Phenoxybenzamine

Phenoxybenzamine

SCHEMBL202823

C[C@@H](COc1ccccc1)N(CCCl)Cc1ccccc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2C

The experimentally established mechanism targets of Phenoxybenzamine. 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
ADRA2B known ✓ P18089 2/20 1.00
ADRA2C known ✓ P18825 2/20 1.00
ADRA1A known ✓ P35348 2/20 1.00
ADRA2A known ✓ P08913 1/20 1.00
SMN1; SMN2 Q16637 3/20 1.00
TSHR P16473 3/20 1.00
ALDH1A1 P00352 2/20 1.00
CYP2D6 P10635 2/20 1.00
SLC6A2 P23975 2/20 1.00
HTR2A P28223 2/20 1.00
SLC6A3 Q01959 2/20 1.00
KCNH2 Q12809 2/20 1.00
SLC22A2 O15244 1/20 1.00
SLC22A1 O15245 1/20 1.00
SLC22A3 O75751 1/20 1.00
ESR1 P03372 1/20 1.00
CHRM2 P08172 1/20 1.00
HTR1A P08908 1/20 1.00
ADORA3 P0DMS8 1/20 1.00
CHRM1 P11229 1/20 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
Phenoxybenzamine SCHEMBL5722 1.00 SMN1; SMN2 (1.00) SMN1; SMN2TSHRALDH1A1CYP2D6ADRA2B
Phenoxybenzamine SCHEMBL50729 0.99 ALDH1A1 (1.00) SMN1; SMN2TSHRALDH1A1CYP2D6ADRA2B
Phenoxybenzamine SCHEMBL1133740 0.97 SMN1; SMN2 (0.94) SMN1; SMN2TSHRALDH1A1CYP2D6ADRA2B
Phenoxybenzamine SCHEMBL14894820 0.90 SMN1; SMN2 (0.81) SMN1; SMN2TSHRALDH1A1CYP2D6ADRA2B
Phenoxybenzamine SCHEMBL11992656 0.87 ALDH1A1 (0.76) SMN1; SMN2TSHRALDH1A1CYP2D6ADRA2B
SCHEMBL15960915 0.87 ALDH1A1 (0.76) SMN1; SMN2TSHRALDH1A1CYP2D6ADRA2B
SCHEMBL19958436 0.85 ALDH1A1 (0.74) SMN1; SMN2TSHRALDH1A1CYP2D6ADRA2B
SCHEMBL11077715 0.85 SMN1; SMN2 (0.74) SMN1; SMN2TSHRALDH1A1CYP2D6ADRA2B
SCHEMBL11682499 0.84 TSHR (0.72) SMN1; SMN2TSHRALDH1A1CYP2D6ADRA2B
SCHEMBL11684275 0.83 SMN1; SMN2 (0.71) SMN1; SMN2TSHRALDH1A1CYP2D6ADRA2B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4232004-A1 FRACTAL FORMULATIONS Nanogyre Sprl (BE) 2023-08-30 EP claimed
WO-2021078412-A1 FRACTAL FORMULATIONS MESSADEK JALLAL (BE) 2021-04-29 WO claimed
US-20200147076-A1 PARENTERAL FORMULATIONS OF LIPOPHILIC PHARMACEUTICAL AGENTS AND METHODS FOR PREPARING AND USING THE SAME PLATFORM BRIGHTWORKS TWO, LTD. (US) 2020-05-14 US claimed
US-20200121652-A1 COMPOUNDS HAVING CASPASE INHIBITORY ACTIVITY, PHARMACEUTICAL AGENT CONTAINING SAID COMPOUNDS AND FOR TREATING OR PREVENTING CORNEAL ENDOTHELIAL SYMPTOMS, DISORDERS, OR DISEASES, AND APPLICATION OF SAID PHARMACEUTICAL AGENT THE DOSHISHA (JP) 2020-04-23 US claimed
EP-3639855-A1 COMPOUNDS HAVING CASPASE INHIBITORY ACTIVITY, PHARMACEUTICAL AGENT CONTAINING SAID COMPOUNDS AND FOR TREATING OR PREVENTING CORNEAL ENDOTHELIAL SYMPTOMS, DISORDERS, OR DISEASES, AND APPLICATION OF SAID PHARMACEUTICAL AGENT The Doshisha (JP) 2020-04-22 EP claimed
US-20190000862-A1 METHODS AND SYSTEMS FOR THE DELIVERY OF A THERAPEUTIC AGENT HANANJA EHF (IS) 2019-01-03 US claimed
US-20180296556-A1 PARENTERAL FORMULATIONS OF LIPOPHILIC PHARMACEUTICAL AGENTS AND METHODS FOR PREPARING AND USING THE SAME PLATFORM BRIGHTWORKS TWO, LTD. (US) 2018-10-18 US claimed
US-20170172971-A1 PARENTERAL FORMULATIONS OF LIPOPHILIC PHARMACEUTICAL AGENTS AND METHODS FOR PREPARING AND USING THE SAME PLATFORM BRIGHTWORKS TWO, LTD. (US) 2017-06-22 US claimed
CN-106610424-A Screening method of acetylated heat shock protein 90 inhibitor 复旦大学 2017-05-03 CN claimed
US-20170112829-A1 USE OF COMPOUNDS BINDING TO THE SIGMA RECEPTOR LIGANDS FOR THE TREATMENT OF NEUROPATHIC PAIN DEVELOPING AS A CONSEQUENCE OF CHEMOTHERAPY LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2017-04-27 US claimed
CN-1260980-A Oral-applied medicine for curing impotence and preparing process thereof JIANG YANG (CN) 2000-07-26 CN claimed
US-5807574-A COMPOSITE WITH POLYETHYLENE WAX ABBOTT LABORATORIES (US) 1998-09-15 US claimed
EP-0818990-A1 HOMOGENEOUS MIXTURES OF LOW TEMPERATURE-MELTING DRUGS AND ADDITIVES FOR CONTROLLED RELEASE Abbott Laboratories (US) 1998-01-21 EP claimed
WO-1996031197-A1 HOMOGENEOUS MIXTURES OF LOW TEMPERATURE-MELTING DRUGS AND ADDITIVES FOR CONTROLLED RELEASE ABBOTT LABORATORIES (US) 1996-10-10 WO claimed
US-5399581-A Method and compositions for treatment of sexual impotence LARAGH JOHN H (US) 1995-03-21 US claimed
US-5261876-A Enhanced peritoneal membrane plasmapheresis MONCRIEF-POPOVICH RESEARCH INSTITUTE, INC. (US) 1993-11-16 US claimed
WO-1992011851-A1 METHOD AND COMPOSITIONS FOR TREATMENT OF SEXUAL IMPOTENCE LARAGH JOHN H (US) 1992-07-23 WO claimed
US-4832684-A PROTEIN REMOVAL; INFUSION OF VASODILATOR THEN DRAINAGE POPOVICH ROBERT P (US) 1989-05-23 US claimed
US-4673385-A INFUSION OF SOLUTION CONTAINING VASODILATOR THEN DRAINAGE FOR TREATMENT OF PLASMA PROTEIN DISEASES POPOVICH ROBERT P 1987-06-16 US claimed
US-4022893-A Treatment for hypertension MOYER JOHN H 1977-05-10 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 (2 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-20190000862-A1 METHODS AND SYSTEMS FOR THE DELIVERY OF A THERAPEUTIC AGENT TMEM205, NUP205, PIGS ADRA2B 2044/4885ADRA2C 1373/4885ADRA1A 1240/4885
US-20200121652-A1 COMPOUNDS HAVING CASPASE INHIBITORY ACTIVITY, PHARMACEUTICAL AGENT CONTAINING SAID COMPOUNDS AND FOR TREATING OR PREVENTING CORNEAL ENDOTHELIAL SYMPTOMS, DISORDERS, OR DISEASES, AND APPLICATION OF SAID PHARMACEUTICAL AGENT TGFB1, CASP3, TGFB2 ADRA2B 3971/4885ADRA2C 4411/4885ADRA1A 4207/4885

“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.