Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4015397

COc1ccc(C2=NN(C3CCNCC3)C(=O)C3CC=CCC23)c2c1OC(C)(C)C2.Cl

nearest known ligand 0.82

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 7)

geneUniProtsupporting neighboursconfidence
PDE4B known ✓ Q07343 18/20 0.82
PDE4D known ✓ Q08499 17/20 0.82
PDE4A known ✓ P27815 16/20 0.82
PDE4C known ✓ Q08493 16/20 0.82
PDE7A known ✓ Q13946 2/20 0.46
PDE3B known ✓ Q13370 1/20 0.46
PDE3A known ✓ Q14432 1/20 0.46

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 SCHEMBL4015395 1.00 PDE4B (0.82) PDE4BPDE4DPDE4APDE4CPDE7A
Hydrochloric Acid SCHEMBL4015390 1.00 PDE4B (0.82) PDE4BPDE4DPDE4APDE4CPDE7A
SCHEMBL6453683 0.99 PDE4B (0.84) PDE4BPDE4DPDE4APDE4CPDE7A
SCHEMBL6453687 0.99 PDE4B (0.84) PDE4BPDE4DPDE4APDE4CPDE7A
Hydrochloric Acid SCHEMBL6470670 0.91 PDE4B (0.68) PDE4BPDE4DPDE4APDE4CPDE7A
Hydrochloric Acid SCHEMBL6470669 0.91 PDE4B (0.68) PDE4BPDE4DPDE4APDE4CPDE7A
SCHEMBL6876779 0.90 PDE4B (1.00) PDE4BPDE4DPDE4APDE4CPDE7A
SCHEMBL6876774 0.90 PDE4B (1.00) PDE4BPDE4DPDE4APDE4CPDE7A
SCHEMBL6876771 0.90 PDE4B (1.00) PDE4BPDE4DPDE4APDE4CPDE7A
SCHEMBL5557664 0.89 PDE4B (0.84) PDE4BPDE4DPDE4APDE4CPDE7A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7531540-B2 Phthalazinone-piperidino-derivatives as PDE4 inhibitors NYCOMED GMBH (DE) 2009-05-12 US disclosed
US-20070129373-A1 Phthalazinone-piperidino-derivatives as PDE4 inhibitors ALTANA PHARMA AG 2007-06-07 US disclosed
US-7220746-B2 Pyrrolidinedione substituted piperidine-phthalazones as PDE4 inhibitors ALTANA PHARMA AG (DE) 2007-05-22 US disclosed
EP-1537100-B1 PYRROLIDINEDIONE SUBSTITUTED PIPERIDINE-PHTHALAZONES AS PDE4 INHIBITORS ALTANA PHARMA AG (DE) 2007-04-25 EP disclosed
US-7179810-B2 Such as 2-{4-[(4aS,8aR)-4-(3,4-dimethoxyphenyl)-1-oxo-4a,5,8,8a-tetrahydro-1H-phthalazin-2-yl]-piperidin-1-yl}-2H-acetamide; phosphodiesterase inhibitors; for treatment of respiratory disorders ALTANA PHARMA AG (DE) 2007-02-20 US disclosed
US-20060160813-A1 Pyrrolidinedione substituted piperidine-phtalazones as pde4 inhibitors ALTANA PHARMA AG (DE) 2006-07-20 US disclosed
US-20050234062-A1 Phthalazinone-piperidino-derivatives as PDE4 inhibitors ALTANA PHARMA AG 2005-10-20 US disclosed
US-6953853-B2 Phospholipase inhbitors; antiinflammatory agents; respiratory system disorders ALTANA PHARMA AG (DE) 2005-10-11 US disclosed
US-20040067946-A1 Phthalatyinone-piperidino-derivatives as pde4 inhibitors TAKEDA GMBH (DE) 2004-04-08 US disclosed
EP-1362044-A1 PHTHALAZINONE-PIPERIDINO-DERIVATIVES AS PDE4 INHIBITORS ALTANA Pharma AG (DE) 2003-11-19 EP disclosed
WO-2002064584-A1 PHTHALAYINONE-PIPERIDINO-DERIVATIVES AS PDE4 INHIBITORS ALTANA PHARMA AG (DE) 2002-08-22 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 (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-20040067946-A1 Phthalatyinone-piperidino-derivatives as pde4 inhibitors PDE4A, PDE4B, PDE5A PDE4B 2/4885PDE4D 9/4885PDE4A 1/4885
US-20060160813-A1 Pyrrolidinedione substituted piperidine-phtalazones as pde4 inhibitors PDE4A, PDE4B, PDE3B PDE4B 2/4885PDE4D 6/4885PDE4A 1/4885
US-20070129373-A1 Phthalazinone-piperidino-derivatives as PDE4 inhibitors PDE4A, PDE4B, PDE5A PDE4B 2/4885PDE4D 6/4885PDE4A 1/4885
US-20050234062-A1 Phthalazinone-piperidino-derivatives as PDE4 inhibitors PDE4A, PDE4B, PDE5A PDE4B 2/4885PDE4D 6/4885PDE4A 1/4885

“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.