Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5565999

Cc1ccc(Nc2ccc[n+](C)c2)cc1O.[Cl-]

nearest known ligand 0.41

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
▸ KDR P35968 7/20 0.41
▸ APOBEC3A P31941 1/20 0.39
▸ APOBEC3G Q9HC16 1/20 0.39
▸ EGFR P00533 5/20 0.39
▸ HSD17B2 P37059 2/20 0.38
▸ RET P07949 1/20 0.38
▸ KIF5B P33176 1/20 0.38
▸ ALDH1A1 P00352 2/20 0.37
▸ FLT1 P17948 1/20 0.36
▸ FLT4 P35916 1/20 0.36
▸ CYP1A2 P05177 2/20 0.36
▸ CYP2D6 P10635 2/20 0.36
▸ CYP2C9 P11712 2/20 0.36
▸ CYP2C19 P33261 2/20 0.36
▸ MEN1 O00255 1/20 0.36
▸ CYP3A4 P08684 1/20 0.36
▸ GAA P10253 1/20 0.36
▸ KMT2A Q03164 1/20 0.36
▸ MAOA P21397 1/20 0.36
▸ MAOB P27338 1/20 0.36

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
SCHEMBL5564793 0.98 KDR (0.40) KDRAPOBEC3AAPOBEC3GEGFRHSD17B2
Iodide SCHEMBL5565778 0.97 KDR (0.41) KDRAPOBEC3AAPOBEC3GEGFRHSD17B2
SCHEMBL5561195 0.87 HSD17B2 (0.38) KDRAPOBEC3AAPOBEC3GEGFRHSD17B2
Hydrochloric Acid SCHEMBL5565982 0.81 ALDH1A1 (0.40) KDREGFRHSD17B2RETKIF5B
Hydrochloric Acid SCHEMBL6130295 0.78 TUBB4A (0.50) EGFRHSD17B2ALDH1A1CYP1A2CYP2D6
Hydrochloric Acid SCHEMBL5566059 0.77 LMNA (0.44) KDRHSD17B2ALDH1A1CYP1A2CYP2D6
SCHEMBL7555415 0.77 HPGD (0.54) KDREGFRALDH1A1MEN1CYP3A4
Fluoride Ion SCHEMBL18740626 0.76 HDAC8 (0.48) APOBEC3AAPOBEC3GALDH1A1CYP2C19L3MBTL1
Bromide SCHEMBL6130243 0.75 TUBB4A (0.50) EGFRHSD17B2ALDH1A1CYP1A2CYP2D6
Iodide SCHEMBL6130228 0.75 TUBB4A (0.50) EGFRHSD17B2ALDH1A1CYP1A2CYP2D6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7229479-B2 Method of coloring porous material CIBA SPECIALTY CHEMICALS CORPORATION (US) 2007-06-12 — — US disclosed
US-20060162095-A1 Method of colouring porous material CIBA SPECIALTY CHEMICALS CORP. 2006-07-27 — — US disclosed
EP-1534226-A1 METHOD OF COLOURING POROUS MATERIAL Ciba SC Holding AG (CH) 2005-06-01 — — EP disclosed
WO-2004019897-A1 METHOD OF COLOURING POROUS MATERIAL CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) 2004-03-11 — — 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-20060162095-A1 Method of colouring porous material ACR, HLA-C, TYR KDR 4077/4885APOBEC3A 1790/4885APOBEC3G 2040/4885

“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.

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