Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4002124

COc1cc(CC(=O)O)cc(OC)c1OC.Cl

nearest known ligand 0.59

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 3/20 0.59
PTGS2 known ✓ P35354 1/20 0.53
HTR2C known ✓ P28335 2/20 0.48
HTR2A known ✓ P28223 1/20 0.48
HTR2B known ✓ P41595 1/20 0.48
HTR1A known ✓ P08908 1/20 0.47
ALDH1A1 P00352 3/20 0.59
TSHR P16473 2/20 0.59
NFKB1 P19838 1/20 0.59
TDP1 Q9NUW8 1/20 0.59
KMT2A Q03164 3/20 0.51
MEN1 O00255 1/20 0.51
CA5A P35218 1/20 0.51
KDM4E B2RXH2 2/20 0.51
HSD17B10 Q99714 2/20 0.50
ALOX15 P16050 1/20 0.50
POLB P06746 1/20 0.50
LMNA P02545 1/20 0.48
SMN1; SMN2 Q16637 1/20 0.48
HPGD P15428 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
SCHEMBL499116 0.98 GAA (0.61) GAAALDH1A1TSHRNFKB1TDP1
SCHEMBL11157934 0.87 GAA (0.54) GAAALDH1A1TSHRNFKB1TDP1
SCHEMBL8080316 0.87 GAA (0.63) GAAALDH1A1TSHRNFKB1TDP1
SCHEMBL6195246 0.85 GAA (0.49) GAAALDH1A1TSHRNFKB1TDP1
SCHEMBL19532894 0.85 GAA (0.56) GAAALDH1A1TSHRNFKB1TDP1
SCHEMBL7046945 0.84 PTGS2 (0.57) GAAALDH1A1PTGS2KMT2AMEN1
SCHEMBL8930355 0.83 CA5A (0.55) GAAALDH1A1TSHRNFKB1TDP1
SCHEMBL9341764 0.83 KMT2A (0.54) GAAALDH1A1PTGS2KMT2AMEN1
SCHEMBL1572690 0.83 GAA (0.47) GAAALDH1A1TSHRNFKB1TDP1
SCHEMBL2307800 0.82 PTGS2 (0.55) GAAALDH1A1PTGS2KMT2AMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7517911-B2 3,4,5-trimethoxy phenyl-based ester compound and preparation method thereof and whitening cosmetic composition containing the same AMOREPACIFIC CORPORATION (KR) 2009-04-14 US disclosed
EP-1430016-B1 3,4,5-TRIMETHOXY PHENYL-BASED ESTER COMPOUND AND PREPARATION METHOD THEREOF AND WHITENING COSMETIC COMPOSITION CONTAINING THE SAME AMOREPACIFIC CORP (KR) 2008-12-17 EP disclosed
US-20060167093-A1 3,4,5-Trimethoxy phenyl-based ester compound and preparation method thereof and whitening cosmetic composition containing the same AMOREPACIFIC CORPORATION (KR) 2006-07-27 US disclosed
EP-1430016-A4 3,4,5-TRIMETHOXY PHENYL-BASED ESTER COMPOUND AND PREPARATION METHOD THEREOF AND WHITENING COSMETIC COMPOSITION CONTAINING THE SAME AMOREPACIFIC CORP (KR) 2006-01-11 EP disclosed
EP-1430016-A1 3,4,5-TRIMETHOXY PHENYL-BASED ESTER COMPOUND AND PREPARATION METHOD THEREOF AND WHITENING COSMETIC COMPOSITION CONTAINING THE SAME Amorepacific Corporation (KR) 2004-06-23 EP disclosed
WO-2003027055-A1 3,4,5-TRIMETHOXY PHENYL-BASED ESTER COMPOUND AND PREPARATION METHOD THEREOF AND WHITENING COSMETIC COMPOSITION CONTAINING THE SAME AMOREPACIFIC CORPORATION (KR) 2003-04-03 WO disclosed
US-4139620-A HYPOTENSIVE AGENTS A. H. ROBINS COMPANY, INC. (US) 1979-02-13 US disclosed
US-4096331-A HYPOTENSIVE A. H. ROBINS COMPANY, INCORPORATED (US) 1978-06-20 US 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-20060167093-A1 3,4,5-Trimethoxy phenyl-based ester compound and preparation method thereof and whitening cosmetic composition containing the same TYR, TH, PAH GAA 485/4885PTGS2 2293/4885HTR2C 1426/4885

“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.