Hydrochloric Acid

Hydrochloric Acid

SCHEMBL250191

C=CCC(N)c1ccccc1.Cl

nearest known ligand 0.55

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 19)

geneUniProtsupporting neighboursconfidence
SCN4A known ✓ P35499 2/20 0.44
DPP4 known ✓ P27487 2/20 0.42
GRIN2D known ✓ O15399 1/20 0.40
GRIN3B known ✓ O60391 1/20 0.40
GRIN1 known ✓ Q05586 1/20 0.40
GRIN2A known ✓ Q12879 1/20 0.40
GRIN2B known ✓ Q13224 1/20 0.40
GRIN2C known ✓ Q14957 1/20 0.40
GRIN3A known ✓ Q8TCU5 1/20 0.40
HTR2A known ✓ P28223 1/20 0.39
CYP2C19 P33261 1/20 0.55
SMN1; SMN2 Q16637 1/20 0.46
KDM4E B2RXH2 1/20 0.45
ALDH1A1 P00352 1/20 0.45
MAPT P10636 1/20 0.45
ALOX15 P16050 1/20 0.45
HSD17B10 Q99714 1/20 0.45
F2 P00734 1/20 0.42
TAAR1 Q96RJ0 1/20 0.39

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 SCHEMBL25188226 1.00 CYP2C19 (0.55) CYP2C19SMN1; SMN2KDM4EALDH1A1MAPT
Hydrochloric Acid SCHEMBL31471464 1.00 CYP2C19 (0.55) CYP2C19SMN1; SMN2KDM4EALDH1A1MAPT
SCHEMBL898390 0.98 CYP2C19 (0.57) CYP2C19SMN1; SMN2KDM4EALDH1A1MAPT
SCHEMBL7406881 0.98 CYP2C19 (0.57) CYP2C19SMN1; SMN2KDM4EALDH1A1MAPT
SCHEMBL4629946 0.98 CYP2C19 (0.57) CYP2C19SMN1; SMN2KDM4EALDH1A1MAPT
SCHEMBL28590509 0.81 CYP2C19 (0.46) CYP2C19SMN1; SMN2ALDH1A1
SCHEMBL22705600 0.80 SCN4A (0.45) SCN4ADPP4F2GRIN2DGRIN3B
Hydrochloric Acid SCHEMBL327082 0.79 DPP4 (0.50) CYP2C19SMN1; SMN2KDM4EALDH1A1MAPT
Hydrochloric Acid SCHEMBL462457 0.79 CYP2C19 (0.43) CYP2C19SCN4ADPP4F2GRIN2D
Hydrochloric Acid SCHEMBL11222348 0.79 CYP2C19 (0.43) CYP2C19SCN4ADPP4F2GRIN2D

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115895631-B Pressure-reducing injection-increasing surfactant composition, and preparation method and application thereof 中国石油化工股份有限公司 2024-01-30 CN claimed
CN-116925724-A Surfactant composition, preparation method and application thereof 中国石油化工股份有限公司 2023-10-24 CN claimed
US-20230150166-A1 METHOD FOR TREATING A WOOD SUBSTRATE PNC BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT 2023-05-18 US claimed
CN-115895631-A Pressure-reducing injection-increasing surfactant composition and preparation method and application thereof 中国石油化工股份有限公司 2023-04-04 CN claimed
CN-114249896-A Allyl-terminated aryl sulfone ether polymer and preparation method thereof 兰溪聪普新材料有限公司 2022-03-29 CN claimed
CN-112680206-A Surfactant composition, and preparation method and application thereof 中国石油化工股份有限公司 2021-04-20 CN claimed
CN-110683996-A Preparation method of tertiary carbonic acid glycidyl ester 于翔 2020-01-14 CN claimed
EP-1584708-B1 Process for the treatment of laser-structured plastic surfaces ENTHONE (US) 2017-01-04 EP claimed
EP-2547777-A2 PROCESSES USING ANTIBIOTIC ALTERNATIVES IN BIOETHANOL PRODUCTION Buckman Laboratories International, Inc (US) 2013-01-23 EP claimed
US-20110230394-A1 Processes Using Antibiotic Alternatives In Bioethanol Production BUCKMAN LABORATORIES INTERNATIONAL, INC. (US) 2011-09-22 US claimed
WO-2011116042-A2 PROCESSES USING ANTIBIOTIC ALTERNATIVES IN BIOETHANOL PRODUCTION BUCKMAN LABORATORIES INTERNATIONAL, INC. (US) 2011-09-22 WO claimed
US-7666254-B1 Borate compositions for wood preservation OSMOSE, INC. (US) 2010-02-23 US claimed
US-7578888-B2 Method for treating laser-structured plastic surfaces ENTHONE INC. (US) 2009-08-25 US claimed
CN-101175800-A Method for improving the insulating capacity of expanded vinyl aromatic polymers and products obtained thereby POLIMERI EUROPA SPA (IT) 2008-05-07 CN claimed
US-20050224092-A1 Method for treating laser-structured plastic surfaces ENTHONE INC. (US) 2005-10-13 US claimed
WO-1995035359-A1 AQUEOUS CLEANING COMPOSITION PEDERSEN ARNE (NO) 1995-12-28 WO claimed
JP-5230406-A None JP disclosed
JP-6220487-A None JP disclosed
US-4510187-A APPLYING A THIN FILM OF DIMETHYLDITALLOWAMMONIUM CHLORIDE; ANTISTATIC AGENTS ROWE IRWIN 1985-04-09 US disclosed
US-4455287-A Method of stabilizing chelated polyvalent metal solutions ARI TECHNOLOGIES, INC. (US) 1984-06-19 US disclosed