Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3012437

CC1=C([Zr+2](=C(c2cccc(C(F)(F)F)c2)c2cccc(C(F)(F)F)c2)C2c3ccccc3-c3ccccc32)C(C)C=C1[Si](C)(C)C.[Cl-].[Cl-]

nearest known ligand 0.34

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 19)

geneUniProtsupporting neighboursconfidence
GAA P10253 2/20 0.34
GPBAR1 Q8TDU6 1/20 0.34
RXFP1 Q9HBX9 1/20 0.32
ALDH1A1 P00352 2/20 0.32
CES2 O00748 1/20 0.32
MEN1 O00255 1/20 0.31
KMT2A Q03164 1/20 0.31
ATM Q13315 1/20 0.31
TLR7 Q9NYK1 2/20 0.31
LMNA P02545 1/20 0.31
RBP4 P02753 1/20 0.31
CNR2 P34972 1/20 0.30
TP53 P04637 1/20 0.30
NPC1 O15118 1/20 0.30
RAB9A P51151 1/20 0.30
POLB P06746 1/20 0.30
TAS1R3 Q7RTX0 1/20 0.30
TAS1R1 Q7RTX1 1/20 0.30
TAS1R2 Q8TE23 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 SCHEMBL3013927 0.90 TP53 (0.33) RXFP1ALDH1A1CES2TP53
Hydrochloric Acid SCHEMBL3002522 0.89 TP53 (0.32) GAARXFP1ALDH1A1TP53POLB
Hydrochloric Acid SCHEMBL3006107 0.88 GAA (0.36) GAAGPBAR1ALDH1A1CES2MEN1
Hydrochloric Acid SCHEMBL2995958 0.86 GAA (0.35) GAAGPBAR1ALDH1A1CES2MEN1
Hydrochloric Acid SCHEMBL3005946 0.86
Hydrochloric Acid SCHEMBL2999936 0.85 NPSR1 (0.34) GAAGPBAR1ALDH1A1CES2MEN1
Hydrochloric Acid SCHEMBL3009835 0.85 ALDH1A1 (0.37) GAAGPBAR1ALDH1A1CES2MEN1
Hydrochloric Acid SCHEMBL3014103 0.83
Hydrochloric Acid SCHEMBL3000698 0.82
Hydrochloric Acid SCHEMBL2999516 0.81 MEN1 (0.34) MEN1KMT2ALMNA

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-20100190941-A1 TRANSITION METAL COMPOUND, CATALYST FOR OLEFIN POLYMERIZATION, AND PROCESS FOR PRODUCING OLEFIN POLYMER MITSUI CHEMICALS, INC. 2010-07-29 US disclosed
US-20090043057-A1 Transition Metal Compound, Catalyst for Olefin Polymerization, and Process for Producing Olefin Polymer MITSUI CHEMICALS , INC. 2009-02-12 US disclosed
EP-1900744-A1 TRANSITION METAL COMPOUND, OLEFIN POLYMERIZATION CATALYST, AND PROCESS FOR PRODUCING OLEFIN POLYMER Mitsui Chemicals, Inc. (JP) 2008-03-19 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-20090043057-A1 Transition Metal Compound, Catalyst for Olefin Polymerization, and Process for Producing Olefin Polymer OR10J3, PYM1, CCNE2 GAA 4612/4885GPBAR1 3842/4885RXFP1 766/4885

“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.