Temiverine

Temiverine

SCHEMBL332032

CCN(CC)CC#CC(C)(C)OC(=O)C(O)(c1ccccc1)C1CCCCC1.Cl

nearest known ligand 0.98

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 Temiverine. 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
CHRM2 known ✓ P08172 6/20 0.69
CHRM1 known ✓ P11229 6/20 0.69
CHRM4 known ✓ P08173 5/20 0.69
CHRM3 known ✓ P20309 5/20 0.69
KCNH2 known ✓ Q12809 2/20 0.69
SLC6A3 known ✓ Q01959 2/20 0.69
ESR1 known ✓ P03372 1/20 0.69
CHRM5 known ✓ P08912 1/20 0.69
ADRA2A known ✓ P08913 1/20 0.69
SLC6A2 known ✓ P23975 1/20 0.69
ADRA1A known ✓ P35348 1/20 0.69
OPRM1 known ✓ P35372 1/20 0.69
DRD3 known ✓ P35462 1/20 0.69
HTR2B known ✓ P41595 1/20 0.69
SIGMAR1 known ✓ Q99720 1/20 0.69
HRH3 known ✓ Q9Y5N1 1/20 0.69
MEN1 O00255 1/20 0.71
RECQL P46063 1/20 0.71
PMP22 Q01453 1/20 0.71
KMT2A Q03164 1/20 0.71

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
Temiverine SCHEMBL5592324 0.99 MEN1 (0.70) MEN1RECQLPMP22KMT2ANPSR1
Hydrochloric Acid SCHEMBL9878351 0.99 MEN1 (0.69) MEN1RECQLPMP22KMT2ANPSR1
Temiverine SCHEMBL120687 0.99 CHRM2 (0.70) MEN1RECQLPMP22KMT2ANPSR1
Temiverine SCHEMBL896437 0.99 CHRM2 (0.70) MEN1RECQLPMP22KMT2ANPSR1
Temiverine SCHEMBL6816326 0.98 CHRM2 (0.69) MEN1RECQLPMP22KMT2ANPSR1
Temiverine SCHEMBL1650105 0.97 CHRM2 (0.68) MEN1RECQLPMP22KMT2ANPSR1
Hydrochloric Acid SCHEMBL9878913 0.92 POLB (0.61) MEN1RECQLPMP22KMT2ANPSR1
Hydrochloric Acid SCHEMBL9878732 0.90 POLB (0.59) MEN1RECQLPMP22KMT2ANPSR1
SCHEMBL7274104 0.86 CHRM2 (0.54) MEN1RECQLPMP22KMT2ANPSR1
SCHEMBL9618325 0.85 POLB (0.54) MEN1RECQLPMP22KMT2ANPSR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1915992-A1 USE OF CYCLOOXYGENASE INHIBITORS AND ANTIMUSCARINIC AGENTS FOR THE TREATMENT OF INCONTINENCE Pharmacia Corporation (US) 2008-04-30 EP claimed
WO-2007072503-A2 COMBINATIONS FOR MANAGING INFLAMMATION AND ASSOCIATED DISORDERS PANACEA BIOTEC LTD. (IN) 2007-06-28 WO claimed
CN-1633283-A Use of cyclooxygenase inhibitors and antimuscarinic agents for the treatment of incontinence PHARMACIA CORP (US) 2005-06-29 CN claimed
EP-1476146-A1 USE OF CYCLOOXYGENASE INHIBITORS AND ANTIMUSCARINIC AGENTS FOR THE TREATMENT OF INCONTINENCE Pharmacia Corporation (US) 2004-11-17 EP claimed
US-20030220310-A1 Epoxy-steroidal aldosterone antagonist and calcium channel blocker combination therapy for treatment of congestive heart failure PHARMACIA CORPORATION 2003-11-27 US claimed
US-20030220312-A1 Epoxy-steroidal aldosterone antagonist and calcium channel blocker combination therapy for treatment of cardiovascular disorders G.D. SEARLE & CO. 2003-11-27 US claimed
US-20030191172-A1 Method of using cyclooxygenase inhibitors and antimuscarinic agents VERSI EBRAHIM (US) 2003-10-09 US claimed
WO-2003070233-A1 USE OF CYCLOOXYGENASE INHIBITORS AND ANTIMUSCARINIC AGENTS FOR THE TREATMENT OF INCONTINENCE PHARMACIA CORPORATION (US) 2003-08-28 WO claimed
WO-2002009761-A9 EPOXY-STEROIDAL ALDOSTERONE ANTAGONIST AND CALCIUM CHANNEL BLOCKER COMBINATION THERAPY FOR TREATMENT OF CONGESTIVE HEART FAILURE PHARMACIA CORP (US) 2003-07-10 WO claimed
US-20030055027-A1 Epoxy-steroidal aldosterone antagonist and calcium channel blocker combination therapy for treatment of congestive heart failure G. D. SEARLE & CO. (US) 2003-03-20 US claimed
US-20020042405-A1 Epoxy-steroidal aldosterone antagonist and calcium channel blocker combination therapy for treatment of congestive heart failure SCHUH JOSEPH R (US) 2002-04-11 US claimed
EP-0359311-B1 Butynylamine derivatives NIPPON SHINYAKU CO LTD (JP) 1997-01-15 EP claimed
US-5036098-A Urogenital disorders NIPPON SHINYAKU CO., LTD. (JP) 1991-07-30 US claimed
EP-4744688-A2 DRUG DELIVERY DEVICES WITH DRUG-PERMEABLE COMPONENT AND METHODS Janssen Biotech, Inc. (US) 2026-05-20 EP disclosed
EP-3285850-B1 DRUG DELIVERY DEVICES WITH DRUG-PERMEABLE COMPONENT AND METHOD OF MANUFACTURING JANSSEN BIOTECH INC (US) 2026-05-06 EP disclosed
US-12576253-B2 Drug delivery device with intravesical tolerability TARIS BIOMEDICAL LLC (US) 2026-03-17 US disclosed
WO-2002009761-A9 EPOXY-STEROIDAL ALDOSTERONE ANTAGONIST AND CALCIUM CHANNEL BLOCKER COMBINATION THERAPY FOR TREATMENT OF CONGESTIVE HEART FAILURE PHARMACIA CORP (US) 2003-07-10 WO disclosed
US-20030055027-A1 Epoxy-steroidal aldosterone antagonist and calcium channel blocker combination therapy for treatment of congestive heart failure G. D. SEARLE & CO. (US) 2003-03-20 US disclosed
US-20020042405-A1 Epoxy-steroidal aldosterone antagonist and calcium channel blocker combination therapy for treatment of congestive heart failure SCHUH JOSEPH R (US) 2002-04-11 US disclosed
US-5036098-A Urogenital disorders NIPPON SHINYAKU CO., LTD. (JP) 1991-07-30 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 (6 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-20030220312-A1 Epoxy-steroidal aldosterone antagonist and calcium channel blocker combination therapy for treatment of cardiovascular disorders NR3C2, PTGER4, PTGER1 CHRM2 1932/4885CHRM1 1610/4885CHRM4 1124/4885
US-20030055027-A1 Epoxy-steroidal aldosterone antagonist and calcium channel blocker combination therapy for treatment of congestive heart failure PTGER1, KCNN4, HCN1 CHRM2 467/4885CHRM1 226/4885CHRM4 415/4885
US-20020042405-A1 Epoxy-steroidal aldosterone antagonist and calcium channel blocker combination therapy for treatment of congestive heart failure KCNN4, NR3C2, EDNRA CHRM2 594/4885CHRM1 533/4885CHRM4 433/4885
US-20030191172-A1 Method of using cyclooxygenase inhibitors and antimuscarinic agents PTGS2, PTGES2, PTGS1 CHRM2 7/4885CHRM1 26/4885CHRM4 34/4885
US-12576253-B2 Drug delivery device with intravesical tolerability ABCB11, SLC6A6, SLC10A2 CHRM2 3492/4885CHRM1 3858/4885CHRM4 4423/4885
US-20030220310-A1 Epoxy-steroidal aldosterone antagonist and calcium channel blocker combination therapy for treatment of congestive heart failure KCNN4, NR3C2, EDNRA CHRM2 594/4885CHRM1 533/4885CHRM4 433/4885

“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.