SCHEMBL299963

SCHEMBL299963

O=P(O)(O)c1ccc2ccccc2c1-c1cccc2ccccc12

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
DNMT1 P26358 1/20 0.43
ACP3 P15309 1/20 0.42
PTK2B Q14289 1/20 0.41
L3MBTL1 Q9Y468 1/20 0.41
WDR5 P61964 1/20 0.41
HDAC8 Q9BY41 1/20 0.41
HDAC6 Q9UBN7 1/20 0.41
GPR84 Q9NQS5 2/20 0.40
TYMP P19971 1/20 0.40
GSK3B P49841 1/20 0.39
ADK P55263 1/20 0.39
CA12 O43570 1/20 0.39
CA2 P00918 1/20 0.39
MMP2 P08253 1/20 0.39
MMP9 P14780 1/20 0.39
MMP8 P22894 1/20 0.39
MMP14 P50281 1/20 0.39
CA14 Q9ULX7 1/20 0.39
ALDH1A1 P00352 2/20 0.39
MEN1 O00255 1/20 0.39

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
Biphenyl SCHEMBL28760132 0.94 ACP3 (0.42) DNMT1ACP3PTK2BL3MBTL1WDR5
SCHEMBL28080572 0.87 WDR5 (0.47) DNMT1ACP3PTK2BL3MBTL1WDR5
SCHEMBL29397823 0.81 GPR84 (0.43) DNMT1ACP3PTK2BL3MBTL1HDAC8
SCHEMBL27902996 0.80 ACP3 (0.46) ACP3PTK2BL3MBTL1HDAC8HDAC6
SCHEMBL6242989 0.80 DNMT1 (0.41) DNMT1L3MBTL1WDR5HDAC8HDAC6
Phosphoric Acid SCHEMBL31219446 0.79 NSD2 (0.51) DNMT1ACP3GPR84MEN1MAPT
Phosphoric Acid SCHEMBL29768762 0.79 NSD2 (0.51) DNMT1ACP3GPR84MEN1MAPT
Phosphoric Acid SCHEMBL3922368 0.79 NSD2 (0.51) DNMT1ACP3GPR84MEN1MAPT
Phosphoric Acid SCHEMBL547015 0.79 ACP3 (0.55) ACP3PTK2BL3MBTL1HDAC8HDAC6
Phosphoric Acid SCHEMBL29911372 0.79 ACP3 (0.55) ACP3PTK2BL3MBTL1HDAC8HDAC6

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 13 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118751288-A Preparation method of propenyl binaphthyl phosphonic acid/Pt-loaded hollow mesoporous nanospheres, product and application thereof 重庆邮电大学 2024-10-11 CN claimed
CN-118751288-A Preparation method of propenyl binaphthyl phosphonic acid/Pt-loaded hollow mesoporous nanospheres, product and application thereof 重庆邮电大学 2024-10-11 CN disclosed
CN-118751288-A Preparation method of propenyl binaphthyl phosphonic acid/Pt-loaded hollow mesoporous nanospheres, product and application thereof 重庆邮电大学 2024-10-11 CN disclosed
CN-108084129-B Method for synthesizing (1S, 5R) -lactone 复旦大学 2022-09-16 CN disclosed
US-11441163-B2 Enzyme-catalyzed synthesis of (1S,5R)-bicyclolactone FUDAN UNIVERSITY (CN) 2022-09-13 US disclosed
US-20210355516-A1 ENZYME-CATALYZED SYNTHESIS OF (1S,5R)-BICYCLOLACTONE FUDAN UNIVERSITY (CN) 2021-11-18 US disclosed
US-10316012-B1 Method of synthesizing (1S, 5R)-lactone FUDAN UNIVERSITY (CN) 2019-06-11 US disclosed
EP-1888604-B1 PROCESS FOR PREPARING (ALPHA S, BETA R)-6-BROMO-ALPHA-[2-(DIMETHYLAMINO)ETHYL]-2-METHOXY-ALPHA-1-NAPHTHALENYL-BETA-PHENYL-3-QUINOLINEETHANOL JANSSEN PHARMACEUTICA NV (BE) 2012-03-14 EP disclosed
EP-0451008-B1 8-Sulfamylmethylene-2-amino tetralins MERRELL DOW PHARMA (US) 1995-06-28 EP disclosed
EP-0451008-A1 8-Sulfamylmethylene-2-amino tetralins MERRELL DOW PHARMACEUTICALS INC. (US) 1991-10-09 EP disclosed
EP-0450238-A1 Novel compounds for the treatment of migraine MERRELL DOW PHARMACEUTICALS INC. (US) 1991-10-09 EP disclosed
EP-0451022-A1 Novel compounds for the treatment of migraine MERRELL DOW PHARMACEUTICALS INC. (US) 1991-10-09 EP disclosed
EP-0447727-A1 Novel 8-sulfamylmethylene-2-amino tetralins MERRELL DOW PHARMACEUTICALS INC. (US) 1991-09-25 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 (1 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-10316012-B1 Method of synthesizing (1S, 5R)-lactone HAO2, HAO1, OXER1 DNMT1 1930/4885ACP3 1077/4885PTK2B 387/4885

“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.