Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4872851

C[SiH](C)[Hf+2](NC(C)(C)C)c1cccc2c1Cc1ccccc1-2.[Cl-].[Cl-]

nearest known ligand 0.39

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.

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 1/20 0.39
RAB9A P51151 1/20 0.39
PNMT P11086 1/20 0.37
DRD2 P14416 1/20 0.33
DRD4 P21917 1/20 0.33
DRD3 P35462 1/20 0.33
HTR7 P34969 1/20 0.32
HTR2B P41595 1/20 0.32
MAOA P21397 1/20 0.31
PGR P06401 1/20 0.30

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

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 SCHEMBL6836898 0.78 NPC1 (0.36) NPC1RAB9APNMTDRD2DRD4
Hydrochloric Acid SCHEMBL5855473 0.77 PNMT (0.37) NPC1RAB9APNMTDRD2DRD4
Hydrochloric Acid SCHEMBL31484316 0.75 RAB9A (0.34) NPC1RAB9APNMTDRD2DRD4
Hydrochloric Acid SCHEMBL6805930 0.75 PNMT (0.35) NPC1RAB9APNMTDRD2DRD4
Hydrochloric Acid SCHEMBL7092707 0.71 NPC1 (0.38) NPC1RAB9APNMT
Hydrochloric Acid SCHEMBL4880319 0.70 NPC1 (0.39) NPC1RAB9APNMTDRD2DRD4
Hydrochloric Acid SCHEMBL10319883 0.70 PNMT (0.47) NPC1RAB9APNMTDRD2DRD4
Hydrochloric Acid SCHEMBL6861252 0.69 PNMT (0.36) NPC1RAB9APNMTDRD2DRD4
Hydrochloric Acid SCHEMBL7782828 0.69 NPC1 (0.49) NPC1RAB9APNMTDRD2DRD4
Hydrochloric Acid SCHEMBL27758449 0.69 NPC1 (0.40) NPC1RAB9APNMTDRD2DRD4

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 10 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119638892-B Catalytic system for preparing cycloolefin copolymer and application thereof 东华大学 2025-05-27 CN claimed
CN-119638892-A Catalytic system for preparing cycloolefin copolymer and application thereof 东华大学 2025-03-18 CN claimed
CN-119638892-B Catalytic system for preparing cycloolefin copolymer and application thereof 东华大学 2025-05-27 CN disclosed
CN-119638892-A Catalytic system for preparing cycloolefin copolymer and application thereof 东华大学 2025-03-18 CN disclosed
US-RE40234-E1 Process for producing crystalline poly-α-olefins with a monocyclopentadienyl transition metal catalyst system EXXONMOBIL CHEMICAL PATENTS, INC. 2008-04-08 US disclosed
US-7041841-B1 Process for producing crystalline poly-α-olefins with a monocyclopentadienyl transition metal catalyst system EXXONMOBIL CHEMICAL PATENTS INC. (US) 2006-05-09 US disclosed
US-6613845-B1 Propylene/ethylene-α-olefin block copolymer and process for producing the same SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2003-09-02 US disclosed
EP-0548277-B1 PROCESS FOR PRODUCING CRYSTALLINE POLY-ALPHA-OLEFINS WITH A MONOCYCLOPENTADIENYL TRANSITION METAL CATALYST SYSTEM EXXONMOBIL CHEM PATENTS INC (US) 2001-11-28 EP disclosed
US-5990242-A Propylene/ethylene-α-olefin block copolymer and process for processing the same SUMITOMO CHEMICAL CO., LTD. (JP) 1999-11-23 US disclosed
US-5026798-A Coordination catalyst EXXON CHEMICAL PATENTS INC. (US) 1991-06-25 US disclosed