Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4842777

C[SiH](C)C1CCCCC1(C(=O)N[Hf+2])C1c2ccccc2-c2ccccc21.[Cl-].[Cl-]

nearest known ligand 0.32

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 17)

geneUniProtsupporting neighboursconfidence
SLC6A3 known ✓ Q01959 1/20 0.32
ACHE known ✓ P22303 1/20 0.31
OPRK1 P41145 1/20 0.32
SLC6A4 P31645 1/20 0.32
KMT2A Q03164 1/20 0.32
MAPK1 P28482 1/20 0.32
POLB P06746 1/20 0.31
TSHR P16473 1/20 0.31
HTT P42858 1/20 0.31
L3MBTL1 Q9Y468 1/20 0.31
BCHE P06276 1/20 0.31
PSEN1 P49768 2/20 0.31
PSEN2 P49810 2/20 0.31
APH1B Q8WW43 2/20 0.31
NCSTN Q92542 2/20 0.31
APH1A Q96BI3 2/20 0.31
PSENEN Q9NZ42 2/20 0.31

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 SCHEMBL7216864 0.88 OPRK1 (0.32) OPRK1SLC6A4SLC6A3KMT2AMAPK1
SCHEMBL9587131 0.87 OPRK1 (0.33) OPRK1SLC6A4SLC6A3KMT2AMAPK1
SCHEMBL6857281 0.63 TSHR (0.34) SLC6A4SLC6A3KMT2APOLBTSHR
Hydrochloric Acid SCHEMBL5852743 0.59 CYP2C19 (0.41) L3MBTL1
SCHEMBL38651516 0.59 BCHE (0.41) SLC6A4SLC6A3BCHEACHE
Hydrochloric Acid SCHEMBL5853853 0.59 CYP2C19 (0.43) L3MBTL1
Hydrochloric Acid SCHEMBL5854814 0.59 CYP2C19 (0.43) L3MBTL1
SCHEMBL25250940 0.58 SLC6A4 (0.51) SLC6A4SLC6A3KMT2ATSHRBCHE
Hydrochloric Acid SCHEMBL5852834 0.57 CYP2C19 (0.41)
Hydrochloric Acid SCHEMBL5852878 0.57 CYP2C19 (0.41)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
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
EP-0548277-A1 PROCESS FOR PRODUCING CRYSTALLINE POLY-ALPHA-OLEFINS WITH A MONOCYCLOPENTADIENYL TRANSITION METAL CATALYST SYSTEM EXXON CHEMICAL PATENTS INC. (US) 1993-06-30 EP disclosed
WO-1992005204-A1 PROCESS FOR PRODUCING CRYSTALLINE POLY-ALPHA-OLEFINS WITH A MONOCYCLOPENTADIENYL TRANSITION METAL CATALYST SYSTEM EXXON CHEMICAL PATENTS INC. (US) 1992-04-02 WO disclosed
US-5026798-A Coordination catalyst EXXON CHEMICAL PATENTS INC. (US) 1991-06-25 US disclosed