Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2404045

Cl.[N-]=[N+]=NS(=O)(=O)c1ccc(C(=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 20)

geneUniProtsupporting neighboursconfidence
CA2 known ✓ P00918 5/20 0.48
F2 P00734 3/20 0.54
PRSS1 P07477 3/20 0.54
PRSS2 P07478 3/20 0.54
PRSS3 P35030 3/20 0.54
CA1 P00915 4/20 0.48
CA12 O43570 4/20 0.48
CA9 Q16790 4/20 0.48
CA14 Q9ULX7 3/20 0.48
CYP2C19 P33261 2/20 0.48
CA3 P07451 1/20 0.48
CA6 P23280 1/20 0.48
CA5A P35218 1/20 0.48
CA7 P43166 1/20 0.48
CA5B Q9Y2D0 1/20 0.48
ALDH1A1 P00352 2/20 0.44
KMT2A Q03164 1/20 0.44
TSHR P16473 2/20 0.43
TP53 P04637 1/20 0.43
HSD17B10 Q99714 1/20 0.41

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
SCHEMBL968758 0.98 F2 (0.56) F2PRSS1PRSS2PRSS3CA2
SCHEMBL10609196 0.93 F2 (0.51) F2PRSS1PRSS2PRSS3CA2
SCHEMBL18087461 0.84 F2 (0.40) F2PRSS1PRSS2PRSS3CA2
SCHEMBL10823807 0.82 CA1 (0.43) F2PRSS1PRSS2PRSS3CA2
SCHEMBL2404043 0.82 ALDH1A1 (0.39) F2PRSS1PRSS2PRSS3CA2
SCHEMBL19887234 0.81 BCL2L1 (0.41) F2PRSS1PRSS2PRSS3CA2
SCHEMBL11668407 0.80 LCK (0.47) F2PRSS1PRSS2PRSS3CA2
SCHEMBL9241270 0.78 F2 (0.60) F2PRSS1PRSS2PRSS3CA2
SCHEMBL9645847 0.77 LMNA (0.46) F2PRSS1PRSS2PRSS3CA2
Ammonia Solution, Strong SCHEMBL11668387 0.77 F2 (0.59) F2PRSS1PRSS2PRSS3CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8853132-B2 Directed synthesis of oligophosphoramidate stereoisomers ROCHE DIAGNOSTICS OPERATIONS, INC. (US) 2014-10-07 US disclosed
US-20140045719-A1 DIRECTED SYNTHESIS OF OLIGOPHOSPHORAMIDATE STEREOISOMERS ROCHE DIAGNOSTICS OPERATIONS, INC. (US) 2014-02-13 US disclosed
US-8569515-B2 Directed synthesis of oligophosphoramidate stereoisomers ROCHE DIAGNOSTICS OPERATIONS, INC. (US) 2013-10-29 US disclosed
EP-2370450-A1 DIRECTED SYNTHESIS OF OLIGOPHOSPHORAMIDATE STEREOISOMERS Roche Diagnostics GmbH (DE) 2011-10-05 EP disclosed
US-20110212861-A1 DIRECTED SYNTHESIS OF OLIGOPHOSPHORAMIDATE STEREOISOMERS ROCHE DIAGNOSTICS GMBH (DE) 2011-09-01 US disclosed
WO-2010060599-A1 DIRECTED SYNTHESIS OF OLIGOPHOSPHORAMIDATE STEREOISOMERS ROCHE DIAGNOSTICS GMBH (DE) 2010-06-03 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-20140045719-A1 DIRECTED SYNTHESIS OF OLIGOPHOSPHORAMIDATE STEREOISOMERS TYMP, TK1, PFAS CA2 743/4885F2 2789/4885PRSS1 572/4885
US-20110212861-A1 DIRECTED SYNTHESIS OF OLIGOPHOSPHORAMIDATE STEREOISOMERS TYMP, TK1, PFAS CA2 743/4885F2 2789/4885PRSS1 572/4885

“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.