Hydrochloric Acid

Hydrochloric Acid

SCHEMBL333804

CC(C)Oc1ccc(C(c2c(C(=O)O)[nH]c3ccc(-c4ccc(C(C)(C)C)cc4)cc23)[N+](C)(C)C(=O)O)cc1.[Cl-]

nearest known ligand 0.42

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
PTGES O14684 3/20 0.42
JAK2 O60674 1/20 0.36
MCL1 Q07820 3/20 0.35
NR1H4 Q96RI1 1/20 0.34
ACACB O00763 2/20 0.34
ACACA Q13085 2/20 0.34
KIF11 P52732 1/20 0.34
GABRA1 P14867 1/20 0.33
GABRG2 P18507 1/20 0.33
GABRB3 P28472 1/20 0.33
GABRA5 P31644 1/20 0.33
GABRA3 P34903 1/20 0.33
GABRA2 P47869 1/20 0.33
GABRA6 Q16445 1/20 0.33
RXRA P19793 1/20 0.33
RXRB P28702 1/20 0.33
MAPT P10636 1/20 0.33
PRKAB2 O43741 1/20 0.33
PRKAG1 P54619 1/20 0.33
PRKAA2 P54646 1/20 0.33

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 SCHEMBL3007569 0.79 PTGES (0.43) PTGESJAK2MCL1NR1H4ACACB
Hydrochloric Acid SCHEMBL3016503 0.79 PTGES (0.41) PTGESJAK2MCL1NR1H4ACACB
Hydrochloric Acid SCHEMBL3007123 0.77 PTGES (0.41) PTGESJAK2MCL1NR1H4ACACB
SCHEMBL5299189 0.76 PTGES (0.52) PTGESJAK2MCL1NR1H4KIF11
Hydrochloric Acid SCHEMBL334148 0.75 PTGES (0.40) PTGESJAK2MCL1MAPTMEN1
SCHEMBL4022950 0.70 ALDH1A1 (0.51) PTGESNR1H4MAPTMEN1POLB
SCHEMBL5212831 0.65 ACACB (0.44) JAK2MCL1ACACBACACAGABRA1
SCHEMBL5204577 0.65 PTGES (0.39) PTGESACACBACACAGABRA1GABRG2
SCHEMBL17404857 0.65 PTPN5 (0.56) PTGESMCL1NR1H4ACACBACACA
Hydrochloric Acid SCHEMBL333803 0.64 PTGES (0.57) PTGESNR1H4

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
US-8097623-B2 1-Aryl-or heteroaryl-3-aryl-or heteroarylindole-2-carboxylic acids or esters: e.g., 5-(4-tert-Butylphenyl)-1,3-bis(4-isopropoxyphenyl)-indole-2-carboxylic acid; inhibition of the activity of microsomal prostaglandin E synthase-1, leukotriene C4 and/or 5-lipoxygenase-activating protein; analgesics BIOLIPOX AB (SE) 2012-01-17 US disclosed
EP-1841735-B1 INDOLES USEFUL IN THE TREATMENT OF INFLAMMATION BIOLIPOX AB (SE) 2011-03-09 EP disclosed
US-20090076004-A1 Indoles Useful in the Treatment of Inflammation BIOLIPOX AB (SE) 2009-03-19 US 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-20090076004-A1 Indoles Useful in the Treatment of Inflammation IDO1, IDO2, AREG PTGES 34/4885JAK2 244/4885MCL1 880/4885

“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.