SCHEMBL3549753

SCHEMBL3549753

C=C1CCc2c(c3ccccc3n2C)C1=O

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR2A P28223 2/20 0.45
HTR2C P28335 2/20 0.45
KDM4E B2RXH2 2/20 0.44
ALOX15 P16050 1/20 0.44
MAPK1 P28482 1/20 0.44
HSD17B10 Q99714 1/20 0.44
KCNH2 Q12809 4/20 0.42
GPR3 P46089 1/20 0.41
CYP3A4 P08684 3/20 0.41
CYP1A2 P05177 3/20 0.41
HTR2B P41595 2/20 0.41
HTR3A P46098 2/20 0.41
CYP2D6 P10635 2/20 0.41
HTR3E A5X5Y0 1/20 0.41
SLC22A2 O15244 1/20 0.41
SLC22A1 O15245 1/20 0.41
SLC22A3 O75751 1/20 0.41
HTR3B O95264 1/20 0.41
CHRNB2 P17787 1/20 0.41
CHRNB4 P30926 1/20 0.41

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
SCHEMBL8270650 0.81 BRD4 (0.32)
SCHEMBL5809427 0.81 AGTR1 (0.39) HTR2C
SCHEMBL984 0.80 HTR2A (0.54) HTR2AHTR2CKDM4EALOX15MAPK1
SCHEMBL7428637 0.74 HTR2A (0.51) HTR2AHTR2CKDM4EALOX15MAPK1
SCHEMBL1146660 0.74 HTR2A (0.51) HTR2AHTR2CKDM4EALOX15MAPK1
SCHEMBL30223533 0.74 HTR2A (0.51) HTR2AHTR2CKDM4EALOX15MAPK1
SCHEMBL13157509 0.73 KCNH2 (0.54) HTR2AHTR2CKDM4EALOX15MAPK1
SCHEMBL918 0.73 BRD4 (0.57) HTR2AHTR2CKDM4EALOX15MAPK1
SCHEMBL13157508 0.72 KCNH2 (0.55) HTR2AHTR2CKDM4EALOX15MAPK1
SCHEMBL19159482 0.71 HTR2A (0.47) HTR2AHTR2CKDM4EALOX15MAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7696356-B2 Process for preparing 1,2,3,9-tetrahydro-9-methyl-3-methylene-4H-carbazol-4-one and ondansetron therefrom TARO PHARMACEUTICAL INDUSTRIES LIMITED (IL) 2010-04-13 US claimed
EP-1828141-A4 A ONE-POT PROCESS FOR THE PREPARATION OF ANTIEMETIC AGENT, 1,2,3,9-TETRAHYDRO-9-METHYL-3[(2-METHYL)-1H-IMIDAZOLE-1-YL)METHYL]-4H-CARBAZOL-4-O IPCA LAB LTD (IN) 2009-04-01 EP claimed
US-20080009635-A1 One-Pot Process for the Preparation of Antiemetic Agent, 1,2,3,9-Tetrahydro-9-Methyl-3[(2-Methyl)-1H-Imidazole-1-Yl)Methyl]-4H-Carbazol-4-O IPCA LABORATORIES LIMITED (IN) 2008-01-10 US claimed
EP-1828141-A1 A ONE-POT PROCESS FOR THE PREPARATION OF ANTIEMETIC AGENT, 1,2,3,9-TETRAHYDRO-9-METHYL-3[(2-METHYL)-1H-IMIDAZOLE-1-YL)METHYL]-4H-CARBAZOL-4-O IPCA Laboratories Limited (IN) 2007-09-05 EP claimed
US-20060252942-A1 Process for preparing 1,2,3,9-tetrahydro-9-methyl-3-[(2-methyl-1H-imidazol-1-YL)methyl]-4H-carbazol-4-one MOLNAR SANDOR 2006-11-09 US claimed
WO-2006046253-A1 A ONE-POT PROCESS FOR THE PREPARATION OF ANTIEMETIC AGENT, 1,2,3,9-TETRAHYDRO-9-METHYL-3[(2-METHYL)-1H-IMIDAZOLE-1-YL)METHYL]-4H-CARBAZOL-4-O IPCA LABORATORIES LIMITED (IN) 2006-05-04 WO claimed
US-20060041004-A1 Process for preparing 1,2,3,9-tetrahydro-9-methyl-3-methylene-4H-carbazol-4-one and ondansetron therefrom TARO PHARMACEUTICAL INDUSTRIES LIMITED (IL) 2006-02-23 US claimed
WO-2006018846-A2 PROCESS FOR PREPARING 1,2,3,9-TETRAHYDRO-9-METHYL-3-METHYLENE-4H- CARBAZOL-4-ONE AND ONDANSETRON THEREFROM TARO PHARMACEUTICAL INDUSTRIES LTD. (IL) 2006-02-23 WO claimed
US-20050020655-A1 Process for preparing 1,2,3,9-tetrahydro-9-methyl-3-[2-methyl-1H-imidazol-1-YL)methyl]-4H-carbazol-4-one TEVA GYOGYSZERGYAR ZARTKORUEN MUKODO RESZVENYTARSASAG (HU) 2005-01-27 US claimed
EP-1499623-A1 PROCESS FOR PREPARING 1,2,3,9-TETRAHYDRO-9-METHYL-3-[(2-METHYL-1H-IMIDAZOL-1-YL)METHYL]-4H-CARBAZOL-4-ONE BIOGAL GYOGYSZERGYAR RT. (HU) 2005-01-26 EP claimed
WO-2003093281-A1 PROCESS FOR PREPARING 1,2,3,9-TETRAHYDRO-9-METHYL-3-[(2-METHYL-1H-IMIDAZOL-1-YL)METHYL]-4H-CARBAZOL-4-ONE BIOGAL GYOGYSZERGYAR RT. (HU) 2003-11-13 WO claimed
US-7696356-B2 Process for preparing 1,2,3,9-tetrahydro-9-methyl-3-methylene-4H-carbazol-4-one and ondansetron therefrom TARO PHARMACEUTICAL INDUSTRIES LIMITED (IL) 2010-04-13 US disclosed
US-7696356-B2 Process for preparing 1,2,3,9-tetrahydro-9-methyl-3-methylene-4H-carbazol-4-one and ondansetron therefrom TARO PHARMACEUTICAL INDUSTRIES LIMITED (IL) 2010-04-13 US disclosed
US-7696356-B2 Process for preparing 1,2,3,9-tetrahydro-9-methyl-3-methylene-4H-carbazol-4-one and ondansetron therefrom TARO PHARMACEUTICAL INDUSTRIES LIMITED (IL) 2010-04-13 US disclosed
US-7696356-B2 Process for preparing 1,2,3,9-tetrahydro-9-methyl-3-methylene-4H-carbazol-4-one and ondansetron therefrom TARO PHARMACEUTICAL INDUSTRIES LIMITED (IL) 2010-04-13 US disclosed
EP-0595111-B1 Carbazolone derivatives and process for preparing the same RICHTER GEDEON VEGYESZET (HU) 1997-09-10 EP disclosed
US-5478949-A Reacting the starting carbazolone with dialkyl oxalate, then formaldehyde and 2-methylimidazole RICHTER GEDEON VEGYESZETI GYAR RT. (HU) 1995-12-26 US disclosed
US-5416221-A ONDANSETRON INTERMEDIATES RICHTER GEDEON VEGYESZETI GYAR RT. (HU) 1995-05-16 US disclosed
EP-0595111-A1 Carbazolone derivatives and process for preparing the same RICHTER GEDEON VEGYESZETI GYAR R.T. (HU) 1994-05-04 EP disclosed
US-4695578-A 1,2,3,9-tetrahydro-3-imidazol-1-ylmethyl-4H-carbazol-4-ones, composition containing them, and method of using them to treat neuronal 5HT function disturbances GLAXO GROUP LIMITED (GB) 1987-09-22 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-20050020655-A1 Process for preparing 1,2,3,9-tetrahydro-9-methyl-3-[2-methyl-1H-imidazol-1-YL)methyl]-4H-carbazol-4-one CYP3A4, HTR4, TPH1 HTR2A 64/4885HTR2C 7/4885KDM4E 475/4885
US-20060041004-A1 Process for preparing 1,2,3,9-tetrahydro-9-methyl-3-methylene-4H-carbazol-4-one and ondansetron therefrom HTR3A, ADORA3, HTR4 HTR2A 22/4885HTR2C 10/4885KDM4E 833/4885
US-20060252942-A1 Process for preparing 1,2,3,9-tetrahydro-9-methyl-3-[(2-methyl-1H-imidazol-1-YL)methyl]-4H-carbazol-4-one SI, CYP3A4, CYP2C19 HTR2A 76/4885HTR2C 10/4885KDM4E 797/4885
US-20080009635-A1 One-Pot Process for the Preparation of Antiemetic Agent, 1,2,3,9-Tetrahydro-9-Methyl-3[(2-Methyl)-1H-Imidazole-1-Yl)Methyl]-4H-Carbazol-4-O CRHR2, HCRTR2, HTR1D HTR2A 14/4885HTR2C 7/4885KDM4E 1490/4885

“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.