Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6904017

Cc1ccc(-c2cccc3c2C=C(c2ccc(C)cn2)C3[Zr+2]C2C(c3ccc(C)cn3)=Cc3c(-c4ccc(C)cc4)cccc32)cc1.[Cl-].[Cl-]

nearest known ligand 0.37

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 20)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 1/20 0.37
CYP2A6 P11509 1/20 0.37
CCR1 P32246 1/20 0.36
CCR5 P51681 1/20 0.36
CCR8 P51685 1/20 0.36
HDAC6 Q9UBN7 1/20 0.36
PTGS2 P35354 2/20 0.32
SYK P43405 1/20 0.32
KDM1A O60341 1/20 0.31
NPC1 O15118 1/20 0.30
TP53 P04637 1/20 0.30
PKM P14618 1/20 0.30
STAT3 P40763 1/20 0.30
STAT1 P42224 1/20 0.30
RAB9A P51151 1/20 0.30
SMN1; SMN2 Q16637 1/20 0.30
KDM4E B2RXH2 1/20 0.30
POLB P06746 1/20 0.30
PPARG P37231 1/20 0.30
MCL1 Q07820 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 SCHEMBL6904132 0.94 CYP3A4 (0.39) CYP3A4CYP2A6CCR1CCR5CCR8
Hydrochloric Acid SCHEMBL6897621 0.92 CYP3A4 (0.33) CYP3A4CYP2A6CCR1CCR5CCR8
Hydrochloric Acid SCHEMBL6903073 0.92 CYP3A4 (0.33) CYP3A4CYP2A6CCR1CCR5CCR8
Hydrochloric Acid SCHEMBL6905100 0.91 DGAT1 (0.33) CYP3A4CYP2A6CCR1CCR5CCR8
Hydrochloric Acid SCHEMBL7733570 0.91 CYP3A4 (0.33) CYP3A4CYP2A6CCR1CCR5CCR8
Hydrochloric Acid SCHEMBL6903825 0.89 SMN1; SMN2 (0.32) CYP3A4CYP2A6CCR1CCR5CCR8
Hydrochloric Acid SCHEMBL6895496 0.88 DHFR (0.35) CYP3A4CYP2A6CCR1CCR5CCR8
Hydrochloric Acid SCHEMBL6903579 0.88 SYK (0.40) CYP3A4CCR1CCR5CCR8SYK
Hydrochloric Acid SCHEMBL6899130 0.88 CYP3A4 (0.30) CYP3A4CYP2A6
Hydrochloric Acid SCHEMBL6902605 0.88 RAB9A (0.39) NPC1TP53STAT3RAB9ASMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1033371-B1 Transition metal compound, catalyst system, process for the preparation thereof and its use for the polymerization of olefins BASELL POLYOLEFINE GMBH (DE) 2004-01-28 EP claimed
US-6458982-B1 CATALYST SYSTEM COMPRISING AT LEAST ONE METALLOCENE AND AT LEAST ONE COCATALYST. ON SUPPORT. TARGOR GMBH (DE) 2002-10-01 US disclosed