Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4890082

CC1=C([Hf+2]c2cccc3c2Cc2ccccc2-3)CC=C1.[Cl-].[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 12)

geneUniProtsupporting neighboursconfidence
PNMT P11086 1/20 0.37
NPC1 O15118 1/20 0.36
RAB9A P51151 1/20 0.36
PGR P06401 1/20 0.33
HTR7 P34969 1/20 0.32
HTR2B P41595 1/20 0.32
MAP3K9 P80192 1/20 0.31
MAP3K11 Q16584 1/20 0.31
DRD2 P14416 1/20 0.31
DRD4 P21917 1/20 0.31
DRD3 P35462 1/20 0.31
MAOA P21397 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 SCHEMBL7753033 0.79 PNMT (0.35) PNMTNPC1RAB9A
Hydrochloric Acid SCHEMBL816978 0.79 PNMT (0.50) PNMTNPC1RAB9APGRHTR7
Hydrochloric Acid SCHEMBL29695725 0.79 PNMT (0.50) PNMTNPC1RAB9APGRHTR7
Iodide SCHEMBL7935539 0.79 PNMT (0.36) PNMTNPC1RAB9A
SCHEMBL8379134 0.76 PNMT (0.50) PNMTNPC1RAB9APGRHTR7
Hydrochloric Acid SCHEMBL3041073 0.75 PNMT (0.39) PNMTNPC1RAB9APGRHTR7
Hydrochloric Acid SCHEMBL4892825 0.74 PNMT (0.35) PNMTNPC1RAB9APGRHTR7
Bromide SCHEMBL7939131 0.72 PNMT (0.39) PNMTNPC1RAB9APGRHTR7
Iodide SCHEMBL7921884 0.72 PNMT (0.39) PNMTNPC1RAB9APGRHTR7
Hydrochloric Acid SCHEMBL2482352 0.70 PNMT (0.37) PNMTNPC1RAB9APGRHTR7

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
EP-1880986-B1 PROCESS FOR PRODUCING SATURATED ALIPHATIC HYDROCARBONS, AND LUBRICANT COMPOSITIONS THEREOF IDEMITSU KOSAN CO (JP) 2013-03-06 EP disclosed
US-8373011-B2 Used in a base oil of lubricant having good low temperature fluidity, low evaporativity, and thermal stability and oxidation stability IDEMITSU KOSAN CO., LTD. (JP) 2013-02-12 US disclosed
US-20080146469-A1 Process for producing saturated aliphatic hydrocarbon compound, and lubricant composition IDEMITSU KOSAN CO., LTD. (JP) 2008-06-19 US disclosed
EP-1880986-A1 PROCESS FOR PRODUCING SATURATED ALIPHATIC HYDROCARBON COMPOUND, AND LUBRICANT COMPOSITION IDEMITSU KOSAN CO., LTD. (JP) 2008-01-23 EP 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-20080146469-A1 Process for producing saturated aliphatic hydrocarbon compound, and lubricant composition ALOX15, ALOX12, ALOX15B PNMT 3641/4885NPC1 2750/4885RAB9A 4124/4885

“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.