SCHEMBL997387

SCHEMBL997387

ClCCC(Cl)OC(Cl)CCCl

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
SCHEMBL11547073 0.78 ALDH1A1 (0.33)
Hydrochloric Acid SCHEMBL8763823 0.76 MAPK1 (0.31)
SCHEMBL11114369 0.73
SCHEMBL8645702 0.73
SCHEMBL11226827 0.71 ALDH1A1 (0.30)
SCHEMBL449310 0.69
SCHEMBL29584437 0.69
SCHEMBL3079563 0.69
SCHEMBL11860922 0.69
SCHEMBL4257430 0.69 TSHR (0.30)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2026103930-A1 IMIDAZOL-2-ONE DERIVATIVE AND PHARMACEUTICAL USE THEREOF 西藏海思科制药有限公司 2026-05-21 WO disclosed
EP-3004282-B1 ENHANCED OIL RECOVERY METHOD EMPLOYING A BIODEGRADABLE BRINE TOLERANT FOAM-FORMING COMPOSITION DOW GLOBAL TECHNOLOGIES LLC (US) 2017-06-21 EP disclosed
EP-3004282-A1 ENHANCED OIL RECOVERY METHOD EMPLOYING A BIODEGRADABLE BRINE TOLERANT FOAM-FORMING COMPOSITION Dow Global Technologies LLC (US) 2016-04-13 EP disclosed
US-20160083643-A1 ENHANCED OIL RECOVERY METHOD EMPLOYING A BIODEGRADABLE BRINE TOLERANT FOAM-FORMING COMPOSITION DOW GLOBAL TECHNOLOGIES LLC (US) 2016-03-24 US disclosed
EP-2454233-B1 SULFONATE SURFACTANTS AND METHODS FOR THEIR PREPARATION AND USE DOW GLOBAL TECHNOLOGIES LLC (US) 2015-02-25 EP disclosed
WO-2014193730-A1 ENHANCED OIL RECOVERY METHOD EMPLOYING A BIODEGRADABLE BRINE TOLERANT FOAM-FORMING COMPOSITION DOW GLOBAL TECHNOLOGIES LLC (US) 2014-12-04 WO disclosed
EP-2623488-B1 Process for olefin etherification DOW GLOBAL TECHNOLOGIES LLC (US) 2014-08-20 EP disclosed
US-8722944-B2 Process for olefin etherification DOW GLOBAL TECHNOLOGIES LLC (US) 2014-05-13 US disclosed
EP-2285763-B1 PROCESS FOR OLEFIN ETHERIFICATION DOW GLOBAL TECHNOLOGIES LLC (US) 2014-05-07 EP disclosed
US-8641816-B2 Vinyl ether compounds and methods of their preparation and use DOW GLOBAL TECHNOLOGIES LLC (US) 2014-02-04 US disclosed
US-6194398-B1 VIRICIDES AGAINST HUMAN IMMUNODEFICIENCY VIRUS, HERPES SIMPLEX VIRUS, HEPATITIS B VIRUS; ANTITUMOR AGENTS; SIDE EFFECT REDUCTION; ORAL ABSORPTION BIOAVAILABILITY; A 2-AMINO-6-HYDROCARBYLTHIO-9-(2-(PHOSPHONOMETHOXY)ETHYL-9H-PURINE MITSUBISHI CHEMICAL CORPORATION (JP) 2001-02-27 US disclosed
US-6037335-A HAVE EXCELLENT ANTIVIRAL ACTIVITY AND ANTINEOPLASTIC ACTIVITY MITSUBISHI CHEMICAL CORPORATION (JP) 2000-03-14 US disclosed
EP-0919562-A1 PHOSPHONATE NUCLEOTIDE COMPOUNDS MITSUBISHI CHEMICAL CORPORATION (JP) 1999-06-02 EP disclosed
EP-0801064-A1 Process for the preparation of 2-(2-(4((4-chlorophenyl)phenylmethyl)-1-piperazinyl)ethoxy)-acetic acid and their salts U C B, S.A. (BE) 1997-10-15 EP disclosed
EP-0632048-A1 Phosphonate-nucleotide ester derivatives Mitsubishi Chemical Corporation (JP) 1995-01-04 EP disclosed
US-4605784-A Process for the preparation of ether-containing chlorides EASTMAN KODAK COMPANY (US) 1986-08-12 US disclosed
US-4166894-A QUATERNARY AMMONIUM COMPOUNDS OR POLYMERS HAVING AMIDE GROUPS CALGON CORPORATION (US) 1979-09-04 US disclosed
US-4156683-A CROWN COMPOUNDS USED AS CHELATING AGENTS SCHERING CORPORATION (US) 1979-05-29 US disclosed
US-4075136-A ELECTROCONDUCTIVE COATING CALGON CORPORATION (US) 1978-02-21 US disclosed
US-3966766-A CHELATING AGENTS SCHERING CORPORATION (US) 1976-06-29 US disclosed