SCHEMBL2861806

SCHEMBL2861806

C=Cc1cc(C=C)c(C)c(C)c1C

nearest known ligand 0.33

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
TP53 P04637 1/20 0.33
TDP1 Q9NUW8 1/20 0.33
ALDH1A1 P00352 1/20 0.31

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
SCHEMBL29618943 0.86 TP53 (0.30) TP53TDP1
SCHEMBL189595 0.86 TP53 (0.30) TP53TDP1
SCHEMBL5229008 0.84
SCHEMBL29279392 0.84 SLC22A8 (0.30)
SCHEMBL4359969 0.82
SCHEMBL3819396 0.82
Hydrochloric Acid SCHEMBL11018648 0.80
SCHEMBL10850669 0.78 ALDH1A1 (0.39) TDP1ALDH1A1
SCHEMBL11661670 0.78 ALDH1A1 (0.38) TP53TDP1ALDH1A1
SCHEMBL31391761 0.78 ALDH1A1 (0.38) TP53TDP1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9360567-B2 Scintillating organic materials and methods for detecting neutron and gamma radiation NANOPTICS, INCORPORATED (US) 2016-06-07 US claimed
US-20140224993-A1 SCINTILLATING ORGANIC MATERIALS AND METHODS FOR DETECTING NEUTRON AND GAMMA RADIATION NANOPTICS, INCORPORATED (US) 2014-08-14 US claimed
US-9759821-B2 Scintillating organic materials and methods for detecting neutron and gamma radiation NANOPTICS, INCORPORATED (US) 2017-09-12 US disclosed
US-9360567-B2 Scintillating organic materials and methods for detecting neutron and gamma radiation NANOPTICS, INCORPORATED (US) 2016-06-07 US disclosed
US-20160154122-A1 Scintillating Organic Materials and Methods For Detecting Neutron and Gamma Radiation NANOPTICS, INCORPORATED 2016-06-02 US disclosed
US-8932628-B2 Modified release formulations of a bupropion salt VALEANT INTERNATIONAL BERMUDA (BM) 2015-01-13 US disclosed
US-7671094-B2 Bupropion hydrobromide and therapeutic applications BIOVAIL LABORATORIES INTERNATIONAL S.R.L. (BB) 2010-03-02 US disclosed
US-7662407-B2 hydrobromide salt; for treatment of depression, nicotine addiction and obesity BIOVAIL LABORATORIES INTERNATIONAL S.R.L. (BB) 2010-02-16 US disclosed
US-7649019-B2 controlled release tablet of bupropion hydrobromide for reducing the ratio of the maximum/minimum plasma bupropion hydrobromide concentration (Cmax/Cmin) while maintaining bupropion plasma levels within the therapeutic window upon administration to a patient; more stable than buproin hcl BIOVAIL LABORATORIES INTERNATIONAL S.R.L. (BB) 2010-01-19 US disclosed
US-7645901-B2 Crystal form; controlled release tablet of bupropion hydrobromide for reducing the ratio of the maximum/minimum plasma bupropion hydrobromide concentration (Cmax/Cmin) while maintaining bupropion plasma levels within the therapeutic window upon administration to a patient; more stable than buproin hcl BIOVAIL LABORATORIES INTERNATIONAL S.R.L. (BB) 2010-01-12 US disclosed
US-7645802-B2 Controlled release, once daily formulation; reducing seizure side effects; antidepressant BIOVAIL LABORATORIES INTERNATIONAL SRL. (BB) 2010-01-12 US disclosed
US-20080057120-A1 controlled release tablet of bupropion hydrobromide for reducing the ratio of the maximum/minimum plasma bupropion hydrobromide concentration (Cmax/Cmin) while maintaining bupropion plasma levels within the therapeutic window upon administration to a patient; more stable than buproin hcl BIOAVAIL LABORATORIES INTERNATIONAL S.R.L. (BB) 2008-03-06 US disclosed
US-20080051606-A1 Crystal form; controlled release tablet of bupropion hydrobromide for reducing the ratio of the maximum/minimum plasma bupropion hydrobromide concentration (Cmax/Cmin) while maintaining bupropion plasma levels within the therapeutic window upon administration to a patient; more stable than buproin hcl BIOAVAIL LABORATORIES INTERNATIONAL S.R.L. (BB) 2008-02-28 US disclosed
US-20080039441-A1 Storage stability; combination forms with antidepressants, antiinflammatories, serotonin reuptake inhibitors, antiemetics, appetite modulators, antivirals, vasodilators and/or pain relievers BIOAVAIL LABORATORIES INTERNATIONAL S.R.L. (BB) 2008-02-14 US disclosed
US-20080038348-A1 Dosage form releases bupropion hydrobromide by dispensing it from a core via at least one passageway in a membrane by pressure created in the core by osmosis and/or by the expansion of a swellable material which forces the bupropion hydrobromide to be dispensed from core BIOAVAIL LABORATORIES INTERNATIONAL S.R.L. (BB) 2008-02-14 US disclosed
US-20080038345-A1 Microparticles having osmotic subcoat; extended release tablets; shelf life; hydrobromide form BIOAVAIL LABORATORIES (BB) 2008-02-14 US disclosed
US-20080033044-A1 Crystal form; controlled release tablet of bupropion hydrobromide for reducing the ratio of the maximum/minimum plasma bupropion hydrobromide concentration (Cmax/Cmin) while maintaining bupropion plasma levels within the therapeutic window upon administration to a patient; more stable than buproin hcl BIOAVAIL LABORATORIES (BB) 2008-02-07 US disclosed
US-20080033043-A1 Crystal form; controlled release tablet of bupropion hydrobromide for reducing the ratio of the maximum/minimum plasma bupropion hydrobromide concentration (Cmax/Cmin) while maintaining bupropion plasma levels within the therapeutic window upon administration to a patient; more stable than buproin hcl BIOAVAIL LABORATORIES INTERNATIONAL S.R.L. (BB) 2008-02-07 US disclosed
US-20070293584-A1 hydrobromide salt; for treatment of depression, nicotine addiction and obesity BIOAVAIL LABORATORIES INTERNATIONAL S.R.L. (BB) 2007-12-20 US disclosed
US-20070281012-A1 MODIFIED RELEASE FORMULATIONS OF A BUPROPION SALT BIOAVAIL LABORATORIES INTERNATIONAL S.R.L. (BB) 2007-12-06 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 (9 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-20080057120-A1 controlled release tablet of bupropion hydrobromide for reducing the ratio of the maximum/minimum plasma bupropion hydrobromide concentration (Cmax/Cmin) while maintaining bupropion plasma levels within the therapeutic window upon administration to a patient; more stable than buproin hcl SLC6A2, BDNF, SLC6A11 TP53 4754/4885TDP1 2444/4885ALDH1A1 3143/4885
US-20080033044-A1 Crystal form; controlled release tablet of bupropion hydrobromide for reducing the ratio of the maximum/minimum plasma bupropion hydrobromide concentration (Cmax/Cmin) while maintaining bupropion plasma levels within the therapeutic window upon administration to a patient; more stable than buproin hcl BDNF, MME, SLC6A11 TP53 4525/4885TDP1 2850/4885ALDH1A1 3922/4885
US-20070281012-A1 MODIFIED RELEASE FORMULATIONS OF A BUPROPION SALT SLC6A2, SLC6A3, SLC6A11 TP53 4820/4885TDP1 570/4885ALDH1A1 2619/4885
US-20080033043-A1 Crystal form; controlled release tablet of bupropion hydrobromide for reducing the ratio of the maximum/minimum plasma bupropion hydrobromide concentration (Cmax/Cmin) while maintaining bupropion plasma levels within the therapeutic window upon administration to a patient; more stable than buproin hcl BDNF, MME, SLC6A11 TP53 4525/4885TDP1 2850/4885ALDH1A1 3922/4885
US-20080051606-A1 Crystal form; controlled release tablet of bupropion hydrobromide for reducing the ratio of the maximum/minimum plasma bupropion hydrobromide concentration (Cmax/Cmin) while maintaining bupropion plasma levels within the therapeutic window upon administration to a patient; more stable than buproin hcl BDNF, MME, SLC6A11 TP53 4525/4885TDP1 2850/4885ALDH1A1 3922/4885
US-20080039441-A1 Storage stability; combination forms with antidepressants, antiinflammatories, serotonin reuptake inhibitors, antiemetics, appetite modulators, antivirals, vasodilators and/or pain relievers SLC6A4, HTR5A, SLC6A2 TP53 4740/4885TDP1 1493/4885ALDH1A1 3089/4885
US-20070293584-A1 hydrobromide salt; for treatment of depression, nicotine addiction and obesity SLC6A3, SLC6A2, SLC6A4 TP53 4780/4885TDP1 1656/4885ALDH1A1 976/4885
US-20080038345-A1 Microparticles having osmotic subcoat; extended release tablets; shelf life; hydrobromide form SLC6A2, SLC6A4, SLC6A3 TP53 4164/4885TDP1 2040/4885ALDH1A1 1530/4885
US-20080038348-A1 Dosage form releases bupropion hydrobromide by dispensing it from a core via at least one passageway in a membrane by pressure created in the core by osmosis and/or by the expansion of a swellable material which forces the bupropion hydrobromide to be dispensed from core SLC6A11, SLC6A1, SLC6A5 TP53 4430/4885TDP1 1139/4885ALDH1A1 1232/4885

“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.