Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5092264

CCCCCCC(CC)C(N)(CC)CC.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 20)

geneUniProtsupporting neighboursconfidence
OPRM1 known ✓ P35372 1/20 0.41
FDPS P14324 1/20 0.42
SPHK1 Q9NYA1 2/20 0.39
DNM1 Q05193 4/20 0.39
LMNA P02545 2/20 0.38
CYP2D6 P10635 2/20 0.36
PLA2G1B P04054 1/20 0.36
PLA2G2A P14555 1/20 0.36
GMNN O75496 1/20 0.36
POLB P06746 1/20 0.36
THPO P40225 1/20 0.36
MTOR P42345 1/20 0.36
BLM P54132 1/20 0.36
KDM4E B2RXH2 1/20 0.36
TP53 P04637 1/20 0.36
CYP1A2 P05177 1/20 0.36
CYP3A4 P08684 1/20 0.36
MAPT P10636 1/20 0.36
CETP P11597 1/20 0.36
HTT P42858 1/20 0.36

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 SCHEMBL5085441 1.00 FDPS (0.42) FDPSOPRM1SPHK1DNM1LMNA
Hydrochloric Acid SCHEMBL5087510 1.00 FDPS (0.42) FDPSOPRM1SPHK1DNM1LMNA
Hydrochloric Acid SCHEMBL5086769 1.00 FDPS (0.42) FDPSOPRM1SPHK1DNM1LMNA
Hydrochloric Acid SCHEMBL5088023 1.00 FDPS (0.42) FDPSOPRM1SPHK1DNM1LMNA
Hydrochloric Acid SCHEMBL5086921 1.00 FDPS (0.42) FDPSOPRM1SPHK1DNM1LMNA
Hydrochloric Acid SCHEMBL5091794 1.00 FDPS (0.42) FDPSOPRM1SPHK1DNM1LMNA
Hydrochloric Acid SCHEMBL5086687 1.00 FDPS (0.42) FDPSOPRM1SPHK1DNM1LMNA
SCHEMBL332946 0.98 FDPS (0.44) FDPSOPRM1SPHK1DNM1LMNA
Hydrochloric Acid SCHEMBL5085440 0.98 OPRM1 (0.42) FDPSOPRM1SPHK1DNM1LMNA
SCHEMBL331848 0.98 FDPS (0.44) FDPSOPRM1SPHK1DNM1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122011219-A Method for preparing nanocellulose through fluid shear induction 昆明理工大学 2026-05-12 CN claimed
EP-2746348-B1 Cellulosic and cellulose ether solutions and their use SE TYLOSE GMBH & CO KG (DE) 2015-10-21 EP claimed
US-8901054-B2 Cellulose and cellulose ether solutions and use thereof SE TYLOSE GMBH & CO., KG (DE) 2014-12-02 US claimed
US-20140171352-A1 CELLULOSE AND CELLULOSE ETHER SOLUTIONS AND USE THEREOF SE TYLOSE GMBH & CO. KG (DE) 2014-06-19 US claimed
EP-4359605-A1 PAPER BAG HAVING BAG CONTENTS Baumit Beteiligungen GmbH (AT) 2024-05-01 EP disclosed
WO-2024004511-A1 SOLVENT TO BE USED FOR DISSOLVING POLYSACCHARIDE, SOLUTION OF POLYSACCHARIDE, AND METHOD FOR PRODUCING MOLDED BODY OF POLYSACCHARIDE USING SAME 旭化成株式会社 2024-01-04 WO disclosed
WO-2023173148-A1 PAPER BAG HAVING BAG CONTENTS BAUMIT BETEILIGUNGEN GMBH (AT) 2023-09-21 WO disclosed
EP-2735581-B1 COMPOSITION AND POLYMER ASAHI CHEMICAL IND (JP) 2021-07-14 EP disclosed
US-9738757-B2 Composition and polymer ASAHI KASEI CHEMICALS CORPORATION (JP) 2017-08-22 US disclosed
US-20160222168-A1 Composition and Polymer ASAHI KASEI CHEMICALS CORPORATION (JP) 2016-08-04 US disclosed
US-9334371-B2 Composition and polymer ASAHI KASEI CHEMICALS CORPORATION (JP) 2016-05-10 US disclosed
EP-1642918-B1 PROCESS FOR PRODUCTION OF BIFUNCTIONAL PHENYLENE ETHER OLIGOMERS MITSUBISHI GAS CHEMICAL CO (JP) 2014-12-24 EP disclosed
US-20140171352-A1 CELLULOSE AND CELLULOSE ETHER SOLUTIONS AND USE THEREOF SE TYLOSE GMBH & CO. KG (DE) 2014-06-19 US disclosed
US-20140171352-A1 CELLULOSE AND CELLULOSE ETHER SOLUTIONS AND USE THEREOF SE TYLOSE GMBH & CO. KG (DE) 2014-06-19 US disclosed
EP-2735581-A1 COMPOSITION AND POLYMER Asahi Kasei Chemicals Corporation (JP) 2014-05-28 EP disclosed
US-20140121293-A1 Composition and Polymer ASAHI KASEI CHEMICALS CORPORATION (JP) 2014-05-01 US disclosed
US-20080214386-A1 Stability; easily separated from solution; surface treatment of catalyst with Group seven compound; reacting epoxide with carbon dioxide NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) 2008-09-04 US disclosed
US-20060160982-A1 Process for the production of bifunctional phenylene ether oligomers MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2006-07-20 US disclosed
EP-1642918-A1 PROCESS FOR PRODUCTION OF BIFUNCTIONAL PHENYLENE ETHER OLIGOMERS MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2006-04-05 EP disclosed
US-4124493-A Catalytic oxidation of mercaptan in petroleum distillate including alkaline reagent and substituted ammonium halide UOP INC. (US) 1978-11-07 US disclosed