Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5115776

CNCCc1ccc(O)cc1.Cl

nearest known ligand 0.95

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
SIGMAR1 known ✓ Q99720 2/20 0.95
ESR1 known ✓ P03372 2/20 0.56
ESR2 known ✓ Q92731 2/20 0.56
SLC6A2 known ✓ P23975 2/20 0.51
SLC6A4 known ✓ P31645 2/20 0.51
OPRM1 known ✓ P35372 2/20 0.51
ADRB3 known ✓ P13945 1/20 0.51
CA2 known ✓ P00918 1/20 0.50
ADRB2 known ✓ P07550 2/20 0.49
ADRB1 known ✓ P08588 1/20 0.49
ADRA1A known ✓ P35348 1/20 0.49
OPRK1 known ✓ P41145 1/20 0.49
SLC6A3 known ✓ Q01959 1/20 0.49
TMEM97 Q5BJF2 2/20 0.95
LMNA P02545 3/20 0.62
MAPT P10636 2/20 0.62
KDM4E B2RXH2 2/20 0.62
BLM P54132 2/20 0.62
GMNN O75496 1/20 0.62
ALDH1A1 P00352 1/20 0.62

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 SCHEMBL27960798 0.98 TMEM97 (0.91) TMEM97SIGMAR1LMNAMAPTKDM4E
SCHEMBL274906 0.98 TMEM97 (1.00) TMEM97SIGMAR1LMNAMAPTKDM4E
Bromide SCHEMBL6337077 0.95 TMEM97 (0.95) TMEM97SIGMAR1LMNAMAPTKDM4E
SCHEMBL11539730 0.95 TMEM97 (0.95) TMEM97SIGMAR1LMNAMAPTKDM4E
Hydrochloric Acid SCHEMBL28659483 0.93 TMEM97 (0.91) TMEM97SIGMAR1LMNAMAPTKDM4E
Nitrous Acid SCHEMBL18329343 0.88 TMEM97 (0.81) TMEM97SIGMAR1LMNAMAPTKDM4E
Tyramine SCHEMBL27589422 0.88 TMEM97 (0.81) TMEM97SIGMAR1LMNAMAPTKDM4E
SCHEMBL579569 0.86 TMEM97 (0.78) TMEM97SIGMAR1LMNAMAPTKDM4E
SCHEMBL10156581 0.85 TAAR1 (0.76) TMEM97SIGMAR1LMNAMAPTKDM4E
Nitric Acid SCHEMBL18329335 0.85 TMEM97 (0.75) TMEM97SIGMAR1LMNAMAPTKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260130363-A1 PEST ANT BAIT COMPOSITIONS AND METHODS THE US SECRETARY OF AGRICULTURE (US) 2026-05-14 US claimed
CN-114853619-B Preparation method of N-methyltyramine hydrochloride suitable for industrial production 神隆医药(常熟)有限公司 2024-05-10 CN claimed
CN-114853619-A Preparation method of N-methyltyramine hydrochloride suitable for industrial production 神隆医药(常熟)有限公司 2022-08-05 CN claimed
CN-113683522-A Preparation method of N-methyltyramine hydrochloride 广汉市派瑞林科技有限责任公司 2021-11-23 CN claimed
CN-106977411-B Synthetic method of N-methyltyramine hydrochloride 苏州永健生物医药有限公司 2020-01-03 CN claimed
CN-106977411-A A kind of synthetic method of N methyltyramines hydrochloride 苏州永健生物医药有限公司 2017-07-25 CN claimed
CN-103755576-A Synthesis method of N-methyl tyramine hydrochloride SHANGHAI XUXIN CHEMICAL CO LTD 2014-04-30 CN claimed
US-20260130363-A1 PEST ANT BAIT COMPOSITIONS AND METHODS THE US SECRETARY OF AGRICULTURE (US) 2026-05-14 US disclosed
EP-3814356-B1 TRIAZOLOTRIAZINE DERIVATIVES AS A2A RECEPTOR ANTAGONISTS ZHEJIANG VIMGREEN PHARMACEUTICALS LTD (CN) 2026-03-11 EP disclosed
CN-120584960-A Application of N-methyltyramine hydrochloride in feed for breeding animals and feed 湖北从力生物科技有限公司 2025-09-05 CN disclosed
CN-120584960-A Application of N-methyltyramine hydrochloride in feed for breeding animals and feed 湖北从力生物科技有限公司 2025-09-05 CN disclosed
US-20250186600-A1 EXCIPIENT COMPOUNDS FOR PROTEIN FORMULATIONS COMERA LIFE SCIENCES, INC. 2025-06-12 US disclosed
CN-114853619-B Preparation method of N-methyltyramine hydrochloride suitable for industrial production 神隆医药(常熟)有限公司 2024-05-10 CN disclosed
US-6794404-B2 BENZIMIDAZOLE DERIVATIVES BOEHRINGER INGELHEIM (CANADA) LTD. (CA) 2004-09-21 US disclosed
US-20030232816-A1 Viral polymerase inhibitors BOEHRINGER INGELHEIM (CANADA) LTD. (CA) 2003-12-18 US disclosed
EP-1301487-A2 VIRAL POLYMERASE INHIBITORS BOEHRINGER INGELHEIM (CANADA) LTD. (CA) 2003-04-16 EP disclosed
US-6479508-B1 INHIBITOR OF RNA DEPENDENT RNA POLYMERASE ACTIVITY OF THE ENZYME NS5B ENCODED BY HEPATITIS C VIRUS FOR TREATMENT AND PREVENTION OF HEPATITIS C INFECTIONS BOEHRINGER INGELHEIM (CANADA) LTD. (CA) 2002-11-12 US disclosed
US-6448281-B1 INHIBITORS OF HEPATITIS C VIRUS REPLICATION; TREATMENT OF HEPATITIS C BOEHRINGER INGELHEIM (CANADA) LTD. (CA) 2002-09-10 US disclosed
US-20020065418-A1 Inhibitors of hepatitis C virus replication; treatment of hepatitis C BOEHRINGER INGELHEIM (CANADA) LTD. (CA) 2002-05-30 US disclosed
WO-2002004425-A2 VIRAL POLYMERASE INHIBITORS BOEHRINGER INGELHEIM (CANADA) LTD. (CA) 2002-01-17 WO 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 (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-20030232816-A1 Viral polymerase inhibitors POLR2H, POLR2E, POLM SIGMAR1 562/4885ESR1 4136/4885ESR2 4459/4885
US-20020065418-A1 Inhibitors of hepatitis C virus replication; treatment of hepatitis C HAVCR2, HCCS, ZC3HAV1 SIGMAR1 266/4885ESR1 4160/4885ESR2 3750/4885
US-20260130363-A1 PEST ANT BAIT COMPOSITIONS AND METHODS AMY1A, STOM, PTMS SIGMAR1 1365/4885ESR1 4351/4885ESR2 4325/4885

“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.