Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7190843

Cl.NNC(=O)CCOc1ccccc1

nearest known ligand 0.69

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
HDAC1 known ✓ Q13547 1/20 0.54
HDAC2 known ✓ Q92769 1/20 0.54
CYP1A2 P05177 3/20 0.65
CYP3A4 P08684 3/20 0.65
CYP2C19 P33261 3/20 0.65
CYP2C9 P11712 2/20 0.65
TSHR P16473 1/20 0.61
RECQL P46063 1/20 0.61
MMP3 P08254 1/20 0.57
RAB9A P51151 5/20 0.56
KMT2A Q03164 5/20 0.56
NPC1 O15118 4/20 0.56
MEN1 O00255 4/20 0.56
TP53 P04637 1/20 0.56
MAPT P10636 4/20 0.55
SMN1; SMN2 Q16637 2/20 0.55
CYP2D6 P10635 2/20 0.55
ALDH1A1 P00352 1/20 0.55
KDM4E B2RXH2 1/20 0.52
TDP1 Q9NUW8 1/20 0.52

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
SCHEMBL4412374 0.98 CYP1A2 (0.67) CYP1A2CYP3A4CYP2C19CYP2C9TSHR
Hydrochloric Acid SCHEMBL5639911 0.91 HDAC1 (0.61) CYP1A2CYP3A4CYP2C19CYP2C9TSHR
SCHEMBL3267877 0.89 HDAC1 (0.63) CYP1A2CYP3A4CYP2C19CYP2C9TSHR
SCHEMBL4411547 0.89 MMP3 (0.54) CYP1A2CYP3A4CYP2C19CYP2C9TSHR
SCHEMBL6189108 0.88 CYP1A2 (0.55) CYP1A2CYP3A4CYP2C19CYP2C9TSHR
Isophthalic Acid SCHEMBL17394551 0.86 SMN1; SMN2 (0.60) CYP1A2CYP3A4CYP2C19CYP2C9TSHR
SCHEMBL4411183 0.86 KDM4E (0.58) CYP1A2CYP3A4CYP2C19CYP2C9TSHR
SCHEMBL4412344 0.84 MMP3 (0.63) CYP1A2CYP3A4CYP2C19CYP2C9TSHR
SCHEMBL4412300 0.84 MMP3 (0.50) CYP1A2CYP3A4CYP2C19CYP2C9TSHR
Hydrochloric Acid SCHEMBL5452550 0.81 ALDH1A1 (0.71) RAB9AKMT2ANPC1MEN1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6586437-B2 Administering (S)-hydroxynefazodone or its salt for therapy of psychosis SEPRACOR INC. 2003-07-01 US disclosed
US-20030083338-A1 Compositions and methods for management of serotonin-mediated disorders SEPRACOR, INC. 2003-05-01 US disclosed
US-6469008-B2 THERAPY OF PSYCHOSIS IN A HUMAN COMPRISING ADMINISTERING (R)-HYDROXYNEFAZODONE OR A PHARMACEUTICALLY ACCEPTABLE SALT SEPRACOR INC. 2002-10-22 US disclosed
WO-2002069951-A2 COMPOSITION CONTAINING A NEFAZONOID SUCH AS NEFAZODONE AND A SEROTONIN-INHIBITOR SUCH AS FLUOXETINE SEPRACOR INC. (US) 2002-09-12 WO disclosed
US-20020077326-A1 Administering (S)-hydroxynefazodone or its salt for therapy of psychosis SEPRACOR INC. 2002-06-20 US disclosed
US-20020058675-A1 (R)-hydroxynefazodone antipsychotic therapy SEPRACOR INC. (US) 2002-05-16 US disclosed
EP-0568437-B1 Antidepressant 3-Halophenylpiperazinyl-propyl Derivatives of Substituted Triazolones and Triazoldiones BRISTOL MYERS SQUIBB CO (US) 2001-02-21 EP disclosed
EP-0568437-A1 Antidepressant 3-Halophenylpiperazinyl-propyl Derivatives of Substituted Triazolones and Triazoldiones Bristol-Myers Squibb Company (US) 1993-11-03 EP disclosed
US-5256664-A Antidepressant 3-halophenylpiperazinylpropyl derivatives of substituted triazolones and triazoldiones BRISTOL-MYERS SQUIBB COMPANY (US) 1993-10-26 US disclosed
US-4575555-A ANTIDEPRESSANTS MEAD JOHNSON & COMPANY (US) 1986-03-11 US disclosed
US-4487773-A ANTISEROTONINE AGENTS MEAD JOHNSON & COMPANY (US) 1984-12-11 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 (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-20020077326-A1 Administering (S)-hydroxynefazodone or its salt for therapy of psychosis SLC6A3, SLC6A2, SLC6A4 HDAC1 1029/4885HDAC2 1160/4885CYP1A2 1827/4885
US-20030083338-A1 Compositions and methods for management of serotonin-mediated disorders HTR5A, TPH1, HTR4 HDAC1 3504/4885HDAC2 3066/4885CYP1A2 305/4885
US-20020058675-A1 (R)-hydroxynefazodone antipsychotic therapy GABRE, GRIN2A, HTR3E HDAC1 1086/4885HDAC2 683/4885CYP1A2 1090/4885

“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.