Racephedrine

Racephedrine

SCHEMBL321655

CN[C@H](C)[C@@H](O)c1ccccc1.Cl

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3SLC6A2

The experimentally established mechanism targets of Racephedrine. 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
▸ ADRA2C known ✓ P18825 2/20 0.96
▸ ADRA1A known ✓ P35348 1/20 0.96
▸ ADRA2A known ✓ P08913 1/20 0.54
▸ SLC6A2 known ✓ P23975 2/20 0.48
▸ KMT2A Q03164 2/20 1.00
▸ MEN1 O00255 1/20 1.00
▸ HBB P68871 1/20 1.00
▸ CYP2D6 P10635 2/20 0.96
▸ CYP2C19 P33261 2/20 0.96
▸ CHRM2 P08172 1/20 0.96
▸ RGS12 O14924 1/20 0.96
▸ GLA P06280 1/20 0.96
▸ CYP3A4 P08684 1/20 0.96
▸ CYP2C9 P11712 1/20 0.96
▸ PKM P14618 1/20 0.96
▸ ALOX15 P16050 1/20 0.96
▸ TSHR P16473 1/20 0.96
▸ ALOX12 P18054 1/20 0.96
▸ NFKB1 P19838 1/20 0.96
▸ HTR2A P28223 1/20 0.96

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
Pseudoephedrine SCHEMBL33285 1.00 KMT2A (1.00) KMT2AMEN1HBBADRA2CCYP2D6
Ephedrine SCHEMBL22822 1.00 KMT2A (1.00) KMT2AMEN1HBBADRA2CCYP2D6
Pseudoephedrine SCHEMBL118099 1.00 KMT2A (1.00) KMT2AMEN1HBBADRA2CCYP2D6
Racephedrine SCHEMBL28253267 1.00 KMT2A (1.00) KMT2AMEN1HBBADRA2CCYP2D6
Racephedrine SCHEMBL22824 1.00 KMT2A (1.00) KMT2AMEN1HBBADRA2CCYP2D6
Racephedrine SCHEMBL22823 1.00 KMT2A (1.00) KMT2AMEN1HBBADRA2CCYP2D6
Racephedrine SCHEMBL27878452 0.98 KMT2A (0.96) KMT2AMEN1HBBADRA2CCYP2D6
Racephedrine SCHEMBL9413942 0.98 KMT2A (0.96) KMT2AMEN1HBBADRA2CCYP2D6
Pseudoephedrine SCHEMBL17004001 0.98 KMT2A (0.96) KMT2AMEN1HBBADRA2CCYP2D6
Racephedrine SCHEMBL8098202 0.98 CYP2D6 (1.00) KMT2AMEN1HBBADRA2CCYP2D6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024040267-A2 DIRECT SYNTHESIS OF N-(3-SUBSTITUTED-CHROMAN-4-YL)-7H- PYRROLO[2,3-D]PYRIMIDIN-4-AMINES AND DERIVATIVES THEREOF MITOKININ, INC. (US) 2024-02-22 — — WO claimed
US-20190145960-A1 COMPOSITIONS, SYSTEMS AND METHODS FOR GENE EXPRESSION NOISE DRUG SCREENING AND USES THEREOF THE J. DAVID GLADSTONE INSTITUTES, A TESTAMENTARY TRUST ESTABLISHED UNDER THE WILL OF J. DAVID GLADSTONE 2019-05-16 — — US claimed
EP-3470536-A1 COMPOSITIONS, SYSTEMS AND METHODS FOR GENE EXPRESSION NOISE DRUG SCREENING AND USES THEREOF The J. David Gladstone Institutes (US) 2019-04-17 — — EP claimed
US-10184933-B2 Compositions, systems and methods for gene expression noise drug screening and uses thereof The J. David Gladstone Industries (US) 2019-01-22 — — US claimed
US-20160245796-A1 COMPOSITIONS, SYSTEMS AND METHODS FOR GENE EXPRESSION NOISE DRUG SCREENING AND USES THEREOF THE J. DAVID GLADSTONE INSTITUTES (US) 2016-08-25 — — US claimed
EP-3052662-A1 COMPOSITIONS, SYSTEMS AND METHODS FOR GENE EXPRESSION NOISE DRUG SCREENING AND USES THEREOF The J. David Gladstone Institutes (US) 2016-08-10 — — EP claimed
WO-2015051035-A1 COMPOSITIONS, SYSTEMS AND METHODS FOR GENE EXPRESSION NOISE DRUG SCREENING AND USES THEREOF THE J. DAVID GLADSTONE INSTITUTES (US) 2015-04-09 — — WO claimed
JP-7165569-A — — None — — JP disclosed
US-20250049722-A1 TRIPULSE RELEASE STIMULANT FORMULATIONS Cingulate Therapeutics LLC (US) 2025-02-13 — — US disclosed
EP-3261625-B1 TRIPULSE RELEASE STIMULANT FORMULATIONS Cingulate Therapeutics LLC (US) 2024-08-14 — — EP disclosed
WO-2024040267-A2 DIRECT SYNTHESIS OF N-(3-SUBSTITUTED-CHROMAN-4-YL)-7H- PYRROLO[2,3-D]PYRIMIDIN-4-AMINES AND DERIVATIVES THEREOF MITOKININ, INC. (US) 2024-02-22 — — WO disclosed
US-20230121531-A1 TRIPULSE RELEASE STIMULANT FORMULATIONS Cingulate Therapeutics LLC (US) 2023-04-20 — — US disclosed
CN-110642721-B Preparation method of selegiline hydrochloride 安徽贝克生物制药有限公司 2022-09-30 — — CN disclosed
CN-1278853-A Gel adhesive, adhesive material containing gel adhesive and adhesive pharmaceutical preparation TEIJIN LTD (JP) 2001-01-03 — — CN disclosed
WO-2000059481-A1 PHARMACEUTICAL DOSAGE FORM FOR PULSATILE DELIVERY OF d-threo-METHYLPHENIDATE AND A SECOND CNS STIMULANT PHARMAQUEST LTD. (BM) 2000-10-12 — — WO disclosed
WO-2000059479-A1 PHARMACEUTICAL DOSAGE FORM FOR PULSATILE DELIVERY OF METHYLPHENIDATE PHARMAQUEST LTD. (BM) 2000-10-12 — — WO disclosed
CN-1054120-C Ephedrine extracting process UNIV QINGHUA (CN) 2000-07-05 — — CN disclosed
CN-1132740-A Ephedrine extracting process UNIV QINGHUA (CN) 1996-10-09 — — CN disclosed
JP-H07165569-A AMELIORANT FOR CEREBRAL FUNCTION TSUMURA & CO 1995-06-27 — — JP disclosed
CN-1043319-A New amine and uses thereof MITSUI PHARMACEUTICALS (JP) 1990-06-27 — — CN disclosed
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