Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7247941

CC1C([Ti+2](C)(C)NC(=O)c2ccccc2)=Cc2c1c1ccccc1c1ccccc21.[Cl-].[Cl-].[SiH4]

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 20)

geneUniProtsupporting neighboursconfidence
RAB9A P51151 4/20 0.32
SMN1; SMN2 Q16637 3/20 0.32
CYP3A4 P08684 3/20 0.32
NPC1 O15118 3/20 0.32
POLB P06746 2/20 0.32
CYP2C9 P11712 2/20 0.32
CYP2C19 P33261 2/20 0.32
HPGD P15428 1/20 0.32
MAPT P10636 1/20 0.32
MEN1 O00255 3/20 0.32
KMT2A Q03164 3/20 0.32
RXFP1 Q9HBX9 1/20 0.32
LMNA P02545 1/20 0.31
HDAC3 O15379 1/20 0.31
CA12 O43570 1/20 0.31
CA1 P00915 1/20 0.31
IDO1 P14902 1/20 0.31
ALOX15 P16050 1/20 0.31
HDAC1 Q13547 1/20 0.31
CA9 Q16790 1/20 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 SCHEMBL7239359 0.79 SMN1; SMN2 (0.37) RAB9ASMN1; SMN2CYP2C19HPGDMAPT
Hydrochloric Acid SCHEMBL7243552 0.76 SMN1; SMN2 (0.33) RAB9ASMN1; SMN2CYP3A4NPC1POLB
Hydrochloric Acid SCHEMBL7173163 0.76
Hydrochloric Acid SCHEMBL7257670 0.76
Hydrochloric Acid SCHEMBL3821780 0.69 NPC1 (0.36) RAB9ASMN1; SMN2CYP3A4NPC1POLB
Hydrochloric Acid SCHEMBL7039631 0.66 ADORA3 (0.32) RAB9ASMN1; SMN2POLBLMNAADORA3
Hydrochloric Acid SCHEMBL7041823 0.65 SMN1; SMN2 (0.32) RAB9ASMN1; SMN2CYP3A4NPC1CYP2C9
SCHEMBL29273718 0.56 HDAC8 (0.60) RAB9ASMN1; SMN2NPC1POLBHPGD
Dibenzoylmethane SCHEMBL28456473 0.55 KMT2A (0.59) RAB9ASMN1; SMN2CYP3A4NPC1CYP2C9
Triphenylene SCHEMBL10947667 0.54 MAPT (0.62) RAB9ASMN1; SMN2CYP3A4NPC1POLB

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
US-6630545-B2 Polymerization catalyst of a metal complex with anionic, polycyclic, fused ring ligand system containing at least 4 fused rings, a cocatalyst and a butadiene or pentadiene THE DOW CHEMICAL COMPANY 2003-10-07 US disclosed
US-20020037981-A1 Polymerization catalyst of a metal complex with anionic, polycyclic, fused ring ligand system containing at least 4 fused rings, a cocatalyst and a butadiene or pentadiene DOW CHEMICAL COMPANY 2002-03-28 US disclosed