Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3978581

CC(N)SSc1ccccn1.Cl

nearest known ligand 0.57

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
GAA known ✓ P10253 1/20 0.34
HRH1 known ✓ P35367 1/20 0.33
GRIN2D known ✓ O15399 1/20 0.33
GRIN3B known ✓ O60391 1/20 0.33
GRIN1 known ✓ Q05586 1/20 0.33
GRIN2A known ✓ Q12879 1/20 0.33
GRIN2B known ✓ Q13224 1/20 0.33
GRIN2C known ✓ Q14957 1/20 0.33
GRIN3A known ✓ Q8TCU5 1/20 0.33
EHMT2 Q96KQ7 1/20 0.57
EHMT1 Q9H9B1 1/20 0.57
APOBEC3G Q9HC16 1/20 0.57
L3MBTL1 Q9Y468 2/20 0.41
HPGD P15428 4/20 0.40
MEN1 O00255 2/20 0.40
KMT2A Q03164 2/20 0.40
TSHR P16473 1/20 0.40
SMN1; SMN2 Q16637 3/20 0.39
HSD17B10 Q99714 2/20 0.39
ALDH1A1 P00352 6/20 0.35

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
SCHEMBL1271372 0.98 EHMT2 (0.59) EHMT2EHMT1APOBEC3GL3MBTL1HPGD
SCHEMBL860540 0.86 EHMT2 (0.64) EHMT2EHMT1APOBEC3GL3MBTL1HPGD
SCHEMBL30195057 0.86 EHMT2 (0.64) EHMT2EHMT1APOBEC3GL3MBTL1HPGD
Hydrochloric Acid SCHEMBL17633942 0.81 EHMT2 (0.50) EHMT2EHMT1APOBEC3GL3MBTL1HPGD
Hydrochloric Acid SCHEMBL10706712 0.81 EHMT2 (0.50) EHMT2EHMT1APOBEC3GL3MBTL1HPGD
SCHEMBL29523202 0.80 EHMT2 (0.55) EHMT2EHMT1APOBEC3GL3MBTL1HPGD
SCHEMBL24599713 0.79 EHMT2 (0.59) EHMT2EHMT1APOBEC3GL3MBTL1HPGD
SCHEMBL15301017 0.79 EHMT2 (0.59) EHMT2EHMT1APOBEC3GL3MBTL1HPGD
SCHEMBL16486465 0.79 EHMT2 (0.59) EHMT2EHMT1APOBEC3GL3MBTL1HPGD
SCHEMBL803314 0.79 EHMT2 (0.59) EHMT2EHMT1APOBEC3GL3MBTL1HPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118139647-A Conjugates of glucagon and AMPK activators 哥本哈根大学 2024-06-04 CN disclosed
EP-1363933-B1 STEROL DERIVATIVES, LIPOSOMES COMPRISING STEROL DERIVATIVES AND METHOD FOR LOADING LIPOSOMES WITH ACTIVE SUBSTANCES NOVOSOM AG (DE) 2009-05-06 EP disclosed
US-20080113017-A1 STEROL DERIVATIVES, LIPOSOMES COMPRISING STEROL DERIVATIVES AND METHOD OF LOADING LIPOSOMES WITH ACTIVE SUBSTANCES NOVOSOM AG (DE) 2008-05-15 US disclosed
US-7312206-B2 Sterol derivatives, liposomes comprising sterol derivatives and method for loading liposomes with active substances NOVOSOM AG (DE) 2007-12-25 US disclosed
EP-1363933-A2 STEROL DERIVATIVES, LIPOSOMES COMPRISING STEROL DERIVATIVES AND METHOD FOR LOADING LIPOSOMES WITH ACTIVE SUBSTANCES Novosom AG (DE) 2003-11-26 EP disclosed
WO-2002066490-A2 CATIONIC STEROL DERIVATIVES, PH-SENSITIVE LIPOSOMES COMPRISING CATIONIC STEROL DERIVATIVES AND METHOD FOR LOADING LIPOSOMES WITH ACTIVE SUBSTANCES NOVOSOM AG (DE) 2002-08-29 WO disclosed
EP-0457250-B1 Novel bifunctional linking compounds, conjugates and methods for their production BRISTOL MYERS SQUIBB CO (US) 1999-07-14 EP disclosed
US-5349066-A Antibodies BRISTOL-MYERS SQUIBB COMPANY (US) 1994-09-20 US disclosed
US-5137877-A N-substituted hydrazine bifuctional derivative; cytotoxic reagent BRISTOL-MYERS SQUIBB (US) 1992-08-11 US disclosed
EP-0457250-A2 Novel bifunctional linking compounds, conjugates and methods for their production BRISTOL-MYERS SQUIBB COMPANY (US) 1991-11-21 EP disclosed