Hydrochloric Acid

Hydrochloric Acid

SCHEMBL8524580

CC1(C)CCCCC(=O)NC1=O.Cl.Cl

nearest known ligand 0.44

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
CRBN known ✓ Q96SW2 6/20 0.44
CYP19A1 known ✓ P11511 5/20 0.31
PDE4D known ✓ Q08499 1/20 0.31
PDE3A known ✓ Q14432 1/20 0.31
FKBP5 Q13451 1/20 0.34
TSHR P16473 2/20 0.34
MEN1 O00255 2/20 0.34
KMT2A Q03164 2/20 0.34
CYP2C19 P33261 1/20 0.34
RAB9A P51151 1/20 0.34
NPSR1 Q6W5P4 1/20 0.33
ALDH1A1 P00352 1/20 0.32
CYP3A4 P08684 2/20 0.31
OR51E2 Q9H255 1/20 0.31
CYP17A1 P05093 1/20 0.31
CYP11A1 P05108 1/20 0.31
TBXAS1 P24557 1/20 0.31
PMP22 Q01453 1/20 0.31
NFKB1 P19838 1/20 0.31
MAPT P10636 1/20 0.31

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 SCHEMBL28637906 1.00 CRBN (0.44) CRBNFKBP5TSHRMEN1KMT2A
Hydrochloric Acid SCHEMBL29738347 0.98 CRBN (0.42) CRBNFKBP5TSHRMEN1KMT2A
SCHEMBL28494495 0.98 CRBN (0.46) CRBNFKBP5TSHRMEN1KMT2A
SCHEMBL229754 0.96 CRBN (0.44) CRBNFKBP5TSHRMEN1KMT2A
Hydrochloric Acid SCHEMBL28883297 0.93 CRBN (0.46) CRBNTSHRMEN1KMT2ACYP2C19
Hydrochloric Acid SCHEMBL27658561 0.93 CRBN (0.46) CRBNTSHRMEN1KMT2ACYP2C19
SCHEMBL20204795 0.91 CRBN (0.48) CRBNFKBP5TSHRMEN1KMT2A
SCHEMBL83187 0.81 CRBN (0.44) CRBNTSHRNPSR1CYP19A1CYP3A4
SCHEMBL5435030 0.73 CRBN (0.48) CRBNFKBP5TSHRMEN1KMT2A
SCHEMBL9576585 0.73 CRBN (0.48) CRBNFKBP5TSHRMEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5891676-A Synthesis and immunogenicity of rotavirus genes using a baculovirus expression system BAYLOR COLLEGE OF MEDICINE (US) 1999-04-06 US disclosed
US-5843733-A Synthesis and immunogenicity of rotavirus genes using a baculovirus expression system BAYLOR COLLEGE OF MEDICINE (US) 1998-12-01 US disclosed
US-5840541-A RECOMBINANT MOLECULE COMPRISING THE POLYHEDRIN GENE PROMOTER OF BACULOVIRUS AND A STRUCTURAL GENE OF A ROTOVIRUS; BIOSYNTHESIS OF ANTIGENIC PROTEIN NS28; USE IN VACCINES, VIRAL DETECTION BAYLOR COLLEGE OF MEDICINE (US) 1998-11-24 US disclosed
US-5827696-A Synthesis and immunogenicity of rotavirus genes using a baculovirus expression system BAYLOR COLLEGE OF MEDICINE (US) 1998-10-27 US disclosed
EP-0273366-B1 The synthesis and immunogenicity of rotavirus genes using a baculovirus expression system BAYLOR COLLEGE MEDICINE (US) 1995-02-22 EP disclosed
US-5186933-A SYNTHESIS AND IMMUNOGENICITY OF ROTAVIRUS GENES USING A BACULOVIRUS EXPRESSION SYSTEM BAYLOR COLLEGE OF MEDICINE (US) 1993-02-16 US disclosed
EP-0273366-A1 The synthesis and immunogenicity of rotavirus genes using a baculovirus expression system BAYLOR COLLEGE OF MEDICINE (US) 1988-07-06 EP disclosed