Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6571402

FC(F)=C(F)[Zn+].[Cl-]

nearest known ligand 0.00

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEBDKRB2CHRM1CHRM2CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNGGUCY1A1GUCY1A2GUCY1B1GUCY1B2NAMPTPTAFRSLC10A2SLC6A2SLC6A3TACR1dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of Hydrochloric Acid. 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
Bromide SCHEMBL4458492 0.89
Iodide SCHEMBL7633134 0.89
Bromide SCHEMBL8196203 0.74
Tetrafluoroethylene SCHEMBL28163430 0.63
SCHEMBL6832083 0.60
Tetrafluoroethylene SCHEMBL821995 0.60
Tetrafluoroethylene SCHEMBL15536 0.60
SCHEMBL43134 0.58
SCHEMBL27777048 0.58
SCHEMBL82518 0.58

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117185898-B Preparation method of hexafluorobutadiene 中化蓝天电子材料(杭州)有限公司 2026-05-19 CN disclosed
US-12612419-B2 Method for producing fluorine-containing (cyclo)alkenyl zinc halide compound DAIKIN INDUSTRIES, LTD. (JP) 2026-04-28 US disclosed
WO-2025124066-A1 PREPARATION METHOD AND PRODUCTION SYSTEM FOR HEXAFLUOROBUTADIENE 中化蓝天电子材料(杭州)有限公司 2025-06-19 WO disclosed
CN-120136664-A Preparation method and production system of hexafluorobutadiene 中化蓝天电子材料(杭州)有限公司 2025-06-13 CN disclosed
CN-119588383-A Ion doped catalyst for synthesizing hexafluoro-1, 3-butadiene, and preparation method and application thereof 湖北广钢气体电子材料有限公司 2025-03-11 CN disclosed
CN-118993838-A Method for preparing hexafluoro-1, 3-butadiene by three-step strategy 湖北广钢气体电子材料有限公司 2024-11-22 CN disclosed
CN-116393092-B Method for separating and purifying hexafluorobutadiene and efficient adsorbent for separating and purifying hexafluorobutadiene 福州绿航环保技术服务有限公司 2024-07-12 CN disclosed
CN-117185898-A Preparation method of hexafluorobutadiene 浙江省化工研究院有限公司 2023-12-08 CN disclosed
CN-116947596-A Preparation method of hexafluorobutadiene 山东华氟化工有限责任公司 2023-10-27 CN disclosed
CN-116393092-A Method for separating and purifying hexafluorobutadiene and efficient adsorbent for separating and purifying hexafluorobutadiene 福州绿航环保技术服务有限公司 2023-07-07 CN disclosed
CN-102634347-A Liquid crystal composition with high optical anisotropy and liquid crystal display element JIANGSU HECHENG DISPLAY TECH 2012-08-15 CN disclosed
CN-102627534-A Compounds including indene and difluoroethylene bridge bond, preparation method thereof and application thereof JIANGSU HECHENG DISPLAY TECH 2012-08-08 CN disclosed
CN-101525267-A Method for preparing hexachlorobutadiene UNIV HENAN TECHNOLOGY 2009-09-09 CN disclosed
CN-101255090-A Synthesis of alpha, beta, beta-trifluorostyrene via in-situ for mation or trifluorovinyl metal halide BALLARD POWER SYSTEMS (CA) 2008-09-03 CN disclosed
CN-100381409-C Synthesis of alpha, beta-trifluorostyrene by in situ formation of trifluorovinyl metal halide BALLARD POWER SYSTEMS (CA) 2008-04-16 CN disclosed
CN-1829673-A Synthesis of alpha, beta-trifluorostyrene by in situ formation of trifluorovinyl metal halide BALLARD POWER SYSTEMS (CA) 2006-09-06 CN disclosed
EP-1463697-A2 SYNTHESIS OF ALFA,BETA,BETA-TRIFLUOROSTYRENE VIA IN-SITU FORMATION OF TRIFLUOROVINYL METAL HALIDE BALLARD POWER SYSTEMS INC. (CA) 2004-10-06 EP disclosed
US-6653515-B2 One pot process comprising reacting tetrafluoroethylene with bases, metal halides and optionally amines to form trifluorovinyl metal complexes, then arylating in the presence of catalysts to form trifluorophenylethylene BALLARD POWER SYSTEMS INC. (CA) 2003-11-25 US disclosed
US-20030144439-A1 Synthesis of alpha, beta, beta-trifluorostyrene via in-situ formation of trifluorovinyl metal halide BALLARD POWER SYSTEMS INC. (CA) 2003-07-31 US disclosed
WO-2003051801-A2 SYNTHESIS OF ALPHA, BETA, BETA-TRIFLUOROSTYRENE VIA IN-SITU FORMATION OF TRIFLUOROVINYL METAL HALIDE BALLARD POWER SYSTEMS INC. (CA) 2003-06-26 WO disclosed