Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6773706

Cl.Cn1cncc1CCN

nearest known ligand 0.96

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
HRH3 known ✓ Q9Y5N1 1/20 0.38
CHRM5 known ✓ P08912 3/20 0.38
CHRM4 known ✓ P08173 2/20 0.36
CHRM1 known ✓ P11229 2/20 0.36
CHRM3 known ✓ P20309 2/20 0.36
CHRM2 known ✓ P08172 1/20 0.36
HTR2A known ✓ P28223 1/20 0.36
TDP1 Q9NUW8 1/20 0.41
LMNA P02545 2/20 0.39
KDM4E B2RXH2 1/20 0.39
MAPT P10636 1/20 0.39
BLM P54132 1/20 0.39
PMP22 Q01453 1/20 0.39
CYP2C9 P11712 3/20 0.38
CYP2C19 P33261 2/20 0.38
TSHR P16473 1/20 0.38
MTOR P42345 1/20 0.38
HRH4 Q9H3N8 1/20 0.38
CYP2A6 P11509 1/20 0.36
CNR1 P21554 1/20 0.36

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 SCHEMBL3001559 1.00 TDP1 (0.41) TDP1LMNAKDM4EMAPTBLM
SCHEMBL946729 0.98
SCHEMBL2171709 0.86 CHRM5 (0.37) LMNAKDM4EMAPTBLMPMP22
SCHEMBL10425365 0.84 CHRM5 (0.43) LMNAKDM4EMAPTBLMPMP22
N-Methylhistamine SCHEMBL25277752 0.82 CYP2C9 (0.70) TDP1CYP2C9CYP2C19TSHRMTOR
SCHEMBL240920 0.80
SCHEMBL4300091 0.78
Hydrochloric Acid SCHEMBL26696161 0.78 TBXAS1 (0.42) LMNAKDM4EMAPTBLMPMP22
SCHEMBL11372674 0.77 L3MBTL1 (0.39) LMNAKDM4EMAPTBLMPMP22
SCHEMBL9597203 0.77

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 14 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112707867-B Novel method for synthesizing 2- (1-methylimidazol-5-yl) ethylamine hydrochloride 苏州莱克施德药业有限公司 2022-03-15 CN claimed
CN-112707867-A Novel method for synthesizing 2- (1-methylimidazol-5-yl) ethylamine hydrochloride 苏州莱克施德药业有限公司 2021-04-27 CN claimed
CN-112707867-B Novel method for synthesizing 2- (1-methylimidazol-5-yl) ethylamine hydrochloride 苏州莱克施德药业有限公司 2022-03-15 CN disclosed
CN-112707867-B Novel method for synthesizing 2- (1-methylimidazol-5-yl) ethylamine hydrochloride 苏州莱克施德药业有限公司 2022-03-15 CN disclosed
CN-112707867-B Novel method for synthesizing 2- (1-methylimidazol-5-yl) ethylamine hydrochloride 苏州莱克施德药业有限公司 2022-03-15 CN disclosed
CN-112707867-A Novel method for synthesizing 2- (1-methylimidazol-5-yl) ethylamine hydrochloride 苏州莱克施德药业有限公司 2021-04-27 CN disclosed
CN-112707867-A Novel method for synthesizing 2- (1-methylimidazol-5-yl) ethylamine hydrochloride 苏州莱克施德药业有限公司 2021-04-27 CN disclosed
CN-112707867-A Novel method for synthesizing 2- (1-methylimidazol-5-yl) ethylamine hydrochloride 苏州莱克施德药业有限公司 2021-04-27 CN disclosed
CN-1326850-C Tricyclic farnesyl protein transferase inhibitors SCHERING CORP (US) 2007-07-18 CN disclosed
US-6740661-B2 TRICYCLIC IMINE CONTAINING COMPOUNDS HAVING IMIDAZOLE SUBSTITUENT; ANTITUMOR AGENTS SCHERING CORPORATION 2004-05-25 US disclosed
US-6372747-B1 ENZYME INHIBITORS AND ANTICARCINOGENIC AGENTS SCHERING CORPORATION 2002-04-16 US disclosed
CN-1334811-A Tricyclic farnesyl protein transferase inhibitors SCHERING CORP (US) 2002-02-06 CN disclosed
EP-1140902-A1 TRICYCLIC FARNESYL PROTEIN TRANSFERASE INHIBITORS SCHERING CORPORATION (US) 2001-10-10 EP disclosed
WO-2000037459-A1 TRICYCLIC FARNESYL PROTEIN TRANSFERASE INHIBITORS SCHERING CORPORATION (US) 2000-06-29 WO disclosed