SCHEMBL982326

SCHEMBL982326

COC(=O)C(O)CCn1cnc2c(N)ncnc21

nearest known ligand 0.58

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.58
ADORA2A P29274 7/20 0.56
ADORA1 P30542 4/20 0.56
ADORA2B P29275 1/20 0.56
ADCY5 O95622 5/20 0.55
NSD3 Q9BZ95 1/20 0.55
LMNA P02545 1/20 0.52
SMN1; SMN2 Q16637 1/20 0.52
PI4KA P42356 1/20 0.51
PI4K2B Q8TCG2 1/20 0.51
PI4K2A Q9BTU6 1/20 0.51
PI4KB Q9UBF8 1/20 0.51
AHCY P23526 2/20 0.51
FGFR1 P11362 1/20 0.51
SLC22A6 Q4U2R8 1/20 0.51

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
SCHEMBL2241928 1.00 ALDH1A1 (0.58) ALDH1A1ADORA2AADORA1ADORA2BADCY5
SCHEMBL14416686 0.89 ALDH1A1 (0.60) ALDH1A1ADORA2AADORA1ADORA2BADCY5
SCHEMBL12948655 0.88 ADORA2A (0.56) ALDH1A1ADORA2AADORA1ADORA2BADCY5
SCHEMBL12922452 0.86 ALDH1A1 (0.62) ALDH1A1ADORA2AADORA1ADORA2BADCY5
SCHEMBL11986908 0.86 ALDH1A1 (0.62) ALDH1A1ADORA2AADORA1ADORA2BADCY5
SCHEMBL982442 0.85 ALDH1A1 (0.76) ALDH1A1ADORA2AADORA1ADORA2BADCY5
SCHEMBL985545 0.80 ADCY5 (0.63) ALDH1A1ADORA2AADORA1ADORA2BADCY5
SCHEMBL8846447 0.80 ALDH1A1 (0.60) ALDH1A1ADORA2AADORA1ADORA2BADCY5
SCHEMBL11986907 0.79 ADORA2A (0.59) ALDH1A1ADORA2AADORA1ADORA2BADCY5
SCHEMBL12922453 0.78 ADORA2A (0.67) ALDH1A1ADORA2AADORA1ADORA2BPI4KA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4735431-A2 MK2 INHIBITORS AND METHODS OF MAKING AND USING THE SAME GILEAD SCIENCES, INC. (US) 2026-05-06 EP claimed
EP-4674484-A2 THIENOPYRROLE COMPOUNDS Gilead Sciences, Inc. (US) 2026-01-07 EP claimed
EP-4291562-B1 THIENOPYRROLE COMPOUNDS GILEAD SCIENCES INC (US) 2025-09-10 EP claimed
US-20250049780-A1 THIENOPYRROLE COMPOUNDS GILEAD SCIENCES, INC. 2025-02-13 US claimed
US-20250051309-A1 MK2 INHIBITORS AND METHODS OF MAKING AND USING THE SAME GILEAD SCIENCES, INC. 2025-02-13 US claimed
WO-2025006568-A2 MK2 INHIBITORS AND METHODS OF MAKING AND USING THE SAME GILEAD SCIENCES, INC. (US) 2025-01-02 WO claimed
US-12070455-B2 Thienopyrrole compounds GILEAD SCIENCES, INC. (US) 2024-08-27 US claimed
EP-4398989-A1 THIENOPYRROLE COMPOUNDS GILEAD SCIENCES, INC. (US) 2024-07-17 EP claimed
CN-117957234-A Thienopyrrole compounds 吉利德科学公司 2024-04-30 CN claimed
US-20240059673-A1 SUBSTITUTED INDOLE COMPOUNDS GILEAD SCIENCES, INC. 2024-02-22 US claimed
WO-2022140326-A1 SUBSTITUTED INDOLE COMPOUNDS GILEAD SCIENCES, INC. (US) 2022-06-30 WO claimed
WO-2022140325-A1 6-SUBSTITUTED INDOLE COMPOUNDS GILEAD SCIENCES, INC. (US) 2022-06-30 WO claimed
EP-1613628-B1 REVERSIBLE INHIBITORS OF S-ADENOSYL-L-HOMOCYSTEINE HYDROLASE AND USES THEREOF GEN ATOMICS (US) 2013-11-20 EP claimed
US-8247549-B2 Method for preparing 4-(6-amino-purin-9-YL)-2(S)-hydroxy-butyric acid methyl ester SHANGHAI INSTITUTE OF MATERIA MEDICA, CHINESE ACADEMY OF SCIENCES (CN) 2012-08-21 US claimed
US-8168643-B2 Multiple sclerosis; hemorrhagic virus infection, autoimmune diseases, autograft rejection, neoplasm, hyperhomocysteineuria, cardiovascular disease, stroke, Alzheimer's disease, or diabetes; can be used in combination with an anti-hemorrhagic viral infection agent, immunosuppressant GENERAL ATOMICS (US) 2012-05-01 US claimed
US-20110201810-A1 Method for Preparing 4-[9-(6-Aminopurine)]-2-(S)-Hydroxyl-Butyric Acid Methyl Ester Shanghai Institute of Materia Medica, Chinese Acad emy of Sciences (CN) 2011-08-18 US claimed
US-7868011-B2 Use of reversible inhibitors of S-adenosyl-L-homocysteine hydrolase for treating lupus GENERAL ATOMICS (US) 2011-01-11 US claimed
EP-2230239-A1 A METHOD FOR PREPARING 4-Ý9-(6-AMINOPURINE)¨-2-(S)-HYDROXYL-BUTYRIC ACID METHYL ESTER SHANGHAI INSTITUTE OF MATERIA MEDICA, CHINESE ACADEMY OF SCIENCES (CN) 2010-09-22 EP claimed
US-7517887-B2 Reversible inhibitors of S-adenosyl-L-homocysteine hydrolase and uses thereof GENERAL ATOMICS (US) 2009-04-14 US claimed
US-20070129386-A1 Reversible inhibitors of S-adenosyl-L-homocysteine hydrolase and uses thereof NINGBO ZIYUAN PHARMACEUTICALS, INC. (CN) 2007-06-07 US claimed

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-20250049780-A1 THIENOPYRROLE COMPOUNDS SSB, TPMT, LCP2 ALDH1A1 2343/4885ADORA2A 290/4885ADORA1 1383/4885
US-20250051309-A1 MK2 INHIBITORS AND METHODS OF MAKING AND USING THE SAME DUSP2, MKNK2, DUSP22 ALDH1A1 4336/4885ADORA2A 2449/4885ADORA1 4465/4885
US-20240059673-A1 SUBSTITUTED INDOLE COMPOUNDS SSB, IDO1, IDO2 ALDH1A1 2448/4885ADORA2A 180/4885ADORA1 936/4885
US-12070455-B2 Thienopyrrole compounds SSB, TPMT, LCP2 ALDH1A1 2343/4885ADORA2A 290/4885ADORA1 1383/4885
US-20110201810-A1 Method for Preparing 4-[9-(6-Aminopurine)]-2-(S)-Hydroxyl-Butyric Acid Methyl Ester TPMT, ATIC, UMPS ALDH1A1 49/4885ADORA2A 208/4885ADORA1 300/4885
US-20070129386-A1 Reversible inhibitors of S-adenosyl-L-homocysteine hydrolase and uses thereof AHCY, AHCYL1, BHMT ALDH1A1 397/4885ADORA2A 72/4885ADORA1 77/4885

“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.