Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1123383

CCCCCCCCCCCCCCCCCCCCCC(N)CCC[Si](OC)(OC)OC.Cl

nearest known ligand 0.52

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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
S1PR2 known ✓ O95136 5/20 0.43
S1PR1 known ✓ P21453 5/20 0.43
S1PR3 known ✓ Q99500 5/20 0.43
S1PR4 known ✓ O95977 4/20 0.43
OPRM1 known ✓ P35372 1/20 0.39
LMNA P02545 2/20 0.49
PLA2G1B P04054 1/20 0.43
PLA2G2A P14555 1/20 0.43
SPHK1 Q9NYA1 2/20 0.37
ALDH1A1 P00352 1/20 0.37
CYP2D6 P10635 2/20 0.35
GMNN O75496 1/20 0.35
POLB P06746 1/20 0.35
THPO P40225 1/20 0.35
MTOR P42345 1/20 0.35
BLM P54132 1/20 0.35
KDM4E B2RXH2 1/20 0.35
TP53 P04637 1/20 0.35
CYP1A2 P05177 1/20 0.35
CYP3A4 P08684 1/20 0.35

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 SCHEMBL1123186 1.00 LMNA (0.49) LMNAS1PR2S1PR1S1PR3S1PR4
Hydrochloric Acid SCHEMBL1333770 1.00 LMNA (0.49) LMNAS1PR2S1PR1S1PR3S1PR4
Hydrochloric Acid SCHEMBL1333797 1.00 LMNA (0.49) LMNAS1PR2S1PR1S1PR3S1PR4
Hydrochloric Acid SCHEMBL1333849 1.00 LMNA (0.49) LMNAS1PR2S1PR1S1PR3S1PR4
Hydrochloric Acid SCHEMBL1334525 1.00 LMNA (0.49) LMNAS1PR2S1PR1S1PR3S1PR4
Hydrochloric Acid SCHEMBL1335393 1.00 LMNA (0.49) LMNAS1PR2S1PR1S1PR3S1PR4
SCHEMBL16447008 0.98 LMNA (0.50) LMNAS1PR2S1PR1S1PR3S1PR4
SCHEMBL2713877 0.98 LMNA (0.50) LMNAS1PR2S1PR1S1PR3S1PR4
Hydrochloric Acid SCHEMBL7909372 0.96 LMNA (0.49) LMNAS1PR2S1PR1S1PR3S1PR4
Hydrochloric Acid SCHEMBL7030381 0.93 LMNA (0.44) LMNAS1PR2S1PR1S1PR3S1PR4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8735618-B2 Solvent-free organosilane quaternary ammonium compositions, method of making and use RESOURCE DEVELOPMENT L.L.C. (US) 2014-05-27 US claimed
EP-2566874-A2 SOLVENT-FREE ORGANOSILANE QUATERNARY AMMONIUM COMPOSITIONS, METHOD OF MAKING AND USE Resource Development L.L.C. (US) 2013-03-13 EP claimed
US-20120125226-A1 Solvent-Free Organosilane Quaternary Ammonium Compositions, Method of Making and Use RESOURCE DEVELOPMENT L.L.C. (US) 2012-05-24 US claimed
US-20110271873-A1 Solvent-Free Organosilane Quaternary Ammonium Compositions, Method of Making and Use Resource Development, LLC (US) 2011-11-10 US claimed
WO-2011140451-A2 SOLVENT-FREE ORGANOSILANE QUATERNARY AMMONIUM COMPOSITIONS, METHOD OF MAKING AND USE RESOURCE DEVELOPMENT L.L.C. (US) 2011-11-10 WO claimed
EP-1997873-B1 Thickened surfactant-free cleasing and multifunctional liquid coating compositions containing nonreactive abrasive solid particles and an organosilane quaternary compound and methods of using RESOURCE DEV LLC (US) 2011-02-09 EP claimed
EP-1942112-B1 Clathrates of an organosilane quaternary ammonium compound and urea and method of use RESOURCE DEV LLC (US) 2010-09-15 EP claimed
EP-4355830-B1 COATING COMPOSITIONS, METHODS OF MAKING AND USING SAME PERFECT CARBON LLC (US) 2026-05-13 EP disclosed
US-20240309227-A1 Coating Compositions, Methods of Making and Using Same PERFECT CARBON LLC 2024-09-19 US disclosed
EP-4355830-A1 COATING COMPOSITIONS, METHODS OF MAKING AND USING SAME Perfect Carbon LLC (US) 2024-04-24 EP disclosed
EP-2566874-B1 SOLVENT-FREE ORGANOSILANE QUATERNARY AMMONIUM COMPOSITIONS, METHOD OF MAKING AND USE RESOURCE DEV LLC (US) 2023-01-18 EP disclosed
WO-2022266545-A1 COATING COMPOSITIONS, METHODS OF MAKING AND USING SAME PERFECT CARBON LLC (US) 2022-12-22 WO disclosed
US-8735618-B2 Solvent-free organosilane quaternary ammonium compositions, method of making and use RESOURCE DEVELOPMENT L.L.C. (US) 2014-05-27 US disclosed
EP-2566874-A2 SOLVENT-FREE ORGANOSILANE QUATERNARY AMMONIUM COMPOSITIONS, METHOD OF MAKING AND USE Resource Development L.L.C. (US) 2013-03-13 EP disclosed
US-20120125226-A1 Solvent-Free Organosilane Quaternary Ammonium Compositions, Method of Making and Use RESOURCE DEVELOPMENT L.L.C. (US) 2012-05-24 US disclosed
US-20110271873-A1 Solvent-Free Organosilane Quaternary Ammonium Compositions, Method of Making and Use Resource Development, LLC (US) 2011-11-10 US disclosed
WO-2011140451-A2 SOLVENT-FREE ORGANOSILANE QUATERNARY AMMONIUM COMPOSITIONS, METHOD OF MAKING AND USE RESOURCE DEVELOPMENT L.L.C. (US) 2011-11-10 WO 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-20120125226-A1 Solvent-Free Organosilane Quaternary Ammonium Compositions, Method of Making and Use VDAC1, CUTA, HVCN1 S1PR2 2897/4885S1PR1 2220/4885S1PR3 2340/4885

“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.