SCHEMBL3201117

SCHEMBL3201117

CN1CCN(c2ccc(Nc3nccc(Nc4cccc(CC#N)c4)n3)cc2C(F)(F)F)CC1.CS(=O)(=O)O

nearest known ligand 0.57

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
CCNA2 P20248 8/20 0.55
CDK2 P24941 8/20 0.55
CCNA1 P78396 8/20 0.55
CDK4 P11802 4/20 0.55
CCND3 P30281 4/20 0.55
GSK3B P49841 4/20 0.55
PIM1 P11309 3/20 0.55
JAK2 O60674 3/20 0.54
JAK3 P52333 2/20 0.53
MTOR P42345 2/20 0.52
TNIK Q9UKE5 1/20 0.51
BRD4 O60885 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
Sulfuric Acid SCHEMBL3208098 0.98 CCNA2 (0.55) CCNA2CDK2CCNA1CDK4CCND3
SCHEMBL3208957 0.95 CCNA2 (0.60) CCNA2CDK2CCNA1CDK4CCND3
SCHEMBL3210167 0.95 CCNA2 (0.55) CCNA2CDK2CCNA1CDK4CCND3
Hydrochloric Acid SCHEMBL3205555 0.95 CCNA2 (0.59) CCNA2CDK2CCNA1CDK4CCND3
SCHEMBL3210186 0.90 PAK1 (0.61) JAK2JAK3TNIKBRD4
Sulfuric Acid SCHEMBL3209435 0.88 PAK1 (0.61) JAK2JAK3TNIKBRD4
SCHEMBL3207950 0.85 PAK1 (0.57) JAK2JAK3TNIKBRD4
SCHEMBL3203546 0.85 PAK1 (0.66) JAK2JAK3TNIK
Hydrochloric Acid SCHEMBL3209167 0.84 PAK1 (0.65) JAK2JAK3TNIK
SCHEMBL13485402 0.84 JAK2 (0.73) JAK2JAK3TNIK

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100029675-A1 Pyrimidine-2, 4-diamine JAK2 Kinase inhibiting anti-inflammation use TOLERO PHARMACEUTICALS, INC. 2010-02-04 US disclosed
WO-2010011349-A2 PYRIMIDINE-2,4-DIAMINE JAK2 KINASE INHIBITING ANTI-INFLAMMATION USE SUPERGEN, INC. (US) 2010-01-28 WO disclosed
EP-2121634-A1 PYRIMIDINE-2,4-DIAMINE DERIVATIVES AND THEIR USE AS JAK2 KINASE INHIBITORS SuperGen, Inc. (US) 2009-11-25 EP disclosed
US-20080214558-A1 PYRIMIDINE-2,4-DIAMINE DERIVATIVES AND THEIR USE AS JAK2 KINASE INHIBITORS SUPERGEN, INC. (US) 2008-09-04 US disclosed
WO-2008106635-A1 PYRIMIDINE-2,4-DIAMINE DERIVATIVES AND THEIR USE AS JAK2 KINASE INHIBITORS SUPERGEN, INC. (US) 2008-09-04 WO 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-20100029675-A1 Pyrimidine-2, 4-diamine JAK2 Kinase inhibiting anti-inflammation use JAK2, JAK1, IRAK4 CCNA2 876/4885CDK2 16/4885CCNA1 1698/4885
US-20080214558-A1 PYRIMIDINE-2,4-DIAMINE DERIVATIVES AND THEIR USE AS JAK2 KINASE INHIBITORS JAK2, JAK1, JAK3 CCNA2 483/4885CDK2 6/4885CCNA1 866/4885

“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.