Hydrochloric Acid

Hydrochloric Acid

SCHEMBL251996

Cl.OCCN1CCN=C1Cc1ccccc1

nearest known ligand 0.72

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
HTR1D known ✓ P28221 1/20 0.44
HTR1B known ✓ P28222 1/20 0.44
TOP2A known ✓ P11388 1/20 0.43
TOP2B known ✓ Q02880 1/20 0.43
DRD4 known ✓ P21917 1/20 0.43
ADRA2A known ✓ P08913 1/20 0.39
ADRA2B known ✓ P18089 1/20 0.39
ADRA2C known ✓ P18825 1/20 0.39
ADRA1D known ✓ P25100 1/20 0.39
ADRA1A known ✓ P35348 1/20 0.39
ADRA1B known ✓ P35368 1/20 0.39
CYP1A2 P05177 2/20 0.72
CYP2D6 P10635 2/20 0.72
TAAR1 Q96RJ0 2/20 0.41
TSHR P16473 2/20 0.39
LMNA P02545 1/20 0.39
KDM4E B2RXH2 1/20 0.36

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
SCHEMBL17965485 0.98 CYP1A2 (0.74) CYP1A2CYP2D6HTR1DHTR1BTOP2A
SCHEMBL13990186 0.84 CYP1A2 (1.00) CYP1A2CYP2D6HTR1DHTR1BDRD4
SCHEMBL11190221 0.83 CYP1A2 (0.74) CYP1A2CYP2D6HTR1DHTR1BDRD4
SCHEMBL10691316 0.81 CYP1A2 (0.82) CYP1A2CYP2D6HTR1DHTR1BDRD4
SCHEMBL11135471 0.80 CYP1A2 (0.71) CYP1A2CYP2D6HTR1DHTR1BDRD4
SCHEMBL23121057 0.80 CYP1A2 (0.70) CYP1A2CYP2D6HTR1DHTR1BDRD4
SCHEMBL10690989 0.78 CYP1A2 (0.67) CYP1A2CYP2D6HTR1DHTR1BDRD4
SCHEMBL2514598 0.75 CYP1A2 (0.63) CYP1A2CYP2D6HTR1DTAAR1TSHR
SCHEMBL28160686 0.74 CYP1A2 (0.58) CYP1A2CYP2D6HTR1DHTR1BDRD4
Hydrochloric Acid SCHEMBL7346644 0.74 HTR1D (0.52) CYP1A2CYP2D6HTR1DHTR1BDRD4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240058434-A1 NANOEMULSION UNIVERSAL INFLUENZA VACCINE BLUEWILLOW BIOLOGICS, INC. (US) 2024-02-22 US claimed
WO-2023133143-A1 INTRANASAL POLYSACCHARIDE CONJUGATE NANOEMULSION VACCINES AND METHODS OF USING THE SAME BLUEWILLOW BIOLOGICS, INC. (US) 2023-07-13 WO claimed
US-20200246449-A1 INTRAVENOUS IMMUNOGLOBULIN COMPOSITIONS SPECIFIC FOR RESPIRATORY SYNCYTIAL VIRUS AND METHODS OF MAKING AND USING THE SAME NANOBIO CORPORATION (US) 2020-08-06 US claimed
US-9492525-B2 Human respiratory syncytial virus vaccine NANOBIO CORPORATION (US) 2016-11-15 US claimed
EP-2729169-A1 HUMAN RESPIRATORY SYNCYTIAL VIRUS VACCINE Nanobio Corporation (US) 2014-05-14 EP claimed
EP-2545937-A1 Nanoemulsion vaccines THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2013-01-16 EP claimed
WO-2013006797-A1 HUMAN RESPIRATORY SYNCYTIAL VIRUS VACCINE NANOBIO CORPORATION (US) 2013-01-10 WO claimed
US-20130011443-A1 HUMAN RESPIRATORY SYNCYTIAL VIRUS VACCINE NANOBIO CORPORATION 2013-01-10 US claimed
US-20120276182-A1 METHODS OF TREATING FUNGAL, YEAST AND MOLD INFECTIONS NANOBIO CORPORATION 2012-11-01 US claimed
US-20120219602-A1 METHODS FOR TREATING HERPES VIRUS INFECTIONS NANOBIO CORPORATION 2012-08-30 US claimed
US-20090304799-A1 NANOEMULSION INFLUENZA VACCINE NANOBIO CORPORATION 2009-12-10 US claimed
US-20090269380-A1 METHODS OF TREATING FUNGAL, YEAST AND MOLD INFECTIONS NANOBIO CORPORATION 2009-10-29 US claimed
US-20090269394-A1 METHODS AND COMPOSITIONS FOR TREATING ONCHOMYCOSIS NANOBIO CORPORATION 2009-10-29 US claimed
WO-2009132342-A1 NANOEMULSIONS FOR TREATING FUNGAL, YEAST AND MOLD INFECTIONS NANOBIO CORPORATION (US) 2009-10-29 WO claimed
WO-2009132343-A1 NANOEMULSIONS FOR TREATING ONCHOMYCOSIS NANOBIO CORPORATION (US) 2009-10-29 WO claimed
WO-2009129470-A2 METHODS FOR TREATING HERPES VIRUS INFECTIONS NANOBIO CORPORATION (US) 2009-10-22 WO claimed
US-20090143476-A1 Antimicrobial Nanoemulsion Compositions and Methods REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2009-06-04 US claimed
US-20090143477-A1 Antimicrobial Nanoemulsion Compositions and Methods REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2009-06-04 US claimed
US-6559189-B2 For decontaminating areas, samples, solutions, and foodstuffs colonized or infected by pathogens and microorganisms REGENTS OF THE UNIVERSITY OF MICHIGAN 2003-05-06 US claimed
US-20020045667-A1 Non-toxic antimicrobial compositions and methods of use THE REGENTS OF THE UNIVERSITY OF MICHIGAN 2002-04-18 US claimed

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-20090269394-A1 METHODS AND COMPOSITIONS FOR TREATING ONCHOMYCOSIS DPM1, ERG28, POLR1C HTR1D 4779/4885HTR1B 4409/4885TOP2A 921/4885
US-20090269380-A1 METHODS OF TREATING FUNGAL, YEAST AND MOLD INFECTIONS DPM1, ERG28, CYP51A1 HTR1D 4701/4885HTR1B 4592/4885TOP2A 1902/4885
US-20120219602-A1 METHODS FOR TREATING HERPES VIRUS INFECTIONS STING1, IFNG, NGF HTR1D 4789/4885HTR1B 4478/4885TOP2A 720/4885
US-20120276182-A1 METHODS OF TREATING FUNGAL, YEAST AND MOLD INFECTIONS DPM1, ERG28, CYP51A1 HTR1D 4701/4885HTR1B 4592/4885TOP2A 1902/4885

“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.