Hydrochloric Acid

Hydrochloric Acid

SCHEMBL19220

Cl.N#CCc1ccncc1

nearest known ligand 0.46

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
PIK3CA known ✓ P42336 1/20 0.39
HRH1 known ✓ P35367 2/20 0.35
HDAC8 known ✓ Q9BY41 1/20 0.34
TNF P01375 1/20 0.46
LOXL2 Q9Y4K0 2/20 0.44
ALDH1A1 P00352 1/20 0.42
CYP1A2 P05177 1/20 0.42
CYP3A4 P08684 1/20 0.42
CYP2D6 P10635 1/20 0.42
CYP2C9 P11712 1/20 0.42
CYP2C19 P33261 1/20 0.42
HSD17B10 Q99714 1/20 0.42
PIK3CG P48736 1/20 0.39
KMT2A Q03164 2/20 0.39
KDM4E B2RXH2 1/20 0.38
TDP1 Q9NUW8 1/20 0.38
SLC22A12 Q96S37 1/20 0.37
ENPP2 Q13822 1/20 0.35
LMNA P02545 1/20 0.35
MAPT P10636 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
SCHEMBL254403 0.97
Iodide SCHEMBL20524267 0.95 TNF (0.46) TNFLOXL2ALDH1A1CYP1A2CYP3A4
Iodomethane SCHEMBL28886765 0.91 TNF (0.44) TNFLOXL2ALDH1A1CYP1A2CYP3A4
SCHEMBL24067260 0.84 TNF (0.54) TNFCYP3A4PIK3CAPIK3CGKMT2A
Pyridine SCHEMBL637184 0.79 KMT2A (0.43) TNFALDH1A1CYP1A2CYP3A4CYP2D6
SCHEMBL2154504 0.78 KMT2A (0.47) TNFLOXL2CYP1A2KMT2AKDM4E
SCHEMBL13907293 0.76 LOXL2 (0.50) LOXL2ALDH1A1CYP1A2CYP3A4CYP2D6
Hydrochloric Acid SCHEMBL4699655 0.74 ENPP2 (0.47) LOXL2ALDH1A1CYP1A2CYP3A4KMT2A
Hydrochloric Acid SCHEMBL28747248 0.74 ENPP2 (0.47) LOXL2ALDH1A1CYP1A2CYP3A4KMT2A
SCHEMBL254617 0.73 MEN1 (0.52) LOXL2ALDH1A1CYP1A2CYP3A4CYP2D6

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 154 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115215841-B Pyridinium-coumarin derivative fluorescent probe and preparation method and application thereof 河南理工大学 2024-01-23 CN claimed
CN-117003781-A Coumarin derivative fluorescent probe and preparation method and application thereof 河南理工大学 2023-11-07 CN claimed
CN-114605318-B Perchlorate visual fluorescent probe molecule and preparation method thereof 中国科学院新疆理化技术研究所 2023-07-07 CN claimed
CN-115215841-A Pyridinium-coumarin derivative fluorescent probe and preparation method and application thereof 河南理工大学 2022-10-21 CN claimed
CN-111484447-B Bipyridyl ligand and preparation method thereof, ruthenium supermolecule self-assembly containing bipyridyl ligand and preparation method and application thereof 江苏师范大学 2022-09-02 CN claimed
CN-113773245-B Water-soluble double-targeting near-infrared fluorescent probe and preparation method thereof 西安交通大学口腔医院 2022-07-01 CN claimed
CN-114605318-A Perchlorate visual fluorescent probe molecule and preparation method thereof 中国科学院新疆理化技术研究所 2022-06-10 CN claimed
CN-113773245-A Water-soluble double-targeting near-infrared fluorescent probe and preparation method thereof 西安交通大学口腔医院 2021-12-10 CN claimed
CN-111484447-A Bipyridyl ligand and preparation method thereof, ruthenium supermolecule self-assembly containing bipyridyl ligand and preparation method and application thereof 江苏师范大学 2020-08-04 CN claimed
CN-107417598-B Fluorescent probe for detecting G-quadruplex DNAs (deoxyribonucleic acids) and preparation method thereof 山西大学 2020-04-17 CN claimed
CN-107501170-B A kind of adjustable aggregation-induced emission type fluorescent material of spectrum and its preparation method and application 陕西师范大学 2019-08-20 CN claimed
CN-107501170-A A kind of adjustable aggregation-induced emission type fluorescent material of spectrum and its preparation method and application 陕西师范大学 2017-12-22 CN claimed
CN-107417598-A Fluorescence probe available for the serobila DNAs of G tetra- detections and preparation method thereof 山西大学 2017-12-01 CN claimed
US-20250084087-A1 BICYCLIC HETEROCYCLES AS MRGPRX2 ANTAGONISTS INCYTE CORPORATION 2025-03-13 US disclosed
WO-2025042730-A1 BICYCLIC HETEROCYCLES AS MRGPRX2 ANTAGONISTS INCYTE CORPORATION (US) 2025-02-27 WO disclosed
US-20240208815-A1 PORPHYRAZINES AS EFFICIENT, CATALYTIC AND SCALABLE METHOD TO PRODUCE CHLORINE DIOXIDE THE TRUSTEES OF PRINCETON UNIVERSITY (US) 2024-06-27 US disclosed
US-5364860-A Naphthyridine compounds which inhibit tyrosine kinase and their pharmaceutical compositions LABORATOIRES UPSA (FR) 1994-11-15 US disclosed
EP-0527181-A4 HETEROCYCLICETHENEDIYL COMPOUNDS WHICH INHIBIT EGF RECEPTOR TYROSINE KINASE 1993-04-07 EP disclosed
EP-0527181-A1 HETEROCYCLICETHENEDIYL COMPOUNDS WHICH INHIBIT EGF RECEPTOR TYROSINE KINASE YISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM (IL) 1993-02-17 EP disclosed
WO-1991016305-A1 HETEROCYCLICETHENEDIYL COMPOUNDS WHICH INHIBIT EGF RECEPTOR TYROSINE KINASE RHONE-POULENC RORER INTERNATIONAL (HOLDINGS), INC. (US) 1991-10-31 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 (2 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-20250084087-A1 BICYCLIC HETEROCYCLES AS MRGPRX2 ANTAGONISTS MRGPRX2, MRGPRX1, MRGPRX4 PIK3CA 2862/4885HRH1 294/4885HDAC8 2182/4885
US-20240208815-A1 PORPHYRAZINES AS EFFICIENT, CATALYTIC AND SCALABLE METHOD TO PRODUCE CHLORINE DIOXIDE PPOX, FECH, CAT PIK3CA 3092/4885HRH1 2379/4885HDAC8 4468/4885

“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.