Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1897057

Cl.N=C(N)NCCC[C@H](N)C(N)=O

nearest known ligand 0.41

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 18)

geneUniProtsupporting neighboursconfidence
DPP7 Q9UHL4 2/20 0.41
OTC P00480 1/20 0.40
NPY4R P50391 10/20 0.40
NPY1R P25929 6/20 0.40
NPY2R P49146 4/20 0.40
NPY5R Q15761 4/20 0.40
ALOX15 P16050 1/20 0.40
MEN1 O00255 1/20 0.39
CYP1A2 P05177 1/20 0.39
KMT2A Q03164 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
DDAH1 O94760 1/20 0.38
GNAI3 P08754 1/20 0.36
GNAO1 P09471 1/20 0.36
GNAI1 P63096 1/20 0.36
NOS3 P29474 1/20 0.35
NOS1 P29475 1/20 0.35
NOS2 P35228 1/20 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
Hydrochloric Acid SCHEMBL29400705 1.00 DPP7 (0.41) DPP7OTCNPY4RNPY1RNPY2R
Hydrochloric Acid SCHEMBL118624 1.00 DPP7 (0.41) DPP7OTCNPY4RNPY1RNPY2R
Hydrochloric Acid SCHEMBL7583819 1.00 DPP7 (0.41) DPP7OTCNPY4RNPY1RNPY2R
Hydrochloric Acid SCHEMBL14831575 1.00 DPP7 (0.41) DPP7OTCNPY4RNPY1RNPY2R
Hydrochloric Acid SCHEMBL123461 1.00 DPP7 (0.41) DPP7OTCNPY4RNPY1RNPY2R
Hydrochloric Acid SCHEMBL30600460 0.98 DPP7 (0.40) DPP7OTCNPY4RNPY1RNPY2R
SCHEMBL598710 0.98 DPP7 (0.42) DPP7OTCNPY4RNPY1RNPY2R
SCHEMBL304115 0.98 DPP7 (0.42) DPP7OTCNPY4RNPY1RNPY2R
SCHEMBL30256813 0.98 DPP7 (0.42) DPP7OTCNPY4RNPY1RNPY2R
SCHEMBL5158398 0.98 DPP7 (0.42) DPP7OTCNPY4RNPY1RNPY2R

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2002098824-A2 IMPROVEMENTS IN ENZYME STABILITY UNISEARCH LIMITED (AU) 2002-12-12 WO claimed
US-11512147-B2 Hyaluronic acid derivative modified with polyethylene glycol CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2022-11-29 US disclosed
EP-3712181-B1 HYALURONIC ACID DERIVATIVE MODIFIED WITH POLYETHYLENE GLYCOL CHUGAI PHARMACEUTICAL CO LTD (JP) 2022-10-26 EP disclosed
US-11389539-B2 Hyaluronic acid derivatives into which cationic and hydrophobic groups are introduced CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2022-07-19 US disclosed
US-20210371548-A1 HYALURONIC ACID DERIVATIVE MODIFIED WITH POLYETHYLENE GLYCOL CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2021-12-02 US disclosed
EP-3712181-A1 HYALURONIC ACID DERIVATIVE MODIFIED WITH POLY(ETHYLENE GLYCOL) Chugai Seiyaku Kabushiki Kaisha (JP) 2020-09-23 EP disclosed
US-20190142959-A1 HYALURONIC ACID DERIVATIVES INTO WHICH CATIONIC AND HYDROPHOBIC GROUPS ARE INTRODUCED CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2019-05-16 US disclosed
EP-3456745-A1 HYALURONIC ACID DERIVATIVE HAVING CATIONIC GROUP AND HYDROPHOBIC GROUP INTRODUCED THEREIN Chugai Seiyaku Kabushiki Kaisha (JP) 2019-03-20 EP disclosed
CN-104662011-B Treat the chroman derivative of mitochondrial disease 康尊知识产权公司 2017-09-29 CN disclosed
CN-104662011-A Chromanyl derivatives for treating mitochondrial disease KHONDRION B V 2015-05-27 CN disclosed
US-8389768-B2 Methods and compositions comprising novel cationic lipids THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) 2013-03-05 US disclosed
US-20110117141-A1 METHODS AND COMPOSITIONS COMPRISING NOVEL CATIONIC LIPIDS THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL 2011-05-19 US disclosed
CN-1279666-A NPY antagonists ASTRAZENECA AB (SE) 2001-01-10 CN disclosed
EP-0680469-A1 AMINOACID DERIVATES, MEDICAMENTS CONTAINING THESE COMPOUNDS AND PROCESS FOR PREPARING THE SAME Dr. Karl Thomae GmbH (DE) 1995-11-08 EP disclosed
WO-1994017035-A1 AMINOACID DERIVATES, MEDICAMENTS CONTAINING THESE COMPOUNDS AND PROCESS FOR PREPARING THE SAME DR. KARL THOMAE GMBH (DE) 1994-08-04 WO 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 (5 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-20110117141-A1 METHODS AND COMPOSITIONS COMPRISING NOVEL CATIONIC LIPIDS LIPA, SGMS1, SGMS2 DPP7 540/4885OTC 754/4885NPY4R 2769/4885
US-11389539-B2 Hyaluronic acid derivatives into which cationic and hydrophobic groups are introduced CD44, MUC1, FUT5 DPP7 2235/4885OTC 4121/4885NPY4R 2573/4885
US-20210371548-A1 HYALURONIC ACID DERIVATIVE MODIFIED WITH POLYETHYLENE GLYCOL CD44, F12, HPSE DPP7 2636/4885OTC 3904/4885NPY4R 2302/4885
US-11512147-B2 Hyaluronic acid derivative modified with polyethylene glycol CD44, F12, HPSE DPP7 2636/4885OTC 3904/4885NPY4R 2302/4885
US-20190142959-A1 HYALURONIC ACID DERIVATIVES INTO WHICH CATIONIC AND HYDROPHOBIC GROUPS ARE INTRODUCED CD44, MUC1, FUT5 DPP7 2235/4885OTC 4121/4885NPY4R 2573/4885

“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.