SCHEMBL8104271

SCHEMBL8104271

CC1OC(=O)C(C)OC1=O.CC1OC(=O)C(C)OC1=O

nearest known ligand 0.41

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
CA1 P00915 1/20 0.41
CA9 Q16790 1/20 0.41
SMN1; SMN2 Q16637 1/20 0.40
MEN1 O00255 1/20 0.38
KMT2A Q03164 1/20 0.38
TAS2R46 P59540 2/20 0.31
MAOA P21397 1/20 0.30
PARP1 P09874 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
SCHEMBL44996 1.00 CA1 (0.41) CA1CA9SMN1; SMN2MEN1KMT2A
SCHEMBL439067 1.00 CA1 (0.41) CA1CA9SMN1; SMN2MEN1KMT2A
SCHEMBL682255 1.00 CA1 (0.41) CA1CA9SMN1; SMN2MEN1KMT2A
SCHEMBL732959 1.00 CA1 (0.41) CA1CA9SMN1; SMN2MEN1KMT2A
SCHEMBL15034 1.00 CA1 (0.41) CA1CA9SMN1; SMN2MEN1KMT2A
SCHEMBL15195848 1.00 CA1 (0.41) CA1CA9SMN1; SMN2MEN1KMT2A
SCHEMBL2860232 1.00 CA1 (0.41) CA1CA9SMN1; SMN2MEN1KMT2A
Methane SCHEMBL1276943 0.96 CA1 (0.39) CA1CA9SMN1; SMN2MEN1KMT2A
SCHEMBL2314693 0.96 CA1 (0.39) CA1CA9SMN1; SMN2MEN1KMT2A
Ammonia Solution, Strong SCHEMBL17351919 0.96 CA1 (0.39) CA1CA9SMN1; SMN2MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109627463-A Hydrogel and pharmaceutical grade protein 深圳诺坦药物技术有限公司 2019-04-16 CN claimed
CN-107320782-B Absorbable bio-medical lactic acid composite material and preparation method thereof 深圳市立心科学有限公司 2018-09-04 CN claimed
CN-107320782-A Absorbable bio-medical lactic acid composite material and preparation method thereof 深圳市立心科学有限公司 2017-11-07 CN claimed
US-11987567-B2 Synthesis method of lactide by confinement effect catalysis of crystalline porous polymer material QINGDAO UNIVERSITY OF SCIENCE AND TECHNOLOGY (CN) 2024-05-21 US disclosed
US-20230094928-A1 Synthesis method of lactide by confinement effect catalysis of crystalline porous polymer material QINGDAO UNIVERSITY OF SCIENCE AND TECHNOLOGY (CN) 2023-03-30 US disclosed
CN-113788937-A Synthetic method of crystalline porous polymer material confined catalytic lactide 青岛科技大学 2021-12-14 CN disclosed
CN-110068546-A Lactide amount in quantifying polymers matrix 普拉克生化公司 2019-07-30 CN disclosed
CN-105229436-B Pressing detection device and touch panel 三井化学株式会社 2019-06-28 CN disclosed
CN-104287797-B For positioning and the method and apparatus of ligament graft fixation object 美多斯国际有限公司 2019-06-18 CN disclosed
CN-105879119-B A kind of compound acellular matrix hydrogel and preparation method thereof 东华大学 2019-06-11 CN disclosed
CN-106084257-B A kind of composite hydrogel and preparation method thereof 东华大学 2019-04-16 CN disclosed
CN-101555243-A Manufacturing method and device of cyclic refined lactic acid dimmer and manufacturing method and device of polylactic acid HITACHI PLANT TECHNOLOGIES LTD (JP) 2009-10-14 CN disclosed
US-6114495-A POLYLACTIDE POLYMER HAVING A NUMBER AVERAGE MOLECULAR WEIGHT OF BETWEEN ABOUT 25,000 AND ABOUT 200,000, LACTIDE, IF PRESENT AT ALL, PRESENT IN CONCENTRATION OF LESS THAN 0.5 WT % BASED ON WEIGHT OF COMPOSITION, DEACTIVATING AGENTS CARGILL INCORPORATED (US) 2000-09-05 US disclosed
US-5686546-A CONTAINER LININGS AT PLASTICS, INC. (CA) 1997-11-11 US disclosed
US-5618911-A RING OPENING POLYMERIZING LACTONE IN THE PRESENCE OF ALIPHATIC CARBOXYLIC ACID; BIODEGRADABILITY TOYO BOSEKI KABUSHIKI KAISHA (JP) 1997-04-08 US disclosed
EP-0722469-A1 CONTINUOUS PROCESS FOR THE MANUFACTURE OF LACTIDE AND LACTIDE POLYMERS CARGILL, INCORPORATED (US) 1996-07-24 EP disclosed
WO-1995009879-A1 CONTINUOUS PROCESS FOR THE MANUFACTURE OF LACTIDE AND LACTIDE POLYMERS CARGILL, INCORPORATED (US) 1995-04-13 WO disclosed
US-5366734-A Implantable or injectable composition with polylactide or copolymer with glycolic acid with polypeptides for sustained release ZENECA LIMITED (GB) 1994-11-22 US disclosed
US-5004602-A Containing Polypeptides IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1991-04-02 US disclosed
US-4767628-A POLYLACTONE AND ACID STABLE POLYPEPTIDE IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1988-08-30 US 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 (2 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-20230094928-A1 Synthesis method of lactide by confinement effect catalysis of crystalline porous polymer material LCT, LDHB, LDHA CA1 34/4885CA9 17/4885SMN1; SMN2 3358/4885
US-11987567-B2 Synthesis method of lactide by confinement effect catalysis of crystalline porous polymer material LCT, LDHB, LDHA CA1 34/4885CA9 17/4885SMN1; SMN2 3358/4885

“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.