(+)-Pentazocine

(+)-Pentazocine

SCHEMBL30132413

CC(C)=CCN1CC[C@]2(C)c3cc(O)ccc3C[C@H]1[C@H]2C

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SIGMAR1

The experimentally established mechanism targets of (+)-Pentazocine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
SIGMAR1 known ✓ Q99720 10/20 1.00
OPRM1 P35372 4/20 1.00
TMEM97 Q5BJF2 4/20 1.00
OPRD1 P41143 3/20 1.00
OPRK1 P41145 3/20 1.00
EBP Q15125 2/20 1.00
CYP1A2 P05177 1/20 0.78
CYP3A4 P08684 1/20 0.78
CYP2D6 P10635 1/20 0.78
TSHR P16473 1/20 0.78
NPSR1 Q6W5P4 1/20 0.76
LMNA P02545 1/20 0.76
PMP22 Q01453 1/20 0.76

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
Pentazocine SCHEMBL2493 1.00 SIGMAR1 (1.00) SIGMAR1OPRM1TMEM97OPRD1OPRK1
(+)-Pentazocine SCHEMBL2492 1.00 SIGMAR1 (1.00) SIGMAR1OPRM1TMEM97OPRD1OPRK1
Rel-Pentazocine SCHEMBL135685 1.00 SIGMAR1 (1.00) SIGMAR1OPRM1TMEM97OPRD1OPRK1
(+)-Pentazocine SCHEMBL16220021 1.00 SIGMAR1 (1.00) SIGMAR1OPRM1TMEM97OPRD1OPRK1
(+)-Pentazocine SCHEMBL16144643 1.00 SIGMAR1 (1.00) SIGMAR1OPRM1TMEM97OPRD1OPRK1
(+)-Pentazocine SCHEMBL18672553 1.00 SIGMAR1 (1.00) SIGMAR1OPRM1TMEM97OPRD1OPRK1
(+)-Pentazocine SCHEMBL4376337 1.00 SIGMAR1 (1.00) SIGMAR1OPRM1TMEM97OPRD1OPRK1
(+)-Pentazocine SCHEMBL680675 1.00 SIGMAR1 (1.00) SIGMAR1OPRM1TMEM97OPRD1OPRK1
(+)-Pentazocine SCHEMBL22865258 1.00 SIGMAR1 (1.00) SIGMAR1OPRM1TMEM97OPRD1OPRK1
Pentazocine SCHEMBL29611805 1.00 SIGMAR1 (1.00) SIGMAR1OPRM1TMEM97OPRD1OPRK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240269230-A1 CYCLOTIDES IN COMBINATION WITH KAPPA OPIOID RECEPTOR LIGANDS FOR MS THERAPY MEDIZINISCHE UNIVERSITAT WIEN (AT) 2024-08-15 US claimed
CN-115697371-A Macrocyclic oligopeptides in combination with kappa opioid receptor ligands for MS therapy 维也纳医科大学 2023-02-03 CN claimed
EP-4121085-A1 CYCLOTIDES IN COMBINATION WITH KAPPA OPIOID RECEPTOR LIGANDS FOR MS THERAPY Medizinische Universität Wien (AT) 2023-01-25 EP claimed
US-20240366513-A1 Methods For Administering Weight Loss Medications NALPROPION PHARMACEUTICALS LLC (US) 2024-11-07 US disclosed
US-20240269230-A1 CYCLOTIDES IN COMBINATION WITH KAPPA OPIOID RECEPTOR LIGANDS FOR MS THERAPY MEDIZINISCHE UNIVERSITAT WIEN (AT) 2024-08-15 US disclosed
US-12048769-B2 Methods for administering weight loss medications NALPROPION PHARMACEUTICALS LLC (US) 2024-07-30 US disclosed
US-20230301922-A1 Layered Pharmaceutical Formulations NALPROPION PHARMACEUTICALS LLC (US) 2023-09-28 US disclosed
CN-115697371-A Macrocyclic oligopeptides in combination with kappa opioid receptor ligands for MS therapy 维也纳医科大学 2023-02-03 CN disclosed
EP-4121085-A1 CYCLOTIDES IN COMBINATION WITH KAPPA OPIOID RECEPTOR LIGANDS FOR MS THERAPY Medizinische Universität Wien (AT) 2023-01-25 EP disclosed