Hydrochloric Acid

Hydrochloric Acid

SCHEMBL236095

Cl.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 SCHEMBL538862 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 323 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116769385-B Anti-cracking anticorrosive paint and preparation method thereof 广东省漆色彩新型材料有限公司 2024-04-26 CN claimed
CN-116769385-A Anti-cracking anticorrosive paint and preparation method thereof 广东蓝风环境科技服务有限公司 2023-09-19 CN claimed
CN-115385823-A Preparation method of 4-aminobenzamidine dihydrochloride 四川青木制药有限公司 2022-11-25 CN claimed
CN-111957073-B Affinity chromatography filler for purifying urokinase, preparation method and application 武汉人福药业有限责任公司 2021-12-24 CN claimed
CN-109052602-B Natural polymeric flocculant for starch wastewater treatment and treatment method thereof 南京大学 2021-04-23 CN claimed
CN-111957073-A Affinity chromatography filler for purifying urokinase, preparation method and application 武汉人福药业有限责任公司 2020-11-20 CN claimed
CN-111606885-A Dabigatran etexilate mesylate and preparation method thereof 安徽鼎旺医药有限公司 2020-09-01 CN claimed
CN-109836412-A A kind of preparation method of dabigatran etexilate methanesulfonate 辽宁博美医药科技有限公司 2019-06-04 CN claimed
CN-109052602-A A kind of natural macromolecule flocculating agent and its processing method for starch wastewater treatment 南京大学 2018-12-21 CN claimed
CN-106083822-B A kind of preparation method of dabigatran etexilate methanesulfonate intermediate 本溪经济开发区博美医药新技术开发有限公司 2018-09-11 CN claimed
CN-104610096-A Diminazene aceturate production method HENAN LINGXIAN PHARMACEUTICAL CO LTD 2015-05-13 CN claimed
CN-101970676-A Compositions for forming immobiized biological layers for sensing ABBOTT POINT OF CARE INC 2011-02-09 CN claimed
EP-1750743-A4 ORAL FORMULATIONS COMPRISING BONE MORPHOGENETIC PROTEINS FOR TREATING METABOLIC BONE DISEASES GLAXOSMITHKLINE ZAGREB (HR) 2009-07-08 EP claimed
US-20070265187-A1 Oral Formulations Comprising Bone Morphogenetic Proteins For Treating Metabolic Bone Diseases GLAXOSMITHKLINE ISTRAZIVACKI CENTAR ZAGREB D.O.O. ZA ISTRAZIVANJE I RAZVOJ (HR) 2007-11-15 US claimed
EP-1750743-A2 ORAL FORMULATIONS COMPRISING BONE MORPHOGENETIC PROTEINS FOR TREATING METABOLIC BONE DISEASES GlaxoSmithKline istrazivacki centar Zagreb d.o.o. (HR) 2007-02-14 EP claimed
WO-2005110465-A2 ORAL FORMULATIONS COMPRISING BONE MORPHOGENETIC PROTEINS FOR TREATING METABOLIC BONE DISEASES GLAXOSMITHKLINE ISTRAZIVACKI CENTAR ZAGREB D.O.O. (HR) 2005-11-24 WO claimed
EP-0839128-B1 PROCESS FOR THE PREPARATION OF ETHYL 3S-[[4-[[4-(AMINOIMINOMETHYL)PHENYL]AMINO]-1,4-DIOXOBUTYL]AMINO]-4-PENTYNOATE SEARLE & CO (US) 2000-04-05 EP claimed
EP-0839128-A1 PROCESS FOR THE PREPARATION OF ETHYL 3S-[[4-[[4-(AMINOIMINOMETHYL)PHENYL]AMINO]-1,4-DIOXOBUTYL]AMINO]-4-PENTYNOATE G.D. SEARLE & CO. (US) 1998-05-06 EP claimed
WO-1997003947-A1 PROCESS FOR THE PREPARATION OF ETHYL 3S-[[4-[[4-(AMINOIMINOMETHYL)PHENYL]AMINO]-1,4-DIOXOBUTYL]AMINO]-4-PENTYNOATE G.D. SEARLE & CO. (US) 1997-02-06 WO claimed
US-5536869-A Process for the preparation of ethyl 3S-[4-[[4-(aminoiminomethyl)phenyl]amino]-1,4-dioxobutyl]amino]-4-pentynoate G. D. SEARLE & CO. (US) 1996-07-16 US claimed