Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1331235

CC(C)NCc1ccccc1.Cl

nearest known ligand 0.63

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
SIGMAR1 known ✓ Q99720 2/20 0.63
HRH1 known ✓ P35367 1/20 0.47
CYP3A4 P08684 2/20 0.56
MAPT P10636 2/20 0.56
KDM4E B2RXH2 1/20 0.56
POLB P06746 1/20 0.53
SMN1; SMN2 Q16637 1/20 0.53
MEN1 O00255 2/20 0.49
KMT2A Q03164 2/20 0.49
ALDH1A1 P00352 2/20 0.47
RAB9A P51151 1/20 0.47
LMNA P02545 1/20 0.47
MAPK1 P28482 1/20 0.47
HTT P42858 1/20 0.47
NPSR1 Q6W5P4 1/20 0.47
ACP3 P15309 2/20 0.47
IDO1 P14902 2/20 0.46
THRB P10828 1/20 0.46
TDP1 Q9NUW8 1/20 0.46

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
SCHEMBL22899588 0.98 SIGMAR1 (0.65) SIGMAR1CYP3A4MAPTKDM4EPOLB
SCHEMBL143708 0.98 SIGMAR1 (0.65) SIGMAR1CYP3A4MAPTKDM4EPOLB
Bromide SCHEMBL1331742 0.95 SIGMAR1 (0.63) SIGMAR1CYP3A4MAPTKDM4EPOLB
Ammonia Solution, Strong SCHEMBL15917374 0.95 SIGMAR1 (0.63) SIGMAR1CYP3A4MAPTKDM4EPOLB
Methyl Alcohol SCHEMBL29261100 0.93 SIGMAR1 (0.61) SIGMAR1CYP3A4MAPTKDM4EPOLB
Hydrochloric Acid SCHEMBL3332713 0.92 SIGMAR1 (0.55) SIGMAR1CYP3A4MAPTKDM4EPOLB
Toluene SCHEMBL27514860 0.92 SMN1; SMN2 (0.61) SIGMAR1CYP3A4MAPTKDM4EPOLB
Alcohol SCHEMBL9136417 0.89 SIGMAR1 (0.57) SIGMAR1CYP3A4MAPTKDM4EPOLB
Hydrochloric Acid SCHEMBL27850743 0.88 SIGMAR1 (0.52) SIGMAR1CYP3A4MAPTKDM4EPOLB
Putrescine SCHEMBL8006412 0.86 SIGMAR1 (0.53) SIGMAR1CYP3A4MAPTKDM4EPOLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107376615-A A kind of highly efficiency compositional desulfurization and decarburization solvent and its application 中国石油集团工程设计有限责任公司 2017-11-24 CN claimed
EP-2729169-A1 HUMAN RESPIRATORY SYNCYTIAL VIRUS VACCINE Nanobio Corporation (US) 2014-05-14 EP claimed
WO-2013006797-A1 HUMAN RESPIRATORY SYNCYTIAL VIRUS VACCINE NANOBIO CORPORATION (US) 2013-01-10 WO claimed
CN-118771989-A Method for catalyzing hydrosilation reduction of amide into amine by using tridentate nitrogen ligand manganese complex 浙江工业大学 2024-10-15 CN disclosed
CN-116887806-A Improved long-wearing sun-proof cosmetic 巴斯夫欧洲公司 2023-10-13 CN disclosed
CN-104629792-B The removal methods of nitride in a kind of heavy oil ZHEJIANG OCEAN UNIVERSITY (CN) 2016-04-27 CN disclosed
CN-104629792-A Method for removing nitride from heavy oil UNIV ZHEJIANG OCEAN 2015-05-20 CN disclosed
US-8962662-B2 Antimicrobial compositions and methods of use thereof BYOCOAT ENTERPRISES, INC. (US) 2015-02-24 US disclosed
US-8586115-B2 Antimicrobial solutions and process related thereto BYOCOAT ENTERPRISES, INC. (US) 2013-11-19 US disclosed
US-20130137732-A1 ANTIMICROBIAL COMPOSITIONS AND METHODS OF USE THEREOF BYOCOAT ENTERPRISES, INC. (US) 2013-05-30 US disclosed
WO-2013074526-A2 ANTIMICROBIAL COMPOSITIONS AND METHODS OF USE THEREOF BYOCOAT ENTERPRISES, INC. (US) 2013-05-23 WO disclosed
WO-2007030104-A1 ANTIMICROBIAL SOLUTIONS AND PROCESS RELATED THERETO BYOCOAT ENTERPRISES, INC. (US) 2007-03-15 WO disclosed
US-20060110506-A1 Antimicrobial solutions and process related thereto BYOCOAT ENTERPRISES, INC. 2006-05-25 US disclosed
US-20050271781-A1 Antimicrobial solutions and process related thereto BYOCOAT ENTERPRISES, INC. 2005-12-08 US disclosed
EP-0065804-B1 PROCESS FOR THE PREPARATION OF N-BENZYL-N-ISOPROPYL PIVALAMIDE HÜLS AKTIENGESELLSCHAFT (DE) 1984-12-12 EP disclosed
EP-0065804-A1 Process for the preparation of N-benzyl-N-isopropyl pivalamide HÜLS AKTIENGESELLSCHAFT (DE) 1982-12-01 EP disclosed
US-4331815-A Process for manufacturing N-benzyl-N-isopropyl amides GULF OIL CORPORATION (US) 1982-05-25 US disclosed
US-4119729-A TREATMENT OF HYPERTENSION MEAD JOHNSON & COMPANY (US) 1978-10-10 US disclosed
US-4067904-A ANTIARRHYTHMIA, HYPOTENSIVE MEAD JOHNSON & COMPANY (US) 1978-01-10 US disclosed
US-3994974-A BRONCHODILATORS YAMANOUCHI PHARMACEUTICAL CO., LTD. (JA) 1976-11-30 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-20130137732-A1 ANTIMICROBIAL COMPOSITIONS AND METHODS OF USE THEREOF KARS1, AAAS, AARS1 SIGMAR1 793/4885HRH1 3366/4885CYP3A4 4251/4885

“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.