Hydrochloric Acid

Hydrochloric Acid

SCHEMBL8469617

CC1=C([Ti+2]NC(=O)C2CCCCCCCCCCC2)C(C)C=C1[SiH](C)C.[Cl-].[Cl-]

nearest known ligand 0.35

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 14)

geneUniProtsupporting neighboursconfidence
PTPN1 P18031 1/20 0.35
LMNA P02545 1/20 0.34
NPSR1 Q6W5P4 1/20 0.34
P2RX7 Q99572 2/20 0.33
KMT2A Q03164 2/20 0.33
RAB9A P51151 2/20 0.33
GAA P10253 1/20 0.33
SMN1; SMN2 Q16637 2/20 0.33
MEN1 O00255 1/20 0.32
HPGD P15428 1/20 0.32
HDAC8 Q9BY41 1/20 0.32
HDAC6 Q9UBN7 1/20 0.32
MAPK1 P28482 1/20 0.32
NPC1 O15118 1/20 0.32

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 SCHEMBL4588710 0.84 PTPN1 (0.38) PTPN1LMNANPSR1P2RX7KMT2A
Hydrochloric Acid SCHEMBL17823015 0.73 HDAC8 (0.37) PTPN1LMNANPSR1P2RX7KMT2A
Hydrochloric Acid SCHEMBL9065698 0.64 LMNA (0.41) PTPN1LMNANPSR1P2RX7KMT2A
Hydrochloric Acid SCHEMBL12817186 0.63 PTPN1 (0.41) PTPN1LMNANPSR1P2RX7KMT2A
SCHEMBL7742360 0.57 HDAC8 (0.54) PTPN1LMNANPSR1KMT2ARAB9A
SCHEMBL24618011 0.54 HDAC8 (0.61) PTPN1LMNANPSR1KMT2ASMN1; SMN2
SCHEMBL13060381 0.54 HDAC8 (0.61) PTPN1LMNANPSR1KMT2ASMN1; SMN2
SCHEMBL6917808 0.54 HDAC8 (0.61) PTPN1LMNANPSR1KMT2ASMN1; SMN2
SCHEMBL21212072 0.54 HDAC8 (0.61) PTPN1LMNANPSR1KMT2ASMN1; SMN2
SCHEMBL1678569 0.54 HDAC8 (0.61) PTPN1LMNANPSR1KMT2ASMN1; 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 6 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0705283-B1 PROCESS FOR PRODUCING AMORPHOUS POLY-$g(a)-OLEFINS WITH A MONOCYCLOPENTADIENYL TRANSITION METAL CATALYST SYSTEM EXXON CHEMICAL PATENTS INC (US) 1999-01-13 EP disclosed
US-5723560-A GROUP 4 OR 5 METAL CATALYST FOR OLEFIN POLYMERIZATION EXXON CHEMICAL PATENTS INC. (US) 1998-03-03 US disclosed
EP-0705283-A1 PROCESS FOR PRODUCING AMORPHOUS POLY-$g(a)-OLEFINS WITH A MONOCYCLOPENTADIENYL TRANSITION METAL CATALYST SYSTEM EXXON CHEMICAL PATENTS INC. (US) 1996-04-10 EP disclosed
US-5504169-A FORMING HIGH MOLECULAR WEIGHT POLYPROPYLENE BY CATALYZING IN PRESENCE OF AN ACTIVATOR AND A TITANIUM CYCLOPENTADIENYL COMPLEXES EXXON CHEMICAL PATENTS INC. (US) 1996-04-02 US disclosed
US-5420217-A Polymerization catalyst and promoter EXXON CHEMICAL PATENTS INC. (US) 1995-05-30 US disclosed
WO-1995000562-A1 PROCESS FOR PRODUCING AMORPHOUS POLY-α-OLEFINS WITH A MONOCYCLOPENTADIENYL TRANSITION METAL CATALYST SYSTEM EXXON CHEMICAL PATENTS INC. (US) 1995-01-05 WO disclosed