Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3279906

CC(N)Cc1ccccc1Cl.Cl

nearest known ligand 0.63

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
SLC6A2 known ✓ P23975 5/20 0.63
SLC6A3 known ✓ Q01959 4/20 0.63
SLC6A4 known ✓ P31645 3/20 0.63
MAOA known ✓ P21397 1/20 0.48
SIGMAR1 known ✓ Q99720 1/20 0.48
ADRB1 known ✓ P08588 1/20 0.44
HTR1A known ✓ P08908 1/20 0.44
ADRA2A known ✓ P08913 1/20 0.44
HTR1D known ✓ P28221 1/20 0.44
HTR1B known ✓ P28222 1/20 0.44
HTR2A known ✓ P28223 1/20 0.44
HTR2C known ✓ P28335 1/20 0.44
HTR1E known ✓ P28566 1/20 0.44
HTR7 known ✓ P34969 1/20 0.44
HTR2B known ✓ P41595 1/20 0.44
HTR6 known ✓ P50406 1/20 0.44
PNMT P11086 3/20 0.50
IDO1 P14902 3/20 0.48
TAAR1 Q96RJ0 3/20 0.48
CYP2A6 P11509 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 SCHEMBL30559556 1.00 SLC6A2 (0.63) SLC6A2SLC6A3SLC6A4PNMTIDO1
SCHEMBL13692527 0.98 SLC6A2 (0.66) SLC6A2SLC6A3SLC6A4PNMTIDO1
SCHEMBL268275 0.98 SLC6A2 (0.66) SLC6A2SLC6A3SLC6A4PNMTIDO1
SCHEMBL8029239 0.98 SLC6A2 (0.66) SLC6A2SLC6A3SLC6A4PNMTIDO1
Methane SCHEMBL20481902 0.96 SLC6A2 (0.63) SLC6A2SLC6A3SLC6A4PNMTIDO1
SCHEMBL2857779 0.82 SLC6A2 (0.61) SLC6A2SLC6A3SLC6A4TAAR1MAOA
SCHEMBL13692532 0.82 PNMT (0.57) SLC6A2SLC6A3SLC6A4PNMTIDO1
SCHEMBL3885817 0.82 PNMT (0.57) SLC6A2SLC6A3SLC6A4PNMTIDO1
SCHEMBL17407624 0.82 SLC6A2 (0.56) SLC6A2SLC6A3SLC6A4PNMTIDO1
Hydrochloric Acid SCHEMBL14660772 0.81 SLC6A2 (0.51) SLC6A2SLC6A3SLC6A4PNMTIDO1

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
EP-4122914-B1 COMPOUND AND METHOD FOR PREPARATION OF LISDEXAMFETAMINE SCI PHARMTECH INC (TW) 2023-08-16 EP disclosed
EP-4215517-A1 COMPOUND AND METHOD FOR PREPARATION OF LISDEXAMFETAMINE SCI Pharmtech Inc. (CN) 2023-07-26 EP disclosed
US-11608312-B1 Compound and method for preparation of lisdexamfetamine SCI PHARMTECH INC. (TW) 2023-03-21 US disclosed
US-20230084232-A1 COMPOUND AND METHOD FOR PREPARATION OF LISDEXAMFETAMINE SCI PHARMTECH INC. (TW) 2023-03-16 US disclosed
EP-4122914-A1 COMPOUND AND METHOD FOR PREPARATION OF LISDEXAMFETAMINE SCI Pharmtech Inc. (CN) 2023-01-25 EP disclosed
WO-2021074309-A1 1-(3-QUINOLYL)-3,4-DIHYDROISOQUINOLINE DERIVATIVES AS FUNGICIDES FOR COMBATING SPECIFIC PHYTOPATHOGENS SYNGENTA CROP PROTECTION AG (CH) 2021-04-22 WO disclosed
US-10544434-B2 Process for the preparation of lisdexamfetamine and related derivatives NORAMCO, INC. (US) 2020-01-28 US disclosed
WO-2017003721-A1 PROCESS FOR THE PREPARATION OF LISDEXAMFETAMINE AND RELATED DERIVATIVES NORAMCO, INC. (US) 2017-01-05 WO disclosed
US-20160376618-A1 PROCESS FOR THE PREPARATION OF LISDEXAMFETAMINE AND RELATED DERIVATIVES NORAMCO, LLC 2016-12-29 US disclosed
US-8614346-B2 Methods and compositions for preparation of amphetamine conjugates and salts thereof CAMBREX CHARLES CITY, INC. (US) 2013-12-24 US disclosed
US-20120190880-A1 METHODS AND COMPOSITIONS FOR PREPARATION OF AMPHETAMINE CONJUGATES AND SALTS THEREOF BLUE OWL CAPITAL CORPORATION, AS NEW AGENT 2012-07-26 US disclosed
WO-2010148305-A1 METHODS AND COMPOSITIONS FOR PREPARATION OF AMPHETAMINE CONJUGATES AND SALTS THEREOF CAMBREX CHARLES CITY, INC. (US) 2010-12-23 WO disclosed
US-7705184-B2 Method of making amphetamine CAMBREX CHARLES CITY, INC. (US) 2010-04-27 US disclosed
US-20090292143-A1 METHOD OF MAKING AMPHETAMINE CAMBREX CHARLES CITY (US) 2009-11-26 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 (6 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-20120190880-A1 METHODS AND COMPOSITIONS FOR PREPARATION OF AMPHETAMINE CONJUGATES AND SALTS THEREOF PNMT, COMT, DDT SLC6A2 25/4885SLC6A3 9/4885SLC6A4 101/4885
US-10544434-B2 Process for the preparation of lisdexamfetamine and related derivatives COMT, MGAM, GAA SLC6A2 14/4885SLC6A3 4/4885SLC6A4 9/4885
US-11608312-B1 Compound and method for preparation of lisdexamfetamine COMT, CYP2D6, SLC6A3 SLC6A2 11/4885SLC6A3 3/4885SLC6A4 54/4885
US-20160376618-A1 PROCESS FOR THE PREPARATION OF LISDEXAMFETAMINE AND RELATED DERIVATIVES COMT, MGAM, GAA SLC6A2 14/4885SLC6A3 4/4885SLC6A4 9/4885
US-20230084232-A1 COMPOUND AND METHOD FOR PREPARATION OF LISDEXAMFETAMINE COMT, CYP2D6, SLC6A3 SLC6A2 11/4885SLC6A3 3/4885SLC6A4 54/4885
US-20090292143-A1 METHOD OF MAKING AMPHETAMINE COMT, PNMT, CES2 SLC6A2 40/4885SLC6A3 7/4885SLC6A4 81/4885

“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.