Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1024140

CCCCCCCCCCCCCCCC[N+](CC)(CC)CC.[Cl-]

nearest known ligand 0.94

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
DNM1 Q05193 6/20 0.94
SLC22A1 O15245 3/20 0.77
ALDH1A1 P00352 1/20 0.72
TP53 P04637 1/20 0.72
CYP3A4 P08684 1/20 0.72
ALOX15 P16050 1/20 0.72
TSHR P16473 1/20 0.72
ALOX12 P18054 1/20 0.72
SMN1; SMN2 Q16637 1/20 0.72
HIF1A Q16665 1/20 0.72
HSD17B10 Q99714 1/20 0.72
SLC22A2 O15244 1/20 0.71
HTT P42858 1/20 0.55
KMT2A Q03164 1/20 0.55

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 SCHEMBL5087508 1.00 DNM1 (0.94) DNM1SLC22A1ALDH1A1TP53CYP3A4
Hydrochloric Acid SCHEMBL967115 1.00 DNM1 (0.94) DNM1SLC22A1ALDH1A1TP53CYP3A4
Hydrochloric Acid SCHEMBL967130 1.00 DNM1 (0.94) DNM1SLC22A1ALDH1A1TP53CYP3A4
Hydrochloric Acid SCHEMBL19873253 1.00 DNM1 (0.94) DNM1SLC22A1ALDH1A1TP53CYP3A4
Hydrochloric Acid SCHEMBL1042158 1.00 DNM1 (0.94) DNM1SLC22A1ALDH1A1TP53CYP3A4
Hydrochloric Acid SCHEMBL19873263 1.00 DNM1 (0.94) DNM1SLC22A1ALDH1A1TP53CYP3A4
Hydrochloric Acid SCHEMBL19873261 1.00 DNM1 (0.94) DNM1SLC22A1ALDH1A1TP53CYP3A4
Hydrochloric Acid SCHEMBL4001962 1.00 DNM1 (0.94) DNM1SLC22A1ALDH1A1TP53CYP3A4
Hydrochloric Acid SCHEMBL22204611 1.00 DNM1 (0.94) DNM1SLC22A1ALDH1A1TP53CYP3A4
Hydrochloric Acid SCHEMBL635917 1.00 DNM1 (0.94) DNM1SLC22A1ALDH1A1TP53CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122005876-A Medical ultrasonic hydrogel and preparation method thereof 华中科技大学同济医学院附属同济医院 2026-05-12 CN claimed
US-12589383-B2 Spherical titanium silicalite molecular sieve catalyst and preparation method therefor Shanghai HuaYi New Material Co., Ltd (CN) 2026-03-31 US claimed
WO-2025094028-A1 CROSSLINKING SYSTEM FOR FLUOROELASTOMERS GUJARAT FLUOROCHEMICALS LIMITED (IN) 2025-05-08 WO claimed
CN-119488885-A Modified porous microsphere, preparation method thereof, separation device and application thereof 中国石油化工股份有限公司 2025-02-21 CN claimed
CN-119488884-A Modified porous microsphere, preparation method thereof, separation device and application thereof 中国石油化工股份有限公司 2025-02-21 CN claimed
CN-118724992-A Synthesis process of estrone 秦皇岛紫竹药业有限公司 2024-10-01 CN claimed
CN-116354359-B Pure silicon MFI structure molecular sieve and preparation method thereof 中国石油天然气股份有限公司 2024-09-10 CN claimed
CN-117965021-A Pure-color 3D printing nylon powder and preparation method thereof 万华化学集团股份有限公司 2024-05-03 CN claimed
CN-117918366-A Pesticide preparation with high adhesiveness to plant leaves 硅羿科技(上海)有限公司 2024-04-26 CN claimed
US-20240100512-A1 Spherical Titanium Silicalite Molecular Sieve Catalyst and Preparation Method Therefor Shanghai HuaYi New Material Co., Ltd (CN) 2024-03-28 US claimed
EP-1311485-A1 PROCESSES FOR PREPARING CILOSTAZOL TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2003-05-21 EP claimed
US-6515128-B2 Dissolving 6-hydroxy-3,4-dihydroquinolinone and a base in water; dissolving a 1-cyclohexyl-5- (4-halobutyl)-tetrazole in water-immiscible solvent, mixing aqueous phase and organic phase in presence of phase transfer catalyst; recovering TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2003-02-04 US claimed
US-20020099213-A1 Processes for preparing cilostazol TEVA PHARMACEUTICALS USA, INC. 2002-07-25 US claimed
WO-2002014283-A1 PROCESSES FOR PREPARING CILOSTAZOL TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2002-02-21 WO claimed
US-6344563-B1 SULFIDING, DEHYDROHALOGENATION, FORMATION OF BOND BETWEEN CARBON AND NITROGEN NORRIS TIMOTHY (US) 2002-02-05 US claimed
CN-1291609-A Method of preparing 5-lipoxidase inhibitor possessing different heterocyclic ring system PFIZER PROD INC (US) 2001-04-18 CN claimed
EP-1081146-A1 Process for making 5-lipoxygenase inhibitors having varied heterocyclic ring systems Pfizer Products Inc. (US) 2001-03-07 EP claimed
EP-1081144-A2 Process for making 5-lipoxygenase inhibitors having varied heterocyclic ring systems Pfizer Products Inc. (US) 2001-03-07 EP claimed
CN-1286251-A Method for preparing 5-lipooxygenase inhibitor having changeable heterocycle system PFIZER PROD INC (US) 2001-03-07 CN claimed
US-3966825-A Process for preparing β-nitroethanethiol SYNTEX (U.S.A.) INC. (US) 1976-06-29 US claimed

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-20020099213-A1 Processes for preparing cilostazol PDE3A, PDE12, PDE5A DNM1 3161/4885SLC22A1 4650/4885ALDH1A1 2070/4885
US-12589383-B2 Spherical titanium silicalite molecular sieve catalyst and preparation method therefor SOST, SSRP1, SEM1 DNM1 1812/4885SLC22A1 4290/4885ALDH1A1 4450/4885

“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.