Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5301741

CCNC(C)Cc1ccc2c(c1)OCO2.Cl

nearest known ligand 0.73

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
SLC6A4 known ✓ P31645 3/20 0.70
SLC6A2 known ✓ P23975 2/20 0.70
SLC6A3 known ✓ Q01959 2/20 0.70
ADRB2 known ✓ P07550 1/20 0.50
ADRB1 known ✓ P08588 1/20 0.50
ADRB3 known ✓ P13945 1/20 0.50
ADRA1D known ✓ P25100 1/20 0.50
ADRA1A known ✓ P35348 1/20 0.50
ADRA1B known ✓ P35368 1/20 0.50
GAA known ✓ P10253 1/20 0.48
TAAR1 Q96RJ0 3/20 0.70
CYP2D6 P10635 2/20 0.70
KDM4E B2RXH2 1/20 0.56
ALDH1A1 P00352 1/20 0.56
TSHR P16473 1/20 0.56
MEN1 O00255 1/20 0.53
KMT2A Q03164 1/20 0.53
CYP3A4 P08684 2/20 0.53
NPSR1 Q6W5P4 1/20 0.52
MAPT P10636 1/20 0.48

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 SCHEMBL30448521 1.00 TAAR1 (0.70) TAAR1SLC6A4SLC6A2SLC6A3CYP2D6
Hydrochloric Acid SCHEMBL35210364 1.00 TAAR1 (0.70) TAAR1SLC6A4SLC6A2SLC6A3CYP2D6
Hydrochloric Acid SCHEMBL25314458 1.00 TAAR1 (0.70) TAAR1SLC6A4SLC6A2SLC6A3CYP2D6
SCHEMBL29350327 0.98 TAAR1 (0.72) TAAR1SLC6A4SLC6A2SLC6A3CYP2D6
SCHEMBL30503037 0.98 TAAR1 (0.72) TAAR1SLC6A4SLC6A2SLC6A3CYP2D6
SCHEMBL30434262 0.98 TAAR1 (0.72) TAAR1SLC6A4SLC6A2SLC6A3CYP2D6
SCHEMBL715096 0.98 TAAR1 (0.72) TAAR1SLC6A4SLC6A2SLC6A3CYP2D6
SCHEMBL25188324 0.98 TAAR1 (0.72) TAAR1SLC6A4SLC6A2SLC6A3CYP2D6
SCHEMBL896903 0.98 TAAR1 (0.72) TAAR1SLC6A4SLC6A2SLC6A3CYP2D6
Hydrochloric Acid SCHEMBL25193660 0.88 SLC6A4 (0.55) TAAR1SLC6A4SLC6A2SLC6A3CYP2D6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12577222-B2 Phenethylamine compounds salts, polymorphic forms and methods of use thereof TERRAN BIOSCIENCES INC. (US) 2026-03-17 US disclosed
US-20240409526-A1 PHENETHYLAMINE COMPOUNDS SALTS, POLYMORPHIC FORMS AND METHODS OF USE THEREOF TERRAN BIOSCIENCES INC (US) 2024-12-12 US disclosed
US-20240327371-A1 PHENETHYLAMINE COMPOUNDS SALTS, POLYMORPHIC FORMS AND METHODS OF USE THEREOF TERRAN BIOSCIENCES INC. (US) 2024-10-03 US disclosed
EP-4433466-A2 PHENETHYLAMINE COMPOUNDS SALTS, POLYMORPHIC FORMS AND METHODS OF USE THEREOF Terran Biosciences Inc. (US) 2024-09-25 EP disclosed
US-11958821-B2 Phenethylamine compounds salts, polymorphic forms and methods of use thereof TERRAN BIOSCIENCES INC. (US) 2024-04-16 US disclosed
US-20230227422-A1 PHENETHYLAMINE COMPOUNDS SALTS, POLYMORPHIC FORMS AND METHODS OF USE THEREOF TERRAN BIOSCIENCES INC. 2023-07-20 US disclosed
WO-2023137446-A1 PRODRUGS OF 3,4-METHYLENEDIOXY- N-ETHYL-AMPHETAMINE (MDEA) AND USES THEREOF TERRAN BIOSCIENCES INC. (US) 2023-07-20 WO disclosed
US-20230202998-A1 PHENETHYLAMINE COMPOUNDS SALTS, POLYMORPHIC FORMS AND METHODS OF USE THEREOF TERRAN BIOSCIENCES INC (US) 2023-06-29 US disclosed
WO-2023092044-A2 PHENETHYLAMINE COMPOUNDS SALTS, POLYMORPHIC FORMS AND METHODS OF USE THEREOF TERRAN BIOSCIENCES, INC. (US) 2023-05-25 WO disclosed
EP-2875362-A1 TEST KIT FOR THE QUANTITATIVE DETERMINATION OF NARCOTIC DRUGS Chiron AS (NO) 2015-05-27 EP disclosed
US-20150025063-A1 Antiparkinsonian Action of Phenylisopropylamines UNIV DUKE (US) 2015-01-22 US disclosed
US-8877802-B2 Antiparkinsonian action of phenylisopropylamines Duke Univerity (US) 2014-11-04 US disclosed
WO-2014013063-A1 TEST KIT FOR THE QUANTITATIVE DETERMINATION OF NARCOTIC DRUGS CHIRON AS (NO) 2014-01-23 WO disclosed
EP-2687854-A1 Test kit for the quantitative determination of narcotic drugs Chiron AS (NO) 2014-01-22 EP disclosed
WO-2007016190-A2 ANTIPARKINSONIAN ACTION OF PHENYLISOPROPYLAMINES DUKE UNIVERSITY (US) 2007-02-08 WO disclosed
US-20070027208-A1 Antiparkinsonian Action of Phenylisopropylamines NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2007-02-01 US 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 (8 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-12577222-B2 Phenethylamine compounds salts, polymorphic forms and methods of use thereof DRD2, DRD1, DRD3 SLC6A4 59/4885SLC6A2 17/4885SLC6A3 5/4885
US-20240409526-A1 PHENETHYLAMINE COMPOUNDS SALTS, POLYMORPHIC FORMS AND METHODS OF USE THEREOF DRD2, DRD3, DRD1 SLC6A4 16/4885SLC6A2 11/4885SLC6A3 4/4885
US-20070027208-A1 Antiparkinsonian Action of Phenylisopropylamines PNMT, SNCA, COMT SLC6A4 178/4885SLC6A2 97/4885SLC6A3 36/4885
US-20150025063-A1 Antiparkinsonian Action of Phenylisopropylamines PNMT, SNCA, COMT SLC6A4 178/4885SLC6A2 97/4885SLC6A3 36/4885
US-20240327371-A1 PHENETHYLAMINE COMPOUNDS SALTS, POLYMORPHIC FORMS AND METHODS OF USE THEREOF DRD2, DRD3, DRD1 SLC6A4 16/4885SLC6A2 11/4885SLC6A3 4/4885
US-20230227422-A1 PHENETHYLAMINE COMPOUNDS SALTS, POLYMORPHIC FORMS AND METHODS OF USE THEREOF DRD2, DRD3, DRD1 SLC6A4 16/4885SLC6A2 11/4885SLC6A3 4/4885
US-20230202998-A1 PHENETHYLAMINE COMPOUNDS SALTS, POLYMORPHIC FORMS AND METHODS OF USE THEREOF DRD2, DRD3, DRD1 SLC6A4 16/4885SLC6A2 11/4885SLC6A3 4/4885
US-11958821-B2 Phenethylamine compounds salts, polymorphic forms and methods of use thereof DRD2, DRD3, DRD1 SLC6A4 16/4885SLC6A2 11/4885SLC6A3 4/4885

“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.