Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1298944

CN1CCC2(CCNCC2)C1.Cl

nearest known ligand 0.44

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
MAOB known ✓ P27338 1/20 0.36
GABRD known ✓ O14764 1/20 0.34
GABRA1 known ✓ P14867 1/20 0.34
GABRB1 known ✓ P18505 1/20 0.34
GABRA5 known ✓ P31644 1/20 0.34
GABRA3 known ✓ P34903 1/20 0.34
GABRA2 known ✓ P47869 1/20 0.34
GABRB2 known ✓ P47870 1/20 0.34
GABRA4 known ✓ P48169 1/20 0.34
DRD2 known ✓ P14416 1/20 0.34
TSHR P16473 6/20 0.44
CYP2D6 P10635 7/20 0.40
CYP3A4 P08684 4/20 0.40
ALDH1A1 P00352 5/20 0.40
CYP1A2 P05177 3/20 0.40
HSD17B10 Q99714 2/20 0.40
USP2 O75604 5/20 0.37
HPGD P15428 1/20 0.37
CYP2C19 P33261 4/20 0.37
KDM1A O60341 1/20 0.36

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 SCHEMBL27007071 1.00 TSHR (0.44) TSHRCYP2D6CYP3A4ALDH1A1CYP1A2
SCHEMBL1753673 0.98 CYP2D6 (0.41) TSHRCYP2D6CYP3A4ALDH1A1CYP1A2
Hydrochloric Acid SCHEMBL19717229 0.87 CYP2D6 (0.49) TSHRCYP2D6CYP3A4ALDH1A1CYP1A2
Hydrochloric Acid SCHEMBL9688286 0.87 TSHR (0.59) TSHRCYP2D6CYP3A4ALDH1A1CYP1A2
Hydrochloric Acid SCHEMBL21058494 0.87 CYP2D6 (0.49) TSHRCYP2D6CYP3A4ALDH1A1CYP1A2
Oxalic Acid SCHEMBL29701092 0.86 USP2 (0.42) TSHRCYP2D6CYP3A4ALDH1A1CYP1A2
Hydrochloric Acid SCHEMBL2761785 0.86 CYP2D6 (0.44) TSHRCYP2D6CYP3A4ALDH1A1CYP1A2
SCHEMBL7711019 0.84 CYP2D6 (0.50) TSHRCYP2D6CYP3A4ALDH1A1CYP1A2
SCHEMBL13879323 0.84 TSHR (0.56) TSHRCYP2D6CYP3A4ALDH1A1CYP1A2
SCHEMBL12457837 0.84 TSHR (0.56) TSHRCYP2D6CYP3A4ALDH1A1CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12257254-B2 Compositions comprising phosphoinositide 3-kinase inhibitors and a second antiproliferative agent CONVALIFE (SHANGHAI) CO. LIMITED (CN) 2025-03-25 US disclosed
US-20240174696-A1 2,8-DIAZASPIRO[4.5]DECANE COMPOUNDS GENENTECH, INC. (US) 2024-05-30 US disclosed
CN-117980297-A Substituted aminopyridine compounds as EGFR inhibitors 柳韩洋行 2024-05-03 CN disclosed
EP-4347594-A1 2, 8-DIAZASPIRO [4.5] DECANE COMPOUNDS Genentech, Inc. (US) 2024-04-10 EP disclosed
CN-117425654-A 2, 8-diazaspiro [4.5] decane compounds 基因泰克公司 2024-01-19 CN disclosed
US-11779586-B2 Compounds comprising tricyclic heterocyclic compounds CONVALIFE (SHANGHAI) CO. LIMITED (CN) 2023-10-10 US disclosed
US-11708378-B2 Tricyclic heterocyclic compounds as phosphoinositide 3-kinase inhibitors CONVALIFE (SHANGHAI) CO. LIMITED (CN) 2023-07-25 US disclosed
US-20230066999-A1 COMPOSITIONS COMPRISING PHOSPHOINOSITIDE 3-KINASE INHIBITORS AND A SECOND ANTIPROLIFERATIVE AGENT KARUS THERAPEUTICS LIMITED (GB) 2023-03-02 US disclosed
EP-3337460-B1 COMPOSITIONS COMPRISING TRICYCLIC HETEROCYCLIC COMPOUNDS CONVALIFE SHANGHAI CO LTD (CN) 2023-02-15 EP disclosed
EP-3337477-B1 COMPOSITIONS COMPRISING PHOSPHOINOSITIDE 3-KINASE INHIBITORS AND A SECOND ANTIPROLIFERATIVE AGENT CONVALIFE SHANGHAI CO LTD (CN) 2023-02-01 EP disclosed
WO-2017029518-A1 COMPOSITIONS COMPRISING TRICYCLIC HETEROCYCLIC COMPOUNDS KARUS THERAPEUTICS LTD (GB) 2017-02-23 WO disclosed
WO-2017029514-A1 COMPOSITIONS COMPRISING A PI3K INHIBITOR AND AN HDAC INHIBITOR KARUS THERAPEUTICS LTD (GB) 2017-02-23 WO disclosed
EP-3105233-A1 TRICYCLIC HETEROCYCLIC COMPOUNDS AS PHOSPHOINOSITIDE 3-KINASE INHIBITORS Karus Therapeutics Limited (GB) 2016-12-21 EP disclosed
US-20160347771-A1 TRICYCLIC HETEROCYCLIC COMPOUNDS AS PHOSPHOINOSITIDE 3-KINASE INHIBITORS CONVALIFE (SHANGHAI) CO. LIMITED (CN) 2016-12-01 US disclosed
WO-2015121657-A1 TRICYCLIC HETEROCYCLIC COMPOUNDS AS PHOSPHOINOSITIDE 3-KINASE INHIBITORS KARUS THERAPEUTICS LTD (GB) 2015-08-20 WO disclosed
US-20140141099-A1 DRUG DISCOVERY METHODS VERTEX PHARMACEUTICALS INCORPORATED 2014-05-22 US disclosed
US-20110269732-A1 DRUG DISCOVERY METHODS VERTEX PHARMACEUTICALS INCORPORATED (US) 2011-11-03 US disclosed
US-20100137305-A1 AMINOPYRIMIDINES USEFUL AS KINASE INHIBITORS VERTEX PHARMACEUTICALS INCORPORATED (US) 2010-06-03 US disclosed
EP-2148931-A2 DRUG DISCOVERY METHODS FOR AURORA KINASE INHIBITORS Vertex Pharmaceuticals Incorporated (US) 2010-02-03 EP disclosed
WO-2008131103-A2 DRUG DISCOVERY METHODS FOR AURORA KINASE INHIBITORS VERTEX PHARMACEUTICALS INCORPORATED (US) 2008-10-30 WO 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 (9 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-11708378-B2 Tricyclic heterocyclic compounds as phosphoinositide 3-kinase inhibitors PIK3CA, PIK3C2A, PIK3C2B MAOB 3319/4885GABRD 4114/4885GABRA1 3716/4885
US-20240174696-A1 2,8-DIAZASPIRO[4.5]DECANE COMPOUNDS LATS1, LATS2, GLS2 MAOB 4583/4885GABRD 69/4885GABRA1 352/4885
US-20100137305-A1 AMINOPYRIMIDINES USEFUL AS KINASE INHIBITORS AURKC, AURKA, AURKB MAOB 2712/4885GABRD 4843/4885GABRA1 4791/4885
US-12257254-B2 Compositions comprising phosphoinositide 3-kinase inhibitors and a second antiproliferative agent MCL1, MYC, XIAP MAOB 3312/4885GABRD 4155/4885GABRA1 3783/4885
US-20160347771-A1 TRICYCLIC HETEROCYCLIC COMPOUNDS AS PHOSPHOINOSITIDE 3-KINASE INHIBITORS PIK3CA, PIK3C2A, PIK3C2B MAOB 3319/4885GABRD 4114/4885GABRA1 3716/4885
US-20140141099-A1 DRUG DISCOVERY METHODS AURKB, AURKC, AURKA MAOB 1367/4885GABRD 4786/4885GABRA1 4402/4885
US-11779586-B2 Compounds comprising tricyclic heterocyclic compounds GRN, GLA, HTT MAOB 703/4885GABRD 1317/4885GABRA1 1684/4885
US-20110269732-A1 DRUG DISCOVERY METHODS AURKB, AURKC, AURKA MAOB 1367/4885GABRD 4786/4885GABRA1 4402/4885
US-20230066999-A1 COMPOSITIONS COMPRISING PHOSPHOINOSITIDE 3-KINASE INHIBITORS AND A SECOND ANTIPROLIFERATIVE AGENT MCL1, MYC, XIAP MAOB 3312/4885GABRD 4155/4885GABRA1 3783/4885

“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.