SCHEMBL700612

SCHEMBL700612

Cl[Zn]c1ccccc1

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
Hydrochloric Acid SCHEMBL15770586 0.97 — —
Iodide SCHEMBL3246741 0.97 — —
Bromide SCHEMBL15771029 0.97 — —
SCHEMBL393949 0.69 ALDH1A1 (0.40) —
SCHEMBL1454329 0.67 — —
Hydrochloric Acid SCHEMBL7924149 0.67 ALDH1A1 (0.38) —
SCHEMBL22027435 0.66 — —
Iodide SCHEMBL4049605 0.65 CA1 (0.36) —
SCHEMBL1141917 0.64 — —
SCHEMBL5846438 0.64 — —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115615967-A Edible plant oil rancidity early-stage rapid determination method based on odor fluorescence sensor 滁州学院 2023-01-17 — — CN claimed
EP-1313560-B1 CATALYST FOR AROMATIC C-O, C-N, and C-C BOND FORMATION UNIV YALE (US) 2007-12-19 — — EP claimed
EP-1313560-A4 CATALYST FOR AROMATIC C-O, C-N, and C-C BOND FORMATION UNIV YALE (US) 2005-02-09 — — EP claimed
EP-1313560-A1 CATALYST FOR AROMATIC C-O, C-N, and C-C BOND FORMATION YALE UNIVERSITY (US) 2003-05-28 — — EP claimed
US-6566572-B2 Subjecting a 9,10- dihalogenoanthracene and a metal or half-metal phenyl compound to a cross-coupling reaction to produce 9,10-diphenylanthracene WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) 2003-05-20 — — US claimed
US-6562989-B2 Bicyclopentyl iron ligand and transition metal catalyst YALE UNIVERSITY 2003-05-13 — — US claimed
US-20030008768-A1 Catalyst for aromatic C-O, C-N, and C-C bond formation NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2003-01-09 — — US claimed
US-20020165411-A1 Sterically hindered phosphine ligands and uses thereof NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2002-11-07 — — US claimed
US-20020162991-A1 Process for producing 9,10-diphenylanthracene WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) 2002-11-07 — — US claimed
WO-2002048160-A1 STERICALLY HINDERED PHOSPHINE LIGANDS AND USES THEREOF YALE UNIVERSITY (US) 2002-06-20 — — WO claimed
WO-2002011883-A1 CATALYST FOR AROMATIC C-O, C-N, and C-C BOND FORMATION YALE UNIVERSITY (US) 2002-02-14 — — WO claimed
EP-1132363-A1 A process for producing 9,10-diphenylanthracene Wako Pure Chemical Industries, Ltd. (JP) 2001-09-12 — — EP claimed
US-6153810-A Highly selective process for making o-arylbenzonitriles OCCIDENTAL CHEMICAL CORPORATION (US) 2000-11-28 — — US claimed
EP-3268129-B1 OLEFIN OLIGOMERISATION PROCESS WITH A CATALYST COMPRISING A CHROMIUM COMPLEX WITH A PHOSPHACYCLE-CONTAINING LIGAND DOW GLOBAL TECHNOLOGIES LLC (US) 2025-06-18 — — EP disclosed
CN-115109579-B Preparation method of quantum dot, quantum dot prepared by quantum dot and application of quantum dot 苏州星烁纳米科技有限公司 2025-01-24 — — CN disclosed
US-11975301-B2 Method of producing nanoparticles DOW SILICONES CORPORATION (US) 2024-05-07 — — US disclosed
US-4085273-A REACTING TRIBUTYL(1-CARBOALKOXY-2,2-DIMETHYL-3-BUTEN-1-YL)TIN WITH ACETYL FLUOBORATE, REACTING PRODUCT WITH METHYL METAL COMPOUND, DEHYDRATING PRODUCT WITH IODINE CATALYSIS THE PROCTER & GAMBLE COMPANY (US) 1978-04-18 — — US disclosed
US-4065480-A Process for preparing substituted cyclopropycarbinyl compounds THE PROCTER & GAMBLE COMPANY (US) 1977-12-27 — — US disclosed
US-3998889-A REACTING AN UNSATURATED ORGANO-TIN COMPOUND WITH AN ORGANIC SULFUR HALIDE THE PROCTER & GAMBLE COMPANY (US) 1976-12-21 — — US disclosed
US-3959324-A PESTICIDE, ANTIINFLAMMATORY THE PROCTER & GAMBLE COMPANY (US) 1976-05-25 — — US disclosed
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