SCHEMBL3415364

SCHEMBL3415364

CC(C)C1COC(c2ccccc2P(c2ccccc2)c2ccccc2)=N1

nearest known ligand 0.58

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 2/20 0.58
MAPT P10636 2/20 0.58
RAB9A P51151 1/20 0.58
SMN1; SMN2 Q16637 1/20 0.58
MEN1 O00255 1/20 0.44
KMT2A Q03164 1/20 0.44
DRD1 P21728 2/20 0.38
MAPK1 P28482 1/20 0.33
POLB P06746 1/20 0.32
HTT P42858 1/20 0.31
RECQL P46063 1/20 0.31
TAAR1 Q96RJ0 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
SCHEMBL29528441 1.00 NPC1 (0.58) NPC1MAPTRAB9ASMN1; SMN2MEN1
SCHEMBL2367798 1.00 NPC1 (0.58) NPC1MAPTRAB9ASMN1; SMN2MEN1
SCHEMBL3954455 1.00 NPC1 (0.58) NPC1MAPTRAB9ASMN1; SMN2MEN1
SCHEMBL2515281 0.89 NPC1 (0.47) NPC1MAPTRAB9ASMN1; SMN2MEN1
SCHEMBL14498451 0.88 NPC1 (0.44) NPC1MAPTRAB9ASMN1; SMN2MEN1
SCHEMBL23944688 0.85 NPC1 (0.43) NPC1MAPTRAB9ASMN1; SMN2MEN1
SCHEMBL22365583 0.85 NPC1 (0.43) NPC1MAPTRAB9ASMN1; SMN2MEN1
SCHEMBL19010013 0.82 NPC1 (0.74) NPC1MAPTRAB9ASMN1; SMN2MEN1
SCHEMBL16325449 0.82 NPC1 (0.56) NPC1MAPTRAB9ASMN1; SMN2MEN1
SCHEMBL21162136 0.82 MAPT (0.47) NPC1MAPTRAB9ASMN1; SMN2DRD1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117024354-B Preparation method of Rui Mi Buti Ni 天津凯莱英制药有限公司 2023-12-08 CN claimed
CN-117024354-A Preparation method of Rui Mi Buti Ni 天津凯莱英制药有限公司 2023-11-10 CN claimed
CN-115141135-A Preparation method of oxindole-acetic acid compound containing 3-bit chiral quaternary carbon center 四川大学 2022-10-04 CN claimed
US-20250333400-A1 CERTAIN PLADIENOLIDE COMPOUNDS AND METHODS OF USE EISAI R&D MANAGEMENT CO., LTD. (JP) 2025-10-30 US disclosed
US-20240368140-A1 CERTAIN PLADIENOLIDE COMPOUNDS AND METHODS OF USE EISAI R&D MANAGEMENT CO., LTD. (JP) 2024-11-07 US disclosed
US-12129249-B2 Method for producing optically active compound DAY ONE BIOPHARMACEUTICALS, INC. (US) 2024-10-29 US disclosed
EP-4406609-A2 METHOD FOR PRODUCING OPTICALLY ACTIVE COMPOUND Day One Biopharmaceuticals, Inc. (US) 2024-07-31 EP disclosed
EP-3439663-B1 METHODS OF TREATING PEDIATRIC CANCERS LOXO ONCOLOGY INC (US) 2024-07-17 EP disclosed
CN-109414442-B Liquid preparation of compound 洛克索肿瘤学股份有限公司 2024-03-29 CN disclosed
US-11926619-B2 Certain pladienolide compounds and methods of use EISAI R & D MANAGEMENT CO., LTD. (JP) 2024-03-12 US disclosed
CN-117447464-A Method for producing optically active compound 首日生物制药公司 2024-01-26 CN disclosed
US-20070117786-A1 Intermediates for the preparation of tricyclic dihydropyrano-imidazo-pyridines derivatives ALTANA PHARMA AG (DE) 2007-05-24 US disclosed
EP-1567464-B1 CATALYTIC HYDROGENERATION OF CARBON-HETEROATOM DOUBLE BONDS SOLVIAS AG (CH) 2007-04-18 EP disclosed
US-7179934-B2 Amino acids with affinity for the α2δ-protein WARNER-LAMBERT COMPANY LLC (US) 2007-02-20 US disclosed
EP-1697358-A1 INTERMEDIATES FOR THE PREPARATION OF TRICYCLIC DIHYDROPYRANO -IMIDAZO -PYRIDINES DERIVATIVES Altana Pharma AG (DE) 2006-09-06 EP disclosed
US-20060084820-A1 Enantioselective, catalytic allylation of ketones and olefins CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 2006-04-20 US disclosed
WO-2005058894-A1 INTERMEDIATES FOR THE PREPARATION OF TRICYCLIC DIHYDROPYRANO -IMIDAZO -PYRIDINES DERIVATIVES ALTANA PHARMA AG (DE) 2005-06-30 WO disclosed
US-20050124668-A1 Amino acids with affinity for the alpha2delta-protein WARNER-LAMBERT COMPANY LLC 2005-06-09 US disclosed
US-20050101643-A1 Amino acids with affinity for the alpha2delta-protein WARNER-LAMBERT COMPANY LLC 2005-05-12 US disclosed
WO-2004031168-A2 PROCESSES AND INTERMEDIATES FOR THE PREPARATION OF OPTICALLY ACTIVE 3-AMINO-1-(2-THIENYL)-1-PROPANOL DERIVATIVES LONZA AG (CH) 2004-04-15 WO 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 (8 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-20060084820-A1 Enantioselective, catalytic allylation of ketones and olefins AKR1C2, TECR, AKR1C4 NPC1 1539/4885MAPT 2756/4885RAB9A 4198/4885
US-20050124668-A1 Amino acids with affinity for the alpha2delta-protein SCN2A, SCN1A, OPRD1 NPC1 3038/4885MAPT 908/4885RAB9A 1165/4885
US-20240368140-A1 CERTAIN PLADIENOLIDE COMPOUNDS AND METHODS OF USE PLAAT5, PLAAT3, PLAAT4 NPC1 1734/4885MAPT 4316/4885RAB9A 704/4885
US-20250333400-A1 CERTAIN PLADIENOLIDE COMPOUNDS AND METHODS OF USE SNRPE, SNRPB2, DDX21 NPC1 1630/4885MAPT 4458/4885RAB9A 2103/4885
US-20070117786-A1 Intermediates for the preparation of tricyclic dihydropyrano-imidazo-pyridines derivatives CYP1A1, CYP3A4, CYP19A1 NPC1 3091/4885MAPT 2451/4885RAB9A 3188/4885
US-20050101643-A1 Amino acids with affinity for the alpha2delta-protein SCN2A, OPRD1, SCN1A NPC1 3111/4885MAPT 1029/4885RAB9A 1183/4885
US-12129249-B2 Method for producing optically active compound DHPS, QDPR, SPR NPC1 2691/4885MAPT 3660/4885RAB9A 1416/4885
US-11926619-B2 Certain pladienolide compounds and methods of use PLAAT5, PLAAT3, PLAAT4 NPC1 1734/4885MAPT 4316/4885RAB9A 704/4885

“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.