SCHEMBL7273282

SCHEMBL7273282

CC(O)C(O)CCCn1c(=O)c2c(ncn2C)n(C)c1=O

nearest known ligand 0.76

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ADORA2B P29275 7/20 0.62
▸ TNF P01375 4/20 0.62
▸ USP2 O75604 1/20 0.62
▸ LMNA P02545 1/20 0.62
▸ CYP1A2 P05177 1/20 0.62
▸ TSHR P16473 1/20 0.62
▸ NFKB1 P19838 1/20 0.62
▸ ACHE P22303 1/20 0.62
▸ PDE4A P27815 1/20 0.62
▸ PMP22 Q01453 1/20 0.62
▸ PDE4B Q07343 1/20 0.62
▸ PDE4C Q08493 1/20 0.62
▸ PDE4D Q08499 1/20 0.62
▸ SMN1; SMN2 Q16637 1/20 0.62
▸ RXFP1 Q9HBX9 1/20 0.62
▸ CHIT1 Q13231 1/20 0.57
▸ CHIA Q9BZP6 1/20 0.57
▸ AKR1B1 P15121 1/20 0.55
▸ GLA P06280 1/20 0.54
▸ BLM P54132 1/20 0.54

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
SCHEMBL6780041 0.90 ADORA2B (0.65) ADORA2BTNFUSP2LMNACYP1A2
Lisofylline SCHEMBL39131 0.86 ADORA2B (0.67) ADORA2BTNFUSP2LMNACYP1A2
Lisofylline SCHEMBL680306 0.86 ADORA2B (0.67) ADORA2BTNFUSP2LMNACYP1A2
Lisofylline, (S)- SCHEMBL1495100 0.86 ADORA2B (0.67) ADORA2BTNFUSP2LMNACYP1A2
SCHEMBL6785799 0.86 ADORA2B (0.64) ADORA2BTNFUSP2LMNACYP1A2
SCHEMBL8061728 0.85 ADORA2B (0.63) ADORA2BTNFUSP2LMNACYP1A2
SCHEMBL8686678 0.85 ADORA2B (0.66) ADORA2BTNFUSP2LMNACYP1A2
SCHEMBL6780377 0.85 ADORA2B (0.62) ADORA2BTNFUSP2LMNACYP1A2
SCHEMBL6780935 0.85 ADORA2B (0.66) ADORA2BTNFUSP2LMNACYP1A2
Lisofylline SCHEMBL10517408 0.85 ADORA2B (0.66) ADORA2BTNFUSP2LMNACYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0484785-B1 Use of xanthines for the preparation of a medicament effective for inhibiting the replication of human retroviruses HOECHST ROUSSEL PHARMA (US) 1996-05-22 — — EP claimed
US-9493463-B2 Substituted xanthine derivatives CONCERT PHARMACEUTICALS, INC. (US) 2016-11-15 — — US disclosed
US-9493463-B2 Substituted xanthine derivatives CONCERT PHARMACEUTICALS, INC. (US) 2016-11-15 — — US disclosed
US-20150322068-A1 SUBSTITUTED XANTHINE DERIVATIVES SUN PHARMACEUTICAL INDUSTRIES, INC. 2015-11-12 — — US disclosed
US-20150322068-A1 SUBSTITUTED XANTHINE DERIVATIVES SUN PHARMACEUTICAL INDUSTRIES, INC. 2015-11-12 — — US disclosed
US-9035050-B2 Substituted xanthine derivatives CONCERT PHARMACEUTICALS, INC. (US) 2015-05-19 — — US disclosed
US-9035050-B2 Substituted xanthine derivatives CONCERT PHARMACEUTICALS, INC. (US) 2015-05-19 — — US disclosed
US-20140296263-A1 SUBSTITUTED XANTHINE DERIVATIVES CONCERT PHARMACEUTICALS, INC. (US) 2014-10-02 — — US disclosed
US-20140296263-A1 SUBSTITUTED XANTHINE DERIVATIVES CONCERT PHARMACEUTICALS, INC. (US) 2014-10-02 — — US disclosed
US-20140121226-A1 SUBSTITUTED XANTHINE DERIVATIVES CONCERT PHARMACEUTICALS, INC. (US) 2014-05-01 — — US disclosed
EP-0573617-A4 — — 1994-02-09 — — EP disclosed
EP-0573617-A1 MODULATION OF CELLULAR RESPONSE TO EXTERNAL STIMULI Fred Hutchinson Cancer Research Center (US) 1993-12-15 — — EP disclosed
WO-1992021344-A2 MODULATION OF CELLULAR RESPONSE TO EXTERNAL STIMULI FRED HUTCHINSON CANCER RESEARCH CENTER (US) 1992-12-10 — — WO disclosed
EP-0493682-A2 Use of xanthines for the preparation of a medicament effective for inhibiting the effects of allograft reaction in humans HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) 1992-07-08 — — EP disclosed
EP-0490181-A1 Use of xanthines for preparation of a medicament having immunosuppressing activity HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) 1992-06-17 — — EP disclosed
EP-0484785-A2 Use of xanthines for the preparation of a medicament effective for inhibiting the replication of human retroviruses HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) 1992-05-13 — — EP disclosed
US-4713455-A FOR OBSTRUCTIVE DISORDERS OF THE RESPIRATORY TRACT HOECHST AKTIENGESELLSCHAFT (DE) 1987-12-15 — — US disclosed
US-4616020-A TREATING OBSTRUCTIVE RESPIRATORY DISEASES HOECHST AKTIENGESELLSCHAFT (DE) 1986-10-07 — — US disclosed
EP-0075850-B1 PHARMACEUTICAL PREPARATIONS CONTAINING VICINAL DIHYDROXYALKYL XANTHINES, PROCESS FOR THE PREPARATION OF THE XANTHINES AND THE APPROPRIATE INTERMEDIATES THEREFOR HOECHST AKTIENGESELLSCHAFT (DE) 1985-12-18 — — EP disclosed
EP-0075850-A2 Pharmaceutical preparations containing vicinal dihydroxyalkyl xanthines, process for the preparation of the xanthines and the appropriate intermediates therefor HOECHST AKTIENGESELLSCHAFT (DE) 1983-04-06 — — 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 (3 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-20150322068-A1 SUBSTITUTED XANTHINE DERIVATIVES XDH, HPRT1, CXCR3 ADORA2B 60/4885TNF 583/4885USP2 4016/4885
US-20140121226-A1 SUBSTITUTED XANTHINE DERIVATIVES XDH, CXCR4, CXCR3 ADORA2B 24/4885TNF 1024/4885USP2 3890/4885
US-20140296263-A1 SUBSTITUTED XANTHINE DERIVATIVES XDH, CXCR3, CXCR4 ADORA2B 179/4885TNF 2183/4885USP2 4406/4885

“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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