Hydrochloric Acid

Hydrochloric Acid

SCHEMBL261263

CCCCC(C)CC[n+]1ccc(N2CCC(C)CC2)cc1.[Cl-]

nearest known ligand 0.38

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
ACHE known ✓ P22303 1/20 0.32
SMN1; SMN2 Q16637 1/20 0.38
USP2 O75604 2/20 0.37
DPP4 P27487 2/20 0.34
CHKA P35790 6/20 0.33
MEN1 O00255 1/20 0.33
GAA P10253 1/20 0.33
KMT2A Q03164 1/20 0.33
NPC1 O15118 1/20 0.32
RAB9A P51151 1/20 0.32
MCL1 Q07820 1/20 0.32
SIGMAR1 Q99720 2/20 0.32
BCHE P06276 1/20 0.32
HPGD P15428 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
Hydrochloric Acid SCHEMBL9676684 0.81 SMN1; SMN2 (0.37) SMN1; SMN2USP2DPP4CHKANPC1
SCHEMBL3040650 0.81 MEN1 (0.50) SMN1; SMN2MEN1KMT2ANPC1RAB9A
Bromide SCHEMBL3040545 0.80 KMT2A (0.49) SMN1; SMN2MEN1KMT2ANPC1RAB9A
SCHEMBL9833857 0.80 SMN1; SMN2 (0.38) SMN1; SMN2USP2DPP4CHKANPC1
Hydrochloric Acid SCHEMBL9838022 0.78 SMN1; SMN2 (0.39) SMN1; SMN2USP2DPP4MEN1GAA
Hydrochloric Acid SCHEMBL9172857 0.71 SMN1; SMN2 (0.37) SMN1; SMN2USP2CHKAMEN1GAA
Hydrochloric Acid SCHEMBL9674296 0.71 USP2 (0.43) SMN1; SMN2USP2CHKAMEN1GAA
Hydrochloric Acid SCHEMBL8959777 0.70 GAA (0.40) SMN1; SMN2USP2CHKAMEN1GAA
Bromide SCHEMBL15923364 0.70 CHKA (0.56) CHKABCHEACHE
SCHEMBL9834829 0.69 USP2 (0.44) SMN1; SMN2USP2CHKAMEN1GAA

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 29 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7268237-B2 Direct dianhydride synthesis GENERAL ELECTRIC COMPANY (US) 2007-09-11 US claimed
US-20060205958-A1 Direct dianhydride synthesis GENERAL ELECTRIC COMPANY 2006-09-14 US claimed
EP-2280963-B1 METHOD OF PURIFYING DIANHYDRIDES, THE DIANHYDRIDES FORMED THEREBY, AND POLYETHERIMIDES FORMED THEREFROM SABIC GLOBAL TECHNOLOGIES BV (NL) 2016-07-20 EP disclosed
CN-105218496-A The method of purifying dianhydride SABIC FOUNDATIONAL GLOBAL TECHNOLOGY CO LTD 2016-01-06 CN disclosed
EP-2097375-B1 METHOD FOR PURIFYING BISIMIDES SABIC INNOVATIVE PLASTICS IP (NL) 2013-04-24 EP disclosed
EP-2089348-B1 METHOD FOR MAKING POLYETHERIMIDES SABIC INNOVATIVE PLASTICS IP (NL) 2013-02-20 EP disclosed
US-8134016-B2 Method for purifying dianhydrides SABIC INNOVATIVE PLASTICS IP B.V. (NL) 2012-03-13 US disclosed
US-8013173-B2 Method of purifying dianhydrides, the dianhydrides formed thereby, and polyetherimides formed therefrom SABIC INNOVATIVE PLASTICS IP B.V. (NL) 2011-09-06 US disclosed
EP-2094691-B1 METHOD FOR PURIFYING DIANHYDRIDES SABIC INNOVATIVE PLASTICS IP (NL) 2011-05-25 EP disclosed
EP-2280963-A1 METHOD OF PURIFYING DIANHYDRIDES, THE DIANHYDRIDES FORMED THEREBY, AND POLYETHERIMIDES FORMED THEREFROM SABIC Innovative Plastics IP B.V. (NL) 2011-02-09 EP disclosed
US-20090247727-A1 Method of Purifying Dianhydrides, the Dianhydrides Formed Thereby, and Polyetherimides Formed Therefrom SHPP GLOBAL TECHNOLOGIES B.V. (NL) 2009-10-01 US disclosed
WO-2008063206-A1 METHOD FOR MAKING POLYETHERIMIDES SABIC INNOVATIVE PLASTICS IP B.V. (NL) 2008-05-29 WO disclosed
WO-2008063208-A1 METHOD FOR PURIFYING BISIMIDES SABIC INNOVATIVE PLASTICS IP B.V. (NL) 2008-05-29 WO disclosed
WO-2008063207-A1 METHOD FOR PURIFYING DIANHYDRIDES SABIC INNOVATIVE PLASTICS IP B.V. (NL) 2008-05-29 WO disclosed
US-7268237-B2 Direct dianhydride synthesis GENERAL ELECTRIC COMPANY (US) 2007-09-11 US disclosed
US-20070073035-A1 Method for making polyetherimides GENERAL ELECTRIC COMPANY (US) 2007-03-29 US disclosed
US-20070073066-A1 Method for purifying dianhydrides GENERAL ELECTRIC COMPANY (US) 2007-03-29 US disclosed
US-20070073063-A1 Method for purifying bisimides GENERAL ELECTRIC COMPANY (US) 2007-03-29 US disclosed
US-20060293528-A1 Method of purifying dianhydrides GENERAL ELECTRIC COMPANY 2006-12-28 US disclosed
US-20060205958-A1 Direct dianhydride synthesis GENERAL ELECTRIC COMPANY 2006-09-14 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 (5 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-20060205958-A1 Direct dianhydride synthesis HDHD5, DOHH, DBH ACHE 1387/4885SMN1; SMN2 4085/4885USP2 3028/4885
US-20070073063-A1 Method for purifying bisimides FHIT, PBRM1, TNS4 ACHE 3216/4885SMN1; SMN2 1842/4885USP2 2508/4885
US-20060293528-A1 Method of purifying dianhydrides CA3, UROD, CA7 ACHE 2507/4885SMN1; SMN2 3053/4885USP2 394/4885
US-20070073066-A1 Method for purifying dianhydrides AQP4, TRRAP, GYPA ACHE 3414/4885SMN1; SMN2 2824/4885USP2 2642/4885
US-20090247727-A1 Method of Purifying Dianhydrides, the Dianhydrides Formed Thereby, and Polyetherimides Formed Therefrom CA7, CA4, CA13 ACHE 3011/4885SMN1; SMN2 4507/4885USP2 78/4885

“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.