Levorphanol

Levorphanol

SCHEMBL14326930

CN1CC[C@]23CCCCC2C1Cc1ccc(O)cc13

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

OPRM1

The experimentally established mechanism targets of Levorphanol. 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
OPRM1 known ✓ P35372 6/20 1.00
GRIN1 Q05586 9/20 1.00
GRIN2A Q12879 9/20 1.00
GRIN2D O15399 8/20 1.00
GRIN3B O60391 8/20 1.00
GRIN2B Q13224 8/20 1.00
GRIN2C Q14957 8/20 1.00
GRIN3A Q8TCU5 8/20 1.00
OPRD1 P41143 5/20 1.00
OPRK1 P41145 5/20 1.00
SLC22A1 O15245 3/20 1.00
SLC6A4 P31645 3/20 1.00
MRGPRX2 Q96LB1 3/20 1.00
CYP2D6 P10635 3/20 1.00
SLC6A2 P23975 3/20 1.00
SCN1A P35498 2/20 1.00
SCN2A Q99250 2/20 1.00
SCN3A Q9NY46 2/20 1.00
ADRA2A P08913 2/20 1.00
KCNH2 Q12809 2/20 1.00

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
Levorphanol SCHEMBL5171217 1.00 GRIN1 (1.00) GRIN1GRIN2AGRIN2DGRIN3BGRIN2B
Levorphanol SCHEMBL24335 1.00 GRIN1 (1.00) GRIN1GRIN2AGRIN2DGRIN3BGRIN2B
Levorphanol SCHEMBL16310821 1.00 GRIN1 (1.00) GRIN1GRIN2AGRIN2DGRIN3BGRIN2B
Levorphanol SCHEMBL3495833 1.00 GRIN1 (1.00) GRIN1GRIN2AGRIN2DGRIN3BGRIN2B
Levorphanol SCHEMBL21095576 1.00 GRIN1 (1.00) GRIN1GRIN2AGRIN2DGRIN3BGRIN2B
Levorphanol SCHEMBL12232844 1.00 GRIN1 (1.00) GRIN1GRIN2AGRIN2DGRIN3BGRIN2B
Levorphanol SCHEMBL22791693 1.00 GRIN1 (1.00) GRIN1GRIN2AGRIN2DGRIN3BGRIN2B
Levorphanol SCHEMBL22722062 1.00 GRIN1 (1.00) GRIN1GRIN2AGRIN2DGRIN3BGRIN2B
Dextrorphan SCHEMBL20535964 1.00 GRIN1 (1.00) GRIN1GRIN2AGRIN2DGRIN3BGRIN2B
Racemorphan SCHEMBL46201 1.00 GRIN1 (1.00) GRIN1GRIN2AGRIN2DGRIN3BGRIN2B

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 13 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9527858-B2 Compounds and compositions for use in phototherapy and in treatment of ocular neovascular disease and cancers MALLINCKRODT LLC (US) 2016-12-27 US disclosed
US-9518062-B2 Compounds and compositions for use in phototherapy and in treatment of ocular neovascular disease and cancers MALLINCKRODT LLC (US) 2016-12-13 US disclosed
US-8987291-B2 Opioid-containing oral pharmaceutical compositions and methods Upsher Smith Laboratories, Inc. (US) 2015-03-24 US disclosed
US-8921386-B1 Opioid salts and formulations exhibiting anti-abuse and anti-dose dumping properties PISGAH LABORATORIES, INC. (US) 2014-12-30 US disclosed
US-20140370006-A1 COMPOUNDS AND COMPOSITIONS FOR USE IN PHOTOTHERAPY AND IN TREATMENT OF OCULAR NEOVASCULAR DISEASE AND CANCERS SpecGx LLC 2014-12-18 US disclosed
US-20140370005-A1 COMPOUNDS AND COMPOSITIONS FOR USE IN PHOTOTHERAPY AND IN TREATMENT OF OCULAR NEOVASCULAR DISEASE AND CANCERS SpecGx LLC 2014-12-18 US disclosed
US-8829020-B2 Compounds and compositions for use in phototherapy and in treatment of ocular neovascular disease and cancers MALLINCKRODT LLC (US) 2014-09-09 US disclosed
US-8748416-B1 Opioid salts and formulations exhibiting anti-abuse and anti-dumping properties PISGAH LABORATORIES, INC. (US) 2014-06-10 US disclosed
US-8569330-B1 Opioid salts and formulations exhibiting anti-abuse and anti-dose dumping properties PISGAH LABORATORIES, INC. (US) 2013-10-29 US disclosed
US-8569329-B1 Opioid salts and formulations exhibiting anti-abuse and anti-dose dumping properties PISGAH LABORATORIES, INC. (US) 2013-10-29 US disclosed
US-8476291-B1 Opioid salts and formulations exhibiting anti-abuse and anti-dumping properties PISGAH LABORATORIES, INC. (US) 2013-07-02 US disclosed
US-20130123293-A1 OPIOID-CONTAINING ORAL PHARMACEUTICAL COMPOSITIONS AND METHODS UPSHER-SMITH LABORATORIES, INC. (US) 2013-05-16 US disclosed
US-8338444-B1 Opioid salts and formulations exhibiting anti-abuse and anti-dose dumping properties PISGAH LABORATORIES, INC. (US) 2012-12-25 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 (3 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-20130123293-A1 OPIOID-CONTAINING ORAL PHARMACEUTICAL COMPOSITIONS AND METHODS OPRK1, OPRM1, OPRL1 OPRM1 2/4885GRIN1 401/4885GRIN2A 374/4885
US-20140370006-A1 COMPOUNDS AND COMPOSITIONS FOR USE IN PHOTOTHERAPY AND IN TREATMENT OF OCULAR NEOVASCULAR DISEASE AND CANCERS VEGFA, OPRL1, OGFR OPRM1 5/4885GRIN1 3441/4885GRIN2A 2767/4885
US-20140370005-A1 COMPOUNDS AND COMPOSITIONS FOR USE IN PHOTOTHERAPY AND IN TREATMENT OF OCULAR NEOVASCULAR DISEASE AND CANCERS VEGFA, OPRL1, OGFR OPRM1 5/4885GRIN1 3441/4885GRIN2A 2767/4885

“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.