Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1980339

CN(C)c1ccccc1C(=O)O.Cl

nearest known ligand 0.69

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
GAA known ✓ P10253 2/20 0.69
CA2 known ✓ P00918 2/20 0.46
GLA known ✓ P06280 2/20 0.45
HDAC8 known ✓ Q9BY41 1/20 0.45
ALDH1A1 P00352 6/20 0.69
MAPT P10636 3/20 0.69
SMN1; SMN2 Q16637 2/20 0.69
TP53 P04637 1/20 0.69
TSHR P16473 1/20 0.69
ALOX15 P16050 1/20 0.54
CNR2 P34972 2/20 0.47
KDM4E B2RXH2 4/20 0.46
HPGD P15428 2/20 0.46
CA12 O43570 2/20 0.46
CA1 P00915 2/20 0.46
CA4 P22748 2/20 0.46
CA7 P43166 2/20 0.46
CA9 Q16790 2/20 0.46
HMGB1 P09429 1/20 0.46
CA6 P23280 1/20 0.46

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
SCHEMBL15240 0.98 ALDH1A1 (0.72) ALDH1A1MAPTSMN1; SMN2GAATP53
SCHEMBL4217683 0.96 ALDH1A1 (0.69) ALDH1A1MAPTSMN1; SMN2GAATP53
Water SCHEMBL11574791 0.96 ALDH1A1 (0.69) ALDH1A1MAPTSMN1; SMN2GAATP53
SCHEMBL6943684 0.96 ALDH1A1 (0.69) ALDH1A1MAPTSMN1; SMN2GAATP53
Phthalic Acid SCHEMBL25407447 0.96 ALDH1A1 (0.69) ALDH1A1MAPTSMN1; SMN2GAATP53
Ethylene SCHEMBL27419882 0.94 ALDH1A1 (0.67) ALDH1A1MAPTSMN1; SMN2GAATP53
Alcohol SCHEMBL19614806 0.90 ALDH1A1 (0.62) ALDH1A1MAPTSMN1; SMN2GAATP53
SCHEMBL27823469 0.88 ALDH1A1 (0.60) ALDH1A1MAPTSMN1; SMN2GAATP53
Anthranilic Acid SCHEMBL1866740 0.87 ALDH1A1 (0.58) ALDH1A1MAPTSMN1; SMN2GAATP53
Methacrylic Acid SCHEMBL22042325 0.87 ALDH1A1 (0.58) ALDH1A1MAPTSMN1; SMN2GAATP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8900796-B2 Acid generator, chemically amplified resist composition, and patterning process SHIN-ETSU CHEMICAL CO., LTD. (JP) 2014-12-02 US disclosed
EP-2634631-A1 Acid generator, chemically amplified resist composition, and patterning process Shin-Etsu Chemical Co., Ltd. (JP) 2013-09-04 EP disclosed
US-20130224657-A1 ACID GENERATOR, CHEMICALLY AMPLIFIED RESIST COMPOSITION, AND PATTERNING PROCESS SHIN-ETSU CHEMICAL CO., LTD. (JP) 2013-08-29 US disclosed
EP-2510041-A1 UV ABSORBING DENTRITIC POLYETHER PREPARED BY POLYMERIZATION OF OXETANES DSM IP Assets B.V. (NL) 2012-10-17 EP disclosed
EP-1637538-B1 CRYSTALLINE CARBAPENEM INTERMEDIATE MEIJI SEIKA PHARMA CO LTD (JP) 2011-08-10 EP disclosed
WO-2011070050-A1 UV ABSORBING DENTRITIC POLYETHER PREPARED BY POLYMERIZATION OF OXETANES DSM IP ASSETS B.V. (NL) 2011-06-16 WO disclosed
US-7482445-B2 Crystalline carbapenem intermediate MEIJI SEIKA KAISHA, LTD. (JP) 2009-01-27 US disclosed
US-20070167620-A1 Crystalline carbapenem intermediate MEIJI SEIKA KAISHA, LTD. (JP) 2007-07-19 US disclosed
EP-1637538-A1 CRYSTALLINE CARBAPENEM INTERMEDIATE MEIJI SEIKA KAISHA LTD. (JP) 2006-03-22 EP 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 (1 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-20070167620-A1 Crystalline carbapenem intermediate TBKBP1, RPS6KB1, TNKS1BP1 GAA 714/4885CA2 2569/4885GLA 1943/4885

“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.