SCHEMBL682450

SCHEMBL682450

PCP

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
Bromide SCHEMBL11778838 0.89
SCHEMBL17486758 0.71
SCHEMBL10984475 0.61
SCHEMBL167536 0.61
SCHEMBL2741523 0.61
SCHEMBL8261613 0.61
SCHEMBL37630 0.61
SCHEMBL8373293 0.61
Water SCHEMBL10882827 0.57
SCHEMBL11171152 0.50

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114096547-B Optically active bisphosphonylmethane, method for producing same, transition metal complex, and asymmetric catalyst 日本化学工业株式会社 2024-04-30 CN claimed
CN-115254158-B Nanocluster metal phosphide-phosphorus-carbon catalyst and preparation and application thereof 中国科学院兰州化学物理研究所 2023-12-22 CN claimed
US-11498935-B2 Optically active bisphosphinomethane, method for producing the same, and transition metal complex and asymmetric catalyst NIPPON CHEMICAL INDUSTRIAL CO., LTD. (JP) 2022-11-15 US claimed
CN-115254158-A Nanocluster metal phosphide-phosphorus-carbon catalyst and preparation and application thereof 中国科学院兰州化学物理研究所 2022-11-01 CN claimed
US-20220204537-A1 OPTICALLY ACTIVE BISPHOSPHINOMETHANE, METHOD FOR PRODUCING THE SAME, AND TRANSITION METAL COMPLEX AND ASYMMETRIC CATALYST NIPPON CHEMICAL INDUSTRIAL CO., LTD. (JP) 2022-06-30 US claimed
CN-114096547-A Optically active bisphosphinylmethane, process for producing the same, transition metal complex, and asymmetric catalyst 日本化学工业株式会社 2022-02-25 CN claimed
EP-1598053-B1 Use of a composition containing at least one phosphine as majority reducing agent to remove the artificial colour of keratinic fibres OREAL (FR) 2006-12-20 EP claimed
EP-1598053-A1 Use of a composition containing at least one phosphine as majority reducing agent to remove the artificial colour of keratinic fibres L'OREAL (FR) 2005-11-23 EP claimed
US-20050251928-A1 Method for stripping artificial color from keratin fibers L'OREAL (FR) 2005-11-17 US claimed
EP-0808908-A1 Leather and its preparation SÜDLEDER GmbH &amp; Co. (DE) 1997-11-26 EP claimed
US-12043781-B2 Liquid-crystalline medium MERCK PATENT GMBH (DE) 2024-07-23 US disclosed
US-20240237382-A1 LIGHT-EMITTING DEVICE AND ELECTRONIC APPARATUS INCLUDING THE SAME SAMSUNG DISPLAY CO., LTD. (KR) 2024-07-11 US disclosed
CN-114096547-B Optically active bisphosphonylmethane, method for producing same, transition metal complex, and asymmetric catalyst 日本化学工业株式会社 2024-04-30 CN disclosed
CN-114096547-B Optically active bisphosphonylmethane, method for producing same, transition metal complex, and asymmetric catalyst 日本化学工业株式会社 2024-04-30 CN disclosed
CN-114096547-B Optically active bisphosphonylmethane, method for producing same, transition metal complex, and asymmetric catalyst 日本化学工业株式会社 2024-04-30 CN disclosed
US-5200539-A Conversion of alpha-olefins to aldehydes LOUISIANA STATE UNIVERSITY BOARD OF SUPERVISORS, A GOVERNING BODY OF LOUISIANA STATE UNIVERSITY AGRICULTURAL AND MECHANICAL COLLEGE (US) 1993-04-06 US disclosed
EP-0221611-A2 Antimicrobial agents and process for their manufacture THE PROCTER & GAMBLE COMPANY (US) 1987-05-13 EP disclosed
US-4474978-A Preparation of carbamates SHELL OIL COMPANY (US) 1984-10-02 US disclosed
US-4181646-A POLYMERIC PHOSPHORUS ESTERS, POLYAMIDES MONSANTO COMPANY (US) 1980-01-01 US disclosed
US-4073829-A POLYESTERS MONSANTO COMPANY (US) 1978-02-14 US disclosed