM-ION BATTERY COMPRISING THE SAME SILA NANOTECHNOLOGIES, INC. (US) 2024-09-26 — — WO claimed
US-20240322244-A1 LOCALIZED HIGH CONCENTRATION ELECTROLYTE AND LITHIUM-ION BATTERY COMPRISING THE SAME SILA NANOTECHNOLOGIES, INC. 2024-09-26 — — US claimed
US-20230265102-A1 PESTICIDALLY ACTIVE HETEROCYCLIC DERIVATIVES WITH SULFUR CONTAINING SUBSTITUENTS SYNGENTA CROP PROTECTION AG (CH) 2023-08-24 — — US claimed
EP-4208447-A1 PESTICIDALLY ACTIVE HETEROCYCLIC DERIVATIVES WITH SULFUR CONTAINING SUBSTITUENTS Syngenta Crop Protection AG (CH) 2023-07-12 — — EP claimed
CN-116234811-A Pesticidally active heterocyclic derivatives with sulfur containing substituents 先正达农作物保护股份公司 2023-06-06 — — CN claimed
EP-4168409-A1 VMAT2 INHIBITORS AND METHODS OF USE Neurocrine Biosciences, Inc. (US) 2023-04-26 — — EP claimed
US-20210330678-A1 PAPD5 INHIBITORS AND METHODS OF USE THEREOF NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2021-10-28 — — US claimed
EP-3846808-A2 PAPD5 INHIBITORS AND METHODS OF USE THEREOF CHILDREN'S MEDICAL CENTER CORPORATION (US) 2021-07-14 — — EP claimed
CN-110386888-A A kind of inexpensive, high yield 1- (thiopurine methyltransferase) cyclopropaneacetic acid production technology 上海红蓝医药科技有限公司 2019-10-29 — — CN claimed
US-20030114458-A1 Antibacterial agents WARNER-LAMBERT COMPANY 2003-06-19 — — US claimed
JP-2002542226-A — — 2002-12-10 — — JP claimed
WO-2002096908-A1 ANTIBACTERIAL AGENTS WARNER-LAMBERT COMPANY LLC (US) 2002-12-05 — — WO claimed
EP-1171421-A1 PROCESS FOR THE PREPARATION OF CYCLOPROPYLACETONITRILE EASTMAN CHEMICAL COMPANY (US) 2002-01-16 — — EP claimed
CN-1072218-C Process for preparing 1- (mercaptomethyl) cyclopropaneacetic acid MERCK & CO INC (US) 2001-10-03 — — CN claimed
US-6191300-B1 REACTING A MIXTURE OF CYCLOPROPYLMETHYL HALIDE, A CYCLOBUTYL HALIDE AND A 4-HALO-1-BUTENE WITH AN ALKALI METAL CYANIDE; RECOVERY OF SUBSTANTIALLY PURE CYCLOPROPYLACETONITRILE AND CYCLOBUTYL HALIDE, EACH HAVING A PURITY &gt;95% EASTMAN CHEMICAL COMPANY 2001-02-20 — — US claimed
WO-2000063163-A1 PROCESS FOR THE PREPARATION OF CYCLOPROPYLACETONITRILE EASTMAN CHEMICAL COMPANY (US) 2000-10-26 — — WO claimed
CN-1172481-A Process for preparation of 1 -(thiomethyl) -cyclopropaneacetic acid MERCK & CO INC (US) 1998-02-04 — — CN claimed
EP-0699182-A1 CYCLOPROPYLACETONITRILE DERIVATIVES, PREPARATION THEREOF AND USE THEREOF AS DRUGS LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 1996-03-06 — — EP claimed
WO-1995025087-A1 CYCLOPROPYLACETONITRILE DERIVATIVES, PREPARATION THEREOF AND USE THEREOF AS DRUGS LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 1995-09-21 — — WO claimed
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