Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2550273

Cl.Nc1cc(O)ccc1O

nearest known ligand 0.54

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
CA2 known ✓ P00918 5/20 0.54
GAA known ✓ P10253 7/20 0.52
HSP90AA1 known ✓ P07900 1/20 0.48
MAOB known ✓ P27338 1/20 0.41
PTGS2 known ✓ P35354 1/20 0.41
ALDH1A1 P00352 12/20 0.54
HSD17B10 Q99714 8/20 0.54
ALOX15 P16050 7/20 0.54
CA12 O43570 5/20 0.54
CA9 Q16790 5/20 0.54
CA14 Q9ULX7 5/20 0.54
CA1 P00915 4/20 0.54
ALOX12 P18054 3/20 0.54
HPGD P15428 3/20 0.54
CA7 P43166 3/20 0.54
SMN1; SMN2 Q16637 2/20 0.54
MAPK1 P28482 1/20 0.54
MAPT P10636 4/20 0.52
MEN1 O00255 3/20 0.52
KMT2A Q03164 3/20 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
Hydrochloric Acid SCHEMBL31310809 1.00 ALDH1A1 (0.54) ALDH1A1HSD17B10ALOX15CA12CA2
SCHEMBL64970 0.97
Bromide SCHEMBL11510703 0.94 ALDH1A1 (0.54) ALDH1A1HSD17B10ALOX15CA12CA2
Water SCHEMBL11319775 0.94 ALDH1A1 (0.54) ALDH1A1HSD17B10ALOX15CA12CA2
SCHEMBL28599140 0.87 ALDH1A1 (0.48) ALDH1A1HSD17B10ALOX15CA12CA2
Methoxymethane SCHEMBL9478417 0.87 ALDH1A1 (0.57) ALDH1A1HSD17B10ALOX15CA12CA2
SCHEMBL10481889 0.85 ALDH1A1 (0.52) ALDH1A1HSD17B10ALOX15CA12CA2
Ether SCHEMBL9342203 0.80 ALDH1A1 (0.47) ALDH1A1HSD17B10ALOX15CA12CA2
SCHEMBL9763212 0.80 ALDH1A1 (0.69) ALDH1A1HSD17B10ALOX15CA12CA2
Hydrochloric Acid SCHEMBL10954400 0.80 CA14 (0.56) ALDH1A1HSD17B10ALOX15CA12CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119125117-A Nitric oxide detection kit with good stability and preparation method thereof 安徽伊普诺康生物技术股份有限公司 2024-12-13 CN claimed
CN-119125117-A Nitric oxide detection kit with good stability and preparation method thereof 安徽伊普诺康生物技术股份有限公司 2024-12-13 CN disclosed
CN-119125117-A Nitric oxide detection kit with good stability and preparation method thereof 安徽伊普诺康生物技术股份有限公司 2024-12-13 CN disclosed
US-12083108-B2 Compounds for targeting mutant huntingtin protein and uses thereof CHDI FOUNDATION, INC. (US) 2024-09-10 US disclosed
CN-112625442-B Cyanate resin composition, prepreg, laminate and printed circuit board 广东盈骅新材料科技有限公司 2023-08-22 CN disclosed
US-20220409600-A1 COMPOUNDS FOR TARGETING MUTANT HUNTINGTIN PROTEIN AND USES THEREOF CHDI FOUNDATION, INC. 2022-12-29 US disclosed
US-11389438-B2 Compounds for targeting mutant huntingtin protein and uses thereof CHDI FOUNDATION, INC. (US) 2022-07-19 US disclosed
CN-112625442-A Cyanate ester resin composition, prepreg, laminate and printed wiring board 广东盈骅新材料科技有限公司 2021-04-09 CN disclosed
US-20200276176-A1 COMPOUNDS FOR TARGETING MUTANT HUNTINGTIN PROTEIN AND USES THEREOF CHDI FOUNDATION, INC. 2020-09-03 US disclosed
CN-110198700-A Compositions comprising resorcinol or derivatives thereof 莱雅公司 2019-09-03 CN disclosed
EP-0124877-B1 COLOR PHOTOGRAPHIC LIGHT-SENSITIVE MATERIALS FUJI PHOTO FILM CO., LTD. (JP) 1988-04-13 EP disclosed
US-4732845-A COLORLESS PHENOLIC AMIDE FUJI PHOTO FILM CO., LTD. (JP) 1988-03-22 US disclosed
US-4584264-A POLYHYDROXYAROMATIC SULFONAMIDE AS STAIN INHIBITOR FUJI PHOTO FILM CO., LTD. (JP) 1986-04-22 US disclosed
US-4547452-A Color diffusion transfer photographic element with sufinic acid FUJI PHOTO FILM CO., LTD. (JP) 1985-10-15 US disclosed
US-4511643-A STYRENESULFINATE POLYMER FUJI PHOTO FILM CO., LTD. (JP) 1985-04-16 US disclosed
EP-0124877-A2 Color photographic light-sensitive materials FUJI PHOTO FILM CO., LTD. (JP) 1984-11-14 EP disclosed
US-4198239-A ACYLAMINO SUBSTITUTED HYDROQUINONES AGFA-GEVAERT, A.G. (DE) 1980-04-15 US disclosed
US-4124393-A PHOTOGRAPHY FUJI PHOTO FILM CO., LTD. (JP) 1978-11-07 US disclosed
US-4032349-A STAIN FREE, COLOR SEPARATIONS FUJI PHOTO FILM CO., LTD. (JA) 1977-06-28 US disclosed
US-3982946-A Bis-azo pyrazolone type dye developer and light-sensitive material FUJI PHOTO FILM CO., LTD. (JA) 1976-09-28 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 (4 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-12083108-B2 Compounds for targeting mutant huntingtin protein and uses thereof HTT, HYPK, UBQLN2 CA2 4736/4885GAA 197/4885HSP90AA1 87/4885
US-11389438-B2 Compounds for targeting mutant huntingtin protein and uses thereof HTT, HYPK, UBQLN2 CA2 4736/4885GAA 197/4885HSP90AA1 87/4885
US-20200276176-A1 COMPOUNDS FOR TARGETING MUTANT HUNTINGTIN PROTEIN AND USES THEREOF HTT, HYPK, UBQLN2 CA2 4736/4885GAA 197/4885HSP90AA1 87/4885
US-20220409600-A1 COMPOUNDS FOR TARGETING MUTANT HUNTINGTIN PROTEIN AND USES THEREOF HTT, HYPK, UBQLN2 CA2 4736/4885GAA 197/4885HSP90AA1 87/4885

“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.