Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5427779

O=[N+]([O-])c1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1.[Cl-]

nearest known ligand 0.51

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
CYP1A2 P05177 1/20 0.51
CYP2C19 P33261 1/20 0.51
ALDH1A1 P00352 3/20 0.50
SNCA P37840 2/20 0.50
PTPRF P10586 1/20 0.50
PTPN2 P17706 1/20 0.50
PTPN1 P18031 1/20 0.50
PTPN11 Q06124 1/20 0.50
LMNA P02545 1/20 0.50
MEN1 O00255 4/20 0.48
KMT2A Q03164 4/20 0.48
SMN1; SMN2 Q16637 2/20 0.48
KDM4E B2RXH2 1/20 0.48
MAPT P10636 1/20 0.48
CRHBP P24387 2/20 0.47
CRHR2 Q13324 2/20 0.47
LOXL2 Q9Y4K0 1/20 0.47
POLB P06746 2/20 0.46
L3MBTL1 Q9Y468 2/20 0.44
ATM Q13315 1/20 0.44

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
SCHEMBL8374037 0.98 CYP1A2 (0.53) CYP1A2CYP2C19ALDH1A1SNCAPTPRF
Bromide SCHEMBL722749 0.97 SNCA (0.53) CYP1A2CYP2C19ALDH1A1SNCAPTPRF
SCHEMBL8379641 0.92 CYP1A2 (0.47) CYP1A2CYP2C19ALDH1A1SNCAPTPRF
SCHEMBL8374699 0.92 CYP1A2 (0.47) CYP1A2CYP2C19ALDH1A1SNCAPTPRF
SCHEMBL8379642 0.85 SNCA (0.44) CYP1A2CYP2C19ALDH1A1SNCAPTPRF
SCHEMBL2085893 0.83 SNCA (0.53) CYP1A2CYP2C19ALDH1A1SNCALMNA
Hydrochloric Acid SCHEMBL7117545 0.82 TSHR (0.54) CYP1A2CYP2C19ALDH1A1LMNAMEN1
Bromide SCHEMBL5828742 0.81 LMNA (0.44) CYP1A2CYP2C19ALDH1A1SNCAPTPRF
Hydrochloric Acid SCHEMBL2446696 0.81 SNCA (0.69) CYP1A2CYP2C19ALDH1A1SNCATSHR
SCHEMBL8374035 0.81 SNCA (0.56) CYP1A2CYP2C19ALDH1A1SNCAMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-3951661-A Silver halide emulsion containing an arylphosphonium salt as antifoggant KONISHIROKU PHOTO INDUSTRY CO. (JA) 1976-04-20 US claimed
US-9409859-B2 Substituted diphenyl derivatives CREATIVE THERAPEUTICS GMBH (DE) 2016-08-09 US disclosed
US-20140005149-A1 Substituted diphenyl derivatives CREATIVE THERAPEUTICS GMBH (DE) 2014-01-02 US disclosed
WO-2012130850-A1 TISSUE TARGETING BY MEANS OF ONCOCIDAL BRIDGED DIPHENYL DERIVATIVES FOR THE SELECTIVE TREATMENT OF SEXUAL ORGAN TUMORS BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2012-10-04 WO disclosed
US-20070099876-A1 Target directed chemotherapy of tumours of the sexual organs TRIN GMBH (CH) 2007-05-03 US disclosed
EP-0800506-B1 SOLVENTLESS PROCESS FOR MAKING 2,6-DIFLUOROBENZONITRILE DOW AGROSCIENCES LLC (US) 1999-12-22 EP disclosed
US-5776718-A Reversible protease inhibitors ARRIS PHARMACEUTICAL CORPORATION (US) 1998-07-07 US disclosed
CN-1174546-A Solventless process for making 2, 6 -difluorobenzonitrile DOWELANCO (US) 1998-02-25 CN disclosed
US-5502235-A FLUORINATON OF 2,6-DICHLOROBENZONITRILE DOWELANCO (US) 1996-03-26 US disclosed
EP-0150433-B1 PROCESS FOR THE PREPARATION OF INSATURATED KETONES BASF Aktiengesellschaft (DE) 1986-12-30 EP disclosed
EP-0150433-A2 Process for the preparation of insaturated ketones BASF Aktiengesellschaft (DE) 1985-08-07 EP disclosed
US-4150105-A 3-Ketosteroid antigenic conjugates, their preparation, antibodies and use BIOLOGICAL DEVELOPMENTS, INC. (US) 1979-04-17 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 (2 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-20070099876-A1 Target directed chemotherapy of tumours of the sexual organs GPER1, SHBG, GNRHR CYP1A2 746/4885CYP2C19 847/4885ALDH1A1 769/4885
US-20140005149-A1 Substituted diphenyl derivatives DPYD, VHL, TP53 CYP1A2 1582/4885CYP2C19 2343/4885ALDH1A1 113/4885

“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.