Guanidine

Guanidine

SCHEMBL8772768

Cc1ccc(S(=O)(=O)CC(=O)O)cc1.N=C(N)N

nearest known ligand 0.69

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2

The experimentally established mechanism targets of Guanidine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 6/20 0.69
RECQL P46063 1/20 0.57
MMP2 P08253 1/20 0.54
MMP7 P09237 1/20 0.54
MMP14 P50281 1/20 0.54
HSD11B1 P28845 1/20 0.53
MAPT P10636 2/20 0.53
LMNA P02545 2/20 0.53
CA12 O43570 2/20 0.50
CA1 P00915 2/20 0.50
CA2 P00918 2/20 0.50
CA9 Q16790 2/20 0.50
KMT2A Q03164 1/20 0.50
HSD17B10 Q99714 1/20 0.49
FFAR1 O14842 1/20 0.48
CYP3A4 P08684 1/20 0.47
CYP2C9 P11712 1/20 0.47
CYP2C19 P33261 1/20 0.47
PKM P14618 2/20 0.47

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
SCHEMBL924405 0.91 ALDH1A1 (0.69) ALDH1A1RECQLMMP2MMP7MMP14
SCHEMBL10338421 0.89 ALDH1A1 (0.67) ALDH1A1RECQLMMP2MMP7MMP14
SCHEMBL10338418 0.89 ALDH1A1 (0.67) ALDH1A1RECQLMMP2MMP7MMP14
Acetic Acid SCHEMBL8984837 0.87 ALDH1A1 (0.65) ALDH1A1RECQLMMP2MMP7MMP14
Guanidine SCHEMBL2286558 0.86 MMP2 (0.54) ALDH1A1MMP2MMP7MMP14HSD11B1
SCHEMBL6651299 0.86 ALDH1A1 (0.62) ALDH1A1RECQLMMP2MMP7MMP14
Guanidine SCHEMBL2279843 0.84 MMP2 (0.65) MMP2MMP7MMP14HSD11B1CA12
Guanidine SCHEMBL2289728 0.83 NPC1 (0.69) ALDH1A1MMP2MMP7MMP14HSD11B1
SCHEMBL608774 0.82 ALDH1A1 (1.00) ALDH1A1RECQLHSD11B1MAPTLMNA
Guanidine SCHEMBL8415495 0.79 HSD11B1 (0.58) ALDH1A1MMP2MMP7MMP14HSD11B1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122085595-A Colored photosensitive resin composition and application thereof 2026-05-26 CN disclosed
CN-122085594-A Positive coloring photosensitive composition and application thereof 2026-05-26 CN disclosed
CN-116262827-A Polyimide precursor resin, photosensitive resin composition and application thereof 北京鼎材科技有限公司 2023-06-16 CN disclosed
CN-115128898-A Photosensitive resin composition and application thereof 北京鼎材科技有限公司 2022-09-30 CN disclosed
CN-114967324-A Diamine compound, resin prepared from same, photosensitive resin composition and application 北京鼎材科技有限公司 2022-08-30 CN disclosed
CN-114967325-A Diamine compound, resin prepared from same, photosensitive resin composition and application 北京鼎材科技有限公司 2022-08-30 CN disclosed
EP-0659581-B1 Stabilized thermal-dye-bleach constructions MINNESOTA MINING & MFG (US) 1997-10-15 EP disclosed
EP-0659581-A2 Stabilized thermal-dye-bleach constructions MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1995-06-28 EP disclosed
US-5395747-A Polylactones as stabilizers in antihalation systems where an anion is thermally generated to decolor dyes formed by scattered light MINNESOTA MINING & MANUFACTURING COMPANY (US) 1995-03-07 US disclosed