The more active members of a proposed class of auxin transport inhibitors have been shown to have the ability to inhibit the active movement of auxin at concentrations where they have Uttle effect on auxin action and no significant auxin activity. They have also been shown to give rise to characteristic biphasic dose-response curves on cress root growth. Based on these physiological similarities and other common physiological properties, it is concluded that they may achieve their effects by a common mode of action which differs from that of other known auxin transport inhibitors. It is suggested that the name "phytotropins" be given to the class of auxin transport inhibitors now defined by a similar mode of action and common chemical properties.It has been shown that a group of chemicals which were known to affect the geotropic response can be defined by a common set of chemical requirements (16) and that these requirements are at least similar to those which can give rise to inhibition of auxin transport ( 18). The group can be divided into eight chemical types, and these are shown in Figure 1. Rules which define the chemical requirements so far known have been formulated (18). In summary, a 2-carboxyphenyl group separated by a conjugated system of atoms from a second aromatic ring may be necessary for a molecule to have high activity.At least one member of each type has been established to be an auxin transport inhibitor, as well as having the additional physiological properties of being able to abolish the root and stem geotropic responses, the phototropic response, and the apical dominance effect. From the close chemical similarity between compounds within each type, it can be inferred that members within each type may act by a similar mode of action. The broader structure-activity correlation, however, implies a relationship between the types (18). It also implies that the mode of action of the group as a whole may be different from other auxin transport inhibitors which do not conform to the chemical parameters. An investigation of this relationship, therefore, would seem warranted, especially since some compounds from within the group, e.g.NPA' III-1; CPD IV-I, and DPX 1840 VIII-I (Fig. 2), have found 'Abbreviations: CFM, methyl-2-chloro-9-hydroxyfluorene-9-carboxylate; CPD, l-(2'-carboxyphenyl)-3-phenylpropane-1,3-dione; CPP, 5-(2'-carboxyphenyl)-3-phenylpyrazole; DPX 1840, 3,3a-dihydro-2-(p-methoxyphenyl)-8H -pyrazolo(5 -1a)isoindol-8-one; NPA, N-(naphth-1-yl)-phthalamic acid; PBA, 2-(1-pyrenoyl)benzoic acid; PCIB, p-chlorophenoxyisobutyric acid; TCBA, 2,3,6-trichlorobenzoic acid; TIBA, 2,3,5-triiodobenzoic acid. use in plant physiological research, together with other auxin transport inhibitors which do not belong to the group, e.g. TIBA IX and the morphactins X (Fig. 2).To enable a class of compounds having similar physiological and chemical properties to be defined, chemicals of known high auxin transport inhibiting activity from within types II through VII were comparatively assessed for re...