Phenobarbital

Phenobarbital

SCHEMBL2120028

CCC1(c2ccccc2)C(=O)NC(=O)NC1=O.Cl

nearest known ligand 0.96

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 Phenobarbital. 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
▸ MMP13 known ✓ P45452 2/20 0.51
▸ MMP8 known ✓ P22894 1/20 0.49
▸ CACNA1F known ✓ O60840 1/20 0.46
▸ HTR2A known ✓ P28223 1/20 0.46
▸ HRH1 known ✓ P35367 1/20 0.46
▸ SCN1A known ✓ P35498 1/20 0.46
▸ SCN4A known ✓ P35499 1/20 0.46
▸ CACNA1D known ✓ Q01668 1/20 0.46
▸ KCNH2 known ✓ Q12809 1/20 0.46
▸ CACNA1S known ✓ Q13698 1/20 0.46
▸ CACNA1C known ✓ Q13936 1/20 0.46
▸ SCN5A known ✓ Q14524 1/20 0.46
▸ SCN2A known ✓ Q99250 1/20 0.46
▸ SCN3A known ✓ Q9NY46 1/20 0.46
▸ MMP2 P08253 6/20 0.77
▸ MMP9 P14780 6/20 0.77
▸ MMP3 P08254 3/20 0.77
▸ KMT2A Q03164 2/20 0.66
▸ MEN1 O00255 1/20 0.66
▸ CYP1A2 P05177 1/20 0.66

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
Phenobarbital SCHEMBL2592325 0.98 MMP2 (0.80) MMP2MMP9MMP3KMT2AMEN1
Phenobarbital SCHEMBL18825042 0.98 MMP2 (0.80) MMP2MMP9MMP3KMT2AMEN1
Phenobarbital SCHEMBL28099657 0.98 MMP2 (0.80) MMP2MMP9MMP3KMT2AMEN1
Phenobarbital SCHEMBL16583 0.98 MMP2 (0.80) MMP2MMP9MMP3KMT2AMEN1
Phenobarbital SCHEMBL6807467 0.96 MMP2 (0.77) MMP2MMP9MMP3KMT2AMEN1
Phenobarbital SCHEMBL3475428 0.96 MMP2 (0.77) MMP2MMP9MMP3KMT2AMEN1
Phenobarbital SCHEMBL352763 0.96 MMP2 (0.77) MMP2MMP9MMP3KMT2AMEN1
Phenobarbital SCHEMBL4193755 0.96 MMP2 (0.77) MMP2MMP9MMP3KMT2AMEN1
Phenobarbital SCHEMBL22032658 0.96 MMP2 (0.77) MMP2MMP9MMP3KMT2AMEN1
Phenobarbital SCHEMBL1322895 0.96 MMP2 (0.77) MMP2MMP9MMP3KMT2AMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240325487-A1 COMPOUNDS AND METHODS FOR INHIBITING PHOSPHATE TRANSPORT ARDELYX, INC. 2024-10-03 — — US disclosed
US-11813304-B2 Compounds and methods for inhibiting phosphate transport ARDELYX, INC. (US) 2023-11-14 — — US disclosed
EP-3884935-B1 COMPOUNDS AND METHODS FOR INHIBITING PHOSPHATE TRANSPORT ARDELYX INC (US) 2023-06-14 — — EP disclosed
CN-114404588-A Compounds and methods for inhibiting phosphate transport 阿德利克斯公司 2022-04-29 — — CN disclosed
CN-105979959-B Compounds and methods for inhibiting phosphate transport 阿德利克斯公司 2021-11-30 — — CN disclosed
EP-3884935-A1 COMPOUNDS AND METHODS FOR INHIBITING PHOSPHATE TRANSPORT Ardelyx, Inc. (US) 2021-09-29 — — EP disclosed
CN-113383075-A Method for determining the pH and calcium concentration or chlorine concentration in a sample 芝加哥大学 2021-09-10 — — CN disclosed
US-20200038475-A1 COMPOUNDS AND METHODS FOR INHIBITING PHOSPHATE TRANSPORT ARDELYX, INC. (US) 2020-02-06 — — US disclosed
EP-3532052-A1 DESIGN AND COMPOSITION OF CELL-STABILIZED PHARMACEUTICAL FORMULATIONS The Regents Of The University Of Michigan (US) 2019-09-04 — — EP disclosed
US-20190262453-A1 DESIGN AND COMPOSITION OF CELL-STABILIZED PHARMACEUTICAL FORMULATIONS THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS 2019-08-29 — — US disclosed
WO-2010138851-A2 E-CADHERIN AS A BIOMARKER OF GASTROESOPHAGEAL REFLUX DISEASE THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) 2010-12-02 — — WO disclosed
US-7749491-B2 Compounds and methods to enhance rAAV transduction UNIVERSITY OF IOWA RESEARCH FOUNDATION (US) 2010-07-06 — — US disclosed
US-20080249050-A1 Compounds and methods to enhance rAAV transduction UNIVERSITY OF IOWA RESEARCH FOUNDATION 2008-10-09 — — US disclosed
EP-1608763-A2 COMPOUNDS AND METHODS TO ENHANCE RAAV TRANSDUCTION UNIVERSITY OF IOWA RESEARCH FOUNDATION (US) 2005-12-28 — — EP disclosed
US-20050037497-A1 Compounds and methods to enhance rAAV transduction NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2005-02-17 — — US disclosed
WO-2004090145-A2 COMPOUNDS AND METHODS TO ENHANCE RAAV TRANSDUCTION UNIVERSITY OF IOWA RESEARCH FOUNDATION (US) 2004-10-21 — — WO disclosed
EP-0901663-A1 SYSTEM AND METHOD FOR AUTOMATIC CRITICAL EVENT NOTIFICATION Cedars-Sinai Medical Center (US) 1999-03-17 — — EP disclosed
WO-1997006499-A1 SYSTEM AND METHOD FOR AUTOMATIC CRITICAL EVENT NOTIFICATION CEDARS-SINAI MEDICAL CENTER (US) 1997-02-20 — — WO disclosed
US-5374537-A Administering organic or inorganic tetrahedral-shaped divalent oxy-anion UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) 1994-12-20 — — US disclosed
US-5189056-A Decrease cell permeability; using sulfonates UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) 1993-02-23 — — US 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-20240325487-A1 COMPOUNDS AND METHODS FOR INHIBITING PHOSPHATE TRANSPORT SLC34A3, SLC34A2, SLC34A1 MMP13 911/4885MMP8 1398/4885CACNA1F 1046/4885
US-11813304-B2 Compounds and methods for inhibiting phosphate transport SLC34A3, SLC34A2, SLC34A1 MMP13 911/4885MMP8 1398/4885CACNA1F 1046/4885
US-20190262453-A1 DESIGN AND COMPOSITION OF CELL-STABILIZED PHARMACEUTICAL FORMULATIONS CALU, ABCG2, ACTB MMP13 919/4885MMP8 2557/4885CACNA1F 3381/4885
US-20200038475-A1 COMPOUNDS AND METHODS FOR INHIBITING PHOSPHATE TRANSPORT SLC34A3, SLC34A2, SLC34A1 MMP13 911/4885MMP8 1398/4885CACNA1F 1046/4885

“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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