Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7200797

Cc1ccc(C[P+](c2ccccc2C)(c2ccccc2C)c2ccccc2C)cc1.[Cl-]

nearest known ligand 0.36

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
ACHE known ✓ P22303 1/20 0.33
CYP19A1 P11511 1/20 0.36
IDO1 P14902 1/20 0.35
POLB P06746 2/20 0.35
LMNA P02545 1/20 0.35
SMN1; SMN2 Q16637 2/20 0.35
SNCA P37840 2/20 0.34
NPSR1 Q6W5P4 1/20 0.34
CYP1A2 P05177 1/20 0.33
CYP2A6 P11509 1/20 0.33
TAAR1 Q96RJ0 1/20 0.33
TSHR P16473 1/20 0.33
MEN1 O00255 1/20 0.33
KMT2A Q03164 1/20 0.33
KDM4E B2RXH2 1/20 0.33
ALDH1A1 P00352 1/20 0.33
RAB9A P51151 1/20 0.33
C3AR1 Q16581 1/20 0.33
HTT P42858 1/20 0.32
CYP2C19 P33261 1/20 0.32

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
Iodide SCHEMBL7197262 0.96 IDO1 (0.35) CYP19A1IDO1POLBLMNASMN1; SMN2
Bromide SCHEMBL7197753 0.96 SNCA (0.37) CYP19A1IDO1POLBLMNASMN1; SMN2
Hydrochloric Acid SCHEMBL6060719 0.88 TAAR1 (0.39) LMNASNCANPSR1CYP2A6TAAR1
Phosphoric Acid SCHEMBL7197915 0.88 FDFT1 (0.37) POLBLMNASMN1; SMN2TSHRMEN1
Acetic Acid SCHEMBL8750064 0.87 SMN1; SMN2 (0.38) POLBSMN1; SMN2MEN1KMT2AALDH1A1
Succinic Acid SCHEMBL7195814 0.84 HDAC3 (0.38) POLBSMN1; SMN2MEN1KMT2AALDH1A1
Acetic Acid SCHEMBL7195823 0.84 SMN1; SMN2 (0.40) POLBSMN1; SMN2MEN1KMT2ARAB9A
Bromide SCHEMBL6060755 0.84 SNCA (0.39) LMNASNCANPSR1CYP2A6TAAR1
Iodide SCHEMBL6060968 0.84 TAAR1 (0.39) LMNASNCANPSR1CYP2A6TAAR1
Hydrochloric Acid SCHEMBL7196439 0.82 L3MBTL1 (0.47) IDO1LMNASMN1; SMN2CYP1A2KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0624173-B2 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS DOW CHEMICAL CO (US) 2003-04-09 EP disclosed
EP-0624173-B1 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS DOW CHEMICAL CO (US) 1997-04-02 EP disclosed
EP-0624173-A1 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS. DOW CHEMICAL CO (US) 1994-11-17 EP disclosed
US-5360886-A Alklyphenylphosphine or phosphonium catalyst THE DOW CHEMICAL COMPANY (US) 1994-11-01 US disclosed
US-5310853-A Epoxy resins THE DOW CHEMICAL COMPANY (US) 1994-05-10 US disclosed
WO-1993015126-A1 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS THE DOW CHEMICAL COMPANY (US) 1993-08-05 WO disclosed
US-5202407-A Phosphonium or phosphine catalyst having at least three alkylphenyl groups attached to phosphorus atom THE DOW CHEMICAL COMPANY (US) 1993-04-13 US disclosed