Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3776804

Cl.Oc1ccc(N2CCc3cc(O)ccc3C2c2ccc(OCCN3CCCC3)cc2)cc1

nearest known ligand 0.87

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
ESR1 known ✓ P03372 18/20 0.87
ESR2 known ✓ Q92731 18/20 0.87
NR3C1 known ✓ P04150 1/20 0.58
CHRM2 known ✓ P08172 1/20 0.58
ADRB1 known ✓ P08588 1/20 0.58
ADRA2A known ✓ P08913 1/20 0.58
CHRM1 known ✓ P11229 1/20 0.58
DRD2 known ✓ P14416 1/20 0.58
ADRA2B known ✓ P18089 1/20 0.58
ADRA2C known ✓ P18825 1/20 0.58
CHRM3 known ✓ P20309 1/20 0.58
SLC6A2 known ✓ P23975 1/20 0.58
HTR2A known ✓ P28223 1/20 0.58
HTR2C known ✓ P28335 1/20 0.58
AVPR2 known ✓ P30518 1/20 0.58
SLC6A4 known ✓ P31645 1/20 0.58
ADRA1A known ✓ P35348 1/20 0.58
PTGS2 known ✓ P35354 1/20 0.58
HRH1 known ✓ P35367 1/20 0.58
DRD3 known ✓ P35462 1/20 0.58

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 SCHEMBL3769936 0.99 ESR1 (0.87) ESR1ESR2MLNRNR1I2NR3C1
Hydrochloric Acid SCHEMBL3776559 0.94 ESR1 (0.98) ESR1ESR2MLNRNR1I2NR3C1
SCHEMBL282599 0.93 ESR1 (0.82) ESR1ESR2
SCHEMBL669065 0.93 ESR1 (1.00) ESR1ESR2MLNRNR1I2NR3C1
SCHEMBL14032457 0.92 ESR1 (0.83) ESR1ESR2
SCHEMBL30583267 0.92 ESR1 (1.00) ESR1ESR2MLNRNR1I2NR3C1
SCHEMBL4325515 0.92 ESR1 (1.00) ESR1ESR2MLNRNR1I2NR3C1
Hydrochloric Acid SCHEMBL3775771 0.87 ESR1 (0.67) ESR1ESR2
Hydrochloric Acid SCHEMBL3805782 0.85 ESR1 (0.67) ESR1ESR2
SCHEMBL3780309 0.85 ESR1 (0.69) ESR1ESR2SLC6A4HRH3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100317712-A1 Estrogen Agonists/Antagonists For Preventing Breast Cancer CAMERON KIMBERLY O 2010-12-16 US disclosed
US-RE39558-E1 5-Substituted-6-cyclic-5,6,7,8-tetrahydronaphthalen 2-ol compounds which are useful for treating osteoporosis PFIZER INC. (US) 2007-04-10 US disclosed
EP-1411049-A1 Estrogen Agonists/Antagonists PFIZER INC. (US) 2004-04-21 EP disclosed
US-20020132816-A1 Estrogen agonists/antagonists for preventing breast cancer CAMERON KIMBERLY O (US) 2002-09-19 US disclosed
US-6441193-B1 INTERMEDIATES SUCH AS 1-(2-(4-(6-METHOXY-3,4-DIHYDRONAPHTHA-LEN-1-YL)PHENOXY)ETHYL)PYRROLIDINE AND COMPOUNDS SUCH AS CIS-6-PHENYL-5-(4-(2-PYRROLIDIN-1-YLETHOXY)PHENYL)-5,6,7,8 -TETRAHYDRONAPHTHALEN-2-OL, HYDROBROMIDE SALT PFIZER INC. 2002-08-27 US disclosed
EP-0802910-B1 ESTROGEN AGONISTS/ANTAGONISTS PFIZER (US) 2002-03-13 EP disclosed
EP-1151998-A1 Estrogen agonists/antagonists PFIZER INC. (US) 2001-11-07 EP disclosed
US-20010025051-A1 Estrogen agonists/antagonists for preventing breast cancer CAMERON KIMBERLY O (US) 2001-09-27 US disclosed
US-6204286-B1 8-(P-(PYRROLIDINYLALKOXY)PHENYL)TETRAHYDRONAPHTHOLS PFIZER INC 2001-03-20 US disclosed
US-6153622-A Estrogen agonists/antagonists PFIZER, INC. (US) 2000-11-28 US disclosed
EP-1004306-A2 Estrogen agonists/antagonists Pfizer Products Inc. (US) 2000-05-31 EP disclosed
EP-0802910-A1 ESTROGEN AGONISTS/ANTAGONISTS PFIZER INC. (US) 1997-10-29 EP disclosed
WO-1996021656-A1 ESTROGEN AGONISTS/ANTAGONISTS PFIZER, INC. (US) 1996-07-18 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 (3 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-20010025051-A1 Estrogen agonists/antagonists for preventing breast cancer GPER1, ESR1, BRCA1 ESR1 2/4885ESR2 4/4885NR3C1 84/4885
US-20100317712-A1 Estrogen Agonists/Antagonists For Preventing Breast Cancer ESR1, GPER1, ESR2 ESR1 1/4885ESR2 3/4885NR3C1 101/4885
US-20020132816-A1 Estrogen agonists/antagonists for preventing breast cancer GPER1, ESR1, BRCA1 ESR1 2/4885ESR2 4/4885NR3C1 84/4885

“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.