Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3280994

Cl.O=C(O)c1ccc(I)c(I)c1I

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
CA2 known ✓ P00918 2/20 0.37
GAA known ✓ P10253 1/20 0.34
ESR2 known ✓ Q92731 1/20 0.34
HDAC8 known ✓ Q9BY41 1/20 0.33
CYP1A2 P05177 1/20 0.46
ALDH1A1 P00352 5/20 0.40
ALOX15 P16050 1/20 0.40
TPMT P51580 2/20 0.39
SELL P14151 1/20 0.38
SELP P16109 1/20 0.38
TSHR P16473 2/20 0.37
CA12 O43570 2/20 0.37
CA1 P00915 2/20 0.37
CA7 P43166 2/20 0.37
CA9 Q16790 2/20 0.37
CA14 Q9ULX7 2/20 0.37
LDHA P00338 1/20 0.36
SMN1; SMN2 Q16637 2/20 0.35
CASP1 P29466 1/20 0.35
KDM4E B2RXH2 2/20 0.34

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
SCHEMBL625273 0.98 CYP1A2 (0.48) CYP1A2ALDH1A1ALOX15TPMTSELL
SCHEMBL28219462 0.98 CYP1A2 (0.48) CYP1A2ALDH1A1ALOX15TPMTSELL
SCHEMBL28485577 0.95 CYP1A2 (0.46) CYP1A2ALDH1A1ALOX15TPMTSELL
SCHEMBL7773866 0.95 CYP1A2 (0.46) CYP1A2ALDH1A1ALOX15TPMTSELL
SCHEMBL28219026 0.89 ALDH1A1 (0.41) CYP1A2ALDH1A1ALOX15TPMTSELL
SCHEMBL3808402 0.87 CYP1A2 (0.58) CYP1A2ALDH1A1ALOX15TPMTSELL
Hexane SCHEMBL28976286 0.84 PPARA (0.45) ALDH1A1TSHRCA12CA9KDM4E
Methacrylic Acid SCHEMBL28059140 0.84 CYP1A2 (0.37) CYP1A2ALDH1A1ALOX15TPMTSELL
2,3,5-Triiodobenzoic Acid SCHEMBL26604178 0.82 TPMT (0.39) CYP1A2ALDH1A1ALOX15TPMTTSHR
SCHEMBL8694537 0.80 CA12 (0.35) CYP1A2CA12CA1CA9TP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8574550-B2 Biocompatible polymeric contrast agents and radiopaque materials for medical services CORDIS CORPORATION 2013-11-05 US disclosed
US-20120252984-A1 BIOCOMPATIBLE POLYMERIC CONTRAST AGENTS AND RADIOPAQUE MATERIALS FOR MEDICAL SERVICES CORDIS CORPORATION (US) 2012-10-04 US disclosed
US-8197796-B2 organic high intensity X-ray contrast agents, dispersed within or conjugated biodegradable polymers, suitable for enhancing the imaging of medical devices, particularly polymeric medical devices and polymeric coatings CORDIS CORPORATION 2012-06-12 US disclosed
US-7704488-B2 Dendritic and star-shaped contrast agents for medical devices and bioabsorbable radiopaque bulk material and method for producing same CORDIS CORPORATION (US) 2010-04-27 US disclosed
EP-2005971-A1 Contrast agents for medical devices Cordis Corporation (US) 2008-12-24 EP disclosed
EP-2005972-A1 Contrast agents for medical devices Cordis Corporation (US) 2008-12-24 EP disclosed
US-20080275210-A1 BIOCOMPATIBLE POLYMERIC CONTRAST AGENTS AND RADIOPAQUE MATERIALS FOR MEDICAL DEVICES CORDIS US CORP 2008-11-06 US disclosed
US-20080177102-A1 DENDRITIC AND STAR-SHAPED CONTRAST AGENTS FOR MEDICAL DEVICES AND BIOABSORBABLE RADIOPAQUE BULK MATERIAL AND METHOD FOR PRODUCING SAME CORDIS US CORP 2008-07-24 US disclosed
US-20060292077-A1 Dendritic and star-shaped contrast agents for medical devices and bioabsorbable radiopaque bulk material and method for producing same CORDIS US CORP 2006-12-28 US disclosed
EP-1702628-A2 Contrast agents for medical devices Cordis Corporation (US) 2006-09-20 EP disclosed
WO-1999056787-A1 SELECTION OF CONTRAST AGENT FROM A COMBINATORIAL LIBRARY NYCOMED IMAGING AS (NO) 1999-11-11 WO disclosed
WO-1999056788-A1 SELECTION OF TARGETED CONTRAST AGENTS FROM A COMBINATORIAL LIBRARY NYCOMED IMAGING AS (NO) 1999-11-11 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 (3 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-20080177102-A1 DENDRITIC AND STAR-SHAPED CONTRAST AGENTS FOR MEDICAL DEVICES AND BIOABSORBABLE RADIOPAQUE BULK MATERIAL AND METHOD FOR PRODUCING SAME MSR1, MYD88, CD209 CA2 2402/4885GAA 2851/4885ESR2 3083/4885
US-20120252984-A1 BIOCOMPATIBLE POLYMERIC CONTRAST AGENTS AND RADIOPAQUE MATERIALS FOR MEDICAL SERVICES CD68, PBRM1, TLR9 CA2 2123/4885GAA 1983/4885ESR2 3927/4885
US-20080275210-A1 BIOCOMPATIBLE POLYMERIC CONTRAST AGENTS AND RADIOPAQUE MATERIALS FOR MEDICAL DEVICES CD68, TLR9, PBRM1 CA2 2385/4885GAA 2186/4885ESR2 3911/4885

“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.