Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1752733

C=CC(c1ccccc1)N(C)C.Cl

nearest known ligand 0.45

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 18)

geneUniProtsupporting neighboursconfidence
HTR2A known ✓ P28223 3/20 0.40
HRH1 known ✓ P35367 3/20 0.40
SLC6A2 known ✓ P23975 1/20 0.36
SLC6A4 known ✓ P31645 1/20 0.36
SLC6A3 known ✓ Q01959 1/20 0.36
LMNA P02545 2/20 0.45
TDP1 Q9NUW8 1/20 0.43
KDM4E B2RXH2 2/20 0.41
ALDH1A1 P00352 1/20 0.41
MEN1 O00255 1/20 0.39
MAPT P10636 1/20 0.39
CYP2C9 P11712 1/20 0.39
KMT2A Q03164 1/20 0.39
MAPK1 P28482 1/20 0.36
PMP22 Q01453 1/20 0.36
SMN1; SMN2 Q16637 1/20 0.36
AOC3 Q16853 7/20 0.35
CYP3A4 P08684 1/20 0.34

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 SCHEMBL28251812 0.98 LMNA (0.44) LMNATDP1KDM4EALDH1A1HTR2A
SCHEMBL290984 0.98 LMNA (0.46) LMNATDP1KDM4EALDH1A1HTR2A
SCHEMBL11324526 0.84 LMNA (0.42) LMNATDP1KDM4EALDH1A1HTR2A
SCHEMBL18493238 0.79 TAAR1 (0.39) LMNATDP1KDM4EALDH1A1HTR2A
SCHEMBL30518068 0.79 SLC6A2 (0.42) LMNATDP1KDM4EALDH1A1HTR2A
SCHEMBL986924 0.78 HTR2A (0.41) LMNATDP1ALDH1A1HTR2AHRH1
SCHEMBL8751571 0.76 LMNA (0.47) LMNATDP1KDM4EALDH1A1MEN1
SCHEMBL7181278 0.76 CYP3A4 (0.35) LMNATDP1KDM4EALDH1A1HTR2A
SCHEMBL689805 0.76 ALDH1A1 (0.42) LMNATDP1KDM4EALDH1A1HTR2A
SCHEMBL12067933 0.76 ALDH1A1 (0.42) LMNATDP1KDM4EALDH1A1HTR2A

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-7968735-B2 Light-emitting biomarker QUIDD (FR) 2011-06-28 US claimed
US-20090041669-A1 Light-Emitting Biomarker QUIDD (FR) 2009-02-12 US claimed
US-4891306-A FLUOROPOLYMER FUJI PHOTO FILM CO., LTD. (JP) 1990-01-02 US claimed
CN-114588270-A Compositions comprising nanoparticles of taxanes and uses thereof DFB索里亚有限责任公司 2022-06-07 CN disclosed
CN-107076674-A Analysis method using SERS and the composition for methods described 庄信万丰股份有限公司 2017-08-18 CN disclosed
US-7968735-B2 Light-emitting biomarker QUIDD (FR) 2011-06-28 US disclosed
US-20090041669-A1 Light-Emitting Biomarker QUIDD (FR) 2009-02-12 US disclosed
WO-2008137773-A1 COMPOSITION FOR IN SITU MANUFACTURE OF INSOLUBLE HYDROXIDE WHEN CLEANING HARD SURFACES AND FOR USE IN AUTOMATIC WAREWASHING MACHINES, AND METHODS FOR MANUFACTURING AND USING ECOLAB INC. (US) 2008-11-13 WO disclosed
US-20080274932-A1 COMPOSITION FOR IN SITU MANUFACTURE OF INSOLUBLE HYDROXIDE WHEN CLEANING HARD SURFACES AND FOR USE IN AUTOMATIC WAREWASHING MACHINES AND METHODS FOR MANUFACTURING AND USING ECOLAB INC. (US) 2008-11-06 US disclosed
US-20060204687-A1 Ink-jet recording sheet KONICA MINOLTA PHOTO IMAGING, INC. (JP) 2006-09-14 US disclosed
EP-1669209-A1 Ink-jet recording sheet and producing method of the same Konica Minolta Photo Imaging, Inc. (JP) 2006-06-14 EP disclosed
EP-0016623-B1 WATER-SOLUBLE POLYMERS CONTAINING QUATERNARY AMMONIUM GROUPS, A PROCESS FOR THEIR PRODUCTION AND THEIR USE IN IMPROVING THE WET STRENGTH OF CELLULOSIC SUBSTRATES MONSANTO COMPANY (US) 1983-12-28 EP disclosed
US-4343730-A WATER AND SEWAGE TREATMENT PETROLITE CORPORATION (US) 1982-08-10 US disclosed
US-4340692-A CATIONIC THERMOSETTING RESINS MONSANTO COMPANY (US) 1982-07-20 US disclosed
US-4312969-A REFLUXING LOW BOILING LIQUID TO DISSIPATE HEAT PETROLITE CORPORATION (US) 1982-01-26 US disclosed
US-4298639-A WATER SOLUBLE, CATIONIC, THERMOSETTING, HAVING GLYCIDYL QUATERNARY AMMONIUM GROUPS FOR APPLICATION TO CELLULOSE SUBSTRATES MONSANTO COMPANY (US) 1981-11-03 US disclosed
US-4233417-A EPICHLOROHYDRIN-TERTIARY AMINE CATIONIC SALT POLYMER IS AN ADDITIVE FOR CELLULOSIC SUBSTRATES MONSANTO COMPANY (US) 1980-11-11 US disclosed
EP-0016623-A1 Water-soluble polymers containing quaternary ammonium groups, a process for their production and their use in improving the wet strength of cellulosic substrates MONSANTO COMPANY (US) 1980-10-01 EP disclosed
US-4035347-A Method for the preparation of dried latex polymer from aqueous emulsion NALCO CHEMICAL COMPANY (US) 1977-07-12 US disclosed
US-4025712-A HYDROLYZING THE EMULSIFIER NALCO CHEMICAL COMPANY (US) 1977-05-24 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 (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-20090041669-A1 Light-Emitting Biomarker ALDH1A2, CYP19A1, GUSB HTR2A 3483/4885HRH1 3865/4885SLC6A2 4172/4885

“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.