Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4636828

Cc1cccc(C(=O)O)c1.[Cl-].[Cl-].[Mg+2]

nearest known ligand 0.65

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
PARP1 P09874 1/20 0.61
POLB P06746 4/20 0.59
SMN1; SMN2 Q16637 1/20 0.58
HDAC8 Q9BY41 1/20 0.57
HDAC6 Q9UBN7 1/20 0.57
TPMT P51580 1/20 0.54
CA12 O43570 1/20 0.54
CA1 P00915 1/20 0.54
CA2 P00918 1/20 0.54
CA6 P23280 1/20 0.54
CA9 Q16790 1/20 0.54
MEN1 O00255 3/20 0.52
KMT2A Q03164 3/20 0.52
TDP1 Q9NUW8 2/20 0.52
KCNK3 O14649 2/20 0.52
KCNK9 Q9NPC2 2/20 0.52
MAPT P10636 2/20 0.52
HSD17B10 Q99714 2/20 0.52
HPGD P15428 2/20 0.52
KDM4E B2RXH2 1/20 0.52

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
SCHEMBL29382709 0.96 PARP1 (0.65) PARP1POLBSMN1; SMN2HDAC8HDAC6
SCHEMBL14406 0.96 PARP1 (0.65) PARP1POLBSMN1; SMN2HDAC8HDAC6
SCHEMBL142937 0.96 PARP1 (0.65) PARP1POLBSMN1; SMN2HDAC8HDAC6
SCHEMBL6907818 0.93 PARP1 (0.63) PARP1POLBSMN1; SMN2HDAC8HDAC6
Ammonia Solution, Strong SCHEMBL1667008 0.93 PARP1 (0.63) PARP1POLBSMN1; SMN2HDAC8HDAC6
SCHEMBL6915713 0.93 PARP1 (0.63) PARP1POLBSMN1; SMN2HDAC8HDAC6
Bromide SCHEMBL6113526 0.93 PARP1 (0.63) PARP1POLBSMN1; SMN2HDAC8HDAC6
SCHEMBL6916592 0.93 PARP1 (0.63) PARP1POLBSMN1; SMN2HDAC8HDAC6
Iodide SCHEMBL6113184 0.93 PARP1 (0.63) PARP1POLBSMN1; SMN2HDAC8HDAC6
SCHEMBL1151724 0.93 PARP1 (0.63) PARP1POLBSMN1; SMN2HDAC8HDAC6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1937614-A1 IRON CATALYZED CROSS-COUPLING REACTIONS OF IMIDOYL DERIVATIVES Arcadia Pharmaceuticals Inc. (US) 2008-07-02 EP disclosed
US-20070106074-A1 Iron catalyzed cross-coupling reactions of imidoyl derivatives ACADIA PHARMACEUTICALS 2007-05-10 US disclosed
WO-2007047776-A1 IRON CATALYZED CROSS-COUPLING REACTIONS OF IMIDOYL DERIVATIVES ACADIA PHARMACEUTICALS INC. (US) 2007-04-26 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20070106074-A1 Iron catalyzed cross-coupling reactions of imidoyl derivatives SDHB, TFRC, SLC40A1 PARP1 3139/4885POLB 1159/4885SMN1; SMN2 3851/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.