Olanzapine

Olanzapine

SCHEMBL1634614

Cc1cc2c(s1)Nc1ccccc1N=C2N1CCN(C)CC1.O.O

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

DRD2DRD3DRD4HTR2AHTR2C

The experimentally established mechanism targets of Olanzapine. 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
DRD2 known ✓ P14416 7/20 0.98
HTR2A known ✓ P28223 5/20 0.98
HTR2C known ✓ P28335 5/20 0.98
DRD4 known ✓ P21917 4/20 0.98
DRD3 known ✓ P35462 3/20 0.98
CHRM1 P11229 10/20 0.98
CHRM2 P08172 5/20 0.98
CHRM4 P08173 5/20 0.98
CHRM5 P08912 5/20 0.98
CHRM3 P20309 5/20 0.98
DRD1 P21728 5/20 0.98
ADRA1D P25100 5/20 0.98
ADRA1A P35348 5/20 0.98
HRH1 P35367 5/20 0.98
ADRA1B P35368 5/20 0.98
HTR2B P41595 5/20 0.98
ADRA2A P08913 4/20 0.98
ADRA2B P18089 4/20 0.98
ADRA2C P18825 4/20 0.98
KCNH2 Q12809 4/20 0.98

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
Olanzapine SCHEMBL5091769 1.00 CHRM1 (0.98) CHRM1DRD2CHRM2CHRM4CHRM5
Olanzapine SCHEMBL1562676 1.00 CHRM1 (0.98) CHRM1DRD2CHRM2CHRM4CHRM5
Olanzapine SCHEMBL1830363 0.99 CHRM1 (0.95) CHRM1DRD2CHRM2CHRM4CHRM5
Olanzapine SCHEMBL16114506 0.99 CHRM1 (0.95) CHRM1DRD2CHRM2CHRM4CHRM5
Olanzapine SCHEMBL28763 0.99 CHRM1 (1.00) CHRM1DRD2CHRM2CHRM4CHRM5
Olanzapine SCHEMBL4775632 0.99 CHRM1 (1.00) CHRM1DRD2CHRM2CHRM4CHRM5
Olanzapine SCHEMBL29358280 0.99 CHRM1 (1.00) CHRM1DRD2CHRM2CHRM4CHRM5
Olanzapine SCHEMBL1376031 0.98 CHRM1 (0.98) CHRM1DRD2CHRM2CHRM4CHRM5
Olanzapine SCHEMBL6461808 0.98 CHRM1 (0.98) CHRM1DRD2CHRM2CHRM4CHRM5
Olanzapine SCHEMBL2222724 0.98 CHRM1 (0.98) CHRM1DRD2CHRM2CHRM4CHRM5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100317849-A1 Process For Producing Pure And Stable Form Of 2-Methyl-4-(4-Methyl-1-Piperazinyl) -10H-Thieno[2,3-B] [1,5] Benzodiazepine JUBILANT ORGANOSYS LTD. (IN) 2010-12-16 US claimed
EP-1994013-A4 PROCESS FOR PRODUCING PURE AND STABLE FORM OF 2-METHYL-4-(4- METHYL- 1 -PIPERAZINYL)-10H-THIENO[2,3-b] [1,5]BENZODIAZEPINE JUBILANT ORGANOSYS LTD (IN) 2009-04-01 EP claimed
EP-1994013-A1 PROCESS FOR PRODUCING PURE AND STABLE FORM OF 2-METHYL-4-(4- METHYL- 1 -PIPERAZINYL)-10H-THIENO[2,3-b] [1,5]BENZODIAZEPINE Jubilant Organosys Limited (IN) 2008-11-26 EP claimed
US-20080009481-A1 Process For Making Form I Of Olanzapine SHASUN CHEMICALS AND DRUGS LIMITED (IN) 2008-01-10 US claimed
WO-2007105225-A1 PROCESS FOR PRODUCING PURE AND STABLE FORM OF 2-METHYL-4-(4- METHYL- 1 -PIPERAZINYL)-10H-THIENO[2,3-b] [ 1,5]BENZODIAZEPINE JUBILANT ORGANOSYS LIMITED (IN) 2007-09-20 WO claimed
US-20070129352-A1 Novel crystal forms, methods for their preparation and method for preparation of olanzapine TEVA PHARMACEUTICAL INDUSTRIES LTD. 2007-06-07 US claimed
EP-1781666-A1 IMPROVED PROCESS FOR MAKING FORM I OF OLANZAPINE. Shasun Chemicals and Drugs Limited (IN) 2007-05-09 EP claimed
EP-1018880-A4 2-METHYL-THIENO-BENZODIAZEPINE FORMULATION LILLY CO ELI (US) 2006-06-14 EP claimed
CN-1239158-C 2-methyl-thieno-benzodiazepine formulation LILLY CO ELI (US) 2006-02-01 CN claimed
WO-2006006185-A1 IMPROVED PROCESS FOR MAKING FORM I OF OLANZAPINE. SHASUN CHEMICALS AND DRUGS LIMITED (IN) 2006-01-19 WO claimed
WO-2002018390-A1 PROCESS FOR PREPARATION OF HYDRATES OF OLANZAPINE AND THEIR CONVERSION INTO CRYSTALLINE FORMS OF OLANZAPINE DR. REDDY'S LABORATORIES LTD. (IN) 2002-03-07 WO claimed
EP-0831098-B1 Intermediates and process for preparing olanzapine LILLY CO ELI (US) 2001-11-21 EP claimed
US-6251895-B1 STABLE CRYSTALLINE DIHYDRATE D OLANZAPINE POLYMORPH ELI LILLY AND COMPANY 2001-06-26 US claimed
CN-1271251-A 2-methyl-thieno-benzodiazepine * formulations LILLY CO ELI (US) 2000-10-25 CN claimed
EP-1018880-A1 2-METHYL-THIENO-BENZODIAZEPINE FORMULATION ELI LILLY AND COMPANY (US) 2000-07-19 EP claimed
US-6020487-A Intermediates and process for preparing olanzapine ELI LILLY AND COMPANY (US) 2000-02-01 US claimed
CN-1234802-A Intermediates and process for preparing olanzapine ELI LILLYAND CO (US) 1999-11-10 CN claimed
WO-1999016313-A1 2-METHYL-THIENO-BENZODIAZEPINE FORMULATION ELI LILLY AND COMPANY (US) 1999-04-08 WO claimed
WO-1998012199-A1 INTERMEDIATES AND PROCESS FOR PREPARING OLANZAPINE ELI LILLY AND COMPANY (US) 1998-03-26 WO claimed
EP-0831098-A2 Intermediates and process for preparing olanzapine ELI LILLY AND COMPANY (US) 1998-03-25 EP claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 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-20080009481-A1 Process For Making Form I Of Olanzapine HTR1A, HTR1D, HTR1B DRD2 26/4885HTR2A 21/4885HTR2C 9/4885

“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.