Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1359562

CCN=C=NCCCN(C)C.Cl.O=C1CCC(=O)N1O

nearest known ligand 0.61

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 2)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 0.61
CYP2D6 P10635 1/20 0.61

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
SCHEMBL490834 0.99 CYP1A2 (0.63) CYP1A2CYP2D6
SCHEMBL29245298 0.90 CYP1A2 (0.55) CYP1A2CYP2D6
Hydrochloric Acid SCHEMBL1850622 0.88 CYP1A2 (0.44) CYP1A2CYP2D6
SCHEMBL2026927 0.86 CYP1A2 (0.45) CYP1A2CYP2D6
Hydrochloric Acid SCHEMBL28461388 0.85 CYP1A2 (0.56) CYP1A2CYP2D6
Hydrochloric Acid SCHEMBL28414077 0.84 CYP1A2 (0.55) CYP1A2CYP2D6
SCHEMBL29245299 0.84 CYP1A2 (0.58) CYP1A2CYP2D6
SCHEMBL4362792 0.81 CYP1A2 (0.38) CYP1A2CYP2D6
Methylpyrrolidone SCHEMBL23037250 0.80 CYP1A2 (0.56) CYP1A2CYP2D6
Methyl Alcohol SCHEMBL29215793 0.80 CYP1A2 (0.88) CYP1A2CYP2D6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118347993-A Ag@EuW based10Preparation of carbohydrate antigen 19-9 (CA 19-9) of PEI 济南大学 2024-07-16 CN claimed
CN-118290611-A Ethylene glycol chitosan-TK-doxorubicin copolymer and polymerization method and application thereof 湖州师范学院 2024-07-05 CN claimed
CN-118267522-A Nanometer liposome crosslinked self-anti-inflammatory polysaccharide injectable hydrogel and preparation method and application thereof 天津大学 2024-07-02 CN claimed
CN-118252986-A Method for preparing anticoagulation coating on surface of substrate and blood contact medical device 上海发微医用材料有限公司 2024-06-28 CN claimed
CN-118217419-A Nanometer drug delivery system for overcoming tumor multidrug resistance and preparation method thereof 山东理工大学 2024-06-21 CN claimed
CN-115343280-B Colorimetric detection test paper for cellulose membrane-based organophosphorus pesticide and preparation method and application thereof 武汉工程大学 2024-06-18 CN claimed
CN-118026985-A Continuous foaming type concrete air entraining agent and preparation method thereof 江苏奥莱特新材料股份有限公司 2024-05-14 CN claimed
CN-114249909-B Micro-nano magnetic polymer microsphere with surface topological structure and preparation method thereof 中国科学院理化技术研究所 2024-05-03 CN claimed
CN-117919447-A PH and thermal response type iron nano-glue and preparation method and application thereof 中国药科大学 2024-04-26 CN claimed
CN-117783239-A MXene-based electrochemical biosensor array and preparation method and application thereof 江苏大学 2024-03-29 CN claimed
US-10288569-B2 Hydrogel, preparation method thereof, and pH sensor comprising the same INDUSTRY-ACADEMIC CORPORATION FOUNDATION YONSEI UNIVERSITY (KR) 2019-05-14 US claimed
EP-3241852-B1 HYALURONIC ACID-BASED AMPHIPHILIC POLYMER, PREPARATION METHOD AND APPLICATION THEREOF BRIGHTGENE BIO MEDICAL TECH CO LTD (CN) 2018-10-17 EP claimed
WO-2018109204-A1 PROCESS FOR THE PREPARATION OF (S)-2-((2-((S)-4-(DIFLUOROMETHYL)-2-OXOOXAZOLIDIN-3-YL)-5,6-DIHYDROBENZO[F]IMIDAZO[1,2-D][1,4]OXAZEPIN-9-YL)AMINO) PROPANAMIDE F. HOFFMANN-LA ROCHE AG (CH) 2018-06-21 WO claimed
US-20180092858-A1 Hyaluronic Acid-Based Amphiphilic Polymer, Preparation Method and Application Thereof BRIGHTGENE BIO-MEDICAL TECHNOLOGY CO., LTD. (CN) 2018-04-05 US claimed
EP-3241852-A1 HYALURONIC ACID-BASED AMPHIPHILIC POLYMER, PREPARATION METHOD AND APPLICATION THEREOF BrightGene Bio-Medical Technology Co., Ltd. (CN) 2017-11-08 EP claimed
US-20170146459-A1 HYDROGEL, PREPARATION METHOD THEREOF, AND pH SENSOR COMPRISING THE SAME INDUSTRY-ACADEMIC COOPERATION FOUNDATION YONSEI UNIVERSITY (KR) 2017-05-25 US claimed
US-20150362437-A1 HYDROGEL, PREPARATION METHOD THEREOF, AND pH SENSOR COMPRISING THE SAME INDUSTRY-ACADEMIC COOPERATION FOUNDATION YONSEI UNIVERSITY (KR) 2015-12-17 US claimed
US-7288661-B2 Process for the synthesis of (2S,3aS,7aS)-1-[(S)-alanyl]-octahydro-1H-indole-2-carboxylic acid compounds and application in the synthesis of perindopril LES LABORATOIRES SERVIER (FR) 2007-10-30 US claimed
US-20070123581-A1 Process for the synthesis of (2s, 3as, 7as)-1-[(s)-alanyl]-octahydro-1h-indole-2-carboxylic acid compounds and application in the synthesis of perindopril LES LABORATOIRES SERVIER (FR) 2007-05-31 US claimed
US-20070093663-A1 Process for the synthesis of perindopril and pharmaceutically acceptable salts thereof. LES LABORATOIRES SERVIER (FR) 2007-04-26 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 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-20180092858-A1 Hyaluronic Acid-Based Amphiphilic Polymer, Preparation Method and Application Thereof CD44, HCAR1, ASGR1 CYP1A2 3687/4885CYP2D6 2761/4885
US-20070093663-A1 Process for the synthesis of perindopril and pharmaceutically acceptable salts thereof. QDPR, REN, ACE CYP1A2 56/4885CYP2D6 5/4885
US-20070123581-A1 Process for the synthesis of (2s, 3as, 7as)-1-[(s)-alanyl]-octahydro-1h-indole-2-carboxylic acid compounds and application in the synthesis of perindopril CYP2S1, TPH1, AGTR1 CYP1A2 23/4885CYP2D6 15/4885

“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.