Phosphine

Phosphine

SCHEMBL1052219

CS(=O)(=O)O.P

nearest known ligand 0.00

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Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of Phosphine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

⚠ 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
Phosphine SCHEMBL28496494 1.00 CA2 (0.54)
Fluoride SCHEMBL28251516 0.95
SCHEMBL128169 0.94
SCHEMBL246838 0.94 CA2 (0.58)
SCHEMBL15109974 0.94
SCHEMBL105 0.94
SCHEMBL8596055 0.94 CA2 (0.58)
SCHEMBL25599 0.94 CA2 (0.58)
Hydrochloric Acid SCHEMBL114313 0.89
SCHEMBL22749161 0.89

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240336833-A1 POLYCANNABINOIDS FOR COMMODITY POLYMERS AND COMMODITY ELECTRONICS UNIVERSITY OF CONNECTICUT 2024-10-10 US claimed
US-11932813-B2 Electrochromic materials; preparation and use thereof UNIVERSITY OF CONNECTICUT (US) 2024-03-19 US claimed
US-20220396728-A1 ELECTROCHROMIC MATERIALS; PREPARATION AND USE THEREOF UNIVERSITY OF CONNECTICUT 2022-12-15 US claimed
WO-2022246027-A1 ELECTROCHROMIC MATERIALS; PREPARATION AND USE THEREOF UNIVERSITY OF CONNECTICUT (US) 2022-11-24 WO claimed
CN-114746383-A Improved process for the preparation of bromochloromethane 赛拓有限责任公司 2022-07-12 CN claimed
CN-107434786-A Benzimidazole compound and preparation method thereof 广东东阳光药业有限公司 2017-12-05 CN claimed
US-9238611-B2 Process for separating aryl carboxylic acids RELIANCE INDUSTRIES LIMITED (IN) 2016-01-19 US claimed
WO-2015166507-A1 A PROCESS FOR PRODUCING AROMATIC DICARBOXYLIC ACIDS RELIANCE INDUSTRIES LIMITED (IN) 2015-11-05 WO claimed
US-20150065748-A1 PROCESS FOR SEPARATING ARYL CARBOXYLIC ACIDS RELIANCE INDUSTRIES LIMITED (IN) 2015-03-05 US claimed
EP-2831027-A1 A PROCESS FOR SEPARATING ARYL CARBOXYLIC ACIDS Reliance Industries Limited (IN) 2015-02-04 EP claimed
WO-2013164852-A1 A PROCESS FOR SEPARATING ARYL CARBOXYLIC ACIDS RELIANCE INDUSTRIES LIMITED (IN) 2013-11-07 WO claimed
WO-2012113778-A1 PROCESS FOR THE HYDROHALOGENATION OF AN ALKYNE AND FOR THE MANUFACTURE OF VINYL CHLORIDE BY HYDROCHLORINATION OF ACETYLENE SOLVAY SA (BE) 2012-08-30 WO claimed
WO-2012084642-A1 MANUFACTURE OF VINYL CHLORIDE BY HYDROCHLORINATION OF ACETYLENE IN THE PRESENCE OF A CATALYTIC SYSTEM CONSISTING OF AT LEAST ONE IONIC LIQUID SOLVAY SA (BE) 2012-06-28 WO claimed
US-20100238534-A1 GEL POLYMERS CONTAINING IONIC LIQUIDS RADMARD BIJAN 2010-09-23 US claimed
US-7626748-B2 Gel polymers containing ionic liquids ARMY, UNITED STATES OF AMERICA AS REPRESENTED BY THE DEPARTMENT OF THE 2009-12-01 US claimed
US-20060203322-A1 Gel polymers containing ionic liquids ARMY, UNITED STATES OF AMERICA AS REPRESENTED BY THE DEPARTMENT OF THE 2006-09-14 US claimed
WO-2006094052-A2 GEL POLYMER ELECTROLYTES TRITON SYSTEMS, INC. (US) 2006-09-08 WO claimed
US-20240336833-A1 POLYCANNABINOIDS FOR COMMODITY POLYMERS AND COMMODITY ELECTRONICS UNIVERSITY OF CONNECTICUT 2024-10-10 US disclosed
US-6187959-B1 AN ONE STEP REACTION OF AN ALCOHOL WITH A TRIARYLPHOSPHINE AND A SULFONIC ACID IN A SOLVENT; SALT FORMATION; A CHEMICAL INTERMEDIATE FOR PREPARING LYCOPENE BASF AKTIENGESELLSCHAFT (DE) 2001-02-13 US disclosed
EP-0895997-A1 Process for the preparation of phosphonium salts BASF AKTIENGESELLSCHAFT (DE) 1999-02-10 EP disclosed