Hydrochloric Acid

Hydrochloric Acid

SCHEMBL538862

Cl.N=C(N)c1ccc(N)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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
PRSS1 P07477 5/20 1.00
F2 P00734 4/20 1.00
PRSS3 P35030 4/20 1.00
APEX1 P27695 1/20 1.00
PLAU P00749 3/20 0.94
MASP2 O00187 1/20 0.94
THPO P40225 1/20 0.94
LMNA P02545 2/20 0.61
BLM P54132 1/20 0.59
PRSS2 P07478 3/20 0.56
C1S P09871 1/20 0.56
RECQL P46063 1/20 0.56
KMT2A Q03164 1/20 0.56
F10 P00742 2/20 0.55
F12 P00748 1/20 0.55
F7 P08709 1/20 0.55
F3 P13726 1/20 0.55
PKM P14618 1/20 0.55
ST14 Q9Y5Y6 1/20 0.54
PRMT5 O14744 1/20 0.54

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 SCHEMBL236095 1.00 PRSS1 (1.00) PRSS1F2PRSS3APEX1PLAU
Hydrochloric Acid SCHEMBL28256621 0.97 PRSS1 (0.95) PRSS1F2PRSS3APEX1PLAU
SCHEMBL150756 0.97 PLAU (1.00) PRSS1F2PRSS3APEX1PLAU
Ammonia Solution, Strong SCHEMBL28058272 0.94 PLAU (0.94) PRSS1F2PRSS3APEX1PLAU
Hydrochloric Acid SCHEMBL30999366 0.88 PRSS1 (0.78) PRSS1F2PRSS3APEX1PLAU
Hydrochloric Acid SCHEMBL392375 0.88 PRSS1 (0.78) PRSS1F2PRSS3APEX1PLAU
Carbamic Acid SCHEMBL28064780 0.87 PLAU (0.81) PRSS1F2PRSS3APEX1PLAU
SCHEMBL537030 0.85 LMNA (0.77) PRSS1F2PRSS3APEX1PLAU
Acetic Acid SCHEMBL7398032 0.84 MASP2 (0.74) PRSS1F2PRSS3APEX1PLAU
Hydrochloric Acid SCHEMBL29182280 0.80 PRSS1 (0.67) PRSS1F2PRSS3APEX1PLAU

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111760556-B Urokinase adsorbent and preparation method and application thereof 江苏尤里卡生物科技有限公司 2023-06-30 CN claimed
CN-113755476-B Preparation method and application of maggot kinase 北京农学院 2023-04-11 CN claimed
CN-113789319-B Method for separating maggot kinase from fly maggots and application thereof 北京农学院 2023-03-28 CN claimed
CN-113789319-A Method for separating maggot kinase from fly maggots and application thereof 北京农学院 2021-12-14 CN claimed
CN-113755476-A Preparation method and application of maggot kinase 北京农学院 2021-12-07 CN claimed
CN-111760556-A Urokinase adsorbent and preparation method and application thereof 江苏尤里卡生物科技有限公司 2020-10-13 CN claimed
CN-108752237-A A kind of new preparation process of p-amino-benzamidine hydrochloride 四川青木制药有限公司 2018-11-06 CN claimed
CN-105330568-B Preparation method for p-aminobenzamidine hydrochloride 山东省医学科学院药物研究所 2017-05-10 CN claimed
CN-104163778-B A kind of method preparing p-amino-benzamidine hydrochloride BANGBU FENGYUAN MEDICINE SCI-TECH DEVELOPMENT CO., LTD. (CN) 2016-03-16 CN claimed
CN-105330568-A Preparation method for p-aminobenzamidine hydrochloride INST OF MATERIA MEDICA SHANDONG ACADEMY OF MEDICAL SCIENCES 2016-02-17 CN claimed
CN-104447408-A Triazoamidine and preparation process thereof HENAN HUIJIN PHARMACEUTICAL CO LTD 2015-03-25 CN claimed
CN-104163778-A Method for preparing p-amino-benzamidine hydrochloride BENGBU BBCA MEDICINE SCIENCE & DEV CO LTD 2014-11-26 CN claimed
CN-101694485-B Method for utilizing affinity column to analyze holoprotein UNIV SHANGHAI JIAOTONG 2013-01-16 CN claimed
CN-101694485-A Method for utilizing affinity column to analyze holoprotein UNIV SHANGHAI JIAOTONG 2010-04-14 CN claimed
US-6420487-B1 POLYMER WITH SPACER AND CATALYST FOR LINKING ENZYME INHIBITOR COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2002-07-16 US claimed
CN-117209508-A Azaphenothiazine compound and preparation method thereof 五邑大学 2023-12-12 CN disclosed
CN-111760556-B Urokinase adsorbent and preparation method and application thereof 江苏尤里卡生物科技有限公司 2023-06-30 CN disclosed
US-4096183-A Styrylsulfonylamidines MEAD JOHNSON & COMPANY (US) 1978-06-20 US disclosed
US-4052455-A ANALGESICS, BLOOD PLATELET AGGREGATION INHIBITORS MEAD JOHNSON & COMPANY (US) 1977-10-04 US disclosed
US-4020268-A Agarose containing affinity matrix materials XEROX CORPORATION (US) 1977-04-26 US disclosed