Hydrochloric Acid

Hydrochloric Acid

SCHEMBL8788681

CCC(CN1CCCC1)C(=O)c1cc(-c2ccccc2)no1.Cl

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
▸ CHRM2 known ✓ P08172 1/20 0.43
▸ CHRM1 known ✓ P11229 1/20 0.43
▸ DRD1 known ✓ P21728 1/20 0.43
▸ SLC6A2 known ✓ P23975 1/20 0.43
▸ ADRA1A known ✓ P35348 1/20 0.43
▸ OPRM1 known ✓ P35372 1/20 0.43
▸ DRD3 known ✓ P35462 1/20 0.43
▸ HRH3 known ✓ Q9Y5N1 1/20 0.43
▸ RAB9A P51151 2/20 0.46
▸ SMN1; SMN2 Q16637 2/20 0.46
▸ PTPN1 P18031 4/20 0.43
▸ CXCR1 P25024 1/20 0.41
▸ MEN1 O00255 3/20 0.41
▸ KMT2A Q03164 3/20 0.41
▸ MAPK1 P28482 1/20 0.41
▸ F2R P25116 1/20 0.41
▸ ALDH1A1 P00352 2/20 0.40
▸ MITF O75030 1/20 0.40
▸ HTT P42858 1/20 0.40
▸ GFER P55789 1/20 0.40

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
SCHEMBL8781882 0.99 RAB9A (0.47) RAB9ASMN1; SMN2CHRM2CHRM1DRD1
SCHEMBL9461390 0.98 RAB9A (0.46) RAB9ASMN1; SMN2CHRM2CHRM1DRD1
Hydrochloric Acid SCHEMBL8880074 0.90 SLC6A4 (0.47) RAB9ASMN1; SMN2CHRM2DRD3HRH3
SCHEMBL8881244 0.89 SLC6A4 (0.48) RAB9ASMN1; SMN2CHRM2DRD3HRH3
Hydrochloric Acid SCHEMBL8882119 0.85 ALDH1A1 (0.48) RAB9ASMN1; SMN2CHRM2CHRM1DRD1
Hydrochloric Acid SCHEMBL8880491 0.84 RAB9A (0.46) RAB9ASMN1; SMN2CHRM2CHRM1DRD1
Hydrochloric Acid SCHEMBL8881755 0.84 PTPN1 (0.47) RAB9ASMN1; SMN2CHRM2CHRM1DRD1
SCHEMBL8880003 0.84 CHRM2 (0.48) RAB9ASMN1; SMN2CHRM2CHRM1DRD1
SCHEMBL8880381 0.83 RAB9A (0.47) RAB9ASMN1; SMN2CHRM2CHRM1DRD1
SCHEMBL27529689 0.83 SMN1; SMN2 (0.49) RAB9ASMN1; SMN2PTPN1MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-8208571-A — — None — — JP disclosed
US-12364842-B2 Activator attachment for blood control catheters BECTON, DICKINSON AND COMPANY (US) 2025-07-22 — — US disclosed
US-20240314779-A1 METHOD BY WHICH TERMINAL TRANSMITS FEEDBACK SIGNAL IN WIRELESS COMMUNICATION SYSTEM, AND APPARATUS THEREFOR LG ELECTRONICS INC. (KR) 2024-09-19 — — US disclosed
US-20240228482-A1 COMPOUNDS, COMPOSITIONS AND METHODS OF TREATING CANCER HOTSPOT THERAPEUTICS, INC. 2024-07-11 — — US disclosed
CN-117751115-A Compounds, compositions, and methods of treating cancer 热点治疗公司 2024-03-22 — — CN disclosed
EP-4323358-A1 COMPOUNDS, COMPOSITIONS AND METHODS OF TREATING CANCER Hotspot Therapeutics, Inc. (US) 2024-02-21 — — EP disclosed
CN-113461640-B LPAR1 inhibitor, medical application and preparation method thereof 中央民族大学 2023-08-11 — — CN disclosed
EP-2763742-B1 PORT VALVE OF A BLOOD CONTROL CATHETER BECTON DICKINSON CO (US) 2022-11-30 — — EP disclosed
CN-112608316-B Pyrazolotriazine adenosine receptor antagonist 厦门宝太生物科技股份有限公司 2022-10-21 — — CN disclosed
WO-2022221704-A1 COMPOUNDS, COMPOSITIONS AND METHODS OF TREATING CANCER HOTSPOT THERAPEUTICS, INC. (US) 2022-10-20 — — WO disclosed
US-20220125427-A1 LOCKING NAIL FOR LOCKING SUTURES AND INTERVENTIONAL REMOTE SUTURE LOCKING DEVICE Hangzhou Valgen Medtech Co., Ltd. (CN) 2022-04-28 — — US disclosed
EP-0501713-B1 Optically active aminoketone derivative and method for preparing same MITSUI TOATSU CHEMICALS (JP) 1997-05-02 — — EP disclosed
US-5602160-A MUSCLE RELAXANT MITSUI TOATSU CHEMICALS INCORPORATED (JP) 1997-02-11 — — US disclosed
JP-H08208571-A RACEMIZATION OF AMINOKETONE DERIVATIVE MITSUI TOATSU CHEM INC 1996-08-13 — — JP disclosed
US-5498619-A MUSCLE RELAXANTS, POLLAKIUREA CURING AGENTS AND MUSCLE SPASMS MITSUI TOATSU CHEMICALS, INCORPORATED (JP) 1996-03-12 — — US disclosed
EP-0414391-B1 Aminoketone derivatives and use thereof MITSUI TOATSU CHEMICALS (JP) 1995-03-15 — — EP disclosed
US-5338857-A Muscle relaxant MITSUI TOATSU CHEMICALS INCORPORATED (JP) 1994-08-16 — — US disclosed
US-5304524-A Asymmetric hydrogenation of aromatic-substituted olefins using organoruthenium catalyst ETHYL CORPORATION (US) 1994-04-19 — — US disclosed
EP-0501713-A1 Optically active aminoketone derivative and method for preparing same MITSUI TOATSU CHEMICALS, Inc. (JP) 1992-09-02 — — EP disclosed
EP-0414391-A2 Aminoketone derivatives and use thereof MITSUI TOATSU CHEMICALS, Inc. (JP) 1991-02-27 — — 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-20240228482-A1 COMPOUNDS, COMPOSITIONS AND METHODS OF TREATING CANCER TP53, CASP3, BAX CHRM2 4434/4885CHRM1 4682/4885DRD1 4676/4885

“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.

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