Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1335628

CCCCCCCC/C=C\CCCCCCCC(N)(CCCCCCCCCCCCCCCC)CCC[Si](OC)(OC)OC.Cl

nearest known ligand 0.41

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
PPARG known ✓ P37231 3/20 0.37
CHRM1 known ✓ P11229 1/20 0.37
TOP1 known ✓ P11387 1/20 0.37
CYP19A1 known ✓ P11511 1/20 0.37
PTGS1 known ✓ P23219 1/20 0.37
SLC6A2 known ✓ P23975 1/20 0.37
FLT3 known ✓ P36888 1/20 0.37
KCNH2 known ✓ Q12809 1/20 0.37
LMNA P02545 2/20 0.41
FAAH O00519 4/20 0.37
TRPV1 Q8NER1 1/20 0.37
TERT O14746 3/20 0.37
PTPN1 P18031 3/20 0.37
PPARD Q03181 3/20 0.37
PPARA Q07869 3/20 0.37
CYP1A2 P05177 2/20 0.37
MAPT P10636 2/20 0.37
CYP2C19 P33261 2/20 0.37
BLM P54132 2/20 0.37
HSD17B10 Q99714 2/20 0.37

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 SCHEMBL766241 0.91 LMNA (0.49) LMNA
Hydrochloric Acid SCHEMBL10611254 0.91 LMNA (0.49) LMNA
SCHEMBL2710658 0.89 LMNA (0.50) LMNA
Fluoride SCHEMBL10882602 0.87 LMNA (0.49) LMNA
SCHEMBL10529239 0.85 LMNA (0.50) LMNA
Hydrochloric Acid SCHEMBL2044459 0.83 FAAH (0.50) LMNAFAAHTRPV1TERTPTPN1
Hydrochloric Acid SCHEMBL2044463 0.83 FAAH (0.50) LMNAFAAHTRPV1TERTPTPN1
Hydrochloric Acid SCHEMBL10591065 0.83 FAAH (0.50) LMNAFAAHTRPV1TERTPTPN1
SCHEMBL2713411 0.82 LMNA (0.53) LMNAFAAHTRPV1TERTPTPN1
SCHEMBL517847 0.82 FAAH (0.52) LMNAFAAHTRPV1TERTPTPN1

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 15 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-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 PPARG 4084/4885CHRM1 171/4885TOP1 1545/4885

“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.