Nordefrin

Nordefrin

SCHEMBL249722

CC(N)C(O)c1ccc(O)c(O)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA2AADRA2BADRA2C

The experimentally established mechanism targets of Nordefrin. 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
ADRA2A known ✓ P08913 2/20 0.52
ADRA2C known ✓ P18825 2/20 0.52
ADRA2B known ✓ P18089 1/20 0.52
TDP1 Q9NUW8 8/20 1.00
KDM4E B2RXH2 7/20 1.00
RECQL P46063 6/20 1.00
MAPT P10636 5/20 1.00
LMNA P02545 5/20 1.00
BLM P54132 4/20 1.00
APEX1 P27695 3/20 1.00
HIF1A Q16665 2/20 1.00
KMT2A Q03164 2/20 1.00
ALOX15 P16050 1/20 1.00
TSHR P16473 1/20 1.00
NFKB1 P19838 1/20 1.00
THPO P40225 1/20 1.00
HSD17B10 Q99714 1/20 1.00
POLB P06746 1/20 1.00
MTOR P42345 1/20 1.00
MAPK1 P28482 2/20 0.62

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
Levonordefrin SCHEMBL6295856 1.00 TDP1 (1.00) TDP1KDM4ERECQLMAPTLMNA
Levonordefrin SCHEMBL14478222 1.00 TDP1 (1.00) TDP1KDM4ERECQLMAPTLMNA
Levonordefrin SCHEMBL14478226 1.00 TDP1 (1.00) TDP1KDM4ERECQLMAPTLMNA
Nordefrin SCHEMBL29693041 1.00 TDP1 (1.00) TDP1KDM4ERECQLMAPTLMNA
Levonordefrin SCHEMBL29410156 1.00 TDP1 (1.00) TDP1KDM4ERECQLMAPTLMNA
Levonordefrin SCHEMBL119171 1.00 TDP1 (1.00) TDP1KDM4ERECQLMAPTLMNA
Levonordefrin SCHEMBL1780761 1.00 TDP1 (1.00) TDP1KDM4ERECQLMAPTLMNA
Nordefrin SCHEMBL316522 0.98 KDM4E (1.00) TDP1KDM4ERECQLMAPTLMNA
Levonordefrin SCHEMBL363800 0.98 KDM4E (1.00) TDP1KDM4ERECQLMAPTLMNA
Nordefrin SCHEMBL5060952 0.98 KDM4E (1.00) TDP1KDM4ERECQLMAPTLMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024249843-A2 GUANFACINE FOR FATIGUE DISORDERS VANDERBILT UNIVERSITY (US) 2024-12-05 WO claimed
US-20240225978-A1 METHODS AND COMPOSITIONS FOR PHARMACOLOGICAL TREATMENT OF BLEPHAROPTOSIS Bokman, Christine Lynn (US) 2024-07-11 US claimed
CN-117100901-A Photoinitiated biological tissue adhesive, gel sheet, preparation method and application 艾弈医疗科技(上海)有限公司 2023-11-24 CN claimed
CN-110143886-B Process for the preparation of beta-arylaminoalkols such as tulobuterol, chlorpropaline, isoadrenaline dichloride and sotalol 北京化工大学 2022-11-01 CN claimed
WO-2020210889-A1 DYE COMPOSITION FOR MARKING ORGANIC TISSUE WITH ANAESTHETIC AND METHOD FOR APPLYING SAME HEXSEL, DORIS MARIA (BR) 2020-10-22 WO claimed
EP-3434271-B1 USE OF PHARMACEUTICAL COMPOSITION FOR THE TREATMENT OF POIKILODERMA OF CIVATTE HEXSEL DORIS MARIA (BR) 2020-08-26 EP claimed
US-10751303-B2 Method for shortening anti-infective therapy duration in subjects with infection INSTITUTE FOR CLINICAL PHARMACODYNAMICS, INC. (US) 2020-08-25 US claimed
US-10617688-B2 Use of pharmaceutical composition for the treatment of skin erythema in poikilodermas NOVA SCIENTIFICA LLC 2020-04-14 US claimed
US-20190269680-A1 USE OF AN ACTIVE SUBSTANCE IN THE TREATMENT OF MELASMA HEXSEL DORIS MARIA (BR) 2019-09-05 US claimed
EP-3498299-A1 COMPOSITIONS AND METHODS FOR TREATING PURPURA Aclaris Therapeutics, Inc. (US) 2019-06-19 EP claimed
US-20020068754-A1 Combination of adrenergic agonist and aryl-cyclo-alkanolamine for relieving chronic pain without adverse side effects OLNEY JOHN W (US) 2002-06-06 US claimed
US-6369114-B1 Administration of an α2-adrenergic receptor agonist to enhance cardiopulmonary resuscitation INSTITUTE OF CRITICAL CARE MEDICINE 2002-04-09 US claimed
US-20020016319-A1 Combined adamantane derivative and adrenergic agonist for relief of chronic pain without adverse side effects OLNEY JOHN W (US) 2002-02-07 US claimed
WO-2001089448-A2 COMBINATION OF ADRENERGIC AGONIST AND NMDA ANTAGONIST FOR RELIEVING CHRONIC PAIN WITHOUT ADVERSE SIDE EFFECTS OLNEY JOHN W (US) 2001-11-29 WO claimed
WO-2001039761-A1 ADMINISTRATION OF AN ALPHA-2 ADRENERGIC RECEPTOR AGONIST TO ENHANCE CARDIOPULMONARY RESUSCITATION INSTITUTE OF CRITICAL CARE MEDICINE (US) 2001-06-07 WO claimed
US-5605911-A NEUROTOXIC SIDE EFFECT INHIBITION WASHINGTON UNIVERSITY (US) 1997-02-25 US claimed
WO-1994000432-A1 ANORECTIC EPINEPHRINE DERIVATIVES THE UNITED STATES OF AMERICA, REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 1994-01-06 WO claimed
EP-0152379-A2 Process for preparing pharmaceutical compositions containing unilamellar liposomes CIBA-GEIGY AG (CH) 1985-08-21 EP claimed
EP-0059057-A1 Treatment of diarrhoea BEECHAM GROUP PLC (GB) 1982-09-01 EP claimed
US-4313956-A Novel sypathomimetic amine prodrugs INTERX RESEARCH CORP. (US) 1982-02-02 US 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-10751303-B2 Method for shortening anti-infective therapy duration in subjects with infection POLR1C, POLI, TYMP ADRA2A 4125/4885ADRA2C 4257/4885ADRA2B 4192/4885

“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.