SCHEMBL4892490

SCHEMBL4892490

CCN(CC)c1cccc(P)c1N(CC)CC

nearest known ligand 0.34

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.34
CYP3A4 P08684 2/20 0.34
TSHR P16473 2/20 0.31
HPGD P15428 1/20 0.30
PSMD14 O00487 1/20 0.30
MAPK1 P28482 1/20 0.30
RECQL P46063 1/20 0.30
GFER P55789 1/20 0.30
TDP1 Q9NUW8 1/20 0.30
L3MBTL1 Q9Y468 1/20 0.30
ALDH1A3 P47895 1/20 0.30

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
SCHEMBL27997994 0.80 TSHR (0.39) ALDH1A1CYP3A4TSHRPSMD14MAPK1
SCHEMBL14860191 0.78 S1PR1 (0.34) ALDH1A1CYP3A4TSHRTDP1
SCHEMBL1953279 0.75 ALDH1A1 (0.42) ALDH1A1CYP3A4TSHRHPGDMAPK1
SCHEMBL2100543 0.75 ALDH1A1 (0.34) ALDH1A1CYP3A4TSHRHPGDPSMD14
SCHEMBL31718395 0.71 TSHR (0.46) ALDH1A1CYP3A4TSHRPSMD14MAPK1
SCHEMBL6299189 0.71 TSHR (0.46) ALDH1A1CYP3A4TSHRPSMD14MAPK1
SCHEMBL29861910 0.70 L3MBTL1 (0.43) ALDH1A1CYP3A4TSHRHPGDPSMD14
SCHEMBL30274134 0.69 TP53 (0.45) ALDH1A1TSHRHPGDTDP1L3MBTL1
SCHEMBL3796130 0.69 GABRA1 (0.40) ALDH1A1CYP3A4TSHRTDP1L3MBTL1
SCHEMBL2104387 0.68 ALDH1A1 (0.30) ALDH1A1CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1598053-B1 Use of a composition containing at least one phosphine as majority reducing agent to remove the artificial colour of keratinic fibres OREAL (FR) 2006-12-20 EP claimed
EP-1598053-A1 Use of a composition containing at least one phosphine as majority reducing agent to remove the artificial colour of keratinic fibres L'OREAL (FR) 2005-11-23 EP claimed
US-20050251928-A1 Method for stripping artificial color from keratin fibers L'OREAL (FR) 2005-11-17 US claimed
US-20260103443-A1 CHEMICAL COMPOUND LMS CO LTD (KR) 2026-04-16 US disclosed
EP-4695222-A1 PROCESS FOR PREPARING ESTERAMIDE COMPOUNDS SPECIALTY OPERATIONS FRANCE (FR) 2026-02-18 EP disclosed
EP-4695220-A1 PROCESSES FOR PRODUCING ALKYL ACRYLATE DIMERS SPECIALTY OPERATIONS FRANCE (FR) 2026-02-18 EP disclosed
US-20250368598-A1 CATALYTIC CARBOXYCARBONYLATION OF ALKENES TO FORM ANHYDRIDES BHATTACHARYA SHRABANTI (US) 2025-12-04 US disclosed
US-20250230119-A1 PROCESSES FOR PRODUCING ALKYL ACRYLATE DIMERS SPECIALTY OPERATIONS FRANCE (FR) 2025-07-17 US disclosed
US-20250197346-A1 COMPOUND FOR OPTICAL ABSORBENT LMS CO., LTD. (KR) 2025-06-19 US disclosed
EP-4543841-A2 CATALYTIC CARBOXYCARBONYLATION OF ALKENES TO FORM ANHYDRIDES The University of North Carolina at Chapel Hill (US) 2025-04-30 EP disclosed
WO-2025073727-A1 USE OF A COMPOSITION FOR IMPROVING ADHESIVE BONDING OF SURFACES, PROCESS FOR BONDING SURFACES SPECIALTY OPERATIONS FRANCE (FR) 2025-04-10 WO disclosed
WO-2006003431-A1 MONODONOR PHOSPHONITE LIGANDS RHODIA UK LIMITED (GB) 2006-01-12 WO disclosed
EP-1598053-A1 Use of a composition containing at least one phosphine as majority reducing agent to remove the artificial colour of keratinic fibres L'OREAL (FR) 2005-11-23 EP disclosed
US-20050251928-A1 Method for stripping artificial color from keratin fibers L'OREAL (FR) 2005-11-17 US disclosed
EP-0871621-A4 ASYMMETRIC SYNTHESIS CATALYZED BY TRANSITION METAL COMPLEXES WITH NEW CHIRAL LIGANDS PENN STATE RES FOUND (US) 1999-10-13 EP disclosed
EP-0871621-A1 ASYMMETRIC SYNTHESIS CATALYZED BY TRANSITION METAL COMPLEXES WITH NEW CHIRAL LIGANDS THE PENN STATE RESEARCH FOUNDATION (US) 1998-10-21 EP disclosed
US-5767276-A Asymmetric synthesis catalyzed by transition metal complexes with new chiral ligands THE PENN STATE RESEARCH FOUNDATION (US) 1998-06-16 US disclosed
WO-1997013763-A1 ASYMMETRIC SYNTHESIS CATALYZED BY TRANSITION METAL COMPLEXES WITH NEW CHIRAL LIGANDS THE PENN STATE RESEARCH FOUNDATION (US) 1997-04-17 WO disclosed
EP-0082057-B1 PROCESS FOR PREPARING PHOSPHINAMIDES, APPLICATIONS AND PRODUCTS SOCIETE NATIONALE ELF AQUITAINE (FR) 1986-04-30 EP disclosed
EP-0082057-A2 Process for preparing phosphinamides, applications and products SOCIETE NATIONALE ELF AQUITAINE (FR) 1983-06-22 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 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-20250368598-A1 CATALYTIC CARBOXYCARBONYLATION OF ALKENES TO FORM ANHYDRIDES CA4, CA12, CA14 ALDH1A1 688/4885CYP3A4 841/4885TSHR 4615/4885
US-20250197346-A1 COMPOUND FOR OPTICAL ABSORBENT CDH1, SUN2, HSF1 ALDH1A1 1614/4885CYP3A4 2405/4885TSHR 4544/4885
US-20260103443-A1 CHEMICAL COMPOUND RAD51, CBR1, NOS1 ALDH1A1 963/4885CYP3A4 222/4885TSHR 2426/4885
US-20050251928-A1 Method for stripping artificial color from keratin fibers KRT18, DSG1, JUP ALDH1A1 4512/4885CYP3A4 4442/4885TSHR 4245/4885
US-20250230119-A1 PROCESSES FOR PRODUCING ALKYL ACRYLATE DIMERS HDHD5, ABHD5, HACL2 ALDH1A1 351/4885CYP3A4 697/4885TSHR 3972/4885

“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.