SCHEMBL3785587

SCHEMBL3785587

O=C(OC[C@H]1OC(OC(=O)c2ccccc2)[C@H](OC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@@H]1OC(=O)c1ccccc1)c1ccccc1

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ PTPN1 P18031 4/20 0.67
▸ F11 P03951 2/20 0.60
▸ USP2 O75604 2/20 0.60
▸ CA1 P00915 2/20 0.60
▸ CA2 P00918 2/20 0.60
▸ MAPK1 P28482 2/20 0.60
▸ TMPRSS2 O15393 1/20 0.60
▸ PDE5A O76074 1/20 0.60
▸ HMGCR P04035 1/20 0.60
▸ CYP1A2 P05177 1/20 0.60
▸ LCK P06239 1/20 0.60
▸ FYN P06241 1/20 0.60
▸ HSPD1 P10809 1/20 0.60
▸ CYP2C9 P11712 1/20 0.60
▸ CA6 P23280 1/20 0.60
▸ TBXAS1 P24557 1/20 0.60
▸ MAPK3 P27361 1/20 0.60
▸ HSPE1 P61604 1/20 0.60
▸ MAPK14 Q16539 1/20 0.60
▸ TST Q16762 1/20 0.60

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
SCHEMBL7642894 1.00 PTPN1 (0.67) PTPN1F11USP2CA1CA2
SCHEMBL18083458 1.00 PTPN1 (0.67) PTPN1F11USP2CA1CA2
SCHEMBL7144957 1.00 PTPN1 (0.67) PTPN1F11USP2CA1CA2
SCHEMBL7251000 1.00 PTPN1 (0.67) PTPN1F11USP2CA1CA2
SCHEMBL19479105 1.00 PTPN1 (0.67) PTPN1F11USP2CA1CA2
SCHEMBL12326369 1.00 PTPN1 (0.67) PTPN1F11USP2CA1CA2
SCHEMBL18068260 1.00 PTPN1 (0.67) PTPN1F11USP2CA1CA2
SCHEMBL16731442 1.00 PTPN1 (0.67) PTPN1F11USP2CA1CA2
SCHEMBL7642890 1.00 PTPN1 (0.67) PTPN1F11USP2CA1CA2
SCHEMBL17633988 1.00 PTPN1 (0.67) PTPN1F11USP2CA1CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108435107-B Preparation and application of DNA affinity nano-microspheres 嘉兴杰赛生物科技有限公司 2020-10-23 — — CN claimed
US-7144453-B2 Composition for preparing porous dielectric thin film containing saccharides porogen SAMSUNG ELECTRONICS CO., LTD. (KR) 2006-12-05 — — US claimed
US-20040121139-A1 Composition for preparing porous dielectric thin film containing saccharides porogen SAMSUNG ELECTRONICS CO., LTD. (KR) 2004-06-24 — — US claimed
EP-1416501-A2 Composition for preparing porous dielectric thin film containing saccharides porogen SAMSUNG ELECTRONICS CO., LTD. (KR) 2004-05-06 — — EP claimed
US-20250333435-A1 TIMOSAPONIN COMPOUNDS GOLDPORP PHARMA LTD (CN) 2025-10-30 — — US disclosed
US-12234258-B2 Timosaponin compounds GOLDPORP PHARMA LIMITED (CN) 2025-02-25 — — US disclosed
US-20220340616-A1 TIMOSAPONIN COMPOUNDS GOLDPORP PHARMA LIMITED (HK) 2022-10-27 — — US disclosed
US-11319338-B2 Timosaponin compounds GOLDPORP PHARMA LIMITED (HK) 2022-05-03 — — US disclosed
US-20150050367-A1 TIMOSAPONIN COMPOUNDS GOLDPORP PHARMA LIMITED (HK) 2015-02-19 — — US disclosed
WO-2013149580-A1 TIMOSAPONIN COMPOUNDS CHE CHIMING (CN) 2013-10-10 — — WO disclosed
US-20100331269-A1 TRITERPENES DERIVATIVES AND USES THEREOF AS ANTITUMOR AGENTS OR ANTI-INFLAMMATORY AGENTS UNIVERSITE DU QUEBEC A CHICOUTIMI (CA) 2010-12-30 — — US disclosed
US-7539038-B2 Nonvolatile nanochannel memory device using organic-inorganic complex mesoporous material SAMSUNG ELECTRONICS CO., LTD. (KR) 2009-05-26 — — US disclosed
US-20060208248-A1 Nonvolatile nanochannel memory device using organic-inorganic complex mesoporous material SAMSUNG ELECTRONICS CO., LTD. (KR) 2006-09-21 — — US disclosed
US-20040121139-A1 Composition for preparing porous dielectric thin film containing saccharides porogen SAMSUNG ELECTRONICS CO., LTD. (KR) 2004-06-24 — — US disclosed
EP-1416501-A2 Composition for preparing porous dielectric thin film containing saccharides porogen SAMSUNG ELECTRONICS CO., LTD. (KR) 2004-05-06 — — EP disclosed
US-6632940-B1 Glycosidic coupling between donor and acceptor in presence of Bronsted or Lewis acid to form glucopyranose-D- glucopyranose LABORATOIRES GOEMAR (FR) 2003-10-14 — — US disclosed
EP-1071692-B1 METHOD FOR LAMINARIBIOSE SYNTHESIS GOEMAR LAB SA (FR) 2002-07-31 — — EP disclosed
EP-1071692-A1 METHOD FOR LAMINARIBIOSE SYNTHESIS LABORATOIRES GOEMAR (FR) 2001-01-31 — — EP disclosed
WO-1999052920-A1 METHOD FOR LAMINARIBIOSE SYNTHESIS LABORATOIRES GOEMAR (FR) 1999-10-21 — — WO disclosed
EP-0306168-A1 Preparation of radiolabeled conjugates IMMUNOMEDICS, INC. (US) 1989-03-08 — — 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 (6 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-12234258-B2 Timosaponin compounds APP, IAPP, BACE1 PTPN1 3996/4885F11 1228/4885USP2 4673/4885
US-20220340616-A1 TIMOSAPONIN COMPOUNDS APP, IAPP, BACE1 PTPN1 3996/4885F11 1228/4885USP2 4673/4885
US-20150050367-A1 TIMOSAPONIN COMPOUNDS APP, IAPP, BACE1 PTPN1 3996/4885F11 1228/4885USP2 4673/4885
US-20100331269-A1 TRITERPENES DERIVATIVES AND USES THEREOF AS ANTITUMOR AGENTS OR ANTI-INFLAMMATORY AGENTS TNF, B3GAT3, ST3GAL3 PTPN1 2783/4885F11 996/4885USP2 3573/4885
US-11319338-B2 Timosaponin compounds APP, IAPP, BACE1 PTPN1 3996/4885F11 1228/4885USP2 4673/4885
US-20250333435-A1 TIMOSAPONIN COMPOUNDS APP, IAPP, BACE1 PTPN1 3996/4885F11 1228/4885USP2 4673/4885

“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.

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