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 12)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | HRH2 known ✓ | P25021 | 1/20 | 0.39 |
| ▸ | CYP1A2 | P05177 | 2/20 | 0.54 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.54 |
| ▸ | ALDH1A1 | P00352 | 3/20 | 0.41 |
| ▸ | TSHR | P16473 | 1/20 | 0.39 |
| ▸ | HRH4 | Q9H3N8 | 2/20 | 0.39 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.39 |
| ▸ | HSD17B10 | Q99714 | 1/20 | 0.38 |
| ▸ | DNM1 | Q05193 | 3/20 | 0.37 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.33 |
| ▸ | BACH1 | O14867 | 1/20 | 0.31 |
| ▸ | MAFK | O60675 | 1/20 | 0.31 |
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Ethane SCHEMBL2545448 | 0.98 | CYP1A2 (0.52) | CYP1A2CYP2D6ALDH1A1TSHRHRH4 | |
| Hydrochloric Acid SCHEMBL28296907 | 0.98 | CYP1A2 (0.52) | CYP1A2CYP2D6ALDH1A1TSHRHRH4 | |
| SCHEMBL301678 | 0.98 | — | — | |
| Carbimide SCHEMBL8927383 | 0.95 | CYP1A2 (0.54) | CYP1A2CYP2D6ALDH1A1TSHRHRH4 | |
| Ethane SCHEMBL8026831 | 0.95 | CYP1A2 (0.54) | CYP1A2CYP2D6ALDH1A1TSHRHRH4 | |
| Ethylene SCHEMBL2344022 | 0.93 | CYP1A2 (0.52) | CYP1A2CYP2D6ALDH1A1TSHRHRH4 | |
| Iodomethane SCHEMBL7521844 | 0.93 | CYP1A2 (0.52) | CYP1A2CYP2D6ALDH1A1TSHRHRH4 | |
| Hydrochloric Acid SCHEMBL28506360 | 0.93 | CYP1A2 (0.47) | CYP1A2CYP2D6ALDH1A1TSHRHRH4 | |
| Alcohol SCHEMBL28266515 | 0.92 | CYP1A2 (0.52) | CYP1A2CYP2D6ALDH1A1TSHRHRH4 | |
| Hydrochloric Acid SCHEMBL839371 | 0.91 | ALDH1A1 (0.48) | CYP1A2CYP2D6ALDH1A1TSHRHRH4 |
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
Appears in 3385 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122011282-A | Polyacrylamide based on molecular chain topological structure regulation and synthesis method thereof | 黑龙江吉地油田服务股份有限公司 | 2026-05-12 | — | — | CN | claimed |
| US-12534703-B2 | Cell culture substrate and manufacturing method therefor | AMOLIFESCIENCE CO., LTD. (KR) | 2026-01-27 | — | — | US | claimed |
| CN-119930540-A | Multi-tenor preparation method of mine | 杭州善礼生物医药科技有限公司 | 2025-05-06 | — | — | CN | claimed |
| CN-119193130-A | Wide-distribution zirconia-aminated carbon quantum dot nano-fluid and preparation and application thereof | 中国石油天然气股份有限公司 | 2024-12-27 | — | — | CN | claimed |
| CN-119015476-A | Preparation method and application of disulfide wet adhesion hydrogel | 赵翌 | 2024-11-26 | — | — | CN | claimed |
| CN-118512634-B | Disulfide wet adhesion patch and preparation and application thereof | 修原(辽宁)生物有限公司 | 2024-10-29 | — | — | CN | claimed |
| WO-2024196171-A1 | CELL CULTURE SUBSTRATE FOR OSTEOCYTE DIFFERENTIATION AND PREPARATION METHOD THEREFOR | 주식회사 아모라이프사이언스 | 2024-09-26 | — | — | WO | claimed |
| EP-3986400-B1 | PROCESSES AND INTERMEDIATES FOR PRODUCING DIAZASPIRO LACTAM COMPOUNDS | NAUREX INC (US) | 2024-08-21 | — | — | EP | claimed |
| CN-118512634-A | Disulfide wet adhesion patch and preparation and application thereof | 修原(辽宁)生物有限公司 | 2024-08-20 | — | — | CN | claimed |
| WO-2024141366-A1 | NEW HYALURONAN HYDROGELS CHEMICALLY CROSSLINKED BY MMP IN-HIBITORS | CONSORZIO INTERUNIVERSITARIO NAZIONALE PER LA SCIENZA E TECNOLOGIA DEI MATERIALI (IT) | 2024-07-04 | — | — | WO | claimed |
| US-20050113584-A1 | On solid support (polyamide) via condensation and dehydration; chromatography | IRM LLC (BM) | 2005-05-26 | — | — | US | claimed |
| WO-2005007678-A2 | METHODS FOR THE PREPARATION OF RHODAMINE | IRM LLC (BM) | 2005-01-27 | — | — | WO | claimed |
| CN-1571785-A | Synthesis of 4- [ (Z) - (4-bromophenyl) (ethoxyimino) methyl ] -1 ' - [ (2, 4-dimethyl-1-oxo-3-pyridyl) carbonyl ] -4 ' -methyl-1, 4 ' -bipiperidine | SCHERING CORP (US) | 2005-01-26 | — | — | CN | claimed |
| CN-1498226-A | Thrombin derivatives and its process for production, anhydrothrombin derivatives and its production method, platelet agglutination-inducing compositions, method of inducing platelet agglutination,... | ɭ����ҵ��ʽ���� | 2004-05-19 | — | — | CN | claimed |
| CN-1382735-A | Somatostatin yolk antibody and its preparing process | INST OF ZOOTECHNICS AND VERTER (CN) | 2002-12-04 | — | — | CN | claimed |
| CN-1035873-C | Preparation of amides and peptides | HOFFMANN LA ROCHE (CH) | 1997-09-17 | — | — | CN | claimed |
| WO-1997023608-A1 | COMPOSITIONS AND METHODS FOR TARGETING GENE DELIVERY VEHICLES USING COVALENTLY BOUND TARGETING ELEMENTS | CHIRON CORPORATION (US) | 1997-07-03 | — | — | WO | claimed |
| CN-1111237-A | Preparation of amides and peptides | HOFFMANN LA ROCHE (CH) | 1995-11-08 | — | — | CN | claimed |
| CN-86101066-A | Process for producing novel trifluoromethyl ketone substituted peptide derivatives | — | 1986-11-05 | — | — | CN | claimed |
| US-4593004-A | Activating with carbodiimide compound | REANAL FINOMVEGYSZERGYAR (HU) | 1986-06-03 | — | — | US | claimed |