SCHEMBL2097116

SCHEMBL2097116

CC(C)CCCP

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
SCHEMBL4814282 0.90 — —
SCHEMBL5717469 0.87 — —
SCHEMBL9794655 0.87 LMNA (0.50) —
SCHEMBL13075202 0.87 LMNA (0.50) —
SCHEMBL6280786 0.87 LMNA (0.50) —
SCHEMBL8652515 0.87 LMNA (0.50) —
SCHEMBL4363756 0.87 LMNA (0.50) —
Bromide SCHEMBL5343457 0.84 LMNA (0.48) —
Hydrochloric Acid SCHEMBL5345632 0.84 LMNA (0.48) —
SCHEMBL6280017 0.77 — —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2022272106-A1 CDK2 INHIBITORS AND METHODS OF USING THE SAME CEDILLA THERAPEUTICS, INC. (US) 2022-12-29 — — WO disclosed
CN-105754099-B Composition and polymer 旭化成株式会社 2018-09-18 — — CN disclosed
EP-2831128-B1 PREPARATION OF FUNCTIONAL POLYMERS USING PHOSPHIDE INITIATORS BRIDGESTONE CORP (JP) 2016-11-30 — — EP disclosed
CN-103502315-B Composition and polymer 旭化成株式会社 2016-08-17 — — CN disclosed
CN-105754099-A Composition and polymer 旭化成株式会社 2016-07-13 — — CN disclosed
US-9163104-B2 Preparation of functional polymers using phosphide initiators BRIDGESTONE CORPORATION (JP) 2015-10-20 — — US disclosed
US-20150065673-A1 Preparation Of Functional Polymers Using Phosphide Initiators BRIDGESTONE CORPORATION (JP) 2015-03-05 — — US disclosed
EP-2831128-A1 PREPARATION OF FUNCTIONAL POLYMERS USING PHOSPHIDE INITIATORS Bridgestone Corporation (JP) 2015-02-04 — — EP disclosed
EP-2702127-A1 PROCESS FOR PRODUCING MONOBRANCHED FATTY ACIDS OR ALKYL ESTERS Croda International PLC (GB) 2014-03-05 — — EP disclosed
CN-103502315-A Composition and polymer ASAHI KASEI CHEMICALS CORP 2014-01-08 — — CN disclosed
WO-2002036639-A2 FLUORINATED ZWITTERIONIC COCATALYST ACTIVATORS FOR OLEFIN POLYMERIZATION EXXONMOBIL CHEMICAL PATENTS INC. (US) 2002-05-10 — — WO disclosed
US-5597776-A ANTAGONIST FOR HERBICIDES BASF AKTIENGESELLSCHAFT (DE) 1997-01-28 — — US disclosed
EP-0599906-B1 HERBICIDES CONTAINING 3-AMINOBENZO B]THIOPHENES AS AN ANTIDOTE BASF AG (DE) 1997-01-15 — — EP disclosed
EP-0552493-B1 Thiochromenone derivatives as antidotes and herbicidal agents containing them BASF AG (DE) 1996-09-11 — — EP disclosed
US-5491123-A Herbicides containing 3-aminobenzo(B)thiophenes as antidotes BASF AKTIENGESELLSCHAFT (DE) 1996-02-13 — — US disclosed
US-5378677-A Applying with cyclohexenone derivative BASF AKTIENGESELLSCHAFT (DE) 1995-01-03 — — US disclosed
EP-0599906-A1 HERBICIDES CONTAINING 3-AMINOBENZO B]THIOPHENES AS AN ANTIDOTE. BASF AG (DE) 1994-06-08 — — EP disclosed
EP-0552493-A1 Thiochromenone derivatives as antidotes and herbicidal agents containing them BASF Aktiengesellschaft (DE) 1993-07-28 — — EP disclosed
EP-0537463-A2 Substituted pyrido(2,3-d)pyrimidines as antidotes BASF Aktiengesellschaft (DE) 1993-04-21 — — EP disclosed
WO-1993004057-A2 HERBICIDES CONTAINING 3-AMINOBENZO[B]THIOPHENES AS AN ANTIDOTE BASF AKTIENGESELLSCHAFT (DE) 1993-03-04 — — WO disclosed
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