Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1930429

Cl.NCCCC[C@H](NC(=O)OCc1ccccc1)C(=O)Oc1ccc([N+](=O)[O-])cc1

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 17)

geneUniProtsupporting neighboursconfidence
HDAC1 known ✓ Q13547 2/20 0.54
HDAC2 known ✓ Q92769 2/20 0.54
ITGB3 known ✓ P05106 4/20 0.52
ITGA2B known ✓ P08514 4/20 0.52
DPP4 known ✓ P27487 2/20 0.47
TGM2 P21980 1/20 0.52
SSTR3 P32745 1/20 0.49
PRSS1 P07477 2/20 0.49
PRSS2 P07478 2/20 0.49
PRSS3 P35030 2/20 0.49
TPSAB1 Q15661 2/20 0.49
CTSL P07711 4/20 0.48
TLR2 O60603 1/20 0.47
DPP8 Q6V1X1 1/20 0.47
SIRT2 Q8IXJ6 1/20 0.47
SIRT1 Q96EB6 1/20 0.47
SIRT3 Q9NTG7 1/20 0.47

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 SCHEMBL28627653 1.00 HDAC1 (0.54) HDAC1HDAC2TGM2ITGB3ITGA2B
SCHEMBL16494584 0.99 HDAC1 (0.55) HDAC1HDAC2TGM2ITGB3ITGA2B
SCHEMBL648254 0.99 HDAC1 (0.55) HDAC1HDAC2TGM2ITGB3ITGA2B
Hydrochloric Acid SCHEMBL23723888 0.97 HDAC1 (0.56) HDAC1HDAC2TGM2ITGB3ITGA2B
SCHEMBL8433172 0.90 HDAC1 (0.65) HDAC1HDAC2TGM2ITGB3ITGA2B
SCHEMBL12091750 0.88 TGM2 (0.57) HDAC1HDAC2TGM2CTSLSIRT2
SCHEMBL2028970 0.88 TGM2 (0.62) HDAC1HDAC2TGM2DPP8SIRT2
SCHEMBL17737201 0.88 ITGB3 (0.58) ITGB3ITGA2BPRSS1PRSS2PRSS3
SCHEMBL12874110 0.87 TGM2 (0.56) HDAC1HDAC2TGM2CTSLSIRT2
SCHEMBL11867081 0.86 CTSL (0.49) HDAC1HDAC2TGM2CTSL

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12168030-B2 Method for producing stable Actinidia deliciosa powder with high level bioactive actinidin enzyme WAITAKI BIOSCIENCES (NZ) 2024-12-17 US disclosed
EP-4099841-A1 METHOD FOR PRODUCING STABLE ACTINIDIA DELICIOSA POWDER WITH HIGH LEVEL BIOACTIVE ACTINIDIN ENZYME Waitaki Biosciences (NZ) 2022-12-14 EP disclosed
CN-109259106-B Method for improving mutton tenderness based on multiple fermentation 福建农林大学 2022-05-10 CN disclosed
CN-109259105-B Method for improving tenderness of duck meat based on multiple fermentation 福建农林大学 2021-09-28 CN disclosed
CN-109259108-B Method for improving beef tenderness based on multiple fermentation 福建农林大学 2021-09-28 CN disclosed
CN-109259110-B Method for improving goose tenderness based on multiple fermentation 福建农林大学 2021-09-24 CN disclosed
US-8506945-B2 Polymers with structure-defined functions SMITH & NEPHEW, PLC. (GB) 2013-08-13 US disclosed
US-20120225962-A1 MOLECULARLY IMPRINTED POLYMERS, METHODS FOR THEIR PRODUCTION AND USES THEREOF MONASH UNIVERSITY (AU) 2012-09-06 US disclosed
US-20110300096-A1 Polymers With Structure-Defined Functions GREENER BRYAN (GB) 2011-12-08 US disclosed
US-7955594-B2 Maleic anhydride-methyl vinyl ether copolymers; polyamic acids; medical implant device, dressing, scaffold, or fluid adhesive for treatment or prophylaxis of wounds; enhanced activity of protease inhibitors and neurotransmitter drugs SMITH & NEPHEW, PLC (GB) 2011-06-07 US disclosed
US-20050032929-A1 Polymers with structure-defined functions SMITH & NEPHEW, PLC (GB) 2005-02-10 US disclosed
EP-1436334-A1 POLYMERS WITH STRUCTURE-DEFINED FUNCTIONS Smith & Nephew PLC (GB) 2004-07-14 EP disclosed
WO-2003027154-A1 POLYMERS WITH STRUCTURE-DEFINED FUNCTIONS SMITH & NEPHEW PLC (GB) 2003-04-03 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-20120225962-A1 MOLECULARLY IMPRINTED POLYMERS, METHODS FOR THEIR PRODUCTION AND USES THEREOF MPI, IDE, NPEPPS HDAC1 1188/4885HDAC2 2050/4885ITGB3 2806/4885
US-20110300096-A1 Polymers With Structure-Defined Functions MMP1, MMP8, ADAM12 HDAC1 688/4885HDAC2 1207/4885ITGB3 332/4885

“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.