Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5700596

CCCN=C(NC(=O)C(C)(C)C)c1ccccc1.CCCN=C(NC(=O)C(C)(C)C)c1ccccc1.[Cl-].[Cl-].[Pd+2]

nearest known ligand 0.40

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
SLC6A3 known ✓ Q01959 1/20 0.36
SMN1; SMN2 Q16637 6/20 0.40
RECQL P46063 1/20 0.40
ALDH1A1 P00352 6/20 0.39
NPC1 O15118 2/20 0.39
RAB9A P51151 2/20 0.39
CYP1A2 P05177 2/20 0.39
CYP3A4 P08684 2/20 0.39
CYP2C9 P11712 2/20 0.39
CYP2C19 P33261 2/20 0.39
ALOX12 P18054 1/20 0.39
LMNA P02545 1/20 0.38
MAPT P10636 3/20 0.37
POLB P06746 3/20 0.37
KDM4E B2RXH2 2/20 0.37
HTT P42858 2/20 0.37
KMT2A Q03164 2/20 0.37
MEN1 O00255 1/20 0.37
GAA P10253 1/20 0.37
AGTR1 P30556 1/20 0.37

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
SCHEMBL5700585 0.97 SMN1; SMN2 (0.42) SMN1; SMN2RECQLALDH1A1NPC1RAB9A
SCHEMBL5700582 0.97 SMN1; SMN2 (0.42) SMN1; SMN2RECQLALDH1A1NPC1RAB9A
Hydrochloric Acid SCHEMBL5700353 0.92 LMNA (0.40) SMN1; SMN2RECQLALDH1A1NPC1RAB9A
SCHEMBL5700600 0.92 SMN1; SMN2 (0.39) SMN1; SMN2RECQLALDH1A1NPC1RAB9A
SCHEMBL5700405 0.89 LMNA (0.41) SMN1; SMN2RECQLALDH1A1NPC1RAB9A
SCHEMBL5700407 0.89 LMNA (0.41) SMN1; SMN2RECQLALDH1A1NPC1RAB9A
Hydrochloric Acid SCHEMBL5700459 0.78 SCN2A (0.51) SMN1; SMN2ALDH1A1NPC1RAB9ACYP1A2
SCHEMBL5836703 0.74 SCN2A (0.53) SMN1; SMN2ALDH1A1NPC1RAB9ACYP1A2
SCHEMBL26558724 0.70 SMN1; SMN2 (0.40) SMN1; SMN2ALDH1A1NPC1RAB9ACYP1A2
SCHEMBL10265496 0.69 LMNA (0.59) SMN1; SMN2RECQLALDH1A1NPC1RAB9A

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-7141687-B2 N'-substituted N-acylamidine metal transition complexes and their use as catalysts BASF AKTIENGESELLSCHAFT (DE) 2006-11-28 US disclosed
EP-1569947-B1 N'-SUBSTITUTED N-ACYLAMIDINE METAL TRANSITION COMPLEXES AND THEIR USE AS CATALYSTS BASF AG (DE) 2006-08-30 EP disclosed
US-20060069275-A1 N'-substituded n-acylamidine metal transition complexes and their use as catalysts BASF AKTIENGESELLSCHAFT (DE) 2006-03-30 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-20060069275-A1 N'-substituded n-acylamidine metal transition complexes and their use as catalysts NR1I3, NR0B1, NR4A1 SLC6A3 756/4885SMN1; SMN2 3235/4885RECQL 1959/4885

“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.