Hydromorphone

Hydromorphone

SCHEMBL1360640

CN1CC[C@]23c4c5ccc(O)c4O[C@H]2C(=O)CC[C@H]3[C@H]1C5.CN1CC[C@]23c4c5ccc(O)c4O[C@H]2[C@@H](O)C=C[C@H]3[C@H]1C5

nearest known ligand 0.79

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

OPRM1

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

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
OPRM1 known ✓ P35372 10/20 0.79
OPRD1 P41143 11/20 0.79
OPRK1 P41145 8/20 0.79
MRGPRX2 Q96LB1 3/20 0.75
SLC22A1 O15245 1/20 0.75
ADRA2A P08913 1/20 0.75
ARRB1 P49407 1/20 0.75
LMNA P02545 1/20 0.61
PDE4D Q08499 1/20 0.61

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
Codeine SCHEMBL250022 0.94 OPRM1 (0.72) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Codeine SCHEMBL3239478 0.94 OPRM1 (0.72) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Ethylmorphine SCHEMBL6471137 0.92 OPRM1 (0.67) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Hydromorphone SCHEMBL16035915 0.92 OPRM1 (0.71) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Hydrocodone SCHEMBL1359279 0.90 OPRM1 (0.78) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Hydromorphone SCHEMBL19107004 0.89 OPRD1 (1.00) OPRD1OPRM1OPRK1MRGPRX2LMNA
Hydromorphone SCHEMBL12368741 0.89 OPRD1 (1.00) OPRD1OPRM1OPRK1MRGPRX2LMNA
Hydromorphone SCHEMBL10031237 0.89 OPRD1 (1.00) OPRD1OPRM1OPRK1MRGPRX2LMNA
Hydromorphone SCHEMBL16024201 0.89 OPRD1 (1.00) OPRD1OPRM1OPRK1MRGPRX2LMNA
Hydromorphone SCHEMBL6798556 0.89 OPRD1 (1.00) OPRD1OPRM1OPRK1MRGPRX2LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20190330328-A1 METHODS OF TREATING NON-RADIOGRAPHIC AXIAL SPONDYLOARTHRITIS USING INTERLEUKIN-17 (IL-17) ANTAGONISTS NOVARTIS PHARMA GMBH (DE) 2019-10-31 US disclosed
CN-110114457-A Generate the method for removing first opiates and NAL- opiates benzyl isoquinoline alkaloid 安思雅公司 2019-08-09 CN disclosed
EP-3365011-A1 METHODS OF TREATING NON-RADIOGRAPHIC AXIAL SPONDYLOARTHRITIS USING INTERLEUKIN-17 (IL-17) ANTAGONISTS Novartis AG (CH) 2018-08-29 EP disclosed
CN-107960102-A The method for producing epimerase and benzyl isoquinoline alkaloid 小利兰·斯坦福大学托管委员会 2018-04-24 CN disclosed
WO-2017068472-A1 METHODS OF TREATING NON-RADIOGRAPHIC AXIAL SPONDYLOARTHRITIS USING INTERLEUKIN-17 (IL-17) ANTAGONISTS NOVARTIS AG (CH) 2017-04-27 WO disclosed
US-8067243-B2 Methods and systems for analyzing medication levels in a sample OREGON MEDICAL LABORATORIES (US) 2011-11-29 US disclosed
US-20100051801-A1 METHODS AND SYSTEMS FOR ANALYZING MEDICATION LEVELS IN A SAMPLE OREGON MEDICAL LABORATORIES 2010-03-04 US disclosed
EP-1399161-A2 SUSTAINED-RELEASE ANALGESIC COMPOUNDS Control Delivery Systems (US) 2004-03-24 EP disclosed
WO-2002098427-A2 SUSTAINED-RELEASE ANALGESIC COMPOUNDS CONTROL DELIVERY SYSTEMS (US) 2002-12-12 WO disclosed
EP-0770387-B1 Pharmaceutical composition containing a local anesthetic and/or centrally acting analgesic BRAUN MELSUNGEN AG (DE) 1999-08-11 EP disclosed
EP-0770387-A1 Pharmaceutical composition containing a local anesthetic and/or centrally acting analgesic B. BRAUN MELSUNGEN AG (DE) 1997-05-02 EP disclosed