Hydrochloric Acid

Hydrochloric Acid

SCHEMBL33975

CC(O)Oc1ccc(N)cc1N.Cl

nearest known ligand 0.49

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 5/20 0.49
ALDH1A1 P00352 9/20 0.49
MAPT P10636 7/20 0.49
KDM4E B2RXH2 5/20 0.49
MEN1 O00255 4/20 0.49
KMT2A Q03164 4/20 0.49
CASP1 P29466 3/20 0.49
POLB P06746 3/20 0.49
USP2 O75604 3/20 0.49
HTT P42858 3/20 0.49
TP53 P04637 1/20 0.49
CASP7 P55210 1/20 0.49
ATM Q13315 1/20 0.49
THRB P10828 2/20 0.37
LMNA P02545 3/20 0.37
CYP2C19 P33261 1/20 0.36
CYP3A4 P08684 1/20 0.34
L3MBTL1 Q9Y468 1/20 0.34
ALOX5 P09917 1/20 0.34
BLM P54132 2/20 0.33

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
Hydrochloric Acid SCHEMBL1426463 1.00 ALDH1A1 (0.49) ALDH1A1MAPTGAAKDM4EMEN1
Hydrochloric Acid SCHEMBL3248993 1.00 ALDH1A1 (0.49) ALDH1A1MAPTGAAKDM4EMEN1
Hydrochloric Acid SCHEMBL10397659 1.00 ALDH1A1 (0.49) ALDH1A1MAPTGAAKDM4EMEN1
Hydrochloric Acid SCHEMBL29836005 1.00 ALDH1A1 (0.49) ALDH1A1MAPTGAAKDM4EMEN1
SCHEMBL129715 0.98 ALDH1A1 (0.46) ALDH1A1MAPTGAAKDM4EMEN1
Hydrochloric Acid SCHEMBL10897913 0.92 ALDH1A1 (0.42) ALDH1A1MAPTGAAKDM4EMEN1
SCHEMBL6946068 0.91 CASP1 (0.41) ALDH1A1MAPTGAAKDM4EMEN1
Hydrochloric Acid SCHEMBL18243321 0.90 ALDH1A1 (0.41) ALDH1A1MAPTGAAKDM4EMEN1
2,4-Diaminophenol SCHEMBL19327373 0.90 ALDH1A1 (0.44) ALDH1A1MAPTGAAKDM4EMEN1
SCHEMBL5870878 0.90 ALDH1A1 (0.40) ALDH1A1MAPTGAAKDM4EMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12396938-B2 Compositions and methods for coloring hair L'OREAL (FR) 2025-08-26 US claimed
US-12268769-B2 Hair coloring compositions L'OREAL (FR) 2025-04-08 US claimed
US-12257330-B2 Hair coloring compositions and methods of use L'OREAL (FR) 2025-03-25 US claimed
US-12109289-B2 Compositions for imparting color and tone to the hair L'OREAL (FR) 2024-10-08 US claimed
CN-117017809-B Dioxygen-free hair dye paste and preparation method thereof 珠海横琴一果投资合伙企业(有限合伙) 2024-07-19 CN claimed
CN-113677322-B Powder cosmetic containing ultraviolet wavelength conversion substance and its preparation method 株式会社资生堂 2024-07-12 CN claimed
EP-3697370-B1 HAIR COLORING COMPOSITION COMPRISING MICROCAPSULES FIRMENICH & CIE (CH) 2024-06-12 EP claimed
CN-117530891-B Hair dye with low irritation and preparation method thereof 佛山市喜妆化妆品有限公司 2024-05-24 CN claimed
US-20240148629-A1 HAIR COLORING COMPOSITIONS L'OREAL (FR) 2024-05-09 US claimed
CN-111417373-B Hair dyeing composition comprising microcapsules 弗门尼舍有限公司 2024-04-12 CN claimed
EP-1120105-B1 Process for the production of 1-(2,5-diaminophenyl)ethanol and use of this compound in oxidative hair dyeing P & G CLAIROL INC (US) 2005-07-27 EP claimed
US-20050039269-A1 Hair colouring compositions BOOTS COMPANY PLC, THE (GB) 2005-02-24 US claimed
CN-1190182-C Intermediates for use in oxidative hair coloring P & G KLEROL INC (US) 2005-02-23 CN claimed
US-6702863-B1 SINGLE PACKAGE AEROSOL CONPRISED OF 5,6-DIHYDROXYINDOLINE, LACCASE, WATER AND PROPELLANT; NONIRRITATING; STORAGE STABLE LION CORPORATION (JP) 2004-03-09 US claimed
CN-1404384-A Novel primary intermediates for use in oxidative hair dyeing P & G KLEROL INC (US) 2003-03-19 CN claimed
US-20020120989-A1 OXIDATION HAIR DYEING AGENT COMPOSITION DOW CORNING CORPORATION 2002-09-05 US claimed
US-6432145-B1 Oxidation hair dyeing agent composition DOW CORNING CORPORATION 2002-08-13 US claimed
US-6342079-B1 1-(2,5-DIPHENYL)ETHANOL FOR HAIR DYES BRISTOL-MYERS SQUIBB COMPANY 2002-01-29 US claimed
WO-2001054656-A1 NOVEL PRIMARY INTERMEDIATE FOR USE IN OXIDATIVE HAIR DYEING P&G-CLAIROL, INC. (US) 2001-08-02 WO claimed
EP-1120105-A2 1-(2,5-diaminophenyl)ethanol and its use in oxidative hair dyeing Bristol-Myers Squibb Company (US) 2001-08-01 EP 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-20240148629-A1 HAIR COLORING COMPOSITIONS PLIN5, GK, PLIN3 GAA 3647/4885ALDH1A1 227/4885MAPT 4097/4885
US-12268769-B2 Hair coloring compositions PLIN5, GK, PLIN3 GAA 3647/4885ALDH1A1 227/4885MAPT 4097/4885
US-12257330-B2 Hair coloring compositions and methods of use SGMS1, PHOSPHO1, SGMS2 GAA 4096/4885ALDH1A1 404/4885MAPT 3030/4885
US-12109289-B2 Compositions for imparting color and tone to the hair TYR, INMT, AADAT GAA 4773/4885ALDH1A1 1168/4885MAPT 596/4885

“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.