Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6894050

CCCCC1=Cc2c(ccc3ccccc23)C1[Zr+2]1(C2C(CCCC)=Cc3c2ccc2ccccc32)C2CCCCC21.[Cl-].[Cl-]

nearest known ligand 0.37

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 14)

geneUniProtsupporting neighboursconfidence
BCHE P06276 2/20 0.37
KDM4E B2RXH2 2/20 0.36
SLC6A4 P31645 2/20 0.33
DRD2 P14416 1/20 0.33
DPP4 P27487 1/20 0.31
GAA P10253 1/20 0.31
TDP1 Q9NUW8 1/20 0.31
L3MBTL1 Q9Y468 1/20 0.31
SLC18A2 Q05940 1/20 0.31
CNR1 P21554 2/20 0.31
NCEH1 Q6PIU2 1/20 0.31
TAAR1 Q96RJ0 1/20 0.30
ALDH1A1 P00352 1/20 0.30
SIGMAR1 Q99720 1/20 0.30

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 SCHEMBL6893651 0.93 KDM4E (0.37) BCHEKDM4ESLC6A4DRD2GAA
Hydrochloric Acid SCHEMBL6885887 0.89 BCHE (0.35) BCHESLC6A4DRD2DPP4CNR1
Hydrochloric Acid SCHEMBL6895104 0.88 KDM4E (0.39) BCHEKDM4ESLC6A4DRD2GAA
Hydrochloric Acid SCHEMBL6892746 0.85 KDM4E (0.37) BCHEKDM4ESLC6A4DRD2DPP4
Hydrochloric Acid SCHEMBL6892084 0.84 KDM4E (0.38) BCHEKDM4ESLC6A4DRD2DPP4
Hydrochloric Acid SCHEMBL6891400 0.84 HTR1A (0.35) BCHE
Hydrochloric Acid SCHEMBL6892890 0.82 KDM4E (0.34) KDM4ESLC18A2
Hydrochloric Acid SCHEMBL6894289 0.82 SLC6A4 (0.34) BCHESLC6A4DRD2SLC18A2
Hydrochloric Acid SCHEMBL6892296 0.81 HTR1A (0.30)
Hydrochloric Acid SCHEMBL6892837 0.79 KDM4E (0.36) BCHEKDM4ESLC6A4DRD2GAA

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-6784305-B2 DERIVATIVES OF ZIRCONOCENE DICHLORIDE IN WHICH THE TWO SUBSTITUTED INDENYL GROUPS ARE JOINED TO ONE ANOTHER VIA A BRIDGE CAN, OWING TO THEIR CONFORMATIONAL RIGIDITY, BE USED AS CATALYSTS FOR THE STEREOSPECIFIC POLYMERIZATION OF OLEFINS BASELL POLYOLEFINE GMBH (DE) 2004-08-31 US disclosed
US-20030199703-A1 Method for producing alkyl-bridged ligand systems and transition metal compounds EQUISTAR CHEMICALS, LP 2003-10-23 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-20030199703-A1 Method for producing alkyl-bridged ligand systems and transition metal compounds ABL1, ICMT, ORAI2 BCHE 4132/4885KDM4E 2918/4885SLC6A4 1973/4885

“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.